African Journal of
Pharmacy and Pharmacology

  • Abbreviation: Afr. J. Pharm. Pharmacol.
  • Language: English
  • ISSN: 1996-0816
  • DOI: 10.5897/AJPP
  • Start Year: 2007
  • Published Articles: 2288

Full Length Research Paper

A review for selecting medicinal plants commonly used for malaria in Uganda

Clement O. Ajayi
  • Clement O. Ajayi
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Anthony A. Elujoba
  • Anthony A. Elujoba
  • Department of Pharmacognosy, Faculty of Pharmacy, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.
  • Google Scholar
Félicien M. Kasali
  • Félicien M. Kasali
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Mercy G. Tenywa
  • Mercy G. Tenywa
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Hedmon Okella
  • Hedmon Okella
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Anke Weisheit
  • Anke Weisheit
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Casim U. Tolo
  • Casim U. Tolo
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar
Patrick E. Ogwang
  • Patrick E. Ogwang
  • Pharm-Biotechnology and Traditional Medicine Center, Mbarara University of Science and Technology, P. O. Box 1410, Mbarara, Uganda.
  • Google Scholar


  •  Received: 25 July 2020
  •  Accepted: 15 September 2020
  •  Published: 31 October 2020

 ABSTRACT

The menace of current cases of parasite resistance to antimalarial drugs, non- availability and accessibility, and the high costs of pharmaceutical products contribute to the high rate of medicinal plants consumption in the treatment of malaria in Uganda. Different ethnobotanical surveys on medicinal plants with antimalarial properties have been conducted across different geographical regions in Uganda in order to identify and select the most commonly used antimalarial plants as candidates in the proposed national herbal pharmacopoeia. The available literature on the medicinal plants used against malaria in the western, central, eastern and northern geographical regions in Uganda was selected from reputable journals using various citation databases as guides. The commonly used antimalarial plants in the regions were searched using relevant journals on previously established ethno-botanical survey. They were then ranked in order of percentage frequency of appearance in the literature from surveys across the country. Fifteen medicinal plants were selected in this way from several antimalarial plants cited. Vernonia amygdalina and Azadirachta indica appeared most (100%), followed by Carica papaya, Mangifera indica and Hoslundia opposita with 80% appearance each across the 4 regions.The medicinal plants from this review were therefore ranked as the most used for treatment of malaria in Uganda and therefore, could be recommended for herbal pharmacopoeial standards development.

Key words: Antimalarial, medicinal plants, antiplasmodial, herbal pharmacopoeial standards.


 INTRODUCTION

Malaria remains one of the major health challenges in developing countries despite the efforts of different organizations including the World Health Organization (WHO), West African Health Organization (WAHO), Centers for Disease Control  and  Prevention  (CDC),  the African Union's Scientific, Technical and Research Commission (AU/STRC) among others to control and eradicate it (WHO, 2018).

It was reported that 219 million cases of malaria occurred  worldwide  in  2017  and  92%  of  these  cases were from African region with 435,000 mortalities. This malaria endemic region was followed by the South-East Asia Region with 5% and the Eastern Mediterranean Region with 2% (WHO, 2017, 2018). The Uganda Malaria Reduction Strategic Plan (UMRSP) reported malaria cases of 1 out of 3 out-patient visits to health facilities and 50% of the in-patient pediatric mortalities are associated with malaria disease yearly (MoH, 2016). The setback to malaria fight has been attributed to non-availability of effective vaccine, resistance to pyrethroid-treated mosquito nets, high costs of antimalarial drugs and the recent widespread chloroquine-resistant Plasmodium falciparum (WHO, 2018).

In malaria chemotherapy, medicinal plants have always played a leading role in drug discovery and such drugs are used in natural form or synthesized or act as structural models for semi-synthetic antimalarial drugs. Quinine was first time isolated from Cinchona bark against malaria in the early 18th century and became a skeleton from which chloroquine (resochin), mefloquine and other similar antimalarial drugs were later synthesized (Achan et al., 2011).

The most successful battle against the sudden appearance of chloroquine-resistant P. falciparum led to the isolation of artemisinin from the Chinese Artemisia annua. Its synthetic chemical derivatives (e.g. artemether, dihydoartemisinin and artesunate) are now combined with existing antimalarial drugs to artemisinin-based combination therapy (ACT) such as artemartemether-lumefantrine, artesunate-amodiaquine, etc. which are referred to as ACT (Chen, 2014). Currently, ACTs remain the recommended choice of drugs for malaria despite recent reports on the P. falciparum resistance in Greater Mekong subregion (GMS) including Cambodia, Lao People’s Democratic Republic, Vietnam, Thailand and Myanmar (WHO, 2018), etc.

Historically (from Cinchona to Artemisia), the plant kingdom remains the source for antimalarial drug discovery. Similar history has shown many current therapeutic drugs (e.g. digoxin, reserpine, morphine, etc.), at conventional health care levels for the management of other diseases from medicinal plants. According to the World Health Organization, 60% of the world’s population depends on traditional medicine and 80% of the people in developing countries depend entirely on traditional medicine practices due to their accessibility, folklore and affordability for their primary health care needs (Chikezie and Ojiako, 2015).

The high acceptability of medicinal plants therefore requires the needs for their national standards which guarantee the consistence, definite identification, reproducible safety, efficacy and qualities as a valuable scientific reference for drug authorities, manufacturers, general public and researchers (WHO, 2011). These plants are normally selected based on their frequent used across   the   country.   This   review   exercise   aimed  at compiling the most used medicinal plants for malaria in Uganda with a view to developing their national standards which will subsequently be used to develop their herbal monographs.


 METHODOLOGY

Literature data collection for the selection of antimalarial medicinal plants

The plants were searched through different search engines including Google Scholar, Institute for Scientific Information, PubMed, Scopus, Hinari, Scientific Information Database, etc., using antimalarial plants, antiplasmodial, malaria endemic, ethnopharmacology and Uganda regions as the keywords.

In this progression, different ethno-botanical survey articles on antimalarial plants in a particular region were first compiled and then ranked based on their frequency of occurrence in literature within the same region. Thereafter, their physical occurrences in the literature from other geographical regions of Uganda were considered. The antimalarial plants, found occurring in at least 2 out of the 4 regions (Central, Eastern, Northern and Western Uganda) and those mentioned in PROMETRA records (Association for the Promotion of Traditional Medicine), Uganda, East Africa, were selected. The following formula was applied to the plant collected prior to their ranking:

Formula: (x/N)×100

Where, x is the total number of appearances ascribed to each antimalarial plant across the regions, while N (5) is the total number of regions together with PROMETRA antimalarial plants.

A comprehensive literature search was thereafter carried out to review the extent of previous studies on each of the selected plants.


 RESULTS AND DISCUSSION

Fifteen medicinal plants belonging to 12 families were found to be commonly used for the control of malaria in Uganda among which 4 species (Bidens pilosa L., Tithonia diversifolia (Hemsl.) A. Gray, Vernonia amygdalina and V. lasiopus O. Hoffm) belonged to the family Asteraceae. V. amygdalina Del. leaf and Azadirachta indica A. Juss. (Meliaceae), being the most used across Uganda with 100% appearance, were followed by Carica papaya L. (Caricaceae), Hoslundia opposita Vahl (Lamiaceae) and Mangifera indica L. (Anacardiaceae) with 80%. B. pilosa L., Cymbopogon citratus (DC.) Stapf. (Poaceae), Justicia betonica L. (Acanthaceae), Markhamia lutea (Benth.) K. Schum. (Bignoniaceae), Moringa oleifera Lam. (Moringaceae), T. diversifolia (Hemsl.) A. Gray, V. lasiopus O. Hoffm showed 60% appearances while Aristolochia elegans Mast. (Aristolochiaceae), Cajanus cajan (L.) Huth (Fabaceae) and Toddalia asiatica (L.) Lam. (Rutaceae) gave 20% appearance representing the least commonly used antimalarial plants across Uganda.

Adia et al. (2014) studied  some medicinal  plants  used for the treatment of malaria by PROMETRA in Central Uganda; about 75% of the traditional medical practitioners (TMPs) of Uganda were interviewed from Mpigi and 25% from Butambala District. Eighty-six medicinal plants from 39 families were reportedly used in the treatment of malaria ailment by the TMPs out of which 32% belonged to Asteraceae, followed by Lamiaceae (24%), Euphorbiaceae (12%) and Poaceae 10%. Out of these, V. amygdalina was the most recorded plant. These plants, used by TMPs, were either used individually (in mono-component remedies) or in combination (in multi-component preparations). The leaf and root are the morphological parts most frequently used and prescribed by the TMPs (Adia et al., 2014).

Tugume et al. (2016) conducted an ethnobotanical survey on medicinal plants used for various ailments in Baganda, Banyarwanda, Basoga, Bagisu, Bakiga, Banyankole, Bagwere and Batoro tribes from Naluvule, Bukuku, Buwoola and Kalagala villages which were mostly Bantu ethnic groups from Central Uganda. The study reported 190 species (from 61 families) in which 20 species were listed for antimalarial herbal remedy and out of which the following 6 species were commonly used in other regions: A. elegans, H. opposita, J. betonica, M. lutea, V. amygdalina and V. lasiopus. In the Central Uganda region, V. amygdalina was highly classified as the most important species in the treatment of malaria. The remedies for malaria treatment were either prepared as decoctions (Table 1) or infusions, each containing single plants or in combination with other plants (Tugume et al., 2016).

The work of Ssegawa and Kasenene (2007) on the medicinal plants of Sango bay area covered: Kaiso, Malabigambo, Namalala, Tero West, Tero East and Kigona forest blocks. One hundred and eighty-six medicinal plants were reported from which 21 plant species were recorded for malaria treatment in this area while in southern part of Uganda, a total of 39 were said to be commonly used for malaria. Among these medicinal plants, A. elegans, A. indica, M. lutea, M. oleifera, V. amygdalina and V. lasiopus were the only species used in the other regions for malaria. Tabuti (2008) studied the medicinal plants used for malaria in selected villages from Budiope County in Eastern Uganda which comprised Busambira and Buseete villages of Kinambogo Parish in the Kamuli district of Eastern Uganda. In his work, 27 medicinal plant species, mainly young leaves, parts of shrubs or trees (singly or in combination), belonging to 16 families, were reportedly used for antimalarial remedies in that County, either as decoctions or infusions (Table 1). The parts are collected and used fresh at no specific time of the day or season. Out of the 27 species reported by Tabuti (2008), 5 species (A. indica, C. cajan, M. indica, M. oleifera and V. amygdalina) were commonly used in other regions of Uganda.

Philip et al. (2017) also studied ethnobotanical survey on medicinal plants used for malaria in Butebo County in the eastern region of Uganda which comprised five sub-Counties: Kakoro, Kabwangasi, Petete, Butebo and Kibale in Pallisa District. In his study, 50 respondents were interviewed, comprising 10 from each sub-County from which 33 plant species belonging to 23 families were reported. Among the 33 medicinal plant species reported, 6 plants were commonly used in other regions which included: A. indica, B. pilosa, C. papaya, C. citratus and M. indica.

In the survey conducted by Anywar et al. (2016), 90 respondents interviewed in three different villages were mainly farmers some of whom are traditional medical practitioners. Twenty medicinal plants from 15 families were reportedly being used for preventing and treating malaria in Cegere sub-County of Uganda and these are mainly herbs. Twelve of the plants are used for the management of malaria, eight for prevention while two are for both prevention and treatment. These plants predominantly belong to Asteraceae and Fabaceae families, and are mostly used as decoctions or infusions (Table 1). The leaves of A. indica, H. opposita, C. papaya, T. diversifolia and M. oleifera (also root) were similarly found useful in antimalarial therapy in other parts of Uganda. The study of Opio et al. (2017) on survey of antimalarial plants in Abukamola, Angeta, Oculoko and Omarari areas of Alebtong District reported 43 antimalarial plants out of which only 3 plants are used in other regions for malaria treatment while other antimalarial plants listed in Alebtong DISTRICT are either used for other ailments or do not appear in other regions.

Kamatenesi et al. (2011) reported 71 medicinal plants used for different ailments in Ngai and Otwal Sub Counties of Oyam District, including four (Acacia hockii De Wild, C. cajan, Ocimum basilicum L., and V. amygdalina) of the listed plant species used for malaria and only two plants (C. cajan and V. amygdalina) appeared in other regions. Hamill et al. (2000) recorded medicinal plants used for general ailments in three districts of south-western Uganda: Rukungiri, Kisoro and Kabale districts of Baganda kingdom. In the first part of the report, 48 plant species were reported from which 6 species were commonly used for malaria in other regions. In the second part among Baganda people of south-western Uganda, all the  medicinal plants studied were summed up to 168 with additional 8 species commonly used for malaria (Hamill et al., 2003).

Katuura et al. (2007)studied medicinal plants used for malaria in Mbarara municipality and Rwampara County from where 20 medicinal plants were reported, out of which 19 species were identified with their leaves or roots being used as decoctions or infusions (Table 1), either individually or in combination. Four of the plant species namely, M. indica, T. assiatica, V. amygdalina and V. lasiopus, commonly  used  for  malaria  treatment  in  this region were also commonly used in other regions of the country.

The results of interview on about 28 traditional birth attendants (TBAs) by Stangeland et al. (2011)in the Nyakayoko sub-County of Mbarara District on medicinal plants commonly-used for malaria, have revealed 56 plant species from 23 families. The leaf part was found to be most widely used but the plants in this sub-County were either used individually or in combination (Table 1). All the medicinal plants used for antimalarial remedies were reported to be commonly used in other regions except, B. pilosa, M. indica and M. oleifera which did not appear in the report of Stangeland (2011).

Asiimwe et al. (2014) reported the use of medicinal plants by the local communities in Western Uganda around Ibanda, Isingiro, Kiruhura and Mbarara districts. The study was conducted on herbalists and traditional birth attendants based on the knowledge, skills, and practices in the use medicinal plants. Out of 231 medicinal plants from 73 families reported as remedies for different ailments, 22 plants were commonly used for malaria in the area and only 5 species (C. cajan, H. opposita, J. betonica, V. amygdalina and V. lasiopus) were commonly used in other geographical regions (Table 1). The leaf or other morphological parts were prepared individually or in combination with other plants as decoction or infusion.

Namukobe et al. (2011) reported 131 plant species from 121 genera, used for different ailments in Kibale National Park which include four parishes (Hiima, Kahangi, Kaswa and Sebitoli) in Hakibale sub-County of Kabarole district. Twenty of the listed plant species are used for malaria out of which only 3 (J. betonica, M. indica and V. amygdalina) are commonly used in other regions for malaria while others are either used for ailments other than malaria or not appearing at all for other regions. Meanwhile, antimalarial and other pharmacological activities of some of the selected medicinal plants have been established and reported as shown in Table 1 with some of their active ingredents, being reported. Also, reports on the safety of some of these plants have been reported with some showing degenerative effects such as nephro-/hepato-toxicity, vacuolar degeneration, necrosis, etc. (Adebayo et al., 2009; Elufioye et al., 2009; Passoni et al., 2013). This review exercise is necessary to select the plants that are commonly used as antimalarial across the country in order to develop their national standards by taking into consideration their botany, safety, efficacy and chemistry.


 CONCLUSION

Through the literature search, fifteen medicinal plants were selected as the most commonly used in Uganda for the treatment  of  malaria  out  of  many  medicinal  plants reported in ethnobotanical surveys across the regions and these plants could be standardized for pharmacopoeial inclusion.


 CONFLICT OF INTERESTS

The authors have not declared any conflict of interests.



 REFERENCES

Achan J, Talisuma AO, Erhart A, Yeka A, Tibenderana JK, Baliraine FN, Rosenthal PJ, D'Alessandro U (2011). Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria. Malaria Journal 10(144):1-12.
Crossref

 

Achenbach H, Waibel R, Nkunya MHH, Weenen H (1992). Antimalarial compounds from Hoslundia opposita. Phytochemistry 31(11):3781-3784.
Crossref

 

Adamu M, Nwosu CO, Agbede RIS (2009). Anti-trypanosomal effects of aqueous extract of Ocimum gratissimum (Lamiaceae) leaf in rats infected with Trypanosoma brucei brucei. African Journal of Traditional, Complementary and Alternative Medicines 6(3):262-267.
Crossref

 

Adebayo JO, Balogun EA, Oyeleke SA (2009). Toxicity study of the aqueous extract of Tithonia diversifolia leaves using selected biochemical parameters in rats. Pharmaceutical Research 1:143-147.

 

Adedapo AA, Aremu OJ, Oyagbemi AA (2014). Anti-oxidant, anti-inflammatory and antinociceptive properties of the acetone leaf extract of Vernonia amygdalina in some laboratory animals. Advanced Pharmaceutical Bulletin 4(2):591-598.

 

Adedapo AA, Falayi OO, Oyagbemi AA (2015). Evaluation of the analgesic, anti-inflammatory, anti-oxidant, phytochemical and toxicological properties of the methanolic leaf extract of commercially processed Moringa oleifera in some laboratory animals. Journal of Basic and Clinical Physiology and Pharmacology 
Crossref

 

Adejumo OE, Kolapo AL, Folarin AO (2012). Moringa oleifera Lam. (Moringaceae) grown in Nigeria: in vitro antisickling activity on deoxygenated erythrocyte cells. Journal of Pharmacy and Bioallied Sciences 4(2):118-123.
Crossref

 

Ademola IO, Eloff JN (2011). Anthelminthic activity of acetone extract and fractions of Vernonia amygdalina against Haemonchus contortus eggs and larvae. Tropical Animal Health and Production 43:521-527.
Crossref

 

Adeneye AA, Agbaje EO (2007). Hypoglycemic and hypolipidemic effects of fresh leaf aqueous extract of Cymbopogon citratus Stapf. in rats. The Journal of Ethnopharmacology 112:440-444.
Crossref

 

Adia MM, Anywar G, Byamukama R, Kamatenesi-Mugisha M, Sekagya Y, Kakudidi EK, Kiremire BT (2014). Medicinal plants used in malaria treatment by PROMETRA herbalists in Uganda. The Journal of Ethnopharmacology 155(1):580-588.
Crossref

 

Agboola OO, Stephen O, Olowooyo JO, Ajao AA, Aregbesola O (2016). Chemical composition and antimicrobial activities of essential oil extracted from Tithonia diversifolia (Asteraceae) flower. Journal of Bioresources and Bioproducts 1:169-176.

 

Aguiyi JC, Obi CI, Gang SS, Igweh AC (2000). Hypoglycaemic activity of Ocimum gratissimum in rats. Fitoterapia 71:444-446.
Crossref

 

Ajaiyeoba EO, Abiodun OO, Falade MO, Ogbole NO, Ashidi JS, Happi CT, Akinboye DO (2006). In vitro cytotoxicity studies of 20 plants used in Nigerian antimalarial ethnomedicine. Phytomedicine 13:295-298.
Crossref

 

Ajao AA, Moteetee AN (2017). Tithonia diversifolia (Hemsl) A. Gray. (Asteraceae: Heliantheae), an invasive plant of significant ethnopharmacological importance: A review. South African Journal of Botany 113:396-403.
Crossref

 

Ajila CM, Aalami M, Leelavathi K, Prasada Rao UJS (2010). Mango peel powder: A potential source of antioxidant and dietary fiber in macaroni preparations. Innovative Food Science and Emerging Technologies 11:219-224.
Crossref

 

Akojie FOB, Fung LWM (1992). Antisickling Activity of Hydroxybenzoic Acids in Cajanus cajan. Planta Medica 58:317-320.
Crossref

 

Alawa CBI, Adamu AM, Gefu JO, Ajanusi OJ, Abdu PA, Chiezey NP, Alawa JN, Bowman DD (2003). In vitro screening of two Nigerian medicinal plants (Vernonia amygdalina and Annona senegalensis) for anthelmintic activity. Veterinary Parasitology 113:73-81.
Crossref

 

Al-malki AL, El-Rabey HA (2015). The antidiabetic effect of low doses of Moringa oleifera Lam. seeds on streptozotocin induced diabetes and diabetic nephropathy in male rats. BioMed Research International 
Crossref

 

Alvarez A, Pomar F, Sevilla MA, Montero MJ (1999). Gastric antisecretory and antiulcer activities of an ethanolic extract of Bidens pilosa L. var. radiata Schult. Bip. Journal of Ethnopharmacology 67:333-340.
Crossref

 

Amalraj T, Ignacimuthu S (1998). Evaluation of the hypoglycaemic effect of Cajanus cajan (seeds) in mice. Indian Journal of Experimental Biology 36:1032-1033.

 

Anand S, Rajan M, Venkateshbabu N, Kandaswamy D, Shravya Y, Rajeswari K (2016). Evaluation of the antibacterial efficacy of Azadirachta indica, Commiphora myrrha, Glycyrrhiza glabra against Enterococcus faecalis using real time PCR. Open Dentistry Journal 10(1):160-165.
Crossref

 

Andrade-Neto VF, Brandão MGL, Oliveira FQ, Casali VWD, Njaine B, Zalis MG, Oliveira LA, Krettli AU (2004). Antimalarial activity of Bidens pilosa L. (Asteraceae) ethanol extracts from wild plants collected in various localities or plants cultivated in humus soil. Phytotherapy Research 18:634-639.
Crossref

 

Anthoney ST, Jackie OK, Miyogo E, Lasiti TT (2016). Bioassay screening of the ethanolic extract of Tithonia diversifolia leaves on selected microorganisms. International Journal of Bioassays 5:4794-4798.
Crossref

 

Anwar F, Latif S, Ashraf M, Gilani AH (2007). Moringa oleifera: A food plant with multiple medicinal uses. Phytotherapy Research 21:17-25.
Crossref

 

Anywar G, van't Klooster CIEA, Willcox M, Nalumansi PA, de Jong J, Rwaburindori P, Kiremire BT (2016). Medicinal plants used in the treatment and prevention of malaria in Cegere sub-county, northern Uganda. Ethnobotany Research and Applications 14:505-516.
Crossref

 

Ashafa OAT, Orekoya LO, Yakubu MT (2012). Toxicity profile of ethanolic extract of Azadirachta indica stem bark in male wistar rats. Asian Pacific Journal of Tropical Biomedicine 2(10):811-817.
Crossref

 

Asiimwe S, Namutebi A, Borg-karlsson A, Mugishaa MK, Oryem-Origa H (2014). Documentation and consensus of indigenous knowledge on medicinal plants used by the local communities of western Uganda. Journal of Natural Product and Plant Resources 4(1):34-42.

 

Atangwho IJ, Egbung GE, Ahmad M, Yam MF, Asmawi MZ (2013). Antioxidant versus anti-diabetic properties of leaves from Vernonia amygdalina Del. growing in Malaysia. Food chemistry 141:3428-3434.
Crossref

 

Atawodi SE, Atawodi JC, Idakwo GA, Pfundstein B, Haubner R, Wurtele G, Bartsch H, Owen RW (2010). Evaluation of the polyphenol content and antioxidant properties of methanol extracts of the leaves, stem, and root barks of Moringa oleifera Lam. Journal of Medicinal Food. 13:710-716.
Crossref

 

Awodele O, Adekunle I, Odoma S, Teixeira JA, Oluseye V (2012). Toxicological evaluation of the aqueous leaf extract of Moringa oleifera Lam. (Moringaceae). Journal of Ethnopharmacology 139(2):330-336.
Crossref

 

Awuku G, Gyan B, Bugyei K, Adjei S, Mahama R, Addo P, Otu-Nyarkoa L, Wiredu EK, Nyarko A (2012). Toxicity potentials of the nutraceutical Moringa oleifera at supra-supplementation levels. Journal of Ethnopharmacology 139(1):265-272.
Crossref

 

Babarinde SA, Akinyemi AO, Usman LA, Odewole AF, Sangodele AO, Iyiola OO (2014). Toxicity and repellency of Hoslundia opposita Vahl (Lamiaceae) leaves essential oil against rust-red flour beetle, Tribolium castaneum Herbst (Coleoptera: Tenebrionidae). Natural Product Research 28(6):365-371.
Crossref

 

Bao XL, Yuan HH, Wang CZ, Fan W, Lan MB (2015). Polysaccharides from Cymbopogon citratus with antitumor and immunomodulatory activity. Pharmaceutical Biology 53(1):117-124.
Crossref

 

Barroso PTW, de Carvalho PP, Rocha TB, Pessoaa FLP, Azevedoc DA, Mendesb MF (2016). Evaluation of the composition of Carica papaya L. seed oil extracted with supercritical CO2. Biotechnology Reports 11:110-116.
Crossref

 

Basha DP, Kuman KP, Teja BB, Subbarao M (2011). Antidiabetic activity on extracts of Mangifera indica in alloxan monohydrate induced diabetic rats. Drug Invention Today 3:165-168.

 

Bassolé IHN, Lamien-Meda A, Bayala B, Obame LC, Ilboudo AJ, Franz C, Novak J, Nebié RC, Dicko MH (2011). Chemical composition and antimicrobial activity of Cymbopogon citratus and Cymbopogon giganteus essential oils alone and in combination. Phytomedicine 18:1070-1074.
Crossref

 

Bbosa GS, Kyegombe DB, Lubega A, Musisi N, Ogwal-Okeng J, Odyek O (2013). Anti-Plasmodium falciparum activity of Aloe dawei and Justicia betonica. African Journal of Pharmacy and Pharmacology 7(31):2258-2263.
Crossref

 

Belay Y (2011). Study of safety and effectiveness of traditional dosage forms of the seed of Aristolochia elegans Mast. against malaria and laboratory investigation of pharmaco-toxicological properties and chemical constituents of its crude extracts. Annals of Tropical Medicine and Parasitology 4(1):33-41.
Crossref

 

Berardini N, Fezer R, Conrad J, Beifuss U, Carle R, Schieber A (2005). Screening of mango (Mangifera indica L.) cultivars for their contents of flavonol O- and xanthone C-glycosides, anthocyanins and pectin. Journal of Agricultural and Food Chemistry 53:1563-1570.
Crossref

 

Bidla G, Titanji VP, Jako B, Bolad A, Berzins K (2004). Antiplasmodial activity of seven plants used in African folk medicine. Indian Journal Pharmacology 36:245-256.

 

Blanco MM, Costa CARA, Freire AO, Santos Jr JG, Costa M (2009). Neurobehavioural effect of essential oil of Cymbopogon citratus in mice. Phytomedicine 16:265-270.
Crossref

 

Brail GA, Ronchi SN, do Nascimento AM, de Lima EM, Romão W, da Costa HB, Scherer R, Ventura JA, Lenz D, Bissoli NS, Endringer DC, de Andrade TU (2014). Antihypertensive effect of Carica papaya via a reduction in ACE activity and improved baroreflex. Planta Medica 80:1580-1587.
Crossref

 

Brandão MGL, Krettli AU, Soares LSR, Nery CGC, Marinuzzi HC. (1997). Antimalarial activity of extracts and fractions from Bidens pilosa and other Bidens species (Asteraceae) correlated with the presence of acetylene and flavonoid compounds. Journal of Ethnopharmacology 57:131-138.
Crossref

 

Brandão MGL, Nery CGC, Mamão MAS, Krettli AU (1998). Two methoxylated flavone glycosides from Bidens pilosa. Phytochemistry 48:397-399.
Crossref

 

Broussalis AM., Ferraro GE., Martino VS., Pinzón R, Coussio JD, Calle AJ (1999). Argentine plants as potential source of insecticidal compounds. Journal of Ethnopharmacology 67:219-223.
Crossref

 

Cáceres A, Cabrera O, Morales O, Mollinedo P, Mendia P (1991). Pharmacological properties of Moringa oleifera. 1. Preliminary screening for antimicrobial activity. Journal of Ethnopharmacology 33:213-216.
Crossref

 

Casanova LM, da Silva D, Sola-Penna M, Camargo LMdM., Celestrini DdM, Tinoco LW, Costa SS (2014). Identification of chicoric acid as a hypoglycemic agent from Ocimum gratissimum leaf extract in a bio-monitoring in vivo study. Fitoterapia 93:132-141.
Crossref

 

Chang JS, Chiang LC, Chen CC, Liu LT, Wang KC, Lin CC (2001). Antileukemic activity of Bidens pilosa L. var. minor (Blume) Sherff and Houttuynia cordata Thunb. American Journal of Chinese Medicine 29:303-312.
Crossref

 

Chang SL, Chiang YM, Chang CLT, Yeh HH, Shyur LF, Kuo YH, Wu TK, Yang WC (2007). Flavonoids, centaurein and centaureidin, from Bidens pilosa, stimulate IFNexpression. Journal of Ethnopharmacology 112:232-236.
Crossref

 

Chatterjee A, Pakrashi SC (1994). The treastise on Indian medicinal plants. CSIR, new Delhi 3:152-153.

 

Chávez-Quintal P, González-Flores T, Rodríguez-Buenfil I, Gallegos-Tintoré S (2011). Antifungal activity in ethanolic extracts of Carica papaya L. cv. maradol leaves and seeds. Indian Journal of Microbiology 51(1):54-60.
Crossref

 

Chen C (2014). Development of antimalarial drugs and their application in China: a historical review. Infectious Diseases of Poverty 3(9):1-10.
Crossref

 

Chiang LC, Chang JS, Chen CC, Ng LT, Lin CC (2003). Anti-Herpes Simplex virus activity of Bidens pilosa and Houttuynia cordata. American Journal of Chinese Medicine 31(3):355-362.
Crossref

 

Chiang LC, Cheng HY, Liu MC, Chiang W, Lin CC (2003). In vitro anti-herpes simplex viruses and anti-adenoviruses activity of twelve traditionally used medicinal plants in Taiwan. Biological and Pharmaceutical Bulletin 26:1600-1604.
Crossref

 

Chieli E, Romiti N, Rodeiro I, Garrido G (2009). In vitro effects of Mangifera indica and polyphenols derived on ABCB1/P-glycoprotein activity. Food and Chemical Toxicology 47:2703-2710.
Crossref

 

Chien SC, Young PH, Hsu YJ, Chen CH, Tien YJ, Shiu SY, Li TH, Yang CW, Marimuthu P, Tsai LFL, Yang WC (2009). Anti-diabetic properties of three common Bidens pilosa variants in Taiwan. Phytochemistry 70:1246-1254.
Crossref

 

Chikezie PC, Ojiako OA (2015). Herbal Medicine: Yesterday, Today and Tomorrow. Alternative and Integrative Medicine 4:195. 
Crossref

 

Chinmoy KB (2007). Possible role of Moringa oleifera Lam. root in epithelial ovarian cancer. Medscape General Medicine 9:26.

 

Chukwuocha UM, Fernández-Rivera O, LegorretaHerrera M (2016). Exploring the antimalarial potential of whole Cymbopogon citratus plant therapy. Journal of Ethnopharmacology 
Crossref

 

Cortés-Rojas DF, Chagas-Paula DA, da Costa FB, Souza CRF, Oliveira WP (2013). Bioactive compounds in Bidens pilosa L. populations: a key step in the standardization of phytopharmaceutical preparations. Revista Brasileira de Farmacognosia 23:28-35.
Crossref

 

Costa RS, Carneiro TCB, Cerqueira-Lima AT, Queiroz NV, Alcântara-Neves NM, Pontes-de-Carvalho LC, Velozo EdS, Oliveira EJ, Figueiredo CA (2012). Ocimum gratissimum Linn. and rosmarinic acid, attenuate eosinophilic airway inflammation in an experimental model of respiratory allergy to Blomia tropicalis. Article in International immunopharmacology 13:126-134.
Crossref

 

Cyril-Olutayo CM, Elujoba AA, Durosinmi MA (2009). Antisickling properties of the fermented mixture of Carica papaya Linn. and Sorgum bicolor (L.) Moench. African Journal of Pharmacy and Pharmacology 3(4):140-143.

 

da Silva JJ, Cerdeira CD, Chavasco JM, Cintra ABP., da Silva CBP, de Mendonça AN, Ishikawa T, Boriollo MFG, Chavasco JK (2014). In vitro screening antibacterial activity of Bidens pilosa L. and Annona crassiflora Mart. against oxacillin resistant Staphylococcus aureus (Orsa) from the aerial environment at the dental clinic. Revista do Instituto de Medicina Tropical de São Paulo 56(4):333-340.

Crossref

Dangi SY, Jolly CI, Narayanan S (2002). Antihypertensive activity of the total alkaloids from the leaves of Moringa oleifera. Pharmaceutical Biology 40:144-148.
Crossref

 
 

De Silva BCJ, Jung WG, Hossain S, Wimalasena SHMP, Pathirana HNKS, Heo GJ (2017). Antimicrobial property of lemongrass (Cymbopogon citratus) oil against pathogenic bacteria isolated from pet turtles. Laboratory Animal Research 33(2):84-91.
Crossref

 
 

Deba F, Xuan TD, Yasuda M, Tawata S (2008). Chemical composition and antioxidant, antibacterial and antifungal activities of the essential oils from Bidens pilosa Linn. var. radiata. Food Control 19:46-352.
Crossref

 
 

Dharani N, Rukunga G, Yenesew A, Mbora A, Mwaura L, Dawson I, Jamnadass R (2010). Common Antimalarial Trees and Shrubs of East Africa: a Description of Species and a Guide to Cultivation and Conservation through Use, Dawson I (ed). The World Agroforestry Centre (ICRAF), Nairobi

 
 

Diallo D, Marston A, Terreaux C, Toure Y, Paulsen BS, Hostettmann K (2001). Screening of Malian medicinal plants for antifungal, larvicidal, molluscidal, antioxidant and radical scavenging activities. Phytotherapy Research 15:401-406.
Crossref

 
 

Dong L, Yang J, Wang X (2004). Analysis of components of volatile oil from Bidens pilosa. Xinxiang Yixueyuan Xuebao 21:179-180.

 
 

dos Santos AO, do Val DR, da Silveira FD, Gomes FI, Freitas HC, de Assis EL, de Almeida DK, da Silva II, Barbosa FG, Mafezoli J, da Silva MR (2018). Antinociceptive, anti-inflammatory and toxicological evaluation of semi-synthetic molecules obtained from a benzyl- isothiocyanate isolated from Moringa oleifera Lam. in a temporomandibular joint inflammatory hypernociception model in rats. Biomedicine and Pharmacotherapy 98:609-618.
Crossref

 

 

Duke JA (1981). Handbook of legumes of world economic importance. Plenum Press, New York.
Crossref

 

Duker-Eshun G, Jaroszewski JW, Asomaning WA, Oppong-Boachie F, Brøgger Christensen S (2004). Antiplasmodial constituents of Cajanus cajan. Phytotherapy Research 18:128-130.
Crossref

 
 

Duraipandiyan V, Ignacimuthu S (2009). Antibacterial and antifungal activity of Flindersine isolated from the traditional medicinal plant, Toddalia asiatica (L.) Lam. Journal of Ethnopharmacology 123:494-498.
Crossref

 
 

Dzotam JK, Touani FK, Kuete V (2016). Antibacterial and antibiotic-modifying activities of three food plants (Xanthosoma mafaffa Lam., Moringa oleifera (L.) Schott and Passiflora edulis Sims) against bacteria. BMC Complement. Alternative Medicine 16(9):1-8.
Crossref

 
 

Ekeke GI, Shode FO (1990). Phenyalanine is the predominant antisickling agent in Cajanus cajan seed extract. Planta Medica 56(1):41-43.
Crossref

 
 

Ekpenyong CE, Akpan E, Nyoh A (2015). Ethnopharmacology, phytochemistry, and biological activities of Cymbopogon citratus (DC.) Stapf extracts. Chinese Journal of Natural Medicines 13(5):0321-0337.
Crossref

 
 

Elufioye TO, Agbedahunsi JM (2004). Antimalarial activities of Tithonia diversifolia (Asteraceae) and Crossopteryx febrifuga (Rubiaceae) on mice in vivo. Journal of Ethnopharmacology 93:167-171.
Crossref

 
 

Elufioye TO, Alatise OI, Fakoya FA, Agbedahunsi JM, Houghton PJ (2009). Toxicity studies of Tithonia diversifolia A. Gray (Asteraceae) in rats. Journal of Ethnopharmacology 122:410-415.
Crossref

 
 

Erasto P, Grierson DS, Afolayan AJ (2006). Bioactive sesquiterpene lactones from the leaves of Vernonia amygdalina. Journal of Ethnopharmacology 106:117-120.
Crossref

 
 

Ezeonwumelu JOC, Omolo RG, Ajayi AM, Agwu E, Tanayen JK, Adiukwu CP, Oyewale AA, Adzu B, Okoruwa AG, Ogbonnia SO (2012). Studies of phytochemical screening, acute toxicity and anti-diarrhoeal effect of aqueous extract of Kenyan Tithonia diversifolia leaves in rats. British Journal of Pharmacology and Toxicology 3(3):127-134.

 
 

Ezike AC, Akah PA, Okoli CC, Chinwe B, Okpala CB (2010). Experimental evidence for the antidiabetic activity of Cajanus cajan leaves in rats. Journal of Basic and Clinical Pharmacy 1(2):81-84.

 
 

Ezike AC, Akah PA, Okoli CO, Ezeuchenne NA, Ezeugwu S (2009). Carica papaya (paw-paw) unripe fruit may be beneficial in ulcer. Journal of Medicinal Food 12(6):1268-1273.
Crossref

 
 

Fandohan P, Gnonlonfin B, Laleye A, Gbenou JD, Darboux R, Moudachirou M (2008). Toxicity and gastric tolerance of essential oils from Cymbopogon citratus, Ocimum gratissimum and Ocimum basilicum in Wistar rats. Food and Chemical Toxicology 46:2493-2497.
Crossref

 
 

Figueirinha A, Cruz MT, Francisco V, Lopes MC, Batista MT (2010). Anti-inflammatory activity of Cymbopogon citratus leaf infusion in lipopolysaccharide-stimulated dendritic cells: contribution of the polyphenols. Journal of Medicinal Food 13(3):681-690.
Crossref

 
 

Fotso AF, Longo F, Désire P, Djomeni D, Kouam SF, Spiteller M, Dongmo AB, Savineau JP (2014). Analgesic and antiinflammatory activities of the ethyl acetate fraction of Bidens pilosa (Asteraceae). Inflammopharmacology 22:105-114.
Crossref

 
 

Francisco V, Costa G, Figueirinha A, Marques C, Pereira P, Neves BM, Lopes MC, García-Rodríguez C, Cruz MT, Batista MT (2013). Anti-inflammatory activity of Cymbopogon citratus leaves infusion via proteasome and nuclear factor-κB pathway inhibition: Contribution of chlorogenic acid. Journal of Ethnopharmacology 148:126-134.
Crossref

 
 

Gadhi CA, Benharref A, Jana M, Brasile AM, Contet-Audonneau N, Fortier B (2001). Antidermathophytic properties of extracts from the leaves of Aristolochia paucinervis Pomel. Phytotherapy Research 15:79-81.
Crossref

 
 

Gangabhavani K, Ravishankar K (2013). Evaluation of analgesic and anti-inflammatory activities of ethanolic extract of whole plant Justicia betonica. World Journal of Pharmacy and Pharmaceutical Sciences 2(6):5218-5228.

 
 

Garcia D, Escalante M, Delgado R, Ubeira FM, Leiro J (2003). Anthelminthic and antiallergic activities of Mangifera indica L. stem bark components Vimang and mangiferin. Phytotherapy Research 17(10):1203-1208.
Crossref

 
 

Gathirwa JW, Rukunga GM, Mwitari PG, Mwikabe NM, Kimani CW, Muthaura CN, Kiboi DM, Nyangacha RM, Omar SA (2011). Traditional herbal antimalarial therapy in Kilifi district, Kenya. Journal of Ethnopharmacology 134(2):434-442.
Crossref

 
 

Gbenou JD, Ahounou JF, Akakpo HB, Laleye A, Yayi E, Gbaguidi F, Baba-Moussa L, Darboux R, Dansou P, Moudachirou M, Kotchoni SO (2013). Phytochemical composition of Cymbopogon citratus and Eucalyptus citriodora essential oils and their anti-inflammatory and analgesic properties on wistar rats. Molecular Biology Reports 40:1127-1134.
Crossref

 
 

Geissberger P, Séquin U (1991). Constituents of Bidens pilosa L.: Do the components found so far explain the use of this plant in traditional medicine? Acta Tropica 48:251-261.
Crossref

 
 

Ghimeray AK, Jin C, Ghimire BK, Cho DH (2009). Antioxidant activity and quantitative estimation of azadirachtin and nimbin in Azadirachta Indica A. Juss grown in foothills of Nepal. African Journal of Biological 8:3084-3091.

 
 

Goffin E, Ziemons E, Mol P, Madureira MC, Martins AP, Cunha AP, Philippe G, Tits M, Angenot L, Frédérich M (2002). In vitro antiplasmodial activity of Tithonia diversifolia and identification of its main active constituent: Tagitinin C. Planta Medica 68:543-545.
Crossref

 
 

Grombone-Guaratini MT, Silva-Brandão KL, Solferini VN, Semir J, Trigo JR (2005). Sesquiterpene and polyacetylene profile of Bidens pilosa complex (Asteraceae: Heliantheae) from southeast of Brazil. Biochemical Systematics and Ecology 33:479-486.
Crossref

 
 

Gu J, Gills JJ, Park EJ, Mata-Greenwood E, Hawthorne ME, Axelrod F, Chavez PI, Fong HHS, Mehta RG, Pezzuto JM, Kinghorn AD (2002). Sesquiterpenoids from Tithonia Diversifolia with potential cancer chemopreventive activity. Journal of Natural Products 65:532-536.
Crossref

 
 

Gundidza GM, Deans SG, Svoboda KP, Mavi S (1992). Antimicrobial activity of essential oil from Hoslundia opposita. Central African Journal of Medicine 38(7):290-293.

 
 

Gurung S, Skalko-Basnet S (2009). Wound healing properties of Carica papaya latex: In vivo evaluation in mice burn model. Journal of Ethnopharmacology 121:338-341.
Crossref

 
 

Hamill FA, Apio S, Mubiru NK, Mosango M, Maganyi OW, Soejarto DD (2000). Traditional herbal drugs of southern Uganda, I. Journal of Ethnopharmacology 70:281-300.
Crossref

 
 

Hamill FA, Apio S, Mubiru NK, Mosango M, Maganyi OW, Soejarto DD (2003). Traditional herbal drugs of southern Uganda, II: literature analysis and antimicrobial assays. Journal of Ethnopharmacology 84:57-78.
Crossref

 
 

Hassan EM, Matlou AA, Abouta ME, Ibrahim NA, Mohamed SM (2016). Assessment of anti-inflammatory, antinociceptive, immunomodulatory, and antioxidant activities of Cajanus cajan L. seeds cultivated in Egypt and its phytochemical composition. Pharmaceutical Biology 54:1380-1391.
Crossref

 
 

Heinrich M, Robles M, West JE, Ortiz de Montellano BR, Rodriguez E (1998). Ethnopharmacology of Mexican Asteraceae (Compositae). Annual Review of Pharmacology and Toxicology 38:539-565.
Crossref

 
 

Hiransai P, Tangpong J, Kumbuar C, Hoonheang N, Rodpech O, Sangsuk P, Kajklangdon U, Inkaow W (2016). Anti-nitric oxide production, anti-proliferation and antioxidant effects of the aqueous extract from Tithonia diversifolia. Asian Pacific Journal of Tropical Biomedicine 6:950-956.
Crossref

 
 

Horiuchi M, Seyama Y (2008). Improvement of the antiinflamatory and antiallergic activity of Bidens pilosa L. var. radiata Scherff treated with enzyme (cellulosine). Journal of Health Sciences 54:294-301.
Crossref

 
 

Hsu YJ, Lee TH, Chang CLT, Huang YT, Yang WC (2009). Anti-hyperglycemic effects and mechanism of Bidens pilosa water extract. Journal of Ethnopharmacology 122:379-383.
Crossref

 
 

Huffman MA, Page JE, Sukhdeo MVK, Gotoh S, Kalunde MS, Towers GHN (1996). Leaf swallowing by chimpanzees: a behavioral adaptation for the control of strong nematode infections. International Journal of Primatology 72:475-503.
Crossref

 
 

Hussein FT, El Sebakhy NA (1974). A phytochemical investigation of the leaves of Aristolochla elegans. Planta Medica 25:310-314.
Crossref

 
 

Ibiba FO, Ezinne OO, Susan DA (2010). Glucose tolerance test in hyperglycaemic guinea pigs treated with aqueous Vernonia amygdalina. Medical Journal of Islamic World Academy of Sciences 18:21-26.

 
 

Igado OO, Glaser J, Ramos-tirado M, BankoÄŸlu EE, Atiba FA., Holzgrabe U, Stopper H, Olopade JO (2017). Isolation of a novel compound (MIMO2) from the methanolic extract of Moringa oleifera leaves: protective effects against vanadium-induced cytotoxity. Drug chemistry Toxicology 
Crossref

 
 

Igile GO, Oleszek W, Burda S, Jurzysta M (1994). Flavonoids from Vernonia amygdalina and their antioxidant ativities. Journal of Agricultural and Food Chemistry 42:2445-2448.
Crossref

 
 

Irudayaraj SS, Sunil C, Duraipandiyan V, Ignacimuthu S (2012). Antidiabetic and antioxidant activities of Toddalia asiatica (L.) Lam. leaves in Streptozotocin induced diabetic rats. Journal of Ethnopharmacology 143:515-523.
Crossref

 
 

Iwalokun BA, Efedede BU, Alabi-Sofunde JA, Oduala T, Magbagbeola OA, Akinwande AI (2006). Hepatoprotective and Antioxidant Activities of Vernonia amygdalina on Acetaminophen-Induced Hepatic Damage in Mice. Journal of Medicinal Food 9(4):524-530.
Crossref

 
 

Jahurul MHA, Zaidul ISM, Ghafoor K, Al-Juhaimi FY, Nyam KL, Norulaini NAN, Sahena F, Mohd Omar AK (2015). Mango (Mangifera indica L.) by-products and their valuable components: A review. Food chemistry 183:173-180.
Crossref

 
 

Jamra N, Das G, Singh P, Haque M (2014). Anthelmintic efficacy of crude neem (Azadirachta indica) leaf powder against bovine strongylosis. Journal of parasitic diseases 39(4):786-788.
Crossref

 
 

Jimenez-Arellanes A, Leon-Diaz R, Meckes M, Tapia A, Molina-Salinas GM, Luna-Herrera J, Yepez-Mulia L (2012). Antiprotozoal and antimycobacterial activities of pure compounds from Aristolochia elegans rhizomes. Evid. Based Complement. Alternative Medicine
Crossref

 
 

Jisaka M, Ohigashi H, Takagaki T, Nozaki H, Tada T, Hirota M, Irie R, Huffman MA, Nishida T, Kaji M, Koshimizu K (1992). Bitter steroids glucosides vernonioside A1, A2 & A3, and related B1 from a possible medicinal plant Vernonia amygdalina, used by wild chimpanzees. Tetrahedron 48:625-632.
Crossref

 
 

Jisaka M, Ohigashi H, Takegawa K, Huffman MA, Koshimizu K (1993). Antitumoral and antimicrobial activities of bitter sesquiterpene lactones of Vernonia amygdalina, a possible medicinal plant used by wild chimpanzees. Bioscience, Biotechnology, and Biochemistry 57(5):833-834.
Crossref

 
 

John-Dewole OO, Oni SO (2013). Phytochemical and antimicrobial studies of extracts from the leaves of Tithonia diversifolia for pharmaceutical importance. IOSR Journal of Pharmaceutical, Chemical and Biological Sciences 6:21-25.
Crossref

 
 

Kamatenesi MM, Acipa A, Oryem-Origa H (2011). Medicinal plants of Otwal and Ngai Sub Counties in Oyam District, Northern Uganda. Journal of Ethnobiology and Ethnomedicine 7:7.
Crossref

 
 

Kanchanapoom T, Noiarsa P, Ruchirawat S, Kasai R, Otsuka H (2004). Triterpenoidal glycosides from Justicia betonica. Phytochemistry 65:2613-2618.
Crossref

 
 

Kariuki HN, Kanui TI, Yenesew A, Patel N, Mbugua PM (2013). Antinocieptive and anti- inflammatory effects of Toddalia asiatica (L) Lam. (Rutaceae) root extract in Swiss albino mice. Pan African Medical Journal 14(133):1-5.
Crossref

 
 

Katuura E, Waako P, Ogwal-Okeng J, Bukenya-Ziraba R (2007). Traditional treatment of malaria in Mbarara District, western Uganda. African Journal of Ecology 45:48-51.
Crossref

 
 

Kayode RMO, Afolayan AJ (2015). Cytotoxicity and effect of extraction methods on the chemical composition of essential oils of Moringa oleifera seeds. Biomed. Biotechnology 16(8):680-689.
Crossref

 
 

Kernan MR, Amarquaye A, Chen JL, Chan J, Sesin DF, Parkinson N, Ye Z, Barrett M, Bales C, Stoddart CA, Sloan B, Blanc P, Limbach C, Mrisho S, Rozhon EJ (1998). Antiviral phenylpropanoid glycosides from the medicinal plant Markhamia lutea. Journal of Natural Products 61:564-570.
Crossref

 
 

Khan MA, Islam MT (2012). Analgesic and cytotoxic activity of Acorus calamus L., Kigelia pinnata L., Mangifera indica L. and Tabernaemontana divaricata L. ournal of Pharmacy and Bioallied Sciences 4(2):149-154.
Crossref

 
 

Khan MR, Kihara M, Omoloso AD (2001). Antimicrobial activity of Bidens pilosa, Bischofia javanica, Elmerillia papuana and Sigesbekia orientalis. Fitoterapia 72:662-665.
Crossref

 
 

Kim H, Banerjee N, Ivanov I, Pfent CM, Prudhomme KR, Bisson WH, Mertens-Talcott SU (2016). Comparison of anti-inflammatory mechanisms of mango (Mangifera indica L.) and pomegranate (Punica granatum L.) in a preclinical model of colitis. Molecular Nutrition Food Research 60(9):1912-1923.
Crossref

 
 

Knodler M, Conrad J, Wenzig EM, Bauer R, Lacorn M, Beifuss U, Schieber A (2008). Anti-inflammatory 5-(11'Z-heptadecenyl)- and 5-(8'Z,11'Z-heptadecadienyl)-resorcinols from mango (Mangifera indica L.) peels. Phytochemistry 69(4):988-993.
Crossref

 
 

Kokwaro JO (1993). Medicinal Plants of East Africa. East African Literature Bureau, Nairobi 212 p.

 
 

Koul JL, Koul S, Singh C, Taneja SC, Shanmugavel M, Kampasi H, Saxena AK, Qazi GN (2003). In vitro cytotoxic elemanolides from Vernonia lasiopus. Planta Medica 69:164-166.
Crossref

 
 

Kumari P, Misra K, Sisodia BS, Faridi U, Srivastava S, Luqman S, Darokar MP, Negi AS, Gupta MM, Singh SC, Kumar JK (2009). A promising anticancer and antimalarial component from the leaves of Bidens pilosa. Planta Medica 75:59-61.
Crossref

 
 

Kupchan SM, Hemingway RJ, Karim A, Werner D (1969). Tumor inhibitors. XLVII. Vernodalin and Vernomydin, two new cytotoxic sesqueterpene lactones from Vernonia amygdalina Journal of Organic Chemistry 34:3908-3911.
Crossref

 
 

Kurian JC (2001). Plants that Heal. 2 ed. Oriental Watchman Publishing House Pune, India 37(55):264-300.

 
 

Kuroda M, Yokosuka A, Kobayashi R, Jitsuno M, Kando H, Nosaka K, Ishii H, Yamori T, Mimaki, Y (2007). Sesquiterpenoids and flavonoids from the aerial parts of Tithonia diversifolia and their cytotoxic activity. Chemical and Pharmaceutical Bulletin 55:1240-1244.
Crossref

 
 

Kusano A, Seyama Y, Usami E, Katayose T, Shibano M., Tsukamoto D, Kusano G (2003). Studies on the antioxidant active constituents of the dried powder from Bidens pilosa L. var. radiata Sch. Nature Medicine 57:100-104.

 
 

Kusemiju TO, Osinubi AA, Noronha CC, Okanlawon AO (2010). Effect of aqueous extract of the bark of Carica papaya on testicular histology in Sprague-Dawley rats. Nigerian Quarterly Journal of Hospital Medicine 20(3):133-137.

 
 

Kviecinski MR, Felipe KB, Schoenfelder T, Wiese LPL, Rossi MH, Gonçalez E, Felicio JD, Filho DW, Pedrosa RC (2008). Study of the antitumor potential of Bidens pilosa (Asteraceae) used in Brazilian folk medicine. Journal of Ethnopharmacology 117:69-75.
Crossref

 
 

Lacroix D, Prado S, Dennis Kamoga D, Kasenene J, Namukobe J, Krief S, Dumontet V, Mouray E, Bodo B, Brunois F (2011). Antiplasmodial and cytotoxic activities of medicinal plants traditionally used in the village of Kiohima, Uganda. Journal of Ethnopharmacology 133:850-855.
Crossref

 
 

Lacroix D, Prado S, Deville A, Krief S, Dumontet V, Kasenene J, Mouray E, Bories C, Bodo B (2009). Hydroperoxy-cycloartane triterpenoids from the leaves of Markhamia lutea, a plant ingested by wild chimpanzees. Phytochemistry 70:1239-1245.
Crossref

 
 

Lai YS, Hsu WH, Huang JJ, Wu SC (2012). Antioxidant and anti-inflammatory effects of pigeon pea (Cajanus cajan L.) extracts on hydrogen peroxide- and lipopolysaccharide-treated RAW264.7 macrophages. Food Function 3:1294-1301.
Crossref

 
 

Lamou B, Taiwe GS, Hamadou A, Houlray J, Atour MM, Tan PV (2016). Antioxidant and antifatigue properties of the aqueous extract of Moringa oleifera in rats subjected to forced swimming endurance test. Oxidative Medicine and Cellular Longevity
Crossref

 
 

Li X, Huang G, Zhao G, Chen W, Li J, Sun L (2013). Two new monoterpenes from Tithonia diversifolia and their anti-hyperglycemic activity. Records of Natural Products 7(4):351-354.

 
 

Linthoingambi W, Singh WS (2013). Antimicrobial activities of different solvent extracts of Tithonia diversifolia (Hemsely) A. Gray. Asian Journal of Plant Science and Research 3:50-54.

 
 

Luo X, Jiang Y, Fronczek FR., Lin C, Izevbigie EB, Lee KS (2011) Isolation and structure determination of a sesquiterpene lactone (vernodalinol) from Vernonia amygdalina extracts. Pharmaceutical Biology 49(5):464-470.
Crossref

 
 

Machado M, Pires P, Dinis AM, Santos-Rosa M, Alves V., Salgueiro L, Cavaleiro C, Sousa MC (2012). Monoterpenic aldehydes as potential anti-Leishmania agents: Activity of Cymbopogon citratus and citral on L. infantum, L. tropica and L. major. Experimental Parasitology 130(3):223-231.
Crossref

 
 

Mahilrajan S, Nandakumar J, Kailayalingam R, Manoharan NA, SriVijeindran S (2014). Screening the antifungal activity of essential oils against decay fungi from palmyrah leaf handicrafts. Biological Research 47(35):1-5.
Crossref

 
 

Maldini M, Maksoud SA, Natella F, Montoro P, Petretto GL, Foddai M, De Nicola GR, Chessa M, Pintore G (2014). Moringa oleifera: study of phenolics and glucosinolates by mass spectrometry. Journal of Mass Spectrometry 49:900-910.
Crossref

 
 

Maniyar Y., Bhixavatimath P. (2015). Antihyperglycemic and hypolipidemic activities of aqueous extract of Carica papaya Linn. leaves in alloxan-induced diabetic rats. Journal of Ayurveda and Integrative Medicine 3(2):70-74.
Crossref

 
 

Martínez-González CL, Martínez L, Martínez-Ortiz EJ, González-Trujano ME, Déciga-Campos M, Ventura-Martínez R, Díaz-Reval I (2017). Moringa oleifera, a species with potential analgesic and anti-inflammatory activities. Biomedicine and Pharmacotherapy 87:482-488.
Crossref

 
 

Matasyoh LG, Matasyoh JC, Wachira FN, Kinyua MG, Muigai AWT, Mukiama TK (2008). Antimicrobial activity of essential oils of Ocimum gratissimum L. from different populations of Kenya. African Journal of Traditional CAM 5(2):187-193.
Crossref

 
 

Mayara TP, Deisiane DB, Christopher DSP, Alex BLR, Ryan DR, Flavia DP, Paula SFS, Núbia PLT, Sheylla SMDA (2016). Antioxidant effect of plant extracts of the leaves of Tithonia diversifolia (Hemsl.) A. Gray on the free radical DPPH. Journal of Chemical and Pharmaceutical Research 8:1182-1189.

 
 

Mbaya AW, Ibrahim UI, ThankGod O, Ladi S (2010). Toxicity and potential anti-trypanosomal activity of ethanolic extract of Azadirachta indica (Maliacae) stem bark: An in vivo and in vitro approach using Trypanosoma brucei. Journal of Ethnopharmacology 128:495-500.
Crossref

 
 

Melariri P, Campbell W, Etusim P, Smith P (2011). Antiplasmodial properties and bioassay-guided fractionation of ethyl acetate extracts from Carica papaya leaves. Journal of Parasitology Research 
Crossref

 
 

Meyer J (2005). Toddalia asiatica (L.) Lam. National Herbarium, Pretoria and South African National Biodiversity Institute, South Africa. 

 
 

Ministry of Health (MoH), Republic of Uganda. (2016). National Malaria Control Program. 

View

 
 

Miura T, Nosaka K, Ishii H, Ishida T (2005). Antidiabetic effect of nitobegiku, the herb Tithonia diversifolia, in KK-Ay diabeticmice. Biological and Pharmaceutical Bulletin 28:2152-2154.
Crossref

 
 

Mohamed ISS, Riffin S (2006). The in-vitro antibacterial activity of methanol and ethanol extracts of Carica papaya flowers and Mangifera indica leaves. Journal of Pharmacological and Toxicological 1:278-283.
Crossref

 
 

Mohan CG, Deepak M, Viswanatha GL, Savinay G, Hanumantharaju V, Rajendra CE, Halemani PD (2013). Anti-oxidant and anti-inflammatory activity of leaf extracts and fractions of Mangifera indica. Asian Pacific Journal of Tropical Medicine 6(4):311-314.
Crossref

 
 

Mohr FBM, Lermen C, Gazim ZC, Gonçalves JE, Alberton O (2017). Antifungal activity, yield, and composition of Ocimum gratissimum essential oil. Genetics and Molecular Research 16(1):gmr16019542.
Crossref

 
 

Morton JF (1976). The pigeon pea (Cajanus cajan Millsp.), a high protein tropical bush legume. Hort Science 11(1):11-19.

 
 

Motsei ML, Lindsey KL, Van Staden J, Jäger AK (2003). Screening of traditionally used South African plants for antifungal activity against Candida albicans. Journal of Ethnopharmacology 86:235-241.
Crossref

 
 

Mujovo SF, Hussein AA, Meyer JJM, Fourie B, Muthivhi T, Lall N (2008). Bioactive compounds from Lippia javanica and Hoslundia opposita. Natural product research 22(12):1047-1054.
Crossref

 
 

Muregi FW, Chhabra SC, Njagi ENM, Lang CC (2003). In vitro antiplasmodial activity of some plants used in Kisii, Kenya against malaria and their chloroquine potentiation effects. Journal of Ethnopharmacology 84:235-239.
Crossref

 
 

Muregi FW, Ishih A, Miyase T, Suzuki T, Kino H, Amano T, Mkoji GM, Terada M (2007). Antimalarial activity of methanolic extracts from plants used in Kenyan ethnomedicine and their interactions with chloroquine (CQ) against a CQ-tolerant rodent parasite, in mice. Journal of Ethnopharmacology 111:190-195.
Crossref

 
 

Murillo AJ, Encarnación DR, Franzblau SG (2001). Antimicrobial and cytotoxic activity of some medicinal plants from Baja California Sur (Mexico). Pharmaceutical Biology 39:445-449.
Crossref

 
 

Muthumani P, Meera R, Devi P, Mohamed SA, Arabath S, Seshu kumar Koduri LV, Manavarthi S (2010). Chemical investigation of Toddalia asiatica Lin. and Cardiospermum halicacabum Lin. International Journal of Drug Form Research 1:224-239.

 
 

Nafiu MO, Akanji MA, Raji ZA, Abdulsalam TA (2014). Phytochemical analysis and in vivo anti-malarial activities of aqueous extracts of Tithonia diversifolia and Parquetina nigrescens leaves in mice. Biokemistri 26:63-68.

 
 

Nakamura CV, Ueda-Nakamura T, Bando E, Melo AFN, Cortez DAG, Filho BPD (1999). Antibacterial activity of Ocimum gratissimum L. essential oil. Memórias do Instituto Oswaldo Cruz 94(5):675-678.
Crossref

 
 

Namukobe J, Kasenene JM, Kiremire BT, Byamukama R, Kamatenesi-Mugisha M, Krief S, Dumontet V, Kabasa JD (2011). Traditional plants used for medicinal purposes by local communities around the Northern sector of Kibale National Park, Uganda. Journal of Ethnopharmacology 136(1):236-245.
Crossref

 
 

Nayak G, Honguntikar SD, Kalthur GS, D'Souza SA, Mutalik S, Setty MM, Kalyankumard R, Krishnamurthy H, Kalthur G, Adiga SK (2016). Ethanolic extract of Moringa oleifera Lam. leaves protect the pre-pubertal spermatogonial cells from cyclophosphamide-induced damage. Journal of Ethnopharmacology 182:101-109.
Crossref

 
 

Nguyen TTT, Shaw PN, Parat MO, Hewavitharana AK (2013). Anticancer activity of Carica papaya: A review. Molecular Nutrition & Food Research 57:153-164.
Crossref

 
 

Nikkon F, Saud A, Rahman MH, Haque ME (2003). In vitro antimicrobial activity of the compound isolated from chloroform extract of Moringa oleifera Lam. Pakistan Journal of Biological Sciences 6:1888-1890.
Crossref

 
 

Nix A, Paull CA, Colgrave M (2015). The flavonoid profile of pigeonpea, Cajanus cajan: a review. Springer Plus. 4(125):1-6.
Crossref

 
 

Njan AA (2004). Herbal medicine in the treatment of malaria: Vernonia amygdalina: an overview of evidence and pharmacology. Toxicity and Drug Testing. Prof. Bill Acree (Ed.), 167-186. ISBN: 978-953-51-0004-1,

 
 

Njan AA, Adzu B, Agaba AG, Byarugaba D, Díaz-llera S, Bangsberg DR (2008). The analgesic and antiplasmodial activities and toxicology of Vernonia amygdalina. Journal of Medicinal Food 11(3):574-581.
Crossref

 
 

Njenga D, Irungu B, Mbaria J, Mutai C (2015). Antiplasmodial, cytotoxic and acute toxicity activities of Vernonia lasiopus O. Hoffman. African Journal of Pharmacology and Therapeutics 4:16-20.

 
 

Nuñez-Sellés AJ, Vélez-Castro HT, Agüero-Agüero J, González-González J, Naddeo F, De Simone F, Rastrelli L (2002). Isolation and quantitative analysis of phenolic antioxidants, free sugars, and polyols from mango (Mangifera indica L.) stem bark aqueous decoction used in Cuba as a nutritional supplement. Journal Agricultural Food chemistry 13:762-766.
Crossref

 
 

Nwodo UU, Ngene AA, Iroegbu CU, Onyedikachi OAL, Chigor V.N., Okoh AI (2011). In vivo evaluation of the antiviral activity of Cajanus cajan on measles virus. Archives of Virology 156:1551-1557.
Crossref

 
 

Odeyemi AT, Agidigbi TS, Adefemi SO, Fasuan SO (2014). Antibacterial activities of crude extracts of Tithonia diversifolia against common environmental pathogenic bacteria. Experimental 20:1421- 1426.

 
 

Oduola T, Adeniyi FAA, Ogunyemi EO, Bello IS, Idowu TO (2006). Antisickling agent in an extract of unripe pawpaw (Carica papaya): is it real? African Journal of Biotechnology 5:1947-1949.

 
 

Oketch-Rabah H.A., Mwangi J.W., Lisgarten J. Mberu E.K. (2000). A new antiplasmodial coumarin from Toddalia asiatica roots. Fitoterapia71:636-640.
Crossref

 
 

Okon UA, Umoren IU (2017). Comparison of antioxidant activity of insulin, Ocimum gratissimum L., and Vernonia amygdalina L. in type 1 diabetic rat model. Journal of Integrative Medicine 15(4):302-309.
Crossref

 
 

Oliveira FQ, Andrade-Neto V, Krettli AU, Brandão MGL (2004). New evidences of antimalarial activity of Bidens pilosa roots extract correlated with polyacetylene and flavonoids. Journal of Ethnopharmacology 93:39-42.
Crossref

 
 

Oliveira RM, Dutra TS, Simionatto E, Ré N, Kassuya CAL. Cardoso CAL (2017). Anti-inflammatory effects of essential oils from Mangifera indica. Genetics and Molecular Research 16(1):gmr16019227.
Crossref

 
 

Olivero-Verbel J, Nerio LS, Stashenko EE (2010). Bioactivity against Tribolium castaneum Herbst (Coleoptera: Tenebrionidae) of Cymbopogon citratus and Eucalyptus citriodora essential oils grown in Colombia. Pest Management Science 66:664-668.
Crossref

 
 

Oloyede OI (2005). Chemical profile of unripe papaya pulp. Pakistan Journal of Nutrition 4(6):379-381.
Crossref

 
 

Olukunle JO, Sogebi AO, Oyewusi JA (2014). Anti-inflammatory and analgesic potential of aqueous leaf extract of Tithonia diversifolia in rodents. Journal of Natural Sciences Engineering and Technology 13:82-90.

 
 

Omoregie ES, Pal A, Sisodia B (2011). In vitro antimalarial and cytotoxic activities of leaf extracts of Vernonia amygdalina (Del.). Nigerian Journal of Basic and Applied Sciences 19(1):121-126.
Crossref

 
 

Opio DR, Andama E, Kureh GT (2017). Ethnobotanical Survey of Antimalarial Plants in Areas of: Abukamola, Angeta, Oculokori and Omarari of Alebtong District in Northern Uganda. European journal of medicinal plants 21(4):1-14.
Crossref

 
 

Orwa JA, Jondiko IJ, Minja RJ, Bekunda M (2008). The use of Toddalia asiatica (L) Lam. (Rutaceae) in traditional medicine practice in East Africa. Journal of Ethnopharmacology 115:2257-2262.
Crossref

 
 

Orwa JA, Ngeny L, Mwikwabe NM, Ondicho J, Jondiko IJO (2013). Antimalarial and safety evaluation of extracts from Toddalia asiatica (L.) Lam. (Rutaceae). Journal of Ethnopharmacology 145(2):587-590.
Crossref

 
 

Otsuki N, Dang NH, Kumagai E, Kondo A, Iwata S, Morimoto C (2010). Aqueous extract of Carica papaya leaves exhibits anti-tumor activity and immunomodulatory effects. Journal of Ethnopharmacology 127:760-767.
Crossref

 
 

Owoyele BV, Adebukola OM, Funmilayo AA, Soladoye AO (2008). Anti-inflammatory activities of ethanolic extract of Carica papaya leaves. Inflammopharmacology 16:168-173.
Crossref

 
 

Oyewole IO, Ibidapo CA, Moronkola DO, Oduola AO, Adeoye GO, Anyasor GN, Obansa JA (2008). Anti-malarial and repellent activities of Tithonia diversifolia (Hemsl.) leaf extracts. Journal of Medicinal Plants Research 2:171-175.

 
 

Pal D, Mishra P, Sachan N, Ghosh AK (2011). Biological activities and medicinal properties of Cajanus cajan (L.) Millsp. Journal of Advanced Pharmaceutical Technology & Research 2(4):207-214.
Crossref

 
 

Pandey AK, Singh P, Tripathi NN (2014). Chemistry and bioactivities of essential oils of some Ocimum species: an overview. Asian Pacific Journal of Tropical Biomedicine 4:682-694.
Crossref

 
 

Pandey S, Cabot PJ, Shaw PN, Hewavitharana AK (2016). Anti-inflammatory and immunomodulatory properties of Carica papaya. Journal of Immunotoxicology 
Crossref

 
 

Parvatkar PT, Parameswaran PS, Bandyopadhyay D, Mukherjee S, Banik BK (2017). Microwave-induced bismuth(III)-catalyzed synthesis of linear indoloquinolines. Tetrahedron Letters 58:2948-2951.
Crossref

 
 

Passoni FD, Oliveira RB, Chagas-Paula DA, Gobbo-Neto L, Da Costa FB (2013). Repeated-dose toxicological studies of Tithonia Diversifolia (Hemsl.) A. Gray and identification of the toxic compounds. Journal of Ethnopharmacology 147:389-394.
Crossref

 
 

Paula-Freire LIG, Andersen ML, Molska GR, Köhn DO, Carlini ELA (2013). Evaluation of the antinociceptive activity of Ocimum gratissimum L. (Lamiaceae) essential oil and its isolated active principles in mice. Phytotherapy Research 27:1220-1224.
Crossref

 
 

Pereira RLC, Ibrahim T, Lucchetti L, Silva AJR, Moraes VLG (1999). Immunosuppressive and anti-inflammatory effects of methanolic extract and the polyacetylene isolated from Bidens pilosa L. Immunopharmacology 43:31-37.
Crossref

 
 

Pereira RP, Fachinetto R, Prestes AdS, Puntel RL, da Silva GNS, Heinzmann BM, Boschetti TK, Athayde ML, Bürger ME, Morel AF, Morsch VM, Rocha JBT (2009). Antioxidant effects of different extracts from Melissa officinalis, Matricaria recutita and Cymbopogon citratus. Neurochemical Research 34:973-983.
Crossref

 
 

Pham VV, Pham TK, Hoang VL, Phan VK (2010). Flavonoid compounds from the plant Bidens pilosa L. (Asteraceae). Tap. Chi. Duoc. Hoc. 50:48-53.

 
 

Philip K, Elizabeth MM, Cheplogoi PK, Samuel KT (2017). Ethnobotanical survey of antimalarial medicinal plants used in Butebo County, Eastern Uganda. European Journal of Medicinal Plants 21(4):1-22
Crossref

 
 

Pierson JT, Monteith GR, Roberts-Thomson SJ, Dietzgen RG, Gidley MJ, Shaw PN (2014). Phytochemical extraction, characterisation and comparative distribution across four mango (Mangifera indica L.) fruit varieties. [Comparative Study]. Food chemistry 149:253-263.
Crossref

 
 

Pinto LA, Cordeiro KW, Carrasco V, Carollo CA, Cardoso CAL, Argadoña EJS, Freitas KdC (2014). Antiulcerogenic activity of Carica papaya seed in rats. Naunyn-Schmiedeberg's Archives of Pharmacology 
Crossref

 
 

Prado Y, Merino N, Acosta J, Herrera JA, Luque Y, Hernández I, Prado E, Garrido G, Delgado R, Rodeiro I (2015). Acute and 28-day subchronic toxicity studies of mangiferin, a glucosyl xanthone isolated from Mangifera indica L. stem bark. Journal of Pharmacy Pharmacognosy Research 3(1):13-23.

 
 

Prashanth GK, Krishnaiah GM (2014). Chemical composition of the leaves of Azadirachta indica Linn (Neem). International Journal of Engineering, Technology Management and Applied Sciences. 1(5):21-31.

 
 

Pulido KDP, Dulcey AJC, Martinez JHI (2017). New caffeic acid derivative from Tithonia diversifolia (Hemsl.) A. Gray butanolic extract and its antioxidant activity. Food Chemistry Toxicology 
Crossref

 
 

Qin J, Chen T, Chen S, Lu Q (2003). Analysis of essential oil of Bidens pilosa L. by GC-MS. Fenxi Ceshi Xuebao 22:85-87.

 
 

Rabelo M, Souza EP, Soares PMG, Miranda AV, Matos FJA, Criddle DN (2003). Antinociceptive properties of the essential oil of Ocimum gratissimum L. (Labiatae) in mice. Brazilian Journal of Medical and Biological Research 36:521-524.
Crossref

 
 

Rachuonyo HO, Ogola PE, Arika W, Nyamai D, Wambani J (2016). In Vitro Antimicrobial Activity of Crude Leaf Extracts from Aloe secundiflora, Bulbine frutescens, Vernonia lasiopus and Tagetes minuta against Salmonella typhi. Journal of Traditional Medicine & Clinical Naturopathy 5:2-4.

 
 

Raj MK, Balachandran C, Duraipandiyan V, Agastian P, Ignacimuthu S (2012). Antimicrobial activity of ulopterol isolated from Toddalia asiatica (L.) Lam.: A traditional medicinal plant. Journal of Ethnopharmacology 140:161-165.
Crossref

 
 

Rastrelli L, Capasso A, Piza C, De Tommasi N, Sorentino L (1997). New protopine and benzyl tetrahydropeotoberberine alkaloids from Aristolochia constricta and their activity on isolated guinea pig ileum. Journal of Natural Products 60:1065-1069.
Crossref

 
 

Rojas JJ, Ochoa VJ, Ocampo SA, Muñoz JF (2006). Screening for antimicrobial activity of ten medicinal plants used in Colombian folkloric medicine: a possible alternative in the treatment of non-nosocomial infections. BMC Complement. Alternative Medicine 6(2):1-6.
Crossref

 
 

Ronchi SN, Brasil GA, do Nascimento AM, de Lima EM, Scherer R, Costa HB, de Andrade TU (2015). Phytochemical and in vitro and in vivo biological investigation on the antihypertensive activity of mango leaves (Mangifera indica L.). Therapeutic Advances in Cardiovascular Disease 9(5):244-256.
Crossref

 
 

Sacchetti G, Maietti S, Muzzoli M, Scaglianti M, Manfredini S, Radice M, Bruni R (2005). Comparative evaluation of 11 essential oils of different origin as functional antioxidants, antiradicals and antimicrobials in foods. Food chemistry 91:621-632.
Crossref

 
 

Sagradas J, Gustavo G, Figueirinha A, Castel-Branco MM, Cabrita AMS, Figueiredo IV, Batista MT (2015). Gastroprotective effect of Cymbopogon citratus infusion on acute ethanol-induced gastric lesions in rats. Journal of Ethnopharmacology 173:134-138.
Crossref

 
 

Sairam K, Hemalatha S, Kumar A, Srinivasan T, Ganesh J, Shankar M, Venkataraman S (2003). Evaluation of anti-diarrhoeal activity in seed extracts of Mangifera indica. Journal of Ethnopharmacology 84(1):11-15.
Crossref

 
 

Salame R, Cheikh-ali Z, Bories C, Poupon E, Champy P (2012). Pyrone and unusually furanone- substituted flavones from the leaves of Hoslundia opposita. Planta Medica 78:1777-1779.
Crossref

 
 

Sánchez-Mendoza ME, Reyes-Ramírez A, Antonio LC, Jiménez LM, RodríguezSilverio J, Arrieta J (2011). Bioassay-guided isolation of an anti-ulcer compound, tagitinin C, from Tithonia diversifolia: role of nitric oxide, prostaglandins and sulfhydryls. Molecules 16:665-674.
Crossref

 
 

Schieber A, Berardini N, Carle R (2003). Identification of flavonol and xanthone glycosides from mango (Mangifera indica L. Cv. ''Tommy Atkins") peels by highperformance liquid chromatography-electrospray ionization mass spectrometry. Journal of Agricultural and Food Chemistry 51:5006-5011.
Crossref

 
 

Severi JA, Lima ZP, Kushima H, Brito AR, Santos LC, Vilegas W, Hiruma-Lima CA (2009). Polyphenols with antiulcerogenic action from aqueous decoction of mango leaves (Mangifera indica L.). Molecules 14(3):1098-1110.
Crossref

 
 

Shan Xf, Meng qf, Kang Yh, Bian Y, Gao Yh, Wang Wl, Qian Ad (2014). Isolation of active compounds from methanol extracts of Toddalia asiatica against Ichthyophthirius multifiliis in goldfish (Carassius auratus). Veterinary Parasitology 199:250-254.
Crossref

 
 

Shi LS, Kuo PC, Tsai YL, Damu AG, Wu TS (2004). The alkaloids and other constituents from the root and stem of Aristolochia elegans. Bioorg. Medicinal Chemistry 12:439446.
Crossref

 
 

Siddique S, Nawaz S, Muhammad F, Akhtar B, Aslam B (2017). Phytochemical screening and in-vitro evaluation of pharmacological activities of peels of Musa sapientum and Carica papaya fruit. Natural Product Research 
Crossref

 
 

Silva C, de B, Guterres SS, Weisheimer V, Schapoval EE (2008). Antifungal activity of the lemongrass oil and citral against Candida spp. Brazilian Journal of Infectious Diseases 12(1):63-66.
Crossref

 
 

Sinha DJ, Nandha KDS, Jaiswal N, Vasudeva A, Tyagi SP, Singh UP (2017). Antibacterial effect of Azadirachta indica (Neem) or Curcuma longa (Turmeric) against Enterococcus faecalis Compared with that of 5 % Sodium Hypochlorite or 2 % Chlorhexidine in vitro. Bull. Tokyo Dental College 58(2):103-109.
Crossref

 
 

Sreelatha S, Padma PR (2009). Antioxidant activity and total phenolic content of Moringa oleifera leav.es in two stages of maturity. Plant Foods Human nutrition 64:303-311.
Crossref

 
 

Ssegawa P, Kasenene JM (2007). Medicinal plant diversity and uses in the Sango bay area, Southern Uganda. Journal of Ethnopharmacology 113:521-540.
Crossref

 
 

Stangeland T, Alele PE, Katuura E, Lye KA (2011). Plants used to treat malaria in Nyakayojo sub-county, western Uganda. Journal of Ethnopharmacology 137(1):154-166.
Crossref

 
 

Stone A (1992). The Neem. Science 15(3):255-107.
Crossref

 
 

Subbaraju GV, Kavitha J, Rajasekhar D, Jimenez JI (2004). Jusbetonin, the first indolo[3,2- ]quinoline alkaloid glycoside from Justicia betonica. Journal of Natural Products 67:461-462.
Crossref

 
 

Sukieum S, Sang-aroon W, Yenjai C (2017). Coumarins and alkaloids from the roots of Toddalia asiatica. Natural Product Research 
Crossref

 
 

Tabuti JRS (2008). Herbal medicines used in the treatment of malaria in Budiope county, Uganda. Journal of Ethnopharmacology 116:33-42.
Crossref

 
 

Tang R, Tian R-h, Cai J-z, Wu J-h, Shen X-l, Hu Y (2017). Acute and sub-chronic toxicity of Cajanus cajan leaf extracts. Pharmaceutical Biology 55(1):1740-1746.
Crossref

 
 

Tanko Y, Magaji GM, Yerima M, Magaji RA, Mohammed A (2008). Anti-nociceptive and anti-inflammatory activities of aqueous leaves extract of Ocimum gratissimum (labiate) in rodents. African Journal of Traditional 5(2):141-146.
Crossref

 
 

Tidjani M, Dupont C, Wepierre J (1989). Anti-inflammatory activity of Azadirachta indica. Planta Medica Phytotherapy 23:259-66.

 
 

Tobinaga S, Sharma MK, Aalbersberg WGL, Watanabe K, Iguchi K, Narui K, Sasatsu M, Waki S (2009). Isolation and identification of a potent antimalarial and antibacterial polyacetylene from Bidens pilosa. Planta Medica 75:624-628.
Crossref

 
 

Trevisan MTS., Silva MGV, Pfundstein B, Spiegelhalder B, Owen RW (2006). Characterization of the volatile pattern and antioxidant capacity of essential oils from different species of the genus Ocimum. Journal of Agricultural and Food Chemistry 54:4377-4382.
Crossref

 
 

Tugume P, Kakudidi EK, Buyinza M, Namaalwa J, Kamatenesi M, Mucunguzi P, Kalema J (2016). Ethnobotanical survey of medicinal plant species used by communities around Mabira Central Forest Reserve, Uganda. Journal of Ethnobiology and Ethnomedicine 12(5):1-28.
Crossref

 
 

Ubillas RP, Mendez CD, Jolad SD, Luo J, King SR, Carlson TJ, Fort DN (2000). Antihyperglycemic acetylenic glucosides from Bidens pilosa. Planta Medica 66:82-83.
Crossref

 
 

Ukpai OM, Amaechi EC (2012). Evaluation of in vivo antimalarial activity of the ethanolic leaf extracts of Chromolaena odorata and Cymbopogon citratus in mice. Nigerian Journal of Biotechnology 24:27-34.

 
 

Usman LA, Zubair MF, Adebayo SA, Oladosu IA, Muhammad NO, Akolade JO (2010) Chemical Composition of Leaf and Fruit Essential Oils of Hoslundia opposita Vahl Grown in Nigeria. American-Eurasian Journal of Agricultural & Environmental Sciences 8(1):40-43.

 
 

Venzon L, Mariano LNB, Somensi LB, Boeing T, de Souza P, Wagner TM, de Andrade SF, Nesello LAN, da Silva LM (2018). Essential oil of Cymbopogon citratus (lemongrass) and geraniol, but not citral, promote gastric healing activity in mice. Biomedicine and Pharmacotherapy 98:118-124.
Crossref

 
 

Viana GSB, Vale TG, Pinho RSN, Matos FJA (2000). Antinociceptive effect of the essential oil from Cymbopogon citratus in mice. Journal of Ethnopharmacology 70:323-327.
Crossref

 
 

Vinitketkumnuen U, Puatanachokchai R, Kongtawelert P, Lertprasertsuke N, Matsushima T (1994). Antimutagenicity of lemon grass (Cymbopogon citratus Stapf) to various known mutagens in salmonella mutation assay. Mutation Research 341:71-75.
Crossref

 
 

Wachira SW, Omar S, Jacob JW, Wahome M, Alborn HT, Spring DR, Masiga DK, Torto B (2014). Toxicity of six plant extracts and two pyridone alkaloids from Ricinus communis against the malaria vector Anopheles gambiae. Parasites and Vectors 7:312.
Crossref

 
 

Wahyuningsih MSH, Mahardika AW, Arief B, Muhammad H (2015). Isolation and identification of potential cytotoxic compound from Kembang bulan (Tithonia diversifolia (Hemsl.) A Gray) leaves. International Journal of Pharmacy and Pharmaceutical Sciences 7:298-301.

 
 

Wang C, Cao M, Shi DX, Yin ZQ, Jia RY, Wang KY, Geng Y, Wang Y, Yao XP, Yang ZR, Zhao J (2013). A 90-day subchronic toxicity study of neem oil, a Azadirachta indica oil, in mice. Human and Experimental Toxicology 32(9):904-913.
Crossref

 
 

Wang F, Xub Y, Liua J (2009). New geranyloxycoumarins from Toddalia asiatica. Journal of Asian Natural Products Research 11:752-756.
Crossref

 
 

Wang J, Yang H, Lin ZW, Sun HD (1997). Flavonoids from Bidens pilosa var. radiata. Phytochemistry 46:1275-1278.
Crossref

 
 

Weenen H, Nkunya MHH, Bray DH, Mwasumbi LB, Kinabo LS, Kilimali VAEB (1990). Antimalarial activity of Tanzanian medicinal plants. Planta Medica 56:368-370.
Crossref

 
 

World Health Organization (WHO) (2011). The World Health Organization. Geneva, Switzerland

 
 

World Health Organization (WHO) (2017). Malaria elimination: report from the inaugural global forum of countries with potential to eliminate malaria by 2020. Wkly Epidemiol Rec.

View

 
 

World Health Organization (WHO) (2018). Antimalarial drug efficacy and drug resistance (updated 27 April 2018) [website]. Geneva: World Health Organization; 2018 

View

 
 

World Health Organization (WHO) (2019). WHO Malaria Policy Advisory Committee (MPAC): meeting report. Geneva: World Health Organization Global Malaria Programme; 2019

 
 

Wu J, Wan Z, Yi J, Wu Y, Peng W, Wu J (2013). Investigation of the extracts from Bidens pilosa Linn. var. radiate Sch. Bip. for antioxidant activities and cytotoxicity against human tumor cells. Journal of Natural Medicines 67:17-26.
Crossref

 
 

Wu L, Chiang Y, Chuang H, Wang S, Yang G, Chen Y, Lai L, Shyur LF (2004). Polyacetylenes function as anti-angiogenic agents. Pharmaceutical Research 21:2112-2119.
Crossref

 
 

Wu LW, Chiang YM, Chuang HC, Lo CP, Yang KY, Wang SY, Shyur LF (2007). A novel polyacetylene significantly inhibits angiogenesis and promotes apoptosis in human endothelial cells through activation of the CDK inhibitors and caspase-7. Planta Medica 73:655-661.
Crossref

 
 

Wu N, Kong Y, Fu Y, Zu Y, Yang Z, Yang M, Peng X, Efferth T (2011). In vitro antioxidant properties, DNA damage protective activity, and xanthine oxidase inhibitory effect of cajaninstilbene acid, a stilbene compound derived from pigeon pea [Cajanus cajan (L.) Millsp.] leaves. Journal of Agricultural and Food Chemistry 59:437-443.
Crossref

 
 

Wu TS, Tsai YL, Damu AG, Kuo PC, Wu PL (2002). Constituents from the Root and Stem of Aristolochia elegans. Journal of Natural Products 65:1522-1525.
Crossref

 
 

Xu CD, Yang X, Lu SG (2007). The invasive plant Tithonia diversifolia in China. Guihaia 27:564-569.

 
 

Yan Y, Liu J, Chen J, Chen J, Qiu M (2015). Three new limonoids from Azadirachta indica. Journal of Asian Natural Products Research 17(1):14-19.
Crossref

 
 

Yedjou C, Izevbigie E, Tchounwou P (2008). Preclinical assessment of Vernonia amygdalina leaf extracts as DNA damaging anti-cancer agent in the management of breast cancer. International Journal of Environmental Research and Public Health 5(5):337-341.
Crossref

 
 

Yemele BM, Krohn K, Hussain H, Dongo E, Schulz B, Hu Q (2006) Tithoniamarin and tithoniamide: a structurally unique isocoumarin dimer and a new ceramide from Tithonia diversifolia. Natural Product Research 20:842-849.
Crossref

 
 

Zamilpa A, Abarca-Vargas R, Ventura-Zapata E, Osuna-Torres L, Zavala MA, Herrera-Ruiz M, Jiménez-Ferrer E, González-Cortazar M (2014). Neolignans from Aristolochia elegans as antagonists of the neurotropic effect of scorpion venom. Journal of Ethnopharmacology 157:156-160.
Crossref

 
 

Zu Yg, Liu Xl, Fua Yj, Wua N, Konga Y, Winkc M (2010). Chemical composition of the SFE-CO2 extracts from Cajanus cajan (L.) Huth and their antimicrobial activity in vitro and in vivo. Phytomedicine 17:1095-1101.
Crossref

 
 

Zulueta MCA, Tada M., Ragasa CY (1995). A diterpene from Bidens pilosa. Phytochemistry 38:1449-1450.
Crossref

 

 




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