Full Length Research Paper
References
|
Aeschbach R, Loliger J, Scott BC, Murcia A, Butler J, Halliwel B, Aruoma OI (1994). Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol. Food Chem. Toxicol. 32(1):31-36. Crossref |
||||
| Agarwal SK, Singh SS, Verma S, Kumar S (1999). Two new anthraquinone derivatives from Rheum emodi. Indian J. Chem. 38B:749-751. | ||||
|
Al-Musayeib N, Perveen S, Fatima I, Nasir M, Hussain A (2011). Antioxidant, Anti-Glycation and anti-inflammatory activities of phenolic constituents from Cordia sinensis. Molecules 16(12):10214-10226. Crossref |
||||
| Amatya S, Tuladhar SM (2005). Eupatoric acid: A novel triterpene from Eupatorium odoratum L. (Asteraceae). Z. Naturforsch. 60b:1006-1011. | ||||
|
Ayyad SE, Abdel-Lateff A, Alarif WM, Patacchioli FR, Badria FA, Ezmirly ST (2012). In vitro and in vivo study of cucurbitacins-type triterpene glucoside from Citrullus colocynthis growing in Saudi Arabia against hepatocellular carcinoma. Environ. Toxicol. Pharmacol. 33:245–251. Crossref |
||||
|
Block S, Baccelli C, Tinant B, Van Meervelt L, Rozenberg R, Habib Jiwan JL, Llabres G, De Pauw-Gillet MC, Quetin-leclercq J (2004). Diterpenes from the leaves of Croton zambesicus. Phytochemistry 65(8):1165-1171. Crossref |
||||
|
Cha TL, Qiu L, Chen CT, Wen Y, Hung MC (2005). Emodin down-regulates androgen receptor and inhibits prostate cancer cell growth. Cancer Res. 65:2287-2295. Crossref |
||||
|
Chang CJ, Ashendel CL, Geahlen RL, McLaughlin JL, Waters DJ (1996), Oncogene signal transduction inhibitors from medicinal plants. In Vivo 10:185-190. Pubmed |
||||
|
Cheng HY, Yang CM, Lin TC, Shieh DE, Lin CC (2006). Ent-epiafzelechin-(4α→8)- epiafzelechin extracted from Cassia javanica inhibits herpes simplex virus type 2 replication. J. Med. Microbiol. 55:201-206. Crossref |
||||
|
Diantini A, Subarnas A, Lestari K, Halimah E, Susilawati Y, Supriyatna, Julaeha E, Achmad TH, Surpadji EW, Yamazaki C, Kobayashi K, Koyama H, Abdulah R (2012). Kaempferol-3-O-rhamnoside isolated from the leaves of Schima wllichii Korth. Inhibits MCF-7 breast cancer cell proliferation through activation of the caspase cascade pathway. Oncol. Lett. 3(5):1069-1072. Pubmed |
||||
|
Fisher GR, Gutierrez PL, Oldcorne MA, Patterson LH (1992). NAD(P)H (quinone acceptor) oxidoreductase (DT-diaphorase)-mediated two-electron reduction of anthraquinone- based antitumor agents and generation of hydroxyl radicals. Biochem. Phrmacol. 43:575-585. Crossref |
||||
|
Gutteridge JMC, Rowley DA, Halliwell B (1981). Superoxide-dependent formation of hydroxyl radicals in the presence of iron salts. Detection of free iron in biological systems by using bleomycin-dependent degradation of DNA. Biochem. J. 199:263-265. Pubmed |
||||
| Hickey M, king C (1997). Common families of flowering plants. Cambridge University Press. pp. 86-95. | ||||
|
Hsiao CJ, Li TK, Chan YL, Hsin LW, Liao CH, Lee CH, Lyu PC, Guh JH (2008). WRC-213, An 1-methionine-conjugated mitoxantrone derivative, displays anticancer activity with reduced cardiotoxicity and drug resistance: Identification of topoisomerase II inhibition and apoptotic machinery in prostate cancers. Biochem. Pharmacol. 75:847-856. Crossref |
||||
|
Joshi CS, Priya ES, Venkataraman S (2007). Acute and subacute toxicity studies on the polyherbal antidiabetic formulation Diakyur in experimental animal models. J. Health Sci. 53(2):245-249. Crossref |
||||
|
Kumavat UC, Shimpi SN, Jagdale SP (2012). Evaluation of hypoglycemic activity of Cassia nodosa leaves in normal and streptozotocin-indused diabetic rats. Int. J. Green Pharm. 6(1):9-13. Crossref |
||||
|
Kuo YC, Sun CM, Ou JC, Tsai WJ (1997). A tumor cell growth inhibitor from Polygonum hypoleucum Ohwi. Life Sci. 61:2335-2344. Crossref |
||||
|
Lissi EA, Modak B, Torres R, Escobar J, Urzua A (1999). Total antioxidant potential of resinous exudates from Heliotropium species, and a comparison of the ABTS and DPPH methods. Free Radic. Res. 30:471-477. Crossref |
||||
|
Mabry TJ, Markham KR, Thomas MB (1970). The Systematic identification of flavonoids. Springer, Berlin. Crossref |
||||
| Malagoli D (2007). A full length protocol to test hemolytic activity of palytoxin on human erythrocytes. Inform. Syst. J. 4(2):92-94. | ||||
|
Markham KR, Terani B (1976). 13C NMR of flavonoids—II: Flavonoids other than flavone and flavonol aglycones. Tetrahedron 32(21):2607-2612. Crossref |
||||
|
Markham KR, Terani B, Stanely R, Geiger H, Mabry TJ (1978). Carbon-13 NMR studies of flavonoids—III: Naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron 34(9):1389-1397. Crossref |
||||
|
Matthes HWD, Luu B, Ourisson G (1980). Cytotoxic components of Zingiber zerumbet, Curcuma zedoaria and C. domestica. Phytochemistry 19(12):2643-2650. Crossref |
||||
|
Mosmann T (1983). Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Methods 65:55-63. Crossref |
||||
|
Nadkarni KM, Nadkarni AK (1976). The Indian Meteria Medica. Bombay. 76. PMid:786854 |
||||
|
Perchellet EM, Magill MJ, Huang X, Dalke DM, Hua DH, Perchellet JP (2000). 1,4- Anthraquinone: An anticancer drug that block nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro. Anticancer Drugs 11:339-352. Crossref |
||||
| Quattrocchi U (2000). CRC World Dictionary of Plant Names. CRC press LLC. Boca Raton, Florida 33431, USA. 1:450. | ||||
| Rizk AM, Heiba HI (1990). Anti-inflammatory and cytotoxic activities of extracts of 30 indigenous plant species growing in Qatar. XVII. Int. J. Crude Drug Res. 28:89-95. | ||||
|
Singh SS, Pandey SC, Singh R, Agarwal SK (2005). 1,8- Dihydroxyanthraquinone derivatives from rhizomes of Rheum emodi Wall. Indian J. Chem. 43B:1494-1496. |
||||
|
Soobrattee MA, Bahorun T, Aruoma OI (2006). Chemopreventive actions of plyphenolic compounds in cancer. BioFactors 27(1-4):19-35. Crossref |
||||
|
Sun HX, Peng XY (2008). Protective effect of triterpenoid fractions from the rhizomes of Astilbe chinensis on cyclophosphamide-induced toxicity in tumor-bearing mice. J. Ethnopharmacol. 119(2):312-317. Crossref |
||||
| Takemura T, Takatsu Y, Kasumi M, Marubashi W, Iwashina T (2005). Flavonoids and their distribution patterns in the flowers of Gladiolus cultivars, Proc. IXth Intl. Symp. on flowers bulbs, Eds.: Okubo H., Miller WB and Chastagner GA, Acta Hort. 487-493. | ||||
| Wealth of India (1963). Raw Material. CSIR. New Delhi. 4:93. | ||||
| Wilson AP (2000). Cytotoxicity and Viability Assays in Animal Cell Culture: A Practical Approach. 3rd ed, Oxford University Press. 1:175-215. | ||||
|
Yadav A, Sharma RA, Singh D, Bhardwaj R (2012). Biochemical estimation of primary metabolites of Cassia nodosa Bunch. Int. J. Biopharm 3(2):65-69. |
||||
|
Zhang L, Chang CJ, Bacus SS, Hung MC (1995). Suppressed transformation and induced differentiation of HER-2/neu-overexpressing breast cancer cells by emodin. Cancer Res. 55:3890-3896. Pubmed |
||||
Copyright © 2024 Author(s) retain the copyright of this article.
This article is published under the terms of the Creative Commons Attribution License 4.0
