Review
References
|
Adianti M, Aoki C, Komoto M, Deng L, Shoji I, Wahyuni TS, Lusida MI, Soetjipto, Fuchino H, Kawahara N, Hotta H (2014). Anti-hepatitis C virus compounds obtained from Glycyrrhiza uralensis and other Glycyrrhiza species. Microbiol Immunol. 58:180-7. crossref |
||||
| Barrero AF, Herrador MM, Arteaga F (1997). Cytotoxic activity of flavonoids from Carthamu arborescens, Ononis natrix ssp. Ramosissima and Centaurea malacitan. Fitoterapia 68:281-283. | ||||
|
Belofsky G, Percivill D, Lewis K, Tegos GP, Ekart J (2004). Phenolic metabolites of Dalea versicolor that enhance antibiotic activity against model pathogenic. J. Nat. Prod. 67:481-484. crossref |
||||
|
Bertl E, Becker H, Eicher T, Herhaus C, Kapadia G, Bartsch H, Gerhauser C (2004). lnhibition of endothelial cell functions by novel potential cancer chemopreventive agents. Biochem. Biophys. Res. Commun. 325:287-95. crossref |
||||
|
Beutler JA, Cardelllna JH, Gray NG, Tanya R, Prather TR (1993).Two new cytotoxic chalcones from Calythropsis aurea. J. Nat. Prod. 56:1718-1722. crossref |
||||
|
Buckwold VE, Wilson RJ, Nalca A, Beer BB, Voss TG, Turpin JA, Buckheit RW (2004). Antiviral activity of hop constituents against a series of DNA and RNA viruses. Antiviral Res. 61:57-62. crossref |
||||
|
Chimenti F, Fioravanti R, Bolasco A,Chimenti P, Secci D, Rossi F, Yá-ez M (2009). Chalcones: A valid scaffold for monoamine oxidases inhibitors. J. Med. Chem. 52:2818–2824. crossref |
||||
|
Cioffi C, Escobar LM, Braca A, Tommasi N (2003). Antioxidant chalcone glycosides and flavanones from Maclura (Chlorophora) tinctoria. J. Nat. Prod. 66:1061-1064. crossref |
||||
|
Cunha GMH, Fontenele JB, Helio V, Junlor N, Sousar FCM, Sílveira ER, Nogueira NAP (2003). Cytotoxic activity of chalcones isolated from Lonchocarpus sericeus (Pocr.) Kunth. Phytoter Res. 17: 155-159. crossref |
||||
|
Daikonya A, Katsuki S, Kitanaka S (2004). Antiallergic agents from natural sources. Inhibition of nitric oxide production by novel chalcone derivatives from Mallotus philippinensis (Euphorbiaceae). Chem. Pharm. Bull. 52:1326-1329. crossref |
||||
|
De Bernonville TD, Guyot S, Paulin J. Gaucher M, Loufrani L, Henrion D, Debre S, Guilet D, Richomme P, Dat JF, Brisset M (2010). Dihydrochalcones: Implication in resistance to oxidative stress and bioactivities against advanced glycation end-products and vasoconstriction. Phytochemistry 71: 443-452. crossref |
||||
|
DellEva R, Ambrosini C, Vannini N, Piaggio G, Albini A, Ferrari N (2007). AKT/NF-kappaB inhibitor xanthohumol targets cell growth and angiogenesis in hematologic malignancies. Cancer 110: 2007-2011. crossref |
||||
| Dhar DN (2003). The Chemistry of Chalcones and Related Compounds. John Wiley, New York. P 1981. | ||||
|
Drewes SE, van Vuuren SF (2008). Antimicrobial acylphloroglucinols and dibenzyloxy flavonoids from flowers of Helichrysum gymnocomum. Phytochemistry 69:1745-1749. crossref |
||||
|
Echeverria C, Santiba-ez JF, Donoso-Tauda O, Escobar CA, Ramirez-Tagle R (2009). Structural antitumoral activity relationships of synthetic chalcones. Int. J. Mol. Sci. 10:221–231. crossref |
||||
|
Go ML, Wu X, Liu XL (2005). Chalcones: An update on cytotoxic and chemoprotective properties. Curr. Med. Chem. 12:483-499. crossref |
||||
|
Jayasinghe L, Bais B, Padmini C, Hara N. Fujimoto Y (2004). Geranyl chalcone derivative with antifungal and radical scavenging properties from the leaves of Artocarpus nobilis. Phytochemistry 65:1287-1290. crossref |
||||
|
Huang H, Ko H, Jin Y, Yang S, Shih Y, Chen I (2012). Dihydrochalcone glucosides and antioxidant activity from the roots of Anneslea fragrans var. lanceolata. Phytochemistry 78: 120-125. crossref |
||||
|
Koorbanally NA, Randrianarivelojosia M, Mulholland DA, van Ufford LQ, van den Berg JJA (2003). Chalcones from the seed of Cedrelopsis grevei (Ptaeroxylaceae). Phytochemistry 62:1225-1229. crossref |
||||
|
Lai SL, Wong PF, Lim TK, Lin Q, Mustafa MR (2015). Cytotoxic mechanisms of Panduratin A on A375 melanoma cells: A quantitative and temporal proteomics analysis. Proteomics crossref |
||||
|
Li L, Zhao X, Luo Y, Jing-Feng Z, Yang X, Zhang H (2011). Novel cytotoxic chalcones from Litsea rubescens and Litsea pedunculata. Bioorg. Med. Chem. Lett. 21:7431-7433. crossref |
||||
|
Liu X, Xu YJ, G0 ML (2008). Functionalized chalcones with basic functionalities have antibacterial activity against drug sensitive Staphylococcus aureus. European J. Med. Chem. 43:1681-1687. crossref |
||||
|
Mojzis J, Varinska L, Mojzisova G, Kostova I, Mirossay L (2008). Antiangiogenic effects of flavonoids and chalcones. Pharmacol. Res. 57:259-265. crossref |
||||
|
Nowakowska Z (2007). A review of anti-infective and anti-inflammatory chalcones. Eur. J. Med. Chem. 42:125-137. crossref |
||||
|
Pascoal AC, Ehrenfried CA, Lopez BG, de Araujo TM, Pascoal VD, Gilioli R, Anhe GF, Ruiz AL, Carvalho JE, Stefanello ME, Salvador MJ (2014). Antiproliferative activity and induction of apoptosis in PC-3 cells by the chalcone cardamonin from Campomanesia adamantium (Myrtaceae) in a bioactivity-guided study. Molecules 19:1843-55. crossref |
||||
|
Patil AD, Freyer AJ, Kíllmer L (2002). Offen, P; Taylor, P.B; Votta, B.J; Johnson, R.K; A new dimer dihydrochalcone and a new prenylated flavone from the bud covers of Artocarpus altilis: Potent inhibitors of cathepsin K. J. Nat. Prod. 65:624-627. crossref |
||||
|
Portet B, Fabre N, Rourny V,Gornitzka H, Bourdy G, Chevalley S, Sauvain M, Valentin A, Moulis C (2007). Activity-guided isolation of antiplasmodial dihydrochalcones and flavanones from Piper hostmannianum var. berbicense. Phytochemistry 68:1312-1320. crossref |
||||
| Rahman MA (2011). Chalcone: A Valuable Insight into the recent advances and potential pharmacological activities. Chem. Sci. 29:1-16. | ||||
|
Resurrección-Magno MHC, Villasenor IM, Harada N (2005). Antihyperglycaemic flavonoids from Syzygium samaran- gense (Blume) Merr.& Perry. Phytother. Res. 19:246-253. crossref |
||||
|
Sabzevari O, Galati G, Moridani M, Siraki A, Obrien P (2004). Molecular cytotoxic mechanisms of anticancer hydrochalcones. Chem Biol Interact. 148:57–67. crossref |
||||
| Seigler D (2002). Plant secondary metabolism. Kluwer academic publishers. Snd Printing. pp. 173-175. | ||||
|
Seo SY, Sharma VK, Sharma N (2003). Mushroom tyrosinase: recent prospects. J. Agric. Food Chem. 51:2837-2853. crossref |
||||
|
Shin JE, Choi EJ, Jin Q, Jin H, Woo E (2011). Chalcones isolated from Angelica keiskei and their inhibition of IL- 6 production in TNF-α- stimulated MG-63 Cell. Arch. Pharm. Res. 34:437-442. crossref |
||||
|
Svetaz L, Tapia A, Lopez SN, Furlan RLE, Petenatti E, Rschmeda-Hirschmann G, Zacchino SA (2004). Antifungal chalcones and new caffeic acid esters from Zuccagnia punctata acting against soybean infecting fungi. J. Agric. Food Chem. 52:3297-3300. crossref |
||||
|
Szliszka E, Czuba ZP, Mazur B, Paradysz A, Krol W (2010). Chalcones and dihydrochalcones augment TRAIL-mediated apoptosis in prostate cancer Cells. Molecules 15:5336-5353. crossref |
||||
|
Tao J, Carol L, Lauren SK, Ramez EY Xiaolin ZG, Hoang BH (2013). Flavokawain B, a kava chalcone, inhibits growth of human osteosarcoma cells through G2/M cell cycle arrest and apoptosis Mol. Cancer 12:55. crossref |
||||
|
Wu J, Li J, Cai Y, Pan Y, Ye F, Zhang Y, Zhao Y, Yang SLX, Liang G (2011). Evaluation and discovery of novel synthetic chalcone deri-vatives as anti- inflammatory agents. J. Med. Chem. 54:8110-8123. crossref |
||||
|
Xu HX, Wan M, Dong H, But P (2000). Ihibitory activity of flavonoids and tannins against HIV-1 protease. Biol. Pharm. Bull. 23:1072-1076. crossref |
||||
|
Zhu XF, Xie BF, Zhou JM, Feng GK, Liu ZC, Wei XY, Zhang FX, Liu MF (2005). Blockade of vascular endothelial growth factor receptor signal pathway and antitumor activity of ON-III (2',4'- dihydroxy-6'-methoxy-3',5'-dimethylchalcone), a component from Chinese herbal medicine. Mol. Pharmacol. 67:1444-1450. crossref |
||||
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