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Parts of Moringa | Extraction method | Experiments | Active compounds | Citation |
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Leaf | Methanol, ethanol, ethyl acetate and chloroform extracts | Cytotoxicity test on U266B1 cells. | Flavonoid and alkaloid group similar to vincristine and vinblastine. | Parvathy & Umamaheshwari (2007) [41] |
Hot water, methanol and hexane extracts | Cytotoxicity test on HeLa cells | Aqueous extract has best anticancer activity. | Nair & Varalakshmi (2011) [42] |
Methanol and dichloromethane extracts | Cytotoxicity test on HepG2, Caco-2 and MCF-7 cells. Quinone reductase induction assay on Hepa-1c1c7 | Dichloromethane extract has best cytotoxic and chemopreventive activity. Active compounds are quercetin, kaempferol, glucosinolate and sulforaphane. | Charoensin (2014) [43] |
Cold water, hot water and 80% ethanol extracts | Cytotoxicity test on AML, ALL and HepG2 cells | Ethanol extract has the best cytotoxicity against AML and ALL. Hot water extract is most cytotoxic towards HepG2 cells. Active compounds are phenolic compounds, especially glycosides. | Khalafalla et al. (2010) [44] |
Cold water extract | Cytotoxicity test on HepG2 cells. In vivo study using hollow fibre assay on HepG2 and A549 cells | Active compounds are water soluble bioactive compounds. | Jung et al. (2015) [45] |
Successive extraction with n-hexane, chloroform, ethyl acetate and 50% methanol. Ethyl acetate extract was further separated into 15 fractions | Cytotoxicity test on HepG2 cells. In vivo studies to determine toxicity. In vivo study with Dalton’s lymphoma ascites (DLA) model | Fraction 1 (F1) from ethyl acetate was the most cytotoxic against HepG2. Active compounds are steroids and phenolic compounds. | Krishnamurthy et al. (2015) [46] |
Hot water extract | Cytotoxic test on KB cells. | Active compounds are polyphenols primarily quercetin and kaempferol. | Sreelatha et al (2011) [47] |
Hot water extract | Cytotoxic test on A549 cells. | Active compounds are glucosinolates, isothiocyanates, niazimicin, niaziminin quercetin, thiocarbamate, carbamates and nitrile glycosides. | Tiloke et al. (2013) [48] |
50% ethanol extract | In vivo study on Swiss albino mice to test radioprotective effects | Active compound is Vitamin C. | Rao et al. (2001) [52] |
Ethanol extract | Cytotoxic test on HCT-8, MDA-MB-231 | Active compounds are D-allose and hexadecanoic acid. | Al-Asmari et al. (2015) [53] |
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Seed | Dried and green seeds ethanol extract partitioned into hexane, ethyl acetate, butanol, and water. | In vivo study of anti-inflammation activity. Antitumor activity tested on ability to inhibit the formation of EBV-EA induced by TPA. | Ethanol extract has best anti-inflammation and antitumor activity. | Guevara et al. (1996) [54] |
Methanol extract | Cytotoxic test on A549, Hep-2,HT-29, and IMR-32. | Active compounds are alkaloids. | Rajesh et al. (2012) [55] |
Ethanol extract whereby the active compounds were isolated with flash column chromatography and further isolated with HPLC. | Tested anticancer activity in vitro with EBV genome-carrying lymphoblastoid cells, Raji cells. Niazimicin tested on mice induced to form tumours. | The active compounds which prevent induction of EBV genome are: β-sitosterol-3-O-glucopyranoside, 4- (α-L-rhamnosyloxy) benzyl isothiocyanate and niazimicin. Niazimicin was able to delay the formation of tumours and reduce the number of tumours in the in vivo study. | Guevara et al. (1999) [56] |
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Bark | Ethanol extract | Cytotoxic test on HCT-8, MDA-MB-231 | Active compounds are Isothiocyanate, hexadecanoic acid and eugenol | Al-Asmari et al. (2015) [53] |
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