Synthesis, Evaluation of Anticancer Activity and QSAR Study of Heterocyclic Esters of Caffeic Acid

AuthorShima Hajmohamad Ebrahim Ketabforooshen
AuthorMohsen Aminien
AuthorMohsen Vosooghien
AuthorAbbas Shafieeen
AuthorEbrahim Azizien
AuthorFarzad Kobarfarden
Issued Date2013-10-31en
AbstractCaffeic acid phenethyl ester (CAPE) suppresses the growth of transformed cells such as human breast cancer cells, hepatocarcinoma , myeloid leukemia, colorectal cancer cells, fibrosarcoma, glioma and melanoma. A group of heterocyclic esters of caffeic acid was synthesized using Mitsunobu reaction and the esters were subjected to further structural modification by electrooxidation of the catechol ring of caffeic acid esters in the presence of sodium benzenesulfinate and sodium toluensulfinate as nucleophiles. Both heterocyclic esters of caffeic acid and their arylsulfonyl derivatives were evaluated for their cytotoxic activity against HeLa, SK-OV-3, and HT-29 cancer cell lines.en
DOIhttps://doi.org/10.22037/ijpr.2013.1355en
KeywordCaffeic aciden
KeywordMitsunobuen
KeywordElectrooxidationen
KeywordCytotoxic activityen
PublisherBrieflandsen
TitleSynthesis, Evaluation of Anticancer Activity and QSAR Study of Heterocyclic Esters of Caffeic Aciden
TypeOriginal Articleen

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