Synthesis and Antitumor Activities of Genistein Analogs
Lurong Zhang
Abstract
Lurong Zhang
Abstract
Twelve genistein analogs were synthesized from p-nitrophenylacetonitrile and phloroglucinol by Friedel-Crafts reaction, cyclization reaction and condensation. Their antitumor activities on MDA-MB-435 cell line and TSU cell line were tested. The results showed that compounds 1b, 1c, 1g and 7 had potent inhibitory effects on TSU cell line and MDA-MB-435 cell line in vitro.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Twelve genistein analogs were synthesized from p-nitrophenylacetonitrile and phloroglucinol by Friedel-Crafts reaction, cyclization reaction and condensation. Their antitumor activities on MDA-MB-435 cell line and TSU cell line were tested. The results showed that compounds 1b, 1c, 1g and 7 had potent inhibitory effects on TSU cell line and MDA-MB-435 cell line in vitro.
Key concepts: Phloroglucinol, Chemistry, Genistein, In vitro, Cell culture, Stereochemistry, Biochemistry, Organic chemistry