α,ß-Didehydrosuberoylanilide hydroxamic acid (DDSAHA) as precursor and possible analogue of the anticancer drug SAHA
HeLa
Hydroxamic acid
Derivative (finance)
Anticancer drug
Alkene
Moiety
DOI:
10.3762/bjoc.15.245
Publication Date:
2019-10-24T06:08:00Z
AUTHORS (4)
ABSTRACT
An alternate synthetic route to the important anticancer drug suberoylanilide hydroxamic acid (SAHA) from its α,ß-didehydro derivative is described. The didehydro obtained through a cross metathesis reaction between suitable terminal alkene and N -benzyloxyacrylamide. Some of derivatives SAHA were preliminarily evaluated for activity towards HeLa cells. administration analogues caused significant decrease in proliferation Furthermore, one showed maximum cytotoxicity with minimum GI 50 value 2.5 µg/mL generation reactive oxygen species (ROS) as some apoptotic features.
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CITATIONS (3)
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