Journal
BIOORGANIC CHEMISTRY
Volume 94, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2019.103384
Keywords
Podophyllotoxin; D-Ring modification; Acid hydrazides; Anti-cancer studies; Tubulin inhibiting agents
Ask authors/readers for more resources
A new series (except compound 3a) of D-ring modified acid hydrazides of podophyllotoxin were synthesized by cleaving of its D-ring with various hydrazines. Furthermore, the synthesized compounds were screened for their anticancer activity against human tumor cell lines i.e., MCF-7, HeLa and A-549 and among the synthesized compounds 3c and 3f have shown significant anticancer activity almost similar to that of standard drug etoposide. Molecular modelling studies were also conducted for active compounds and found that the free energies obtained were in good agreement with the observed IC50 values.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available