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Discovery and structure–activity relationships of (2-(arylthio)benzylideneamino)guanidines as a novel series of potent apoptosis inducers

Authors :
Zhang, Han-Zhong
Crogan-Grundy, Candace
May, Chris
Drewe, John
Tseng, Ben
Cai, Sui Xiong
Source :
Bioorganic & Medicinal Chemistry. Apr2009, Vol. 17 Issue 7, p2852-2858. 7p.
Publication Year :
2009

Abstract

Abstract: 1-(2-(2,5-Dimethoxyphenylthio)benzylidene)semicarbazide (2a) was discovered as a potent apoptosis inducer through our cell based HTS assay. SAR study led to the discovery of a more aqueous soluble analog (2-(2,5-dimethoxyphenylthio)-6-methoxybenzylideneamino)guanidine (5e) with EC50 value of 60nM in the caspase activation assay and GI50 value of 62nM in the growth inhibition assay in T47D cells. Compound 5e was found to be an inhibitor of tubulin polymerization and efficacious in a MX-1 breast tumor model. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
09680896
Volume :
17
Issue :
7
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
37227931
Full Text :
https://doi.org/10.1016/j.bmc.2009.02.029