dc.contributor.author |
Kumar, Shailesh |
|
dc.contributor.author |
Deshpande, Shreekant |
|
dc.contributor.author |
Kitchlu, Shakti |
|
dc.contributor.author |
Chandra, Vishal |
|
dc.contributor.author |
Dwivedi, Anila |
|
dc.contributor.author |
Nayak, V L |
|
dc.contributor.author |
Konwar, Rituraj |
|
dc.contributor.author |
Prabhakar, Y S |
|
dc.contributor.author |
Sahu, D P |
|
dc.date.accessioned |
2012-04-18T11:55:25Z |
|
dc.date.available |
2012-04-18T11:55:25Z |
|
dc.date.issued |
2009 |
|
dc.identifier.citation |
Bioorganic & Medicinal Chemistry 2009, 17(19), 6832–6840 |
en |
dc.identifier.uri |
http://hdl.handle.net/123456789/758 |
|
dc.description.abstract |
A novel class of 2,3,4-triarylbenzopyrans has been synthesized and were evaluated for their selective estrogen receptor rmodulation and anti-proliferative activities. 10a and 11c exhibited 73.91 and 69.24 % inhibition as estrogen antagonistic activity respectively. 11a showed lowest MIC at 6.971µM against MCF-7 cell line and 10h showed lowest MIC at 6.971µM against MDA-MB-231 cell line |
en |
dc.format.extent |
995030 bytes |
|
dc.format.mimetype |
application/pdf |
|
dc.language.iso |
en |
en |
dc.relation.ispartofseries |
CDRI Communication No.7778 |
en |
dc.subject |
SERMs |
en |
dc.subject |
Estradiol |
en |
dc.subject |
2,3,4-triarylbenzopyrans |
en |
dc.title |
Synthesis and biological evaluation of 2,3,4-triarylbenzopyran derivatives as SERM and therapeutic agent for breast cancer† |
en |
dc.type |
Article |
en |