| 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 |