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Synthesis and structure guided evaluation of estrogen agonist and antagonist activities of some new tetrazolyl indole derivatives.

作者信息

Singh Uma Sharan, Shankar Ravi, Yadav Gaya P, Kharkwal Geetika, Dwivedi Anila, Keshri Govind, Singh M M, Moulik P R, Hajela K

机构信息

Medicinal and Process Chemistry Division, Central Drug Research Institute, Lucknow 226001, India.

出版信息

Eur J Med Chem. 2008 Oct;43(10):2149-58. doi: 10.1016/j.ejmech.2007.10.035. Epub 2007 Nov 17.

DOI:10.1016/j.ejmech.2007.10.035
PMID:18155810
Abstract

Several regioisomeric tetrazolyl indole derivatives with structurally modified alkyl substituents at the tetracyclic indole nitrogen containing N-ethyl amino tetrazole moiety have been synthesized and screened for their ER binding affinity, agonist (estrogenic), antagonist (antiestrogenic) and anti-implantation activities. N-2 regioisomers were found to be moderately antagonists and one compound showed 100% contraceptive efficacy at 10 mg/kg dose. Molecular docking studies carried out in comparison to estradiol and raloxifene showed different binding modes of the two regioisomers to the binding site.

摘要

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