| Literature DB >> 28435524 |
Jakub Staroń1, Stefan Mordalski1, Dawid Warszycki1, Grzegorz Satała1, Adam Hogendorf1, Andrzej J Bojarski1.
Abstract
In this letter, we report the synthesis of a pyrano[2,3,4-cd]indole chemical scaffold designed through a tandem bioisostere generation/virtual screening protocol in search of 5-HT6R ligands. The discovered chemical scaffold resulted in the design of highly active basic and nonbasic 5-HT6R ligands (5-HT6R Ki = 1 nM for basic compound 6b and 5-HT6R Ki = 4 nM for its neutral analog 7b). Additionally, molecular modeling suggested that the hydroxyl group of nonbasic ligands 7a-7d forms hydrogen bonds with aspartic acid D3×32 or D7.36×35.Entities:
Keywords: 5-HT6; Serotonin; bioisosteres; molecular modeling; nonbasic; virtual screening
Year: 2017 PMID: 28435524 PMCID: PMC5392774 DOI: 10.1021/acsmedchemlett.6b00482
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345