| Literature DB >> 25147430 |
Seung B Ha1, Neli Melman2, Kenneth A Jacobson2, Vasu Nair1.
Abstract
N6-Substituted adenosine analogues containing cyclic hydrazines or chiral hydroxy (ar)alkyl groups, designed to interact with the S2 and S3 receptor subregions, have been synthesized and their binding to the adenosine A1 and A2A receptors have been investigated. Examples of both types of compounds were found to exhibit highly selective binding (Ki in low nM range) to the rat A1 receptor.Entities:
Year: 1997 PMID: 25147430 PMCID: PMC4138058 DOI: 10.1016/S0960-894X(97)10177-9
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823