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NEW BASE-ALTERED ADENOSINE ANALOGUES: SYNTHESIS AND AFFINITY AT ADENOSINE A(1) and A(2A) RECEPTORS

N(6)-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 A(1) and A(2A) receptors have been investigated. Examples of both types of compo...

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Bibliografische gegevens
Hoofdauteurs: Ha, Seung B., Melman, Neli, Jacobson, Kenneth A., Nair, Vasu
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1997
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4138058/
https://ncbi.nlm.nih.gov/pubmed/25147430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0960-894X(97)10177-9
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