Acyl-Hydrazide Derivatives of a Xanthine Carboxylic Congener (XCC) as Selective Antagonists at Human A(2B) Adenosine Receptors

The structure–activity relationships (SAR) of 8-phenyl-1,3-dipropylxanthine derivatives in binding to recombinant human A(2B) adenosine receptors were explored, in order to identify selective antagonists. Based on the finding of receptor selectivity in MRS 1204, containing an N-hydroxysuccinimide es...

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Detalles Bibliográficos
Autores principales: Kim, Yong-Chul, Karton, Yishai, Ji, Xiao-duo, Melman, Neli, Linden, Joel, Jacobson, Kenneth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 1999
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196953/
https://www.ncbi.nlm.nih.gov/pubmed/35790094
http://dx.doi.org/10.1002/(sici)1098-2299(199908)47:4<178::aid-ddr4>3.0.co;2-l

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196953/
https://www.ncbi.nlm.nih.gov/pubmed/35790094
http://dx.doi.org/10.1002/(sici)1098-2299(199908)47:4<178::aid-ddr4>3.0.co;2-l

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