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The role of 5-arylalkylamino- and 5-piperazino- moieties on the 7-aminopyrazolo[4,3-d]pyrimidine core in affecting adenosine A(1) and A(2A) receptor affinity and selectivity profiles
New 7-amino-2-phenylpyrazolo[4,3-d]pyrimidine derivatives, substituted at the 5-position with aryl(alkyl)amino- and 4-substituted-piperazin-1-yl- moieties, were synthesized with the aim of targeting human (h) adenosine A(1) and/or A(2A) receptor subtypes. On the whole, the novel derivatives 1–24 sha...
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| Vydáno v: | J Enzyme Inhib Med Chem |
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| Hlavní autoři: | , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6009979/ https://ncbi.nlm.nih.gov/pubmed/28114825 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2016.1247060 |
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