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APORPHINOID ANTAGONISTS OF 5-HT(2A) RECEPTORS: FURTHER EVALUATION OF RING A SUBSTITUENTS AND THE SIZE OF RING C

A series of ring A modified analogs of nantenine as well as structural variants in ring C were synthesized and evaluated for antagonist activity at 5-HT(2A) and α(1A) receptors. Halogenation improves 5-HT(2A) antagonist potency in molecules containing a C1 methoxyl/C2 methoxyl or C1 methoxyl/C2 hydr...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Ponnala, Shashikanth, Kapadia, Nirav, Navarro, Hernán A., Harding, Wayne W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4197079/
https://ncbi.nlm.nih.gov/pubmed/24766771
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cbdd.12345
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