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Biochemical and pharmacological characterization of an extremely potent and selective nonpeptide cholecystokinin antagonist.

3S(-)-N-(2,3-dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4- benzodiazepine-3-yl)-1H-indole-2-carboxamide (L-364,718) interacted in a competitive manner with rat pancreatic cholecystokinin (CCK) receptors as determined by Scatchard analysis of the specific binding of 125I-labeled CCK. The affinity of L-364,...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Chang, R S, Lotti, V J
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1986
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC323856/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3014520/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.83.13.4923
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