Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptors.

1. The interaction at tachykinin receptors of a series of novel cyclic hexapeptides has been examined by use of radioligand binding assays (NK1 and NK3 sites in rat cortex, NK2 sites in hamster urinary bladder) and functional pharmacological assays (guinea-pig ileum, rat vas deferens and rat portal...

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Hlavní autoři: McKnight, A. T., Maguire, J. J., Elliott, N. J., Fletcher, A. E., Foster, A. C., Tridgett, R., Williams, B. J., Longmore, J., Iversen, L. L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1991
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1908569/
https://ncbi.nlm.nih.gov/pubmed/1665732
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