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Merck
CN

Orally active, nonpeptide oxytocin antagonists.

Journal of medicinal chemistry (1992-10-16)
B E Evans, J L Leighton, K E Rittle, K F Gilbert, G F Lundell, N P Gould, D W Hobbs, R M DiPardo, D F Veber, D J Pettibone
摘要

The first nonpeptide antagonists of the neurohypophyseal hormone, oxytocin (OT) are described. Derivatives of the spiroindenepiperidine ring system, these compounds include L-366,509, an orally bioavailable OT antagonist with good in vivo duration. The potential use of these agents for treatment of preterm labor and their significance as new nonpeptide ligands for peptide receptors are discussed.

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Sigma-Aldrich
(1S)-(+)-10-樟脑磺酰氯, 97%