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Nonpeptide oxytocin antagonists: potent, orally bioavailable analogs of L-371,257 containing a 1-R-(pyridyl)ethyl ether terminus.
Kuo, M S; Bock, M G; Freidinger, R M; Guidotti, M T; Lis, E V; Pawluczyk, J M; Perlow, D S; Pettibone, D J; Quigley, A G; Reiss, D R; Williams, P D; Woyden, C J.
Afiliação
  • Kuo MS; Department of Medicinal Chemistry, Merck Research Laboratories, West Point, PA 19486, USA.
Bioorg Med Chem Lett ; 8(21): 3081-6, 1998 Nov 03.
Article em En | MEDLINE | ID: mdl-9873680
Structure-activity studies on the oxytocin antagonist 1 (L-371,257) have identified a new series of high affinity, receptor-selective OT antagonists in which the N-acetyl-4-piperidinyl ether terminus in 1 has been replaced with a 1-(aryl)ethoxy group.
Assuntos
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Base de dados: MEDLINE Assunto principal: Oxazinas / Piperidinas / Ocitocina Limite: Animals / Female / Humans Idioma: En Ano de publicação: 1998 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Oxazinas / Piperidinas / Ocitocina Limite: Animals / Female / Humans Idioma: En Ano de publicação: 1998 Tipo de documento: Article