Efficient design, synthesis and structure–activity relationship studies of 1-(3′-substituted propyl)-4-arylpiperidines as non-peptide antagonists of nociceptin/orphanin FQ receptor: biological activities, metabolic stabilities and hERG channel bindings期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Efficient design, synthesis and structure–activity relationship studies of 1-(3′-substituted propyl)-4-arylpiperidines as non-peptide antagonists of nociceptin/orphanin FQ receptor: biological activities, metabolic stabilities and hERG channel bindings

Authors:	Shigeo Hayashi Katsuyo Ohashi Eriko Nakata Chie Emoto

Institution:	1. Nagoya Laboratories, Pfizer Global Research & Development, Pfizer Japan Inc., 5-2 Taketoyo, Aichi, 470-2393, Japan

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