PF-06767832 | 1859081-58-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: PF-06767832
• 英文别名: N-[(3R,4S)-3-hydroxyoxan-4-yl]-5-methyl-4-[[4-(1,3-thiazol-4-yl)phenyl]methyl]pyridine-2-carboxamide
• CAS: 1859081-58-5
• 化学式: C₂₂H₂₃N₃O₃S
• 分子量: 409.509
• InChiKey: VVZZHFMLRHJXTO-RXVVDRJESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  113
• 氢给体数：
  2
• 氢受体数：
  6

安全信息

• WGK Germany：
  3

反应信息

• 作为反应物：
  描述：

  PF-06767832 在 还原型辅酶II(NADPH)四钠盐 、 magnesium chloride 作用下， 以 aq. phosphate buffer 为溶剂， 反应 1.0h， 生成 N-[(3R,4S)-2,3-dihydroxyoxan-4-yl]-5-methyl-4-[[4-(1,3-thiazol-4-yl)phenyl]methyl]pyridine-2-carboxamide
  参考文献：
  名称：

  Harnessing biosynthesis and quantitative NMR for late stage functionalization of lead molecules: Application to the M1 positive allosteric modulator (PAM) program

  摘要：

  A facile method for late stage diversification of lead molecules for the M1 PAM program using biosynthesis is described. Liver microsomes from several species are screened to identify a high turnover system. Subsequent incubations using less than 1 mg of substrate generate nanomole quantities of drug metabolites that are purified, characterized by microcryoprobe NMR spectroscopy, and quantified to known concentrations to enable rapid biology testing. The late-stage diversification of lead compounds provides rapid SAR feedback to the medicinal chemistry design cycle. (C) 2018 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2018.04.054

文献信息

• [EN] PYRIDINE DERIVATIVES AS MUSCARINIC M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS<br/>[FR] DÉRIVÉS DE LA PYRIDINE EN TANT QUE MODULATEURS ALLOSTÉRIQUES POSITIFS DU RÉCEPTEUR M1 MUSCARINIQUE
  申请人：PFIZER

  公开号：WO2016009297A1

  公开（公告）日：2016-01-21

  The present invention provides, in part, compounds of Formula I: (I) N-oxides thereof, and pharmaceutically acceptable salts of the compounds or N-oxides; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds,N-oxides, or salts, and their uses for treating M1-mediated (or M1-associated) disorders including, e.g., Alzheimer's disease, schizophrenia (e.g., its cognitive and negative symptoms), pain, addiction, and a sleep disorder.

  本发明部分提供了以下化合物的公式I：（I）其N-氧化物，以及该化合物或N-氧化物的药用盐；用于制备的工艺；用于制备的中间体；以及含有这些化合物、N-氧化物或盐的组合物，以及它们用于治疗M1介导（或与M1相关）疾病的用途，例如阿尔茨海默病、精神分裂症（例如其认知和消极症状）、疼痛、成瘾和睡眠障碍。
• PYRIDINE DERIVATIVES AS MUSCARINIC M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
  申请人：PFIZER INC.

  公开号：US20160016907A1

  公开（公告）日：2016-01-21

  The present invention provides, in part, compounds of Formula I: N-oxides thereof, and pharmaceutically acceptable salts of the compounds or N-oxides; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds, N-oxides, or salts, and their uses for treating M1-mediated (or M1-associated) disorders including, e.g., Alzheimer's disease, schizophrenia (e.g., its cognitive and negative symptoms), pain, addiction, and a sleep disorder.

  本发明提供了部分式I的化合物，其N-氧化物以及该化合物或N-氧化物的药学上可接受的盐；制备过程；制备中使用的中间体；以及含有这样的化合物、N-氧化物或盐的组合物，以及它们用于治疗M1介导（或M1相关）疾病，包括例如阿尔茨海默病，精神分裂症（例如其认知和消极症状），疼痛，成瘾和睡眠障碍。