4-oxo-4-phenyl-N-m-tolyl-butyramide | 36775-82-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-oxo-4-phenyl-N-m-tolyl-butyramide
• 英文别名: N-(3-methylphenyl)-4-oxo-4-phenylbutanamide
• CAS: 36775-82-3
• 化学式: C₁₇H₁₇NO₂
• 分子量: 267.327
• InChiKey: LTMMPGSTYVLYMK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  46.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-oxo-4-phenyl-N-m-tolyl-butyramide 在 五氯化磷 、 叠氮基三甲基硅烷 作用下， 以 二氯甲烷 为溶剂， 反应 0.25h， 生成 1-phenyl-3-(1-m-tolyl-1H-tetrazol-5-yl)-propan-1-one
  参考文献：
  名称：

  WO2007/29021

  摘要：

  公开号：
• 作为产物：
  描述：

  3-甲基苯胺 、 3-苯丙烯溴酸酯 在 N,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下， 以 二氯甲烷 为溶剂， 反应 0.33h， 生成 4-oxo-4-phenyl-N-m-tolyl-butyramide
  参考文献：
  名称：

  Modulation of 11β-hydroxysteroid dehydrogenase type 1 activity by 1,5-substituted 1H-tetrazoles

  摘要：

  Inhibitors of 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD1) show promise as drugs to treat metabolic disease and CNS disorders such as cognitive impairment. A series of 1,5-substituted 1H-tetrazole 11 beta-HSD1 inhibitors has been discovered and chemically modified. Compounds are selective for 11 beta-HSD1 over 11 beta-HSD2 and possess good cellular potency in human and murine 11 beta-HSD1 assays. A range of in vitro stabilities are observed in human liver microsome assays. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.04.055

文献信息

• WO2007/29021
  申请人：——

  公开号：——

  公开（公告）日：——
• [EN] 1,5-SUBSTITUTED TETRAZOLES AS THERAPEUTIC COMPOUNDS<br/>[FR] TETRAZOLES 1,5-SUBSTITUÉS EN TANT QUE COMPOSÉS THÉRAPEUTIQUES
  申请人：UNIV EDINBURGH

  公开号：WO2007029021A1

  公开（公告）日：2007-03-15

  [EN] The present invention pertains to certain 1,5-substituted-1H-tetrazole compounds that, inter alia, inhibit 11ß- hydroxysteroid dehydrogenase type 1 (11ß-HSD1). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, bothin vitro and in vivo, to inhibit 11ß-hydroxysteroid dehydrogenase type 1; to treat conditions that are ameliorated by the inhibition of 11ß-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes conditions such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS conditions such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.
  [FR] La présente invention concerne certains composés 1H-tétrazole 1,5 substitués qui, notamment, inhibent la 11ß-hydroxystéroïde déshydrogénase de type 1(11ß-HSD1). Cette invention concerne également des compositions pharmaceutiques comprenant ces composés et l'utilisation de ces composés et compositions, tant in vitro qu'in vivo, afin d'inhiber la 11ß-hydroxystéroïde déshydrogénase de type 1; afin de traiter des pathologies atténuées par l'inhibition de la 11ß-hydroxystéroïde déshydrogénase de type 1; afin de traiter le syndrome métabolique, qui inclut des affections telles que le diabète de type 2 et l'obésité, ainsi que des pathologies associées, notamment l'insulinorésistance, l'hypertension, les troubles lipidiques et les pathologies cardiovasculaires telles que les maladies cardiaques ischémiques (coronariennes) ; afin de traiter des affections du SNC telles que le déficit cognitif léger et la démence précoce, y compris la maladie d'Alzheimer; etc.
• Modulation of 11β-hydroxysteroid dehydrogenase type 1 activity by 1,5-substituted 1H-tetrazoles
  作者：Scott P. Webster、Margaret Binnie、Kirsty M.M. McConnell、Karen Sooy、Peter Ward、Michael F. Greaney、Andy Vinter、T. David Pallin、Hazel J. Dyke、Matthew I.A. Gill、Ines Warner、Jonathan R. Seckl、Brian R. Walker

  DOI：10.1016/j.bmcl.2010.04.055

  日期：2010.6

  Inhibitors of 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD1) show promise as drugs to treat metabolic disease and CNS disorders such as cognitive impairment. A series of 1,5-substituted 1H-tetrazole 11 beta-HSD1 inhibitors has been discovered and chemically modified. Compounds are selective for 11 beta-HSD1 over 11 beta-HSD2 and possess good cellular potency in human and murine 11 beta-HSD1 assays. A range of in vitro stabilities are observed in human liver microsome assays. (C) 2010 Elsevier Ltd. All rights reserved.