ethyl hydrogen (4R)-4-(2-phenylethyl)glutarate | 82924-27-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: ethyl hydrogen (4R)-4-(2-phenylethyl)glutarate
• 英文别名: (4R)-4-ethoxycarbonyl-6-phenylhexanoic acid
• CAS: 82924-27-4
• 化学式: C₁₅H₂₀O₄
• 分子量: 264.321
• InChiKey: FLQCJPXCMAFVCK-CYBMUJFWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  19
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  63.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  ethyl hydrogen (4R)-4-(2-phenylethyl)glutarate 在 吡啶 、 草酰氯 作用下， 反应 3.0h， 生成 1-(4-carboethoxy-4R-phenethylbutanoyl)-indoline-2S-carboxylic acid
  参考文献：
  名称：

  Angiotensin converting enzyme inhibitors: 1-glutarylindoline-2-carboxylic acid derivatives

  摘要：

  The preparation of a series of 1-glutarylindoline-2(S)-carboxylic acid derivatives, 6a-v and 21a-c, is described. The above compounds were tested for inhibition of angiotensin converting enzyme. The structure-activity relationship of the series is also discussed. Compound 6u, the most potent member of the series, had an in vitro IC50 of 4.8 X 10(-9) M. Compound 6v, an ethyl ester of 6u, lowered blood pressure 70 mm in spontaneous hypertensive rats at an oral dose of 30 mg/kg.

  DOI：

  10.1021/jm00363a012
• 作为产物：
  描述：

  ethyl 2R-allyl-4phenyl-butyrate 生成 ethyl hydrogen (4R)-4-(2-phenylethyl)glutarate
  参考文献：
  名称：

  Angiotensin converting enzyme inhibitors: 1-glutarylindoline-2-carboxylic acid derivatives

  摘要：

  The preparation of a series of 1-glutarylindoline-2(S)-carboxylic acid derivatives, 6a-v and 21a-c, is described. The above compounds were tested for inhibition of angiotensin converting enzyme. The structure-activity relationship of the series is also discussed. Compound 6u, the most potent member of the series, had an in vitro IC50 of 4.8 X 10(-9) M. Compound 6v, an ethyl ester of 6u, lowered blood pressure 70 mm in spontaneous hypertensive rats at an oral dose of 30 mg/kg.

  DOI：

  10.1021/jm00363a012

文献信息

• 1-CARBOXYALKANOYLPERHYDROINDOLE-2-CARBOXYLIC ACIDS AND DERIVATIVES
  申请人：CIBA-GEIGY AG

  公开号：EP0105919A1

  公开（公告）日：1984-04-25
• US4479963A
  申请人：——

  公开号：US4479963A

  公开（公告）日：1984-10-30
• [EN] 1-CARBOXYALKANOYLPERHYDROINDOLE-2-CARBOXYLIC ACIDS AND DERIVATIVES
  申请人：CIBA-GEIGY AG

  公开号：WO1983003828A1

  公开（公告）日：1983-11-10

  (EN) The perhydrindoles of formula I, wherein R4 represents hydrogen or lower alkyl; R5 represents lower alkyl; or R5 represents lower alkyl substituted by optionally substituted phenyl; t is 0 or 1; esters, amides and salts thereof, are useful as antihypertensive and cardioactive agents.(FR) Perhydroindols correspondant à la formule (I), où R4 représente de l'hydrogène ou un alkyle inférieur; R5 représente un alkyle inférieur ou R5 représente un alkyle inférieur substitué par un phényle facultativement substitué; t vaut 0 ou 1. Ces composés, ainsi que leurs esters, leurs amides et leurs sels, sont utiles en tant qu'agents antihypertensifs et cardio-actifs.
• Angiotensin converting enzyme inhibitors: 1-glutarylindoline-2-carboxylic acid derivatives
  作者：Norbert Gruenfeld、James L. Stanton、Andrew M. Yuan、Frank H. Ebetino、Leslie J. Browne、Candido Gude、Charles F. Huebner

  DOI：10.1021/jm00363a012

  日期：1983.9

  The preparation of a series of 1-glutarylindoline-2(S)-carboxylic acid derivatives, 6a-v and 21a-c, is described. The above compounds were tested for inhibition of angiotensin converting enzyme. The structure-activity relationship of the series is also discussed. Compound 6u, the most potent member of the series, had an in vitro IC50 of 4.8 X 10(-9) M. Compound 6v, an ethyl ester of 6u, lowered blood pressure 70 mm in spontaneous hypertensive rats at an oral dose of 30 mg/kg.