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4-(2,2-dimethyl-1-oxopropyl)-N-(2-propenyloxy)benzamide | 157465-48-0

中文名称
——
中文别名
——
英文名称
4-(2,2-dimethyl-1-oxopropyl)-N-(2-propenyloxy)benzamide
英文别名
4-(2,2-dimethylpropanoyl)-N-prop-2-enoxybenzamide
4-(2,2-dimethyl-1-oxopropyl)-N-(2-propenyloxy)benzamide化学式
CAS
157465-48-0
化学式
C15H19NO3
mdl
——
分子量
261.321
InChiKey
MYSHCWODYAWQSA-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    19
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(2,2-dimethyl-1-oxopropyl)-N-(2-propenyloxy)benzamide四氧化锇 、 m-bisulfite 、 potassium hydride 、 N-甲基吗啉氧化物 作用下, 反应 0.5h, 生成 4-(2,2-dimethyl-1-oxopropyl)benzoic acid anhydride with N-(2,3-dihydroxypropoxy)-4-(2,2-dimethyl-1-oxopropyl)benzenecarboximidic acid
    参考文献:
    名称:
    Hypoglycemic Prodrugs of 4-(2,2-Dimethyl-1-oxopropyl)benzoic Acid
    摘要:
    SAH 51-641 (1) is a potent hypoglycemic agent, which acts by inhibiting hepatic gluconeogenesis. It is a prodrug of 4-(2,2-dimethyl-1-oxopropyl)benzoic acid (2) and 4-(2,2-dimethyl-1-hydroxy propyl)benzoic acid (3), which sequester coenzyme A (CoA) in the mitochondria, and inhibits medium-chain acyltransferase. 1-3 and 4-tert-butylbenzoic acid all cause testicular degeneration in rats at pharmacologically active doses. 14b (FOX 988) is a prodrug of 3, which is metabolized in the liver at a rate sufficient enough to have hypoglycemic potency (an ED50 of 65 mu mol/kg, 28 mg/kg/day, for glucose lowering), yet by avoiding significant escape of the metabolite 3 to the systemic circulation, it avoids the testicular toxicity at doses up to 1500 mu mol/kg/day. 14b was selected for clinical studies.
    DOI:
    10.1021/jm980438y
  • 作为产物:
    参考文献:
    名称:
    Hypoglycemic Prodrugs of 4-(2,2-Dimethyl-1-oxopropyl)benzoic Acid
    摘要:
    SAH 51-641 (1) is a potent hypoglycemic agent, which acts by inhibiting hepatic gluconeogenesis. It is a prodrug of 4-(2,2-dimethyl-1-oxopropyl)benzoic acid (2) and 4-(2,2-dimethyl-1-hydroxy propyl)benzoic acid (3), which sequester coenzyme A (CoA) in the mitochondria, and inhibits medium-chain acyltransferase. 1-3 and 4-tert-butylbenzoic acid all cause testicular degeneration in rats at pharmacologically active doses. 14b (FOX 988) is a prodrug of 3, which is metabolized in the liver at a rate sufficient enough to have hypoglycemic potency (an ED50 of 65 mu mol/kg, 28 mg/kg/day, for glucose lowering), yet by avoiding significant escape of the metabolite 3 to the systemic circulation, it avoids the testicular toxicity at doses up to 1500 mu mol/kg/day. 14b was selected for clinical studies.
    DOI:
    10.1021/jm980438y
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文献信息

  • US5319123A
    申请人:——
    公开号:US5319123A
    公开(公告)日:1994-06-07
  • Hypoglycemic Prodrugs of 4-(2,2-Dimethyl-1-oxopropyl)benzoic Acid
    作者:Thomas D. Aicher、Gregory R. Bebernitz、Philip A. Bell、Leonard J. Brand、Jeremy G. Dain、Rhonda Deems、William S. Fillers、James E. Foley、Douglas C. Knorr、Jeffrey Nadelson、Dario A. Otero、Ronald Simpson、Robert J. Strohschein、Douglas A. Young
    DOI:10.1021/jm980438y
    日期:1999.1.1
    SAH 51-641 (1) is a potent hypoglycemic agent, which acts by inhibiting hepatic gluconeogenesis. It is a prodrug of 4-(2,2-dimethyl-1-oxopropyl)benzoic acid (2) and 4-(2,2-dimethyl-1-hydroxy propyl)benzoic acid (3), which sequester coenzyme A (CoA) in the mitochondria, and inhibits medium-chain acyltransferase. 1-3 and 4-tert-butylbenzoic acid all cause testicular degeneration in rats at pharmacologically active doses. 14b (FOX 988) is a prodrug of 3, which is metabolized in the liver at a rate sufficient enough to have hypoglycemic potency (an ED50 of 65 mu mol/kg, 28 mg/kg/day, for glucose lowering), yet by avoiding significant escape of the metabolite 3 to the systemic circulation, it avoids the testicular toxicity at doses up to 1500 mu mol/kg/day. 14b was selected for clinical studies.
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