(+)-Mebudipine | 1226774-08-8

• 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: (+)-Mebudipine
• 英文别名: tert-butyl methyl 4(R)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate；(-)-nebudipine；5-O-tert-butyl 3-O-methyl (4R)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
• CAS: 1226774-08-8
• 化学式: C₂₀H₂₄N₂O₆
• 分子量: 388.42
• InChiKey: YXPRKGBMFPQBDH-QGZVFWFLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  110
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  (+/-)-Mebudipine 在 二氧化碳 作用下， 以 乙醇 为溶剂， 生成 (+)-Mebudipine 、 (-)-Mebudipine
  参考文献：
  名称：

  Stereochemical Requirements for the Mineralocorticoid Receptor Antagonist Activity of Dihydropyridines

  摘要：

  A number of known 1,4-dihydropyridine CCBs were identified as having comparable potency to the steroidal MR antagonist eplerenone. Chiral resolution of mebudipine revealed that MR and CCB activity reside in opposite enantiomers. Small molecule X-ray crystal structures showed that the C4 stereochemistry of optimized selective MR analogues, e.g. 5, is consistent with MR-active mebudipine. Molecular modeling supports a binding pose consistent with that previously proposed for DHP diesters.

  DOI：

  10.1021/jm1002827

文献信息

• Stereochemical Requirements for the Mineralocorticoid Receptor Antagonist Activity of Dihydropyridines
  作者：Graciela B. Arhancet、Scott S. Woodard、Jessica D. Dietz、Danny J. Garland、Grace M. Wagner、Kaliappan Iyanar、Joe T. Collins、James R. Blinn、Randal E. Numann、Xiao Hu、Horng-Chih Huang

  DOI：10.1021/jm1002827

  日期：2010.5.27

  A number of known 1,4-dihydropyridine CCBs were identified as having comparable potency to the steroidal MR antagonist eplerenone. Chiral resolution of mebudipine revealed that MR and CCB activity reside in opposite enantiomers. Small molecule X-ray crystal structures showed that the C4 stereochemistry of optimized selective MR analogues, e.g. 5, is consistent with MR-active mebudipine. Molecular modeling supports a binding pose consistent with that previously proposed for DHP diesters.