| 1265624-82-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• CAS: 1265624-82-5
• 化学式: C₂₇H₃₃F₃N₂O₄S
• 分子量: 538.631
• InChiKey: KVTMYUXPWDQIDC-RNXOBYDBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.49
• 重原子数：
  37.0
• 可旋转键数：
  8.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.52
• 拓扑面积：
  86.71
• 氢给体数：
  2.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  、 甲基磺酰氯 在 三乙胺 作用下， 以75%的产率得到
  参考文献：
  名称：

  Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors

  摘要：

  The synthesis and SAR of a series of 4,4-disubstituted cyclohexylbenzamide inhibitors of 11 beta-HSD1 are described. Optimization rapidly led to potent, highly selective, and orally bioavailable inhibitors demonstrating efficacy in both rat and non-human primate ex vivo pharmacodynamic models. (c) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.10.129

文献信息

• Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
  作者：Daqing Sun、Zhulun Wang、Seb Caille、Michael DeGraffenreid、Felix Gonzalez-Lopez de Turiso、Randall Hungate、Juan C. Jaen、Ben Jiang、Lisa D. Julian、Ron Kelly、Dustin L. McMinn、Jacob Kaizerman、Yosup Rew、Athena Sudom、Hua Tu、Stefania Ursu、Nigel Walker、Maren Willcockson、Xuelei Yan、Qiuping Ye、Jay P. Powers

  DOI：10.1016/j.bmcl.2010.10.129

  日期：2011.1

  The synthesis and SAR of a series of 4,4-disubstituted cyclohexylbenzamide inhibitors of 11 beta-HSD1 are described. Optimization rapidly led to potent, highly selective, and orally bioavailable inhibitors demonstrating efficacy in both rat and non-human primate ex vivo pharmacodynamic models. (c) 2010 Elsevier Ltd. All rights reserved.