Tert-butyl 4-[(4-chlorophenyl)methyl-[(5-nitrothiophen-2-yl)methyl]amino]piperidine-1-carboxylate | 1384516-26-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: Tert-butyl 4-[(4-chlorophenyl)methyl-[(5-nitrothiophen-2-yl)methyl]amino]piperidine-1-carboxylate
• CAS: 1384516-26-0
• 化学式: C₂₂H₂₈ClN₃O₄S
• 分子量: 466.001
• InChiKey: VJALLRWRAIRMTL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  31
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  107
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  5-硝基噻吩-2-甲醛 在 三乙酰氧基硼氢化钠 、 溶剂黄146 作用下， 以 1,2-二氯乙烷 为溶剂， 生成 Tert-butyl 4-[(4-chlorophenyl)methyl-[(5-nitrothiophen-2-yl)methyl]amino]piperidine-1-carboxylate
  参考文献：
  名称：

  Small molecule tertiary amines as agonists of the nuclear hormone receptor Rev-erbα

  摘要：

  The structure-activity relationship study of a small molecule Rev-erb alpha agonist is reported. The potency and efficacy of the agonists in a cell-based assay were optimized as compared to the initial lead. Modest mouse pharmacokinetics coupled with an improved in vitro profile make 12e a suitable in vivo probe to interrogate the functions of Rev-erba in animal models of disease (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.04.126

文献信息

• Small molecule tertiary amines as agonists of the nuclear hormone receptor Rev-erbα
  作者：Youseung Shin、Romain Noel、Subhashis Banerjee、Douglas Kojetin、Xinyi Song、Yuanjun He、Li Lin、Michael D. Cameron、Thomas P. Burris、Theodore M. Kamenecka

  DOI：10.1016/j.bmcl.2012.04.126

  日期：2012.7

  The structure-activity relationship study of a small molecule Rev-erb alpha agonist is reported. The potency and efficacy of the agonists in a cell-based assay were optimized as compared to the initial lead. Modest mouse pharmacokinetics coupled with an improved in vitro profile make 12e a suitable in vivo probe to interrogate the functions of Rev-erba in animal models of disease (C) 2012 Elsevier Ltd. All rights reserved.