1-(2,4-Dimethylbenzenesulfonyl)piperidine-4-carboxylic acid | 757192-81-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(2,4-Dimethylbenzenesulfonyl)piperidine-4-carboxylic acid
• 英文别名: 1-(2,4-dimethylphenyl)sulfonylpiperidine-4-carboxylic acid
• CAS: 757192-81-7
• 化学式: C₁₄H₁₉NO₄S
• mdl: MFCD06340098
• 分子量: 297.375
• InChiKey: HXHCPNPCXHOMLI-UHFFFAOYSA-N

物化性质

• 沸点：
  489.2±55.0 °C(Predicted)
• 密度：
  1.295±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  83.1
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  1-(2,4-Dimethylbenzenesulfonyl)piperidine-4-carboxylic acid 、 3,5-二氯苯胺 在 4-二甲氨基吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 生成 N-(3,5-dichlorophenyl)-1-(2,4-dimethylphenyl)sulfonylpiperidine-4-carboxamide
  参考文献：
  名称：

  Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

  摘要：

  A series of potent amide non-urea inhibitors of soluble epoxide hydrolase (sEH) is disclosed. The inhibition of soluble epoxide hydrolase leads to elevated levels of epoxyeicosatrienoic acids (EETs), and thus inhibitors of sEH represent one of a novel approach to the development of vasodilatory and anti-inflammatory drugs. Structure-activities studies guided optimization of a lead compound, identified through high-throughput screening, gave rise to sub-nanomolar inhibitors of human sEH with stability in human liver microsomal assay suitable for preclinical development. Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2012.11.084
• 作为产物：
  描述：

  4-哌啶甲酸甲酯 在 水 、 三乙胺 、 lithium hydroxide 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 48.0h， 生成 1-(2,4-Dimethylbenzenesulfonyl)piperidine-4-carboxylic acid
  参考文献：
  名称：

  Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors

  摘要：

  A series of potent amide non-urea inhibitors of soluble epoxide hydrolase (sEH) is disclosed. The inhibition of soluble epoxide hydrolase leads to elevated levels of epoxyeicosatrienoic acids (EETs), and thus inhibitors of sEH represent one of a novel approach to the development of vasodilatory and anti-inflammatory drugs. Structure-activities studies guided optimization of a lead compound, identified through high-throughput screening, gave rise to sub-nanomolar inhibitors of human sEH with stability in human liver microsomal assay suitable for preclinical development. Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2012.11.084

文献信息

• [EN] POTENT NON-UREA INHIBITORS OF SOLUBLE EPOXIDE HYDROLASE<br/>[FR] PUISSANTS INHIBITEURS NON-URÉE DE L'ÉPOXYDE-HYDROLASE SOLUBLE
  申请人：UNIV COLUMBIA

  公开号：WO2013112751A1

  公开（公告）日：2013-08-01

  The present invention relates to compounds that exhibit vasodilatory and anti-inflammatory effects by inhibiting the activity of soluble epoxide hydrolase (sEH). The present invention is also directed to methods of identifying such compounds, and use of such compounds for the treatment of diseases related to dysfunction of vasodilation, inflammation, and/or endothelial cells. In particular non-limiting embodiments, components of the invention may be used to treat hypertension.

  本发明涉及通过抑制可溶性环氧化物水解酶（sEH）的活性而表现出扩血管和抗炎作用的化合物。本发明还涉及识别此类化合物的方法，以及利用这些化合物治疗与血管舒张功能障碍、炎症和/或内皮细胞功能障碍相关的疾病的方法。在特定的非限制性实施例中，本发明的组分可用于治疗高血压。
• POTENT NON-UREA INHIBITORS OF SOLUBLE EPOXIDE HYDROLASE
  申请人：The Trustees of Columbia University in the City of New York

  公开号：US20140336193A1

  公开（公告）日：2014-11-13

  The present invention relates to compounds that exhibit vasodilatory and anti-inflammatory effects by inhibiting the activity of soluble epoxide hydrolase (sEH). The present invention is also directed to methods of identifying such compounds, and use of such compounds for the treatment of diseases related to dysfunction of vasodilation, inflammation, and/or endothelial cells. In particular non-limiting embodiments, components of the invention may be used to treat hypertension.
• Synthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors
  作者：Stevan Pecic、Svetlana Pakhomova、Marcia E. Newcomer、Christophe Morisseau、Bruce D. Hammock、Zhengxiang Zhu、Alison Rinderspacher、Shi-Xian Deng

  DOI：10.1016/j.bmcl.2012.11.084

  日期：2013.1

  A series of potent amide non-urea inhibitors of soluble epoxide hydrolase (sEH) is disclosed. The inhibition of soluble epoxide hydrolase leads to elevated levels of epoxyeicosatrienoic acids (EETs), and thus inhibitors of sEH represent one of a novel approach to the development of vasodilatory and anti-inflammatory drugs. Structure-activities studies guided optimization of a lead compound, identified through high-throughput screening, gave rise to sub-nanomolar inhibitors of human sEH with stability in human liver microsomal assay suitable for preclinical development. Published by Elsevier Ltd.