3-[2-methyl-4-({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methoxy)phenyl]propanoic acid

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 苯丙酸
• 英文名称: 3-[2-methyl-4-({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methoxy)phenyl]propanoic acid
• 英文别名: 3-{2-Methyl-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-phenyl}-propionic acid；3-[2-methyl-4-[[4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methoxy]phenyl]propanoic acid
• 化学式: C₂₂H₂₀F₃NO₃S
• 分子量: 435.467
• InChiKey: RSLROHSQFVXOLQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  30
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  87.7
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  4-(三氟甲基)硫代苯甲酰胺 在 lithium hydroxide 、 lithium aluminium tetrahydride 、 caesium carbonate 、 甲基磺酰氯 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 16.0h， 生成 3-[2-methyl-4-({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methoxy)phenyl]propanoic acid
  参考文献：
  名称：

  Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ)—synthesis and biological activity

  摘要：

  We report the synthesis and biological activity of a new series of small molecule agonists of the human Peroxisome Proliferator-Activated Receptor delta (PPARdelta). Several hits were identified from our original libraries containing lipophilic carboxylic acids. Optimization of these hits by structure-guided design led to 7k (GW501516) and 71 (GW0742), which shows an EC50 Of 1.1 nM against PPARdelta with 1000-fold selectivity over the other human subtypes. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00207-5

文献信息

• Activator of PPAR delta
  申请人：——

  公开号：US20030203947A1

  公开（公告）日：2003-10-30

  Compounds of Formula (I) are disclosed. These compounds include selective activators of human PPAR delta.

  公式（I）的化合物已被披露。这些化合物包括人类PPAR delta的选择性激活剂。
• [EN] THIAZOLE AND OXAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE<br/>[FR] DERIVES DE THIAZOL ET D'OXAZOLE ET UTILISATION PHARMACEUTIQUE DE CEUX-CI
  申请人：GLAXO GROUP LTD

  公开号：WO2001000603A1

  公开（公告）日：2001-01-04

  Compounds of Formula (I) are disclosed. These compounds include selective activators of human PPAR delta.

  本发明公开了化学式(I)的化合物。这些化合物包括选择性激活人类PPAR delta的激动剂。
• ACTIVATING AGENT FOR PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR DELTA
  申请人：Sakuma Shogo

  公开号：US20090298896A1

  公开（公告）日：2009-12-03

  A compound represented by the following general formula (II) or a salt thereof is used as an activator of PPARδ. wherein G a is O, CH 2 or the like; A a is thiazole, oxazole, or thiophene, which can have a substituent such as C 1-8 alkyl, C 1-8 alkoxy, halogen, C 1-8 alkyl substituted with halogen or the like; B a is a C 1-8 alkylene or C 2-8 alkenylene chain; and each of R 1a and R 2a independently is hydrogen, C 1-8 alkyl, C 1-8 alkoxy, halogen, C 1-8 alkyl substituted with halogen or the like.

  以下通式（II）所代表的化合物或其盐被用作PPARδ的激活剂。其中G是O，CH2或类似物；A是噻唑、噁唑或噻吩，可以具有C1-8烷基、C1-8烷氧基、卤素、C1-8卤代烷基或类似物的取代基；B是C1-8烷基或C2-8烯基烷链；R1a和R2a各自独立地是氢、C1-8烷基、C1-8烷氧基、卤素、C1-8卤代烷基或类似物。
• ACTIVATING AGENT FOR PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR
  申请人：Nippon Chemiphar Co., Ltd.

  公开号：EP2014652A1

  公开（公告）日：2009-01-14

  A compound represented by the following general formula (II) or a salt thereof is used as an activator of PPARδ. wherein Ga is O, CH2 or the like; Aa is thiazole, oxazole, or thiophene, which can have a substituent such as C1-8 alkyl, C1-8 alkoxy, halogen, C1-8 alkyl substituted with halogen or the like; Ba is a C1-8 alkylene or C2-8 alkenylene chain; and each of R1a and R2a independently is hydrogen, C1-8 alkyl, C1-8 alkoxy, halogen, C1-8 alkyl substituted with halogen or the like.

  以下通式 (II) 所代表的化合物或其盐可用作 PPARδ 的激活剂。 其中 Ga 是 O、CH2 或类似物； Aa 是噻唑、噁唑或噻吩，可具有取代基，如 C1-8 烷基、C1-8 烷氧基、卤素、被卤素取代的 C1-8 烷基或类似物； Ba 是 C1-8 烯链或 C2-8 烯链；以及 R1a 和 R2a 各自独立地为氢、C1-8 烷基、C1-8 烷氧基、卤素、被卤素取代的 C1-8 烷基或类似基团。
• Compositions and methods for promoting intestinal stem cell and/or non-stem progenitor cell function
  申请人：Whitehead Institute for Biomedical Research

  公开号：US10426757B2

  公开（公告）日：2019-10-01

  Disclosed herein are novel methods and compositions useful for promoting intestinal stem cell function. The methods and compositions are particularly useful for stimulating the proliferation of and/or self-renewal of intestinal stem cells, as well as for minimizing, preventing, or ameliorating cellular damage resulting from incidental or accidental exposure to radiation (e.g., cancer radiation therapy).

  本文公开了有助于促进肠道干细胞功能的新型方法和组合物。这些方法和组合物特别适用于刺激肠道干细胞的增殖和/或自我更新，以及最大限度地减少、预防或改善因偶然或意外暴露于辐射（如癌症放射治疗）而造成的细胞损伤。