5-(3-chloro-4-(2-cyclohexylethoxy)benzyl)thiazolidine-2,4-dione | 1234322-90-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 5-(3-chloro-4-(2-cyclohexylethoxy)benzyl)thiazolidine-2,4-dione
• 英文别名: 5-[[3-chloro-4-(2-cyclohexylethoxy)phenyl]methyl]-1,3-thiazolidine-2,4-dione
• CAS: 1234322-90-7
• 化学式: C₁₈H₂₂ClNO₃S
• 分子量: 367.897
• InChiKey: LXRMEKYGJPHJTB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  24
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  80.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  5-[3-chloro-4-(2-cyclohexylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione 在 cobalt(II) chloride hexahydrate sodium tetrahydroborate 、 水 、 二甲基乙二醛肟 、 sodium hydroxide 、 溶剂黄146 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以79%的产率得到5-(3-chloro-4-(2-cyclohexylethoxy)benzyl)thiazolidine-2,4-dione
  参考文献：
  名称：

  NOVEL THIAZOLIDINEDIONE DERIVATIVE AND USE THEREOF

  摘要：

  本发明涉及由以下式（I）表示的新型噻唑烷二酮衍生物及其用途。更具体地说，本发明涉及由以下式（I）表示的新型噻唑烷二酮衍生物以及包含其的药物组合物。根据本发明的式（I）的新型噻唑烷二酮衍生物可以通过抑制分解前列腺素的15-羟基前列腺素脱氢酶（15-PGDH）的活性，有效用于预防或治疗心血管疾病、胃肠道疾病和肾脏疾病，同时也用于预防脱发和促进头发生长，以及促进骨生成和伤口愈合。

  公开号：

  US20110269954A1

文献信息

• [EN] METHODS OF REJUVENATING AGED TISSUE BY INHIBITING 15-HYDROXYPROSTAGLANDIN DEHYDROGENASE (15-PGDH)<br/>[FR] MÉTHODES DE RAJEUNISSEMENT DE TISSUS ÂGÉS PAR L'INHIBITION DE LA 15-HYDROXYPROSTAGLANDINE DÉSHYDROGÉNASE (15-PGDH)
  申请人：UNIV LELAND STANFORD JUNIOR

  公开号：WO2020252146A1

  公开（公告）日：2020-12-17

  The present disclosure provides compositions and methods based on the identification of 15-hydroxyprostaglandin dehydrogenase (15-PGDH) as a therapeutic target in aging, dystrophic muscle to improve muscle atrophy, increase muscle mass, function and strength. Further provided herein are compositions and methods for the rejuvenation of aged tissue. In particular, 15-PGDH inhibitors, such as SW033291, are used to elevate the levels of prostaglandin E2 (PGE2) in the muscle or tissue.

  本公开提供了基于将15-羟基前列腺素脱氢酶（15-PGDH）识别为老化、营养不良肌肉中的治疗靶点的组合物和方法，以改善肌肉萎缩，增加肌肉质量、功能和力量。此外，还提供了用于恢复老化组织的组合物和方法。具体而言，使用15-PGDH抑制剂，如SW033291，来提高肌肉或组织中前列腺素E2（PGE2）的水平。
• Thiazolidinedione derivative and use thereof
  申请人：Cho Hoon

  公开号：US08637558B2

  公开（公告）日：2014-01-28

  The present invention relates to novel thiazolidinedione derivatives expressed by the following formula (I) and the uses thereof. More specifically, the present invention relates to novel thiazolidinedione derivatives expressed by the following formula (I) and a pharmaceutical composition comprising the same. The novel thiazolidinedione derivatives of formula (I) according to the present invention can be effectively used for the prevention or treatment of cardiovascular disease, gastrointestinal disease and renal disease by inhibiting the activity of 15-hydroxyprostaglandin dehydrogenase (15-PGDH) that decomposes prostaglandins as well as useful for the prevention of hair loss and the stimulation of hair growth, and osteogenic stimulation and wound healing.

  本发明涉及以下式(I)所表示的新型噻唑烷二酮衍生物及其用途。更具体地说，本发明涉及以下式(I)所表示的新型噻唑烷二酮衍生物及其制备的药物组合物。根据本发明的新型噻唑烷二酮衍生物可以有效用于抑制降解前列腺素的15-羟基前列腺素脱氢酶（15-PGDH）的活性，从而预防或治疗心血管疾病、胃肠道疾病和肾脏疾病，并且有助于预防脱发和促进头发生长，以及促进骨生成和伤口愈合。
• METHODS OF REJUVENATING AGED TISSUE BY INHIBITING 15-HYDROXYPROSTAGLANDIN DEHYDROGENASE (15-PGDH)
  申请人：The Board of Trustees of the Leland Stanford Junior University

  公开号：EP3982957A1

  公开（公告）日：2022-04-20
• US8637558B2
  申请人：——

  公开号：US8637558B2

  公开（公告）日：2014-01-28
• [EN] COMPOSITION FOR CONTROLLING HARMFUL ALGAE<br/>[FR] COMPOSITION POUR CONTRÔLER DES ALGUES NUISIBLES
  申请人：IND ACADEMIC COOP

  公开号：WO2010090458A2

  公开（公告）日：2010-08-12

  본 발명은 영양염류로 인한 유해조류의 이상 증식을 방지하기 위한 유해조류 방제용 조성물에 관한 것이다. 보다 구체적으로 본 발명은 하기 화학식 1로 표시되는 화합물 또는 그의 염을 포함하는 유해조류 방제용 조성물에 관한 것이다. 본 발명에 따른 화학식 1의 화합물을 포함하는 조성물은 해양, 하천 또는 강 등에서 녹조 및 적조와 같은 조류의 이상 증식을 유발하는 녹조류, 남조류, 규조류, 유글레노이드류, 편모조류 및 황녹색조류의 생장 및 증식을 억제하는 살조 효과가 우수하므로 녹조 및 적조 피해를 예방하고 수질오염을 방지하는데 매우 유용하게 사용될 수 있다.