1-(2-Chlorophenyl)-3-pyridin-3-yl-4,5-dihydropyrazolo[4,3-g][1,3]benzothiazol-7-amine | 883865-08-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 1-(2-Chlorophenyl)-3-pyridin-3-yl-4,5-dihydropyrazolo[4,3-g][1,3]benzothiazol-7-amine
• CAS: 883865-08-5
• 化学式: C₁₉H₁₄ClN₅S
• 分子量: 379.873
• InChiKey: RDMPRKXBPKIVTH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  26
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  97.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  o-isopentyloxyphenyl isocyanate 、 1-(2-Chlorophenyl)-3-pyridin-3-yl-4,5-dihydropyrazolo[4,3-g][1,3]benzothiazol-7-amine 以 N,N-二甲基甲酰胺 为溶剂， 以7.7%的产率得到1-[1-(2-Chlorophenyl)-3-pyridin-3-yl-4,5-dihydropyrazolo[4,3-g][1,3]benzothiazol-7-yl]-3-[2-(3-methylbutoxy)phenyl]urea
  参考文献：
  名称：

  EP2426135

  摘要：

  公开号：
• 作为产物：
  描述：

  N-[1-(2-chloro-phenyl)-3-pyridin-3-yl-4,5-dihydro-1H-pyrazolo[3',4':3,4]benzo[1,2-d]thiazol-7-yl]-acetamide 在 盐酸 、 水 、 sodium hydroxide 作用下， 以16%的产率得到1-(2-Chlorophenyl)-3-pyridin-3-yl-4,5-dihydropyrazolo[4,3-g][1,3]benzothiazol-7-amine
  参考文献：
  名称：

  EP2426135

  摘要：

  公开号：

文献信息

• Thiazolyl-dihydro-indazole
  申请人：Betzemeier Bodo

  公开号：US20060100254A1

  公开（公告）日：2006-05-11

  The present invention encompasses compounds of the general formula (1) in which R 1 to R 3 are defined as in Claim 1, which are suitable for treating diseases which are characterized by excessive or anomalous cell proliferation, and their use for producing a pharmaceutical having the abovementioned properties.

  本发明涵盖一般式（1）中定义如权利要求1中的R1至R3的化合物，这些化合物适用于治疗由过度或异常细胞增殖特征的疾病，并且它们用于制造具有上述特性的药物。
• THIAZOLYL-DIHYDRO-INDAZOLES
  申请人：BETZEMEIER Bodo

  公开号：US20100113414A1

  公开（公告）日：2010-05-06

  The present invention encompasses compounds of the general formula (1) in which R 1 to R 3 are defined as in claim 1 , which are suitable for treating diseases which are characterized by excessive or anomalous cell proliferation, and their use for producing a pharmaceutical having the abovementioned properties.

  本发明涵盖了通式（1）中定义如权利要求1中的R1至R3的化合物，适用于治疗以过度或异常细胞增殖为特征的疾病，并且它们的用途用于制备具有上述特性的药物。
• UREA DERIVATIVE HAVING PI3K INHIBITORY ACTIVITY
  申请人：Shionogi & Co., Ltd.

  公开号：EP2426135A1

  公开（公告）日：2012-03-07

  Provided is a compound or a pharmaceutically acceptable salt thereof which inhibits the activity of PI3K to regulate many biological processes including the growth, differentiation, survival, proliferation, migration, metabolism, and the like of cells and is therefore useful for the prophylaxis/therapy of diseases including inflammatory diseases, arteriosclerosis, vascular/circulatory diseases, cancer/tumors, immune system diseases, cell proliferative diseases, infectious diseases, and the like. The above problem was solved by providing a urea derivative shown in the present specification, or a pharmaceutically acceptable salt thereof.

  本发明提供了一种化合物或其药学上可接受的盐，可抑制 PI3K 的活性，从而调节许多生物过程，包括细胞的生长、分化、存活、增殖、迁移、新陈代谢等，因此可用于疾病的预防/治疗，包括炎症性疾病、动脉硬化、血管/循环系统疾病、癌症/肿瘤、免疫系统疾病、细胞增殖性疾病、传染性疾病等。通过提供本说明书所示的脲衍生物或其药学上可接受的盐，上述问题得以解决。
• UREA DERIVATIVES HAVING PI3K-INHIBITING ACTIVITY
  申请人：Taniyama Daisuke

  公开号：US20120071475A1

  公开（公告）日：2012-03-22

  Provided is a compound or a pharmaceutically acceptable salt thereof which inhibits the activity of PI3K to regulate many biological processes including the growth, differentiation, survival, proliferation, migration, metabolism, and the like of cells and is therefore useful for the prophylaxis/therapy of diseases including inflammatory diseases, arteriosclerosis, vascular/circulatory diseases, cancer/tumors, immune system diseases, cell proliferative diseases, infectious diseases, and the like. The above problem was solved by providing a urea derivative shown in the present specification, or a pharmaceutically acceptable salt thereof.
• US7691888B2
  申请人：——

  公开号：US7691888B2

  公开（公告）日：2010-04-06