N-(4-{2-[(5-isopropyl-1,3-thiazol-2-yl)amino]-1-methyl-2-oxoethyl}phenyl)nicotinamide | 492445-44-0

• 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: N-(4-{2-[(5-isopropyl-1,3-thiazol-2-yl)amino]-1-methyl-2-oxoethyl}phenyl)nicotinamide
• 英文别名: N-[4-[1-oxo-1-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]propan-2-yl]phenyl]pyridine-3-carboxamide
• CAS: 492445-44-0
• 化学式: C₂₁H₂₂N₄O₂S
• 分子量: 394.497
• InChiKey: YYFRUJBCSFDVJP-UHFFFAOYSA-N

物化性质

• 密度：
  1.291±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  112
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• Phenylacetamido-thiazole derivatives, process for the preparation and their use as antitumor agents
  申请人：——

  公开号：US20040235919A1

  公开（公告）日：2004-11-25

  Compounds represented by formula (I), as defined in the description, wherein R is a hydrogen atom or a methyl group and R1 is a group as defined in the specification, or a pharmaceutically acceptable salt thereof, are disclosed; the said compounds are useful in the treatment of cell proliferative disorders, e.g. cancer, associated with an altered cell cycle dependent kinase activity.

  公式(I)所代表的化合物，如描述中所定义，其中R是氢原子或甲基基团，R1是规范中定义的基团，或其药用盐，均已披露；所述化合物在治疗细胞增殖紊乱疾病（如癌症）方面具有用途，与细胞周期依赖性激酶活性异常有关。
• Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents
  申请人：Pfizer Italia S.r.l.

  公开号：EP1724270A2

  公开（公告）日：2006-11-22

  Compounds represented by formula (I), as defined in the description, wherein R is a hydrogen atom or a methyl group and R1 is a group as defined in the specification, or a pharmaceutically acceptable salt thereof, are disclosed; the said compounds are useful in the treatment of cell proliferative disorders, e.g. cancer, associated with an altered cell cycle dependent kinase activity.

  本发明公开了式(I)所代表的化合物，如说明书中所定义，其中R是氢原子或甲基，R1是如说明书中所定义的基团，或其药学上可接受的盐；所述化合物可用于治疗与细胞周期依赖性激酶活性改变有关的细胞增殖性疾病，如癌症。
• PHENYLACETAMIDO-THIAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS
  申请人：Pfizer Italia S.r.l.

  公开号：EP1406899B1

  公开（公告）日：2006-11-15
• THIOPYRANE-4-ONES AS DNA PROTEIN KINASE INHIBITORS
  申请人：CANCER RESEARCH TECHNOLOGY LIMITED

  公开号：EP1416936A1

  公开（公告）日：2004-05-12
• [EN] THIOPYRANE-4-ONES AS DNA PROTEIN KINASE INHIBITORS<br/>[FR] THIOPYRANE-4-ONES UTILISES COMME INHIBITEURS D'UNE PROTEINE KINASE DEPENDANTE DE L'ADN
  申请人：CANCER REC TECH LTD

  公开号：WO2003015790A1

  公开（公告）日：2003-02-27

  The present invention provides compounds of formula (I) and isomers, salts, solvates, chemically protected forms, and prodrugs thereof, wherein R?1 and R2¿ are independently hydrogen, an option ally substituted C¿1-7? alkyl group, C3-20 heterocyclyl group, or C5-20 aryl group, or may together form, along with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring having from 4 to 8 ring atoms; and R?3¿ is an optionally substituted C¿3-20? heterocyclyl or C5-20 aryl group, and their use as pharmaceuticals, particularly in treating diseases which are retroviral mediated or ameliorated by the inhibition of DNA-PK.