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5-chloro-N-[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-yl]-6-(4-hydroxypiperidino)nicotinamide | 778572-93-3

中文名称
——
中文别名
——
英文名称
5-chloro-N-[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-yl]-6-(4-hydroxypiperidino)nicotinamide
英文别名
4-(Decarboxy)-4-hydroxy-avatrombopag;5-chloro-N-[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)-1,3-thiazol-2-yl]-6-(4-hydroxypiperidin-1-yl)pyridine-3-carboxamide
5-chloro-N-[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-yl]-6-(4-hydroxypiperidino)nicotinamide化学式
CAS
778572-93-3
化学式
C28H34Cl2N6O2S2
mdl
——
分子量
621.655
InChiKey
JLDDJJNSCVWAKW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    40
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    141
  • 氢给体数:
    2
  • 氢受体数:
    9

文献信息

  • 2-Acylaminothiazole derivative or salt thereof
    申请人:Sugasawa Keizo
    公开号:US20050153977A1
    公开(公告)日:2005-07-14
    A 2-acylaminothiazole derivative or a pharmaceutically acceptable salt thereof having an excellent effect of proliferating human c-mpl-Ba/F3 cells and an activity of increasing platelets based on the effect of promoting the formation of megakaryocytic colonies. A compound or a pharmaceutically acceptable salt thereof useful in treating thrombocytopenia.
    一种2-酰胺基噻唑生物或其药学上可接受的盐,具有优异的促进人类c-mpl-Ba / F3细胞增殖和增加血小板活性的作用,基于促进巨核细胞集落形成的效果。一种化合物或其药学上可接受的盐,用于治疗血小板减少症。
  • 2-ACYLAMINOTHIAZOLE DERIVATIVE OR SALT THEREOF
    申请人:Astellas Pharma Inc.
    公开号:EP1466912B1
    公开(公告)日:2013-04-24
  • Compositions and methods for treating thrombocytopenia
    申请人:Suzuki Ken-Ichi
    公开号:US20070203153A1
    公开(公告)日:2007-08-30
    The present invention in certain embodiments is directed to a pharmaceutical dosage form comprising a therapeutically effective amount of a first agent that agonizes a human TPO receptor by binding to the rhTPO binding site of the human TPO receptor; and a therapeutically effective amount of a second agent that agonizes the human TPO receptor by binding to a binding site of the human TPO receptor distinct from the rhTPO binding site.
  • US7638536B2
    申请人:——
    公开号:US7638536B2
    公开(公告)日:2009-12-29
  • US8338429B2
    申请人:——
    公开号:US8338429B2
    公开(公告)日:2012-12-25
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