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4-hydroxy-4-(5-methyl-1,3-thiazol-2-yl)cyclohexanone | 857650-93-2

中文名称
——
中文别名
——
英文名称
4-hydroxy-4-(5-methyl-1,3-thiazol-2-yl)cyclohexanone
英文别名
4-hydroxy-4-(5-methyl-thiazol-2-yl)-cyclohexanone;4-hydroxy-4-(5-methyl-1,3-thiazol-2-yl)cyclohexan-1-one
4-hydroxy-4-(5-methyl-1,3-thiazol-2-yl)cyclohexanone化学式
CAS
857650-93-2
化学式
C10H13NO2S
mdl
——
分子量
211.285
InChiKey
GKXJQZCGEPZWTF-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):
    0.5
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] A METHOD OF TREATING LIVER FIBROSIS<br/>[FR] MÉTHODE DE TRAITEMENT DE LA FIBROSE HÉPATIQUE
    申请人:PFIZER LTD
    公开号:WO2012114223A1
    公开(公告)日:2012-08-30
    The present invention relates to a method of treating hepatis C and/or liver fibroisis with 3-cycloalkylaminopyrrolidine derivatives of the present invention.
    本发明涉及一种使用本发明中的3-环烷基吡咯烷衍生物治疗丙型肝炎和/或肝纤维化的方法。
  • CYCLOHEXYL-AZETIDINYL ANTAGONISTS OF CCR2
    申请人:Zhang Xuqing
    公开号:US20110306592A1
    公开(公告)日:2011-12-15
    The present invention comprises compounds of Formula (I). wherein: R 1 , R 2 , X, and Z are as defined in the specification. The invention also comprises a method of preventing, treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is type II diabetes, obesity and asthma. The invention also comprises a method of inhibiting CCR2 activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula (I).
    本发明包括式(I)的化合物。其中:R1、R2、X和Z如规范中所定义。该发明还包括一种预防、治疗或改善综合症、紊乱或疾病的方法,其中所述综合症、紊乱或疾病为II型糖尿病、肥胖和哮喘。该发明还包括通过给哺乳动物施用至少一种式(I)化合物的治疗有效量来抑制CCR2活性的方法。
  • 3-Cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors
    申请人:Xue Chu-Biao
    公开号:US20050192302A1
    公开(公告)日:2005-09-01
    The present invention relates to 3-cycloalkylaminopyrrolidine derivatives of the formula I: (wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , X, Y and Z are as defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of chemokine receptors and more specifically as modulators of the CCR2 and/or CCR5 receptor. The compounds and compositions of the invention may bind to chemokine receptors, e.g., the CCR2 and/or CCR5 chemokine receptors, and are useful for treating diseases associated with chemokine, e.g., CCR2 and/or CCR5, activity, such as atherosclerosis, restenosis, lupus, organ transplant rejection and rheumatoid arthritis.
    本发明涉及公式I的3-环烷胺基吡咯烷衍生物:(其中R1、R2、R3、R4、R5、R6、R7、X、Y和Z如本文所定义),这些衍生物可用作化学因子受体活性的调节剂。特别是,这些化合物可用作化学因子受体的调节剂,更具体地作为CCR2和/或CCR5受体的调节剂。本发明的化合物和组合物可能结合化学因子受体,例如CCR2和/或CCR5化学因子受体,并且可用于治疗与化学因子(例如CCR2和/或CCR5)活性相关的疾病,如动脉粥样硬化、再狭窄、狼疮、器官移植排斥和类风湿性关节炎。
  • 4-AZETIDINYL-1-HETEROARYL-CYCLOHEXANOL ANTAGONISTS OF CCR2
    申请人:Zhang Xuqing
    公开号:US20100144695A1
    公开(公告)日:2010-06-10
    The present invention comprises compounds of Formula (I). wherein: R 1 , R 2 , R 3 , and R 4 are as defined in the specification. The invention also comprises pharmaceutical compositions comprising the compounds of formula (I) and methods of preventing, treating or ameliorating a CCR2 mediated syndrome, disorder or disease, for example, type II diabetes, obesity or asthma, by administering the compounds of formula (I).
    本发明涉及式(I)的化合物。其中:R1、R2、R3和R4如规范中所定义。该发明还涉及包含式(I)化合物的药物组合物,以及通过给予式(I)化合物来预防、治疗或改善CCR2介导的综合症、疾病或疾病的方法,例如II型糖尿病、肥胖或哮喘。
  • 3-(4-heteroarylcyclohexylamino)cyclopentanecarboxamides as modulators of chemokine receptors
    申请人:Incyte Corporation
    公开号:US07307086B2
    公开(公告)日:2007-12-11
    The present invention is directed to compounds of Formula I: which are modulators of chemokine receptors. The compounds of the invention, and compositions thereof, are useful in the treatment of diseases related to chemokine receptor expression and/or activity.
    本发明涉及化合物I型的调节化学因子受体的作用,该发明的化合物及其组合物在治疗与化学因子受体表达和/或活性相关的疾病方面具有用处。
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