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2-Chloro-7-methyl[1,3]thiazolo[4,5-b]pyridine | 1190927-30-0

中文名称
——
中文别名
——
英文名称
2-Chloro-7-methyl[1,3]thiazolo[4,5-b]pyridine
英文别名
2-Chloro-7-methyl-[1,3]thiazolo[4,5-b]pyridine
2-Chloro-7-methyl[1,3]thiazolo[4,5-b]pyridine化学式
CAS
1190927-30-0
化学式
C7H5ClN2S
mdl
——
分子量
184.649
InChiKey
XFRYNQUEHMJPJB-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):
    3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-(哌啶-1-基甲基)苯酚2-Chloro-7-methyl[1,3]thiazolo[4,5-b]pyridinepotassium carbonate 作用下, 以 乙腈 为溶剂, 以53%的产率得到7-Methyl-2-[4-(piperidin-1-ylmethyl)phenoxy][1,3]thiazolo[4,5-b]pyridine
    参考文献:
    名称:
    Azabenzthiazole inhibitors of leukotriene A4 hydrolase
    摘要:
    Previously, benzthiazole containing LTA4H inhibitors were discovered that were potent (1-3), but were associated with the potential for a hERG liability. Utilizing medicinal chemistry first principles (e. g., introducing rigidity, lowering cLogD) a new benzthiazole series was designed, congeners of 1-3, which led to compounds 7a, 7c, 12a-d which exhibited LTA4H IC50 = 3-6 nM and hERG Dofetilide Binding IC50 = 8.9-> >10 mu M. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.10.036
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文献信息

  • [EN] COMPOUNDS WITH TWO FUSED BICYCLIC HETEROARYL MOIETIES AS MODULATORS OF LEUKOTRIENE A4 HYDROLASE<br/>[FR] COMPOSÉS POSSÉDANT DEUX GROUPEMENTS HÉTÉROARYLE BICYCLIQUES CONDENSÉS EN TANT QUE MODULATEURS DE LA LEUCOTRIÈNE A4 HYDROLASE
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2010132599A1
    公开(公告)日:2010-11-18
    Compounds with two fused bicyclic heteroaryl moieties of formula I and their pharmaceutical compositions, and methods of using them as leukotriene A4 hydrolase (LTA4H) modulators and for the treatment of diseases, disorders and conditions mediated by LTA4H.
    具有式I中两个融合的双环杂环芳基部分的化合物及其药物组合物,以及将它们用作白三烯A4水解酶(LTA4H)调节剂,并用于治疗由LTA4H介导的疾病、紊乱和病况的方法。
  • Thiazolopyridin-2-yloxy-phenyl and thiazolopyrazin-2-yloxy-phenyl amines as modulators of leukotriene A4 hydrolase
    申请人:Bacani Genesis M.
    公开号:US20090258854A1
    公开(公告)日:2009-10-15
    Thiazolopyridin-2-yloxy-phenyl and thiazolopyrazin-2-yloxy-phenyl amine compounds are described, which are useful as LTA4 hydrolase (LTA4H) modulators. Such compounds may be used in pharmaceutical compositions and methods for modulation of LTA4H and for the treatment of disease states, disorders, and conditions mediated by LTA4 hydrolase activity.
    描述了噻唑吡啶-2-氧基苯基和噻唑吡嗪-2-氧基苯基胺化合物,这些化合物可作为LTA4水解酶(LTA4H)调节剂。这些化合物可以用于制备药物组合物,用于调节LTA4H并治疗由LTA4水解酶活性介导的疾病状态、疾病和症状。
  • Thyazolopyridin-2-yloxy-phenyl and thiazolopyrazin-2-yloxy-phenyl amines as modulators of leukotriene A4 hydrolase
    申请人:Bacani Genesis M.
    公开号:US20110159563A1
    公开(公告)日:2011-06-30
    Thiazolopyridin-2-yloxy-phenyl and thiazolopyrazin-2-yloxy-phenyl amine compounds are described, which are useful as LTA4 hydrolase (LTA4H) modulators. Such compounds may be used in pharmaceutical compositions and methods for modulation of LTA4H and for the treatment of disease states, disorders, and conditions mediated by LTA4 hydrolase activity.
    本文介绍了一种Thiazolopyridin-2-yloxy-phenyl和thiazolopyrazin-2-yloxy-phenyl胺类化合物,这些化合物可用作LTA4水解酶(LTA4H)调节剂。这些化合物可以用于制备药物组合物和方法,用于调节LTA4H并治疗由LTA4水解酶活性介导的疾病状态、疾患和病情。
  • COMPOUNDS WITH TWO FUSED BICYCLIC HETEROARYL MOIETIES AS MODULATORS OF LEUKOTRIENE A4 HYDROLASE
    申请人:Bacani Genesis
    公开号:US20100292208A1
    公开(公告)日:2010-11-18
    Compounds with two fused bicyclic heteroaryl moieties and their pharmaceutical compositions, and methods of using them as leukotriene A 4 hydrolase (LTA 4 H) modulators and for the treatment of diseases, disorders and conditions mediated by LTA 4 H.
    具有两个融合的杂环芳基基团的化合物及其制药组合物,以及将它们用作白三烯A4水解酶(LTA4H)调节剂的方法,以及用于治疗由LTA4H介导的疾病,障碍和情况的方法。
  • THIAZOLOPYRIDIN-2-YLOXY-PHENYL AND THIAZOLOPYRAZIN-2-YLOXY-PHENYL AMINES AS MODULATORS OF LEUKOTRIENE A4 HYDROLASE
    申请人:Janssen Pharmaceutica, N.V.
    公开号:EP2268646B1
    公开(公告)日:2013-10-02
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