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cis-2-(4-Aminocyclohexyl)propan-2-ol;hydrochloride | 2387569-41-5

中文名称
——
中文别名
——
英文名称
cis-2-(4-Aminocyclohexyl)propan-2-ol;hydrochloride
英文别名
2-(4-aminocyclohexyl)propan-2-ol;hydrochloride
cis-2-(4-Aminocyclohexyl)propan-2-ol;hydrochloride化学式
CAS
2387569-41-5
化学式
C9H19NO*ClH
mdl
——
分子量
193.717
InChiKey
BMAQQHDLYHZJFN-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):
    1.7
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    3
  • 氢受体数:
    2

反应信息

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文献信息

  • AMINOTRIAZOLOPYRIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
    申请人:Bahmanyar Sogole
    公开号:US20100093698A1
    公开(公告)日:2010-04-15
    Provided herein are Heteroaryl Compounds of formula (I): wherein R 1 and R 2 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing inflammatory conditions or cancer, and conditions treatable or preventable by inhibition of a kinase or a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a subject in need thereof.
    本文提供了公式(I)的杂环芳基化合物:其中R1和R2如本文所定义,包含有效量杂环芳基化合物的组合物,以及用于治疗或预防炎症性疾病或癌症的方法,以及通过抑制激酶或激酶途径治疗或预防的疾病,包括向需要的受试者施用有效量杂环芳基化合物。
  • AMINOTRIAZOLOPYRIDINES AND THEIR USE AS KINASE INHIBITORS
    申请人:Signal Pharmaceuticals, LLC
    公开号:EP2344494B1
    公开(公告)日:2016-04-20
  • QUINOLINE-3-CARBOXAMIDES AS H-PGDS INHIBITORS
    申请人:Astex Therapeutics Limited
    公开号:EP3390384B1
    公开(公告)日:2021-09-15
  • CHEMICAL COMPOUNDS
    申请人:GlaxoSmithKline Intellectual Property Development Limited
    公开号:US20210238162A1
    公开(公告)日:2021-08-05
    The present invention relates to compounds of Formula (XI): wherein R 1a , R 2a , R 3a , R 4a , R 5a , R 6a , and Aa are as defined herein, and pharmaceutically acceptable salts thereof. The compounds of the present invention are inhibitors of hematopoietic prostaglandin D synthase (H-PGDS) inhibitors and can be useful in the treatment of Duchenne Muscular Dystrophy. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting H-PGDS activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.
  • US8299056B2
    申请人:——
    公开号:US8299056B2
    公开(公告)日:2012-10-30
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