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3-ethoxy-1-ethyl-1H-pyrazol-4-amine | 1356543-57-1

中文名称
——
中文别名
——
英文名称
3-ethoxy-1-ethyl-1H-pyrazol-4-amine
英文别名
3-ethoxy-1-ethylpyrazol-4-amine
3-ethoxy-1-ethyl-1H-pyrazol-4-amine化学式
CAS
1356543-57-1
化学式
C7H13N3O
mdl
——
分子量
155.2
InChiKey
JTKWRXVNTQNPOL-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:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    53.1
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] COMPOUNDS AND METHODS FOR INHIBITING JAK<br/>[FR] COMPOSÉS ET PROCÉDÉS D'INHIBITION DE JAK
    申请人:ASTRAZENECA AB
    公开号:WO2017050938A1
    公开(公告)日:2017-03-30
    Disclosed are compounds of formula (I), pharmaceutical compositions comprising such compounds and methods/uses of using the same, for example, for treating a JAK-related disorder, such as cancer, cancer cachexia or an immune disorder: (I) wherein R1 is methyl or ethyl; R2 is selected from methyl, ethyl, methoxy and ethoxy; R3 is selected from hydrogen, chlorine, fluorine, bromine and methyl; R4 is selected from methyl, ethyl and -CH2OCH3; R5 and R6 are each individually methyl or hydrogen; and R7 is selected from methyl, ethyl, -(CH2)2OH and –(CH2)2OCH3, or a pharmaceutically acceptable salt thereof.
    公开的是公式(I)的化合物,包括含有这些化合物的药物组合物以及使用这些化合物的方法/用途,例如用于治疗JAK相关疾病,如癌症、癌症恶病质或免疫紊乱:(I)其中R1是甲基或乙基;R2选择自甲基、乙基、甲基和乙基;R3选择自甲基;R4选择自甲基、乙基和- OCH3;R5和R6分别是甲基;R7选择自甲基、乙基、-(CH2)2OH和-( )2OCH3,或其药用盐。
  • Compounds and methods for inhibiting JAK
    申请人:Dizal (Jiangsu) Pharmaceutical Co., Ltd.
    公开号:US10167276B2
    公开(公告)日:2019-01-01
    Disclosed are compounds of formula (I), pharmaceutical compositions comprising such compounds and methods/uses of using the same, for example, for treating a JAK-related disorder, such as cancer, cancer cachexia or an immune disorder: wherein R1 is methyl or ethyl; R2 is selected from methyl, ethyl, methoxy and ethoxy; R3 is selected from hydrogen, chlorine, fluorine, bromine and methyl; R4 is selected from methyl, ethyl and —CH2OCH3; R5 and R6 are each individually methyl or hydrogen; and R7 is selected from methyl, ethyl, —(CH2)2OH and —(CH2)2OCH3, or a pharmaceutically acceptable salt thereof.
    公开了式(I)化合物、包含此类化合物的药物组合物以及使用此类化合物的方法/用途,例如,用于治疗与JAK相关的疾病,如癌症、癌症恶病质或免疫紊乱: 其中 R1 是甲基或乙基 R2 选自甲基、乙基、甲基和乙基; R3 选自甲基; R4 选自甲基、乙基和- OCH3; R5 和 R6 分别为甲基;以及 R7 选自甲基、乙基、-(CH2)2OH 和-( )2OCH3 或其药学上可接受的盐。
  • COMPOUNDS AND METHODS FOR INHIBITING JAK
    申请人:AstraZeneca AB
    公开号:US20170320857A1
    公开(公告)日:2017-11-09
    Disclosed are compounds of formula (I), pharmaceutical compositions comprising such compounds and methods/uses of using the same, for example, for treating a JAK-related disorder, such as cancer, cancer cachexia or an immune disorder: wherein R 1 is methyl or ethyl; R 2 is selected from methyl, ethyl, methoxy and ethoxy; R 3 is selected from hydrogen, chlorine, fluorine, bromine and methyl; R 4 is selected from methyl, ethyl and —CH 2 OCH 3 ; R 5 and R 6 are each individually methyl or hydrogen; and R 7 is selected from methyl, ethyl, —(CH 2 ) 2 OH and —(CH 2 ) 2 OCH 3 , or a pharmaceutically acceptable salt thereof.
  • US9714236B2
    申请人:——
    公开号:US9714236B2
    公开(公告)日:2017-07-25
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