摩熵化学
数据开放平台 数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(4-(5-(5-amino-1-(6,7-dimethoxyquinazolin-4-yl)-1H-1,2,4-triazol-3-ylamino)-2-chlorophenyl)piperazin-1-yl)ethanone | 1037797-84-4

中文名称
——
中文别名
——
英文名称
1-(4-(5-(5-amino-1-(6,7-dimethoxyquinazolin-4-yl)-1H-1,2,4-triazol-3-ylamino)-2-chlorophenyl)piperazin-1-yl)ethanone
英文别名
1-[4-[5-[[5-Amino-1-(6,7-dimethoxyquinazolin-4-yl)-1,2,4-triazol-3-yl]amino]-2-chlorophenyl]piperazin-1-yl]ethanone
1-(4-(5-(5-amino-1-(6,7-dimethoxyquinazolin-4-yl)-1H-1,2,4-triazol-3-ylamino)-2-chlorophenyl)piperazin-1-yl)ethanone化学式
CAS
1037797-84-4
化学式
C24H26ClN9O3
mdl
——
分子量
523.982
InChiKey
DUKDOIDZRBVCGV-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):
    3.1
  • 重原子数:
    37
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    137
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • [EN] COMPOUNDS WHICH INHIBIT THE GLYCINE TRANSPORTER AND USES THEREOF IN MEDICINE<br/>[FR] COMPOSÉS QUI INHIBENT LE TRANSPORTEUR DE GLYCINE ET SES UTILISATIONS EN MÉDECINE
    申请人:GLAXO GROUP LTD
    公开号:WO2009034062A1
    公开(公告)日:2009-03-19
    Compounds of Formula (I) and salts thereof are provided: wherein the groups are as defined in the specification. Uses of the compounds as medicaments, and in the manufacture of medicament for treating neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder are also disclosed. The invention further comprises processes to make these compounds and pharmaceutical formulations thereof.
    提供了化合物(I)的公式及其盐:其中所述基团如规范中定义。还披露了将这些化合物用作药物,以及用于治疗神经系统和神经精神障碍的药物的制造方法,特别是精神病、痴呆或注意力缺陷障碍。该发明还包括制备这些化合物和药物配方的过程。
  • SUBSTITUTED TRIAZOLES USEFUL AS AXL INHIBITORS
    申请人:Goff Dane
    公开号:US20080188474A1
    公开(公告)日:2008-08-07
    Substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.
    本发明揭示了替代三唑和含有该化合物的制药组合物,其在抑制受体蛋白酪氨酸激酶Axl的活性方面是有用的。还揭示了使用该化合物治疗与Axl活性相关的疾病或病况的方法。
  • Substituted triazoles useful as AXL inhibitors
    申请人:Rigel Pharmaceuticals, Inc.
    公开号:EP2476679A2
    公开(公告)日:2012-07-18
    Substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.
    所公开的取代三唑类化合物和含有这些化合物的药物组合物有助于抑制受体蛋白酪氨酸激酶 Axl 的活性。还公开了使用这些化合物治疗与 Axl 活性相关的疾病或病症的方法。
  • Substituted triazoles useful as Axl inhibitors
    申请人:Rigel Pharmaceuticals, Inc.
    公开号:US10166216B2
    公开(公告)日:2019-01-01
    Substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.
    所公开的取代三唑类化合物和含有这些化合物的药物组合物有助于抑制受体蛋白酪氨酸激酶 Axl 的活性。还公开了使用这些化合物治疗与 Axl 活性相关的疾病或病症的方法。
  • US8906922B2
    申请人:——
    公开号:US8906922B2
    公开(公告)日:2014-12-09
查看更多