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7-(2-hydroxypropan-2-yl)-3-methyl-4-(2-methyl-3-(4-oxoquinazolin-3(4H)-yl)phenyl)-9H-pyrido[3,4-b]indole-1-carboxamide | 1352837-00-3

中文名称
——
中文别名
——
英文名称
7-(2-hydroxypropan-2-yl)-3-methyl-4-(2-methyl-3-(4-oxoquinazolin-3(4H)-yl)phenyl)-9H-pyrido[3,4-b]indole-1-carboxamide
英文别名
7-(2-hydroxypropan-2-yl)-3-methyl-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-9H-pyrido[3,4-b]indole-1-carboxamide
7-(2-hydroxypropan-2-yl)-3-methyl-4-(2-methyl-3-(4-oxoquinazolin-3(4H)-yl)phenyl)-9H-pyrido[3,4-b]indole-1-carboxamide化学式
CAS
1352837-00-3
化学式
C31H27N5O3
mdl
——
分子量
517.587
InChiKey
GTPUWISDBGFVHJ-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):
    4.1
  • 重原子数:
    39
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    125
  • 氢给体数:
    3
  • 氢受体数:
    5

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

  • SUBSTITUTED TETRAHYDROCARBAZOLE AND CARBAZOLE CARBOXAMIDE COMPOUNDS
    申请人:Bristol-Myers Squibb Company
    公开号:US20140378475A1
    公开(公告)日:2014-12-25
    Disclosed are compounds of Formula (I) wherein: the two dotted lines represent either two single or two double bonds; Q is: R 1 is F, Cl, —CN, or —CH 3 ; R 2 is Cl or —CH 3 ; R 3 is —C(CH 3 ) 2 OH or —CH 2 CH 2 OH; R a is H or —CH 3 ; each R b is independently F, Cl, —CH 3 , and/or —OCH 3 ; and n is zero, 1, or 2. Also disclosed are methods of using such compounds as inhibitors of Bruton's tyrosine kinase (Btk), and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.
    公开的是Formula (I)的化合物,其中:两条虚线代表两个单键或两个双键;Q是:R1是F、Cl、—CN或—CH3;R2是Cl或—CH3;R3是—C(CH3)2OH或—CH2CH2OH;Ra是H或—CH3;每个Rb独立地是F、Cl、—CH3和/或—OCH3;n为零、1或2。还公开了将这些化合物用作Bruton酪氨酸激酶(Btk)抑制剂的方法,以及包含这些化合物的药物组合物。这些化合物在治疗、预防或减缓多种治疗领域的疾病或疾病的进展方面非常有用,如自身免疫疾病和血管疾病。
  • [EN] CARBAZOLE CARBOXAMIDE COMPOUNDS USEFUL AS KINASE INHIBITORS<br/>[FR] COMPOSÉS DE CARBAZOLE-CARBOXAMIDE UTILES COMME INHIBITEURS DE KINASES
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2014210087A1
    公开(公告)日:2014-12-31
    Disclosed are compounds of Formula (I); and salts thereof, wherein:Formula (II); Q is: R1 is -C(CH3)2OH, -NHC(=0)C(CH3)3, -N(CH3)2, or -CH2Rd; R2 is CI or -CH3; R3 is H, F, or -CH3; Ra is H or -CH3; Rb is H, F, CI, or -OCH3 Rc is H or F; and Rd is -OH, -OCH3, -NHC(=0)CH3, or fORMULA (III), Also disclosed are methods of using such compounds as inhibitors of Bruton's tyrosine kinase (Btk), and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.
    公开了Formula (I)的化合物及其盐,其中:Formula (II);Q是:R1为-C(CH3)2OH,-NHC(=0)C(CH3)3,-N(CH3)2,或-CH2Rd;R2为CI或-CH3;R3为H,F或-CH3;Ra为H或-CH3;Rb为H,F,CI或-OCH3;Rc为H或F;Rd为-OH,-OCH3,-NHC(=0)CH3,或Formula (III)。还公开了使用这些化合物作为Bruton酪氨酸激酶(Btk)抑制剂的方法,以及包含这些化合物的药物组合物。这些化合物在治疗、预防或减缓各种治疗领域的疾病或障碍方面具有用途,如自身免疫疾病和血管疾病。
  • Carboline carboxamide compounds useful as kinase inhibitors
    申请人:Liu Chunjian
    公开号:US08685969B2
    公开(公告)日:2014-04-01
    Compounds having formula (I), and enantiomers, and diastereomers, stereoisomers, pharmaceutically-acceptable salts thereof, formula (I) are useful as kinase modulators, including Btk modulation.
    化合物的公式为(I),其对映异构体、顺反异构体、立体异构体、药物可接受的盐,公式(I)可用作激酶调节剂,包括Btk调节。
  • CARBOLINE CARBOXAMIDE COMPOUNDS USEFUL AS KINASE INHIBITORS
    申请人:Liu Chunjian
    公开号:US20130096118A1
    公开(公告)日:2013-04-18
    Compounds having formula (I), and enantiomers, and diastereomers, stereoisomers, pharmaceutically-acceptable salts thereof, formula (I) are useful as kinase modulators, including Btk modulation.
    具有公式(I)的化合物,其对映异构体,顺反异构体,立体异构体,以及其药学上可接受的盐,公式(I)对于激酶调节剂非常有用,包括Btk调节。
  • SUBSTITUTED TETRAHYDROCARBAZOLE AND CARBAZOLES CARBOXAMIDE COMPOUNDS
    申请人:Bristol-Myers Squibb Company
    公开号:US20160194338A1
    公开(公告)日:2016-07-07
    Disclosed are compounds of Formula (I) wherein: the two dotted lines represent either two single or two double bonds; Q is: R 1 is F, Cl, —CN, or —CH 3 ; R 2 is C 1 or —CH 3 ; R 3 is —C(CH 3 ) 2 OH or —CH 2 CH 2 OH; R a is H or —CH 3 ; each R b is independently F, Cl, —CH 3 , and/or —OCH 3 ; and n is zero, 1, or 2. Also disclosed are methods of using such compounds as inhibitors of Bruton's tyrosine kinase (Btk), and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.
    本发明涉及式(I)的化合物,其中:两个点状线代表两个单键或两个双键;Q为:R1为F、Cl、—CN或—CH3;R2为C1或—CH3;R3为—C(CH3)2OH或—CH2CH2OH;Ra为H或—CH3;每个Rb独立地为F、Cl、—CH3和/或—OCH3;n为零、1或2。本发明还涉及使用这些化合物作为布鲁顿酪氨酸激酶(Btk)抑制剂的方法,以及包含这些化合物的制药组合物。这些化合物在治疗、预防或减缓多种治疗领域的疾病或疾病进展方面是有用的,例如自身免疫性疾病和血管疾病。
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