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6-[4-(dimethylamino)phenyl]-1H-indazol-3-amine | 627859-70-5

中文名称
——
中文别名
——
英文名称
6-[4-(dimethylamino)phenyl]-1H-indazol-3-amine
英文别名
3-amino-6-[4-(dimethylamino)phenyl]-1H-indazole
6-[4-(dimethylamino)phenyl]-1H-indazol-3-amine化学式
CAS
627859-70-5
化学式
C15H16N4
mdl
——
分子量
252.319
InChiKey
AMNNNXKKWJWAMV-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:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    57.9
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Aminoindazole derivatives and intermediates, preparation thereof, and pharmaceutical compositions thereof
    申请人:——
    公开号:US20040014802A1
    公开(公告)日:2004-01-22
    The present invention relates to the novel indazole derivatives of general formula (I): 1 in which: R is either O, S or NH; R3 is an alkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, aryl, heterocycle, cycloalkyl, alkenyl, etc. radical; these radicals being optionally substituted with one or more substituents; R4, R5, R6 and R7 are chosen, independently of each other, from the following radicals: hydrogen, halogen, CN, NO 2 , NH 2 , OH, COOH, C(O)OR8, —O—C(O)R8, NR8R9, NHC(O)R8, C(O)NR8R9, NHC(S)R8, C(S)NR8R9, SR8, S(O)R8, SO 2 R8, NHSO 2 R8, SO 2 NR8R9, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, heterocycle, cycloalkyl, alkenyl, etc.; these radicals being optionally substituted with one or more substituents.
    本发明涉及一般式(I)的新型吲唑生物: 1 其中:R为O、S或NH;R3为烷基、芳基、芳基烷基、杂芳基、杂芳基烷基、芳基、杂环、环烷基、烯基等基团;这些基团可以选择性地被一个或多个取代基取代;R4、R5、R6和R7分别选择自以下基团:氢、卤素、CN、NO 2 、NH 2 、OH、COOH、C(O)OR8、—O—C(O)R8、NR8R9、NHC(O)R8、C(O)NR8R9、NHC(S)R8、C(S)NR8R9、SR8、S(O)R8、SO 2 R8、NHSO 2 R8、SO 2 NR8R9、三甲基、三甲氧基、烷基、烷氧基、芳基、芳基烷基、杂芳基、杂芳基烷基、杂环、环烷基、烯基等;这些基团可以选择性地被一个或多个取代基取代。
  • Aminoindazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
    申请人:Martina Katia
    公开号:US20060106083A1
    公开(公告)日:2006-05-18
    Compounds which are indazole derivatives and pharmaceutically acceptable salts thereof, together with pharmaceutical compositions comprising them, as well as combinatorial libraries of indazole derivatives, as set forth in the specification, are disclosed; these compounds or compositions may be useful in the treatment of diseases caused by and/or associated with an altered protein kinase activity such as cancer, cell proliferative disorders, Alzheimer's disease, viral infections, auto-immune diseases and neurodegenerative disorders.
    这些是关于吲唑生物及其药用盐的化合物,以及包含它们的药物组合物,以及吲唑生物的组合化合物库的说明;这些化合物或组合物可能在治疗由改变的蛋白激酶活性引起和/或与之相关的疾病方面有用,如癌症、细胞增殖紊乱、阿尔茨海默病、病毒感染、自身免疫疾病和神经退行性疾病。
  • 3-Aminoindazoles
    申请人:Dorsch Dieter
    公开号:US20070232620A1
    公开(公告)日:2007-10-04
    Novel 3-aminoindazoles of the formula (I) are SGK inhibitors and can be used for the treatment of SGK-induced diseases and conditions, such as diabetes, obesity, metabolic syndrome (dyslipidaemia), systemic and pulmonary hypertonia, cardiovascular diseases and renal diseases, generally in fibrosis and inflammatory processes of any type.
    公式(I)的新型3-氨基吲唑是SGK抑制剂,可用于治疗由SGK引起的疾病和症状,如糖尿病、肥胖症、代谢综合征(脂质代谢紊乱)、全身和肺动脉高压、心血管疾病和肾脏疾病,通常用于任何类型的纤维化和炎症过程。
  • [EN] AMINOINDAZOLE DERIVATIVES ACTIVE AS KINASE INHIBITORS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM<br/>[FR] DERIVES D'AMINOINDAZOLE AGISSANT COMME INHIBITEURS DE KINASE, METHODE D'OBTENTION ET COMPOSITIONS PHARMACEUTIQUES LES RENFERMANT
    申请人:PHARMACIA ITALIA SPA
    公开号:WO2003097610A1
    公开(公告)日:2003-11-27
    Compounds which are indazole derivatives and pharmaceutically acceptable salts thereof together with pharmaceutical compositions comprising them, as well as combinatorial libraries of indazole derivatives, as set forth in the specification, are disclosed; these compounds or compositions may be useful in the treatment of diseases caused by and/or associated with an altered protein kinase activity such as cancer, cell proliferative disorders, Alzheimer's disease, viral infections, auto-immune diseases and neurodegenerative disorders.
    本发明公开了吲唑生物化合物及其药学上可接受的盐,以及包括它们的制药组合物,以及吲唑生物的组合化学库,这些化合物或组合物可能有用于治疗由于和/或与蛋白激酶活性改变相关的疾病,如癌症,细胞增殖性疾病,阿尔茨海默病,病毒感染,自身免疫疾病和神经退行性疾病。
  • DERIVES D'AMINOINDAZOLES COMME INHIBITEURS DE PROTEINE-KINASE
    申请人:Aventis Pharma S.A.
    公开号:EP1487804B1
    公开(公告)日:2014-02-26
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