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6-氨基-3-羟基(1h)吲唑 | 59673-74-4

中文名称
6-氨基-3-羟基(1h)吲唑
中文别名
1,2-二氢-6-氨基-吲唑-3-酮;3-羟基-6-氨基-1H-吲唑
英文名称
6-amino-1,2-dihydro-3H-indazol-3-one
英文别名
6-amino-1,2-dihydroindazol-3-one
6-氨基-3-羟基(1h)吲唑化学式
CAS
59673-74-4
化学式
C7H7N3O
mdl
——
分子量
149.152
InChiKey
RVEOZWSYDIHKIB-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

物化性质

  • 沸点:
    278.9±19.0 °C(Predicted)
  • 密度:
    1.363±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    67.2
  • 氢给体数:
    3
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

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

  • Fused heterocyclic compounds useful as kinase modulators
    申请人:Vaccaro Wayne
    公开号:US20070078136A1
    公开(公告)日:2007-04-05
    Compounds having the formula (1), and enantiomers, and diastereomers, pharmaceutically-acceptable salts, thereof, are usefuil as kinase modulators, including MK2 modulation, wherein one of E and F is a nitrogen atom and the other of E and F is a carbon atom, Z is N or CR 3 , and R 1 , R 2 , R 3 , X and Y are as defined herein.
    具有化学式(1)的化合物,以及其对映体、非对映体、药用可接受的盐,可用作激酶调节剂,包括MK2调节,其中E和F中的一个是氮原子,另一个是碳原子,Z是N或CR3,R1、R2、R3、X和Y如本文所定义。
  • Substituted Oxopyridine Derivatives and Use Thereof in the Treatment of Cardiovascular Disorders
    申请人:BAYER PHARMA AKTIENGESELLSCHAFT
    公开号:US20160052884A1
    公开(公告)日:2016-02-25
    The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.
    这项发明涉及替代的氧代吡啶衍生物及其制备方法,以及它们用于制备用于治疗和/或预防疾病的药物,特别是心血管疾病,优选是血栓性或血栓栓塞性疾病、肿以及眼科疾病。
  • FUSED HETEROCYCLIC COMPOUNDS USEFUL AS KINASE MODULATORS
    申请人:Vaccaro Wayne
    公开号:US20080045536A1
    公开(公告)日:2008-02-21
    Compounds having the formula (I), and enantiomers, and diastereomers, pharmaceutically-acceptable salts, thereof, are useful as kinase modulators, including MK2 modulation, wherein one of E and F is a nitrogen atom and the other of E and F is a carbon atom, Z is N or CR 3 , and R 1 , R 2 , R 3 , X and Y are as defined herein.
    具有公式(I)的化合物,其对映异构体,顺反异构体和药学上可接受的盐,对于激酶调节剂是有用的,包括MK2调节剂,其中E和F中的一个是氮原子,另一个是碳原子,Z是N或CR3,而R1,R2,R3,X和Y如此定义。
  • SUBSTITUTED ALKYLAMINE DERIVATIVES AND METHODS OF USE
    申请人:CHEN Guoqing
    公开号:US20120065185A1
    公开(公告)日:2012-03-15
    Selected heterocyclic compounds are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like.
    选择的杂环化合物对于预防和治疗疾病,如血管生成介导的疾病是有效的。该发明涵盖了新型化合物、类似物、前药和其药学上可接受的衍生物、药物组合物以及预防和治疗涉及癌症等疾病和其他疾病或病症的方法。
  • Substituted aryl-amine derivatives and methods of use
    申请人:Yuan Chester Chenguang
    公开号:US20090143355A1
    公开(公告)日:2009-06-04
    Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds of Formula I and II wherein R, R 1 and R 2 for each formula are defined herein. The invention further includes analogs, prodrugs and pharmaceutically acceptable salts and derivatives of Formulas I and II, as well as pharmaceutical compositions, medicaments and methods thereof for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选择的胺类化合物可用于预防和治疗一些疾病,例如血管生成介导的疾病。本发明涵盖了公式I和II的新化合物,其中公式中的R、R1和R2已在此定义。本发明还包括公式I和II的类似物、前药和药物可接受的盐和衍生物,以及用于预防和治疗涉及癌症等疾病和其他病症或状况的药物组合物、药物和方法。本发明还涉及制备这些化合物的过程以及在这些过程中有用的中间体。
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