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2-methoxyquinoline-3-carbohydrazide | 1561822-95-4

中文名称
——
中文别名
——
英文名称
2-methoxyquinoline-3-carbohydrazide
英文别名
2-Methoxyquinoline-3-carbohydrazide
2-methoxyquinoline-3-carbohydrazide化学式
CAS
1561822-95-4
化学式
C11H11N3O2
mdl
——
分子量
217.227
InChiKey
DCRKVBCXIMAPKT-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):
    1
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    77.2
  • 氢给体数:
    2
  • 氢受体数:
    4

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

  • [EN] COMPOUNDS FOR USE IN THE TREATMENT OF KINETOPLASTID INFECTION<br/>[FR] COMPOSÉS UTILISÉS POUR TRAITER UNE INFECTION CINÉTOPLASTIDE
    申请人:IRBM SCIENCE PARK S P A
    公开号:WO2018115275A1
    公开(公告)日:2018-06-28
    The present invention relates to a class of novel heterocyclic compounds, to pharmaceutical compositions comprising the compounds and their use in the treatment of kinetoplastid infections.
    本发明涉及一类新颖的杂环化合物,以及包含这些化合物的药物组合物及其在治疗运动毛虫感染中的用途。
  • COMPOUNDS FOR USE IN THE TREATMENT OF DISORDERS THAT ARE AMELIORATED BY INHIBITION OF HDAC
    申请人:IRBM - Science Park S.p.A.
    公开号:US20150218112A1
    公开(公告)日:2015-08-06
    The present invention relates to compounds of formula (I) and (IV), and pharmaceutically acceptable salts, tautomers, stereoisomers thereof, which are inhibitors of histone deacetylase (HDAC). The compounds of the present invention are for use in the treatment of disorders that are ameliorated by inhibition of HDAC such as cancer and hemoglobinopathies like β-thalassemia or sickle cell anemia.
    本发明涉及式(I)和式(IV)的化合物,以及其药学上可接受的盐、互变异构体和立体异构体,它们是组蛋白去乙酰化酶(HDAC)的抑制剂。本发明的化合物用于治疗由HDAC抑制改善的疾病,例如癌症和血红蛋白病,如β-地中海贫血或镰状细胞贫血。
  • Compounds for use in the treatment of disorders that are ameliorated by inhibition of HDAC
    申请人:IRBM—Science Park S.p.A.
    公开号:US09371295B2
    公开(公告)日:2016-06-21
    The present invention relates to compounds of formula (I) and (IV), and pharmaceutically acceptable salts, tautomers, stereoisomers thereof, which are inhibitors of histone deacetylase (HDAC). The compounds of the present invention are for use in the treatment of disorders that are ameliorated by inhibition of HDAC such as cancer and hemoglobinopathies like β-thalassemia or sickle cell anemia.
    本发明涉及公式(I)和(IV)的化合物以及其药学上可接受的盐、互变异构体和立体异构体,它们是组蛋白去乙酰化酶(HDAC)的抑制剂。本发明的化合物可用于治疗通过抑制HDAC改善的疾病,例如癌症和血红蛋白病,如β-地中海贫血或镰状细胞贫血。
  • Compounds for use in the treatment of kinetoplastid infection
    申请人:C.N.C.C.S. S.c.a.r.l. COLLEZIONE NAZIONALE DEI COMPOSTI CHIMICI E CENTRO SCREENING
    公开号:US10815222B2
    公开(公告)日:2020-10-27
    The present invention relates to a class of novel heterocyclic compounds, to pharmaceutical compositions containing the compounds and their use in the treatment of kinetoplastid infections.
    本发明涉及一类新型杂环化合物、含有该化合物的药物组合物及其在治疗奇梭菌感染中的用途。
  • COMPOUNDS FOR USE IN THE TREATMENT OF KINETOPLASTID INFECTION
    申请人:C.N.C.C.S. S.c.a.r.l. Collezione Nazionale Dei Composti Chimici e Centro Screening
    公开号:EP3558980B1
    公开(公告)日:2021-01-27
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