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7-Methylpyrazolo[5,1-c][1,2,4]triazine

中文名称
——
中文别名
——
英文名称
7-Methylpyrazolo[5,1-c][1,2,4]triazine
英文别名
7-methylpyrazolo[5,1-c][1,2,4]triazine
7-Methylpyrazolo[5,1-c][1,2,4]triazine化学式
CAS
——
化学式
C6H6N4
mdl
——
分子量
134.14
InChiKey
HUXQMVQJQDSICF-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):
    -0.3
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Methods for treating neisseria gonorrhoeae infection with substituted 1,2-dihydro-2A,5,8A-triazaacenaphthylene-3,8-diones
    申请人:GlaxoSmithKline Intellectual Property Development Limited
    公开号:US10702521B2
    公开(公告)日:2020-07-07
    The present invention relates to methods for treating Neisseria Gonorrhoeae infection which comprises administering to a subject in need thereof novel 1,2-dihydro-2a,5,8a-triazaacenaphthylene-3,8-dione compounds: or pharmaceutically acceptable salts thereof and/or corresponding pharmaceutical compositions.
    本发明涉及治疗淋病双球菌感染的方法,包括向需要的受试者施用新型1,2-二氢-2a,5,8a-三氮杂蒽-3,8-二酮化合物:或其药学上可接受的盐和/或相应的药物组合物。
  • [EN] TRICYCLIC NITROGEN CONTAINING COMPOUNDS FOR TREATING NEISSERIA GONORRHOEA INFECTION<br/>[FR] COMPOSÉS CONTENANT DE L'AZOTE TRICYCLIQUE POUR LE TRAITEMENT DE L'INFECTION À NEISSERIA GONORRHOEAE
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2016027249A1
    公开(公告)日:2016-02-25
    The present invention relates to methods for treating Neisseria gonorrhoeae infection which comprises administering to a subject in need thereof novel Tricyclic nitrogen containing compounds and corresponding pharmaceutical compositions as described herein.
    本发明涉及一种治疗淋病奈瑟氏菌感染的方法,包括向需要该方法的受试者施用本文所述的新型三环氮含量化合物及相应的药物组成。
  • PRMT5 INHIBITORS AND USES THEREOF
    申请人:Epizyme, Inc.
    公开号:US20150191432A1
    公开(公告)日:2015-07-09
    Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.
    本文描述了公式(I)的化合物,其药学上可接受的盐和制药组合物。本发明的化合物对于抑制PRMT5活性是有用的。还描述了使用这些化合物治疗PRMT5介导的疾病的方法。
  • TETRAHYDRO- AND DIHYDRO-ISOQUINOLINE PRMT5 INHIBITORS AND USES THEREOF
    申请人:EPIZYME, INC.
    公开号:US20150344434A1
    公开(公告)日:2015-12-03
    Described herein are compounds of Formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5 mediated disorders are also described.
    本文描述了公式(A)的化合物,其药学上可接受的盐以及它们的药物组合物。本发明的化合物对于抑制PRMT5活性是有用的。还描述了使用这些化合物治疗PRMT5介导的疾病的方法。
  • PRMT5 INHIBITORS CONTAINING A DIHYDRO- OR TETRAHYDROISOQUINOLINE AND USES THEREOF
    申请人:EPIZYME, INC.
    公开号:US20150344433A1
    公开(公告)日:2015-12-03
    Described herein are compounds of Formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.
    本文描述了公式(A)的化合物,其药学上可接受的盐和药物组合物。本发明的化合物可用于抑制PRMT5活性。还描述了使用这些化合物治疗PRMT5介导的疾病的方法。
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