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5-Amino-3-<2-aminoaethyl>-indazol | 98953-79-8

中文名称
——
中文别名
——
英文名称
5-Amino-3-<2-aminoaethyl>-indazol
英文别名
3-(2-amino-ethyl)-1(2)H-indazol-5-ylamine;3-(2-aminoethyl)-2H-indazol-5-amine
5-Amino-3-<2-aminoaethyl>-indazol化学式
CAS
98953-79-8
化学式
C9H12N4
mdl
——
分子量
176.221
InChiKey
LCZLUYVSHLDANC-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):
    0.2
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    80.7
  • 氢给体数:
    3
  • 氢受体数:
    3

文献信息

  • Substitited indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds, their prepartion and use in medicaments
    申请人:Esteve Laboratorios Dr. Esteve S.A.
    公开号:EP1676841A1
    公开(公告)日:2006-07-05
    The present invention relates to substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds of general formula I, a process for their preparation, medicaments comprising said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds as well as the use of said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds for the preparation of medicaments, which are particularly suitable for the prophylaxis and/or treatment of disorders or diseases that are at least partially mediated via 5-HT6 receptors.
    本发明涉及通式I的取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物,其制备方法,包含所述取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物的药物,以及利用所述取代吲唑磺胺基和2,3-二氢吲唑磺胺基化合物制备药物,该药物特别适用于预防和/或治疗至少部分通过5-HT6受体介导的疾病或疾病。
  • Substituted Indazolyl Sulfonamide and 2,3-Dihydro-Indolyl Sulfonamide Compounds, their Preparation and Use in Medicaments
    申请人:Merce Vidal Ramon
    公开号:US20090005417A1
    公开(公告)日:2009-01-01
    The present invention relates to substituted indazolyl sulfonamide and 2,3-dihydroindolyl sulfonamide compounds of general formula I, a process for their preparation, medicaments comprising said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds as well as the use of said substituted indazolyl sulfonamide and 2,3-dihydro-indolyl sulfonamide compounds for the preparation of medicaments, which are particularly suitable for the prophylaxis and/or treatment of disorders or diseases that are at least partially mediated via 5-HT 6 receptors.
    本发明涉及一般式I的取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物,以及它们的制备方法、包含所述取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物的药物,以及利用所述取代的吲唑磺酰胺和2,3-二氢吲哚磺酰胺化合物制备药物,特别适用于预防和/或治疗通过5-HT6受体介导的至少部分疾病或疾病的用途。
  • Combination of a NMDA-receptor ligand and a compound with 5-HT6 receptor affinity
    申请人:LABORATORIOS DEL DR. ESTEVE, S.A.
    公开号:EP1902733A1
    公开(公告)日:2008-03-26
    The present invention relates to an active substance combination comprising at least one compound with 5-HT6 receptor affinity, and at least NMDA-receptor ligand, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种由至少一种具有 5-HT6 受体亲和力的化合物和至少一种 NMDA 受体配体组成的活性物质组合、一种包含所述活性物质组合的药物,以及使用所述活性物质组合制造药物。
  • SUBSTITUTED INDAZOLYL SULFONAMIDE AND 2,3-DIHYDRO-INDOLYL SULFONAMIDE COMPOUNDS, THEIR PREPARATION AND USE IN MEDICAMENTS
    申请人:LABORATORIOS DEL DR. ESTEVE, S.A.
    公开号:EP1869002A1
    公开(公告)日:2007-12-26
  • COMBINATION OF A CHOLINESTERASE INHIBITOR AND A COMPOUND WITH 5-HT6 RECEPTOR AFFINITY
    申请人:Laboratorios Del. Dr. Esteve, S.A.
    公开号:EP2040755A1
    公开(公告)日:2009-04-01
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