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2-(3-chloro-6-methoxy-indazol-1-yl)-1-methyl-ethylamine | 362512-19-4

中文名称
——
中文别名
——
英文名称
2-(3-chloro-6-methoxy-indazol-1-yl)-1-methyl-ethylamine
英文别名
1-(3-Chloro-6-methoxyindazol-1-yl)propan-2-amine
2-(3-chloro-6-methoxy-indazol-1-yl)-1-methyl-ethylamine化学式
CAS
362512-19-4
化学式
C11H14ClN3O
mdl
——
分子量
239.705
InChiKey
PNHDUSKIMUKQDR-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):
    1.9
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    53.1
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • Ophthalmic compositions for treating ocular hypertension
    申请人:——
    公开号:US20040097575A1
    公开(公告)日:2004-05-20
    This invention relates to potent potassium channel blocker compounds of Formula I or a formulation thereof for the treatment of glaucoma and other conditions which leads to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use of such compounds to provide a neuroprotective effect to the eye of mammalian species, particularly humans.
    这项发明涉及公式I的强效钾通道阻滞剂化合物或其制剂,用于治疗青光眼和其他导致患者眼内压升高的疾病。该发明还涉及使用这些化合物为哺乳动物,特别是人类的眼提供神经保护作用。
  • [EN] OPHTHALMIC COMPOSITIONS FOR TREATING OCULAR HYPERTENSION<br/>[FR] COMPOSITIONS OPHTALMIQUES TRAITANT L'HYPERTENSION OCULAIRE
    申请人:MERCK & CO INC
    公开号:WO2005026128A1
    公开(公告)日:2005-03-24
    This invention relates to potent potassium channel blocker compounds of Formula (I) or a formulation thereof for the treatment of glaucoma and other conditions which leads to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use of such compounds to provide a neuroprotective effect to the eye of mammalian species, particularly humans, or a pharmaceutically acceptable salt, in vivo hydrolysable ester, enantiomer, diastereomer or mixture thereof: formula (II) represents C6-10 aryl or C3-10 heterocyclyl, said aryl or heterocyclyl optionally substituted with 1-3 groups selected from Ra; Z represents (CH2)nPO(OR)(OR*).
    这项发明涉及公式(I)的强效钾通道阻滞剂化合物或其制剂,用于治疗青光眼和其他导致患者眼内压升高的疾病。该发明还涉及利用这些化合物为哺乳动物,特别是人类的眼提供神经保护作用,或其药用可接受的盐、体内可水解酯、对映体、二对映体或其混合物的用途:公式(II)代表C6-10芳基或C3-10杂环烷基,所述芳基或杂环烷基可选择地取代为1-3个Ra基团;Z代表(CH2)nPO(OR)(OR*)。
  • Pyrroloquinoline Derivatives And Their Use As Protein Kinases Inhibitors
    申请人:Bienayme Hugues
    公开号:US20090042876A1
    公开(公告)日:2009-02-12
    The present invention relates to inhibitors of protein kinases of formula I: which can be used in the treatment of various diseases, notably cancer, inflammation or disorders of the central nervous system. It also relates to pharmaceutical compositions containing the compounds according to the invention and their use in therapy.
    本发明涉及式I的蛋白激酶抑制剂,可用于治疗各种疾病,特别是癌症、炎症或中枢神经系统疾病。还涉及含有根据本发明的化合物的药物组合物及其在治疗中的应用。
  • [EN] OPHTHALMIC COMPOSITIONS FOR TREATING OCULAR HYPERTENSION<br/>[FR] COMPOSITIONS OPHTALMIQUES POUR TRAITER L'HYPERTENSION OCULAIRE
    申请人:MERCK & CO INC
    公开号:WO2005025568A1
    公开(公告)日:2005-03-24
    This invention relates to potent potassium channel blocker compounds of structural Formula I or a formulation thereof for the treatment of glaucoma and other conditions which leads to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use of such compounds to provide a neuroprotective effect to the eye of mammalian species, particularly humans.
    这项发明涉及结构式I的强效钾通道阻滞剂化合物或其制剂,用于治疗青光眼和其他导致患者眼内压升高的疾病。该发明还涉及利用这些化合物为哺乳动物,特别是人类的眼提供神经保护作用。
  • EP4 receptor agonist, compositions and methods thereof
    申请人:——
    公开号:US20040198701A1
    公开(公告)日:2004-10-07
    This invention relates to potent selective agonists of the EP 4 subtype of prostaglandin E2 receptors, their use or a formulation thereof in the treatment of glaucoma and other conditions, which are related to elevated intraocular pressure in the eye of a patient. This invention further relates to the use of the compounds of this invention for mediating the bone modeling and remodeling processes of the osteoblasts and osteoclasts.
    这项发明涉及到前列腺素E2受体EP4亚型的强效选择性激动剂,以及它们在治疗青光眼和其他与患者眼内高眼压相关的疾病中的使用或配方。此发明还涉及将本发明的化合物用于介导成骨细胞和破骨细胞的骨建模和重塑过程。
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