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N-(2-methoxyethyl)pyrazin-2-amine | 894808-32-3

中文名称
——
中文别名
——
英文名称
N-(2-methoxyethyl)pyrazin-2-amine
英文别名
——
N-(2-methoxyethyl)pyrazin-2-amine化学式
CAS
894808-32-3
化学式
C7H11N3O
mdl
MFCD11123102
分子量
153.184
InChiKey
SQHNPLCTJPREES-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):
    0.4
  • 重原子数:
    11
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    47
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    2,3-Diaminopyrazines as rho kinase inhibitors
    摘要:
    Inhibition of rho kinase ( ROCK) has been recognized as an important target for a number of diseases, including glaucoma. Herein we report SAR development around two hits from a kinase library that led to the discovery of the ROCK inhibitor compound 38. In vitro and in vivo analysis of this compound, including its effects in a monkey model of glaucoma will be discussed. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.12.012
  • 作为产物:
    参考文献:
    名称:
    2,3-Diaminopyrazines as rho kinase inhibitors
    摘要:
    Inhibition of rho kinase ( ROCK) has been recognized as an important target for a number of diseases, including glaucoma. Herein we report SAR development around two hits from a kinase library that led to the discovery of the ROCK inhibitor compound 38. In vitro and in vivo analysis of this compound, including its effects in a monkey model of glaucoma will be discussed. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.12.012
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文献信息

  • Aminopyrazine analogs for treating glaucoma and other rho kinase-mediated diseases and conditions
    申请人:Hellberg R. Mark
    公开号:US20060142307A1
    公开(公告)日:2006-06-29
    Methods for using aminopyrazine analogs to treat rho kinase-mediated diseases or rho kinase-mediated conditions, including controlling intraocular pressure and treating glaucoma, are disclosed. Ophthalmic pharmaceutical compositions useful in the treatment of eye diseases such as glaucoma, and additionally useful for controlling intraocular pressure, the compositions comprising an effective amount of aminopyrazine analogs, are also disclosed.
    使用氨基吡唑类似物治疗rho激酶介导的疾病或rho激酶介导的状况的方法被披露。这些疾病或状况包括控制眼内压和治疗青光眼。还披露了用于治疗眼疾如青光眼以及用于控制眼内压的眼科药物组合物,该组合物包含有效量的氨基吡唑类似物。
  • AMINOPYRAZINE ANALOGS FOR TREATING GLAUCOMA AND OTHER RHO KINASE-MEDIATED DISEASES AND CONDITIONS
    申请人:Hellberg Mark
    公开号:US20080269249A2
    公开(公告)日:2008-10-30
    Methods for using aminopyrazine analogs to treat rho kinase-mediated diseases or rho kinase-mediated conditions, including controlling intraocular pressure and treating glaucoma, are disclosed. Ophthalmic pharmaceutical compositions useful in the treatment of eye diseases such as glaucoma, and additionally useful for controlling intraocular pressure, the compositions comprising an effective amount of aminopyrazine analogs, are also disclosed.
    本发明公开了使用氨基吡嗪类似物治疗rho激酶介导的疾病或rho激酶介导的状况的方法,包括控制眼压和治疗青光眼。本发明还公开了用于治疗眼部疾病(如青光眼)和控制眼压的眼科药物组合物,该组合物包括有效量的氨基吡嗪类似物。
  • AMINOPYRAZINE ANALOGS FOR TREATING GLAUCOMA AND OTHER RHO KINASE-MEDIATED DISEASES
    申请人:Novartis AG
    公开号:EP1830853B1
    公开(公告)日:2011-08-10
  • 2,3-Diaminopyrazines as rho kinase inhibitors
    作者:Alan J. Henderson、Mark Hadden、Cheng Guo、Neema Douglas、Helene Decornez、Mark R. Hellberg、Andrew Rusinko、Marsha McLaughlin、Naj Sharif、Colene Drace、Raj Patil
    DOI:10.1016/j.bmcl.2009.12.012
    日期:2010.2
    Inhibition of rho kinase ( ROCK) has been recognized as an important target for a number of diseases, including glaucoma. Herein we report SAR development around two hits from a kinase library that led to the discovery of the ROCK inhibitor compound 38. In vitro and in vivo analysis of this compound, including its effects in a monkey model of glaucoma will be discussed. (C) 2009 Elsevier Ltd. All rights reserved.
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