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2-propionamidoisonicotinic acid | 1173066-86-8

中文名称
——
中文别名
——
英文名称
2-propionamidoisonicotinic acid
英文别名
2-(propanoylamino)pyridine-4-carboxylic acid
2-propionamidoisonicotinic acid化学式
CAS
1173066-86-8
化学式
C9H10N2O3
mdl
——
分子量
194.19
InChiKey
SFLVVAYXHGROMU-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:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    79.3
  • 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

  • 作为产物:
    描述:
    2-氨基异烟酸甲酯吡啶 、 sodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成 2-propionamidoisonicotinic acid
    参考文献:
    名称:
    [EN] HETEROCYCLIC DERIVATIVES AS Nav1.7 and Nav1.8 BLOCKERS
    [FR] DÉRIVÉS HÉTÉROCYLCIQUES UTILISÉS EN TANT QUE BLOQUEURS NAV1.7 ET NAV1.8
    摘要:
    本发明涉及具有阻断活性的杂环衍生物,其作用于Nav1.7和Nav1.8通道的电压门控钠通道,并且在处理或预防涉及电压门控钠通道的疾病和疾病方面具有用途。该发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及电压门控钠通道的疾病方面的用途。
    公开号:
    WO2020138271A1
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文献信息

  • [EN] AMIDE DERIVATIVES AS Nav1.7 and Nav1.8 BLOCKERS<br/>[FR] DÉRIVÉS D'AMIDE UTILISÉS EN TANT QUE BLOQUEURS DE NAV1,7 ET DE NAV1,8
    申请人:RAQUALIA PHARMA INC
    公开号:WO2018235851A1
    公开(公告)日:2018-12-27
    The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the Nav1.7 and Nav1.8 channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及酰胺衍生物,具有对Nav1.7和Nav1.8通道的阻塞活性,并且在涉及电压门控钠通道的疾病和疾病的治疗或预防中有用。该发明还涉及包含这些化合物的药物组合物,以及在涉及电压门控钠通道的疾病的预防或治疗中使用这些化合物和组合物。
  • [EN] ARYLAMIDE DERIVATIVES AS TTX-S BLOCKERS<br/>[FR] DÉRIVÉS D'ARYLAMIDE EN TANT QU'AGENTS BLOQUANTS DE TTX-S
    申请人:RAQUALIA PHARMA INC
    公开号:WO2012053186A1
    公开(公告)日:2012-04-26
    The present invention relates to arylamide derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及具有对电压门控钠通道(如TTX-S通道)具有阻塞活性的芳基酰胺衍生物,用于治疗或预防涉及电压门控钠通道的疾病和疾病。该发明还涉及包含这些化合物的药物组合物以及在预防或治疗涉及电压门控钠通道的这类疾病中使用这些化合物和组合物。
  • ARYLAMIDE DERIVATIVES AS TTX-S BLOCKERS
    申请人:Yamagishi Tatsuya
    公开号:US20140336377A1
    公开(公告)日:2014-11-13
    The present invention relates to arylamide derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及一种芳基酰胺衍生物,其具有阻断电压门控钠通道(如TTX-S通道)的活性,并且在涉及电压门控钠通道的疾病和疾病的治疗或预防中有用。本发明还涉及包含这些化合物的制药组合物以及这些化合物和组合物在涉及电压门控钠通道的这种疾病的预防或治疗中的使用。
  • Arylamide derivatives as TTX-S blockers
    申请人:Yamagishi Tatsuya
    公开号:US09302991B2
    公开(公告)日:2016-04-05
    The present invention relates to arylamide derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及芳基酰胺衍生物,其具有阻断电压门控钠通道(TTX-S通道)的活性,并且在治疗或预防涉及电压门控钠通道的疾病和疾病方面有用。本发明还涉及包含这些化合物的制药组合物以及在预防或治疗涉及电压门控钠通道的疾病方面使用这些化合物和组合物。
  • Amide derivatives as Nav1.7 and Nav1.8 blockers
    申请人:RaQualia Pharma Inc.
    公开号:US11154544B2
    公开(公告)日:2021-10-26
    The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the Nav1.7 and Nav1.8 channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及对电压门控钠通道(如 Nav1.7 和 Nav1.8 通道)具有阻断活性的酰胺衍生物,它们可用于治疗或预防涉及电压门控钠通道的紊乱和疾病。本发明还涉及包含这些化合物的药物组合物,以及这些化合物和组合物在预防或治疗涉及电压门控钠通道的此类疾病中的用途。
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