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6-Ethyl-5,6,7,8-tetrahydro-1,6-naphthyridin-2(1H)-one

中文名称
——
中文别名
——
英文名称
6-Ethyl-5,6,7,8-tetrahydro-1,6-naphthyridin-2(1H)-one
英文别名
6-ethyl-1,5,7,8-tetrahydro-1,6-naphthyridin-2-one
6-Ethyl-5,6,7,8-tetrahydro-1,6-naphthyridin-2(1H)-one化学式
CAS
——
化学式
C10H14N2O
mdl
——
分子量
178.23
InChiKey
ZXOKVMGXRMHCOU-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
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Compounds as autotaxin inhibitors and pharmaceutical compositions comprising the same
    申请人:LegoChem Biosciences, Inc.
    公开号:US10961242B2
    公开(公告)日:2021-03-30
    The present invention relates to novel compounds as autotoxin inhibitors for treatment and prophylaxis of conditions or a disorder caused by autotaxin activation or increased concentration of lysophosphatidic acid, and also a pharmaceutical composition containing the same. The novel compounds of the present invention are autotoxin inhibitors, and by inhibiting the production of lysophosphatidic acid, they are useful for treatment or prophylaxis of cardiovascular disorder, cancer, metabolic disorder, kidney disorder, liver disorder, inflammatory disorder, nervous system disorder, respiratory system disorder, fibrotic disease, ocular disorder, cholestatic and other forms of chronic pruritus, or acute or chronic organ transplant rejection.
    本发明涉及作为自体毒素抑制剂的新型化合物,用于治疗和预防由自体毒素激活或溶血磷脂酸浓度升高引起的病症或紊乱,以及含有本发明的药物组合物。 本发明的新型化合物是自体毒素抑制剂,通过抑制溶血磷脂酸的产生,可用于治疗或预防心血管疾病、癌症、代谢紊乱、肾脏疾病、肝脏疾病、炎症性疾病、神经系统疾病、呼吸系统疾病、纤维化疾病、眼部疾病、胆汁淤积性和其他形式的慢性瘙痒症,或急性或慢性器官移植排斥反应。
  • NOVEL COMPOUNDS AS AUTOTAXIN INHIBITORS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME
    申请人:LegoChem Biosciences, Inc.
    公开号:US20200172542A1
    公开(公告)日:2020-06-04
    The present invention relates to novel compounds as autotoxin inhibitors for treatment and prophylaxis of conditions or a disorder caused by autotaxin activation or increased concentration of lysophosphatidic acid, and also a pharmaceutical composition containing the same. The novel compounds of the present invention are autotoxin inhibitors, and by inhibiting the production of lysophosphatidic acid, they are useful for treatment or prophylaxis of cardiovascular disorder, cancer, metabolic disorder, kidney disorder, liver disorder, inflammatory disorder, nervous system disorder, respiratory system disorder, fibrotic disease, ocular disorder, cholestatic and other forms of chronic pruritus, or acute or chronic organ transplant rejection.
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