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1-methyl-7-methoxy-2-oxo-8-pentyloxy-1,2-dihydroquinoline-3-carboxylic acid methyl ester | 282089-48-9

中文名称
——
中文别名
——
英文名称
1-methyl-7-methoxy-2-oxo-8-pentyloxy-1,2-dihydroquinoline-3-carboxylic acid methyl ester
英文别名
Methyl 7-methoxy-1-methyl-2-oxo-8-pentoxyquinoline-3-carboxylate
1-methyl-7-methoxy-2-oxo-8-pentyloxy-1,2-dihydroquinoline-3-carboxylic acid methyl ester化学式
CAS
282089-48-9
化学式
C18H23NO5
mdl
——
分子量
333.384
InChiKey
UBIPCIUUNYZMLF-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):
    3.3
  • 重原子数:
    24
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    65.1
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • Antipruritics
    申请人:Yasui Kiyoshi
    公开号:US20050101590A1
    公开(公告)日:2005-05-12
    It is intended to provide antipruritics (drugs to control itching, antiitch agents and drugs to stop itching). It is found out that a compound having an agonistic activity to the cannabinoid receptor shows an antipruritics effect.
    这意味着它旨在提供止痒药(用于控制瘙痒的药物,抗瘙痒剂和止痒药)。研究发现,具有激动性作用的大麻素受体的化合物具有止痒效果。
  • 2-oxoquinoline compounds and pharmaceutical uses thereof
    申请人:——
    公开号:US20030191069A1
    公开(公告)日:2003-10-09
    A 2-oxoquinoline compound or its pharmaceutically acceptable salt of general formula [I]: 1 (wherein each symbol in the formula is as determined in the description), and its pharmaceutical use. The compound [I] of the present invention and its pharmaceutically acceptable salts selectively act on cannabinoid receptors, particularly on peripheral type cannabinoid receptors, and have fewer side effects on the central nervous system, having great immunosuppressive action, anti-inflammatory action or antiallergic action. Therefore, these compounds are useful as cannabinoid receptors (particularly peripheral type cannabinoid receptors) modulator, immunosuppressants, anti-inflammatory agents, and antiallergic agents.
    一种2-氧基喹啉化合物或其药学上可接受的盐,其通式为[I]:1(其中公式中的每个符号如说明中所确定的那样),以及其医药用途。本发明的化合物[I]及其药学上可接受的盐,能够选择性地作用于大麻素受体,特别是外周型大麻素受体,并且对中枢神经系统的副作用较少,具有很强的免疫抑制作用、抗炎作用或抗过敏作用。因此,这些化合物可用作大麻素受体(特别是外周型大麻素受体)调节剂、免疫抑制剂、抗炎剂和抗过敏剂。
  • 2-OXOQUINOLINE COMPOUNDS AND MEDICINAL USES THEREOF
    申请人:Japan Tobacco Inc.
    公开号:EP1142877A1
    公开(公告)日:2001-10-10
    A 2-oxoquinoline compound or its pharmaceutically acceptable salt of general formula [I]: (wherein each symbol in the formula is as determined in the description), and its pharmaceutical use. The compound [I] of the present invention and its pharmaceutically acceptable salts selectively act on cannabinoid receptors, particularly on peripheral type cannabinoid receptors, and have fewer side effects on the central nervous system, having great immunosuppressive action, anti-inflammatory action or antiallergic action. Therefore, these compounds are useful as cannabinoid receptors (particularly peripheral type cannabinoid receptors) modulator, immunosuppressants, anti-inflammatory agents, and antiallergic agents.
    通式[I]的 2-氧代喹啉化合物或其药学上可接受的盐: (其中式中各符号由说明中确定)及其药物用途。 本发明的化合物[I]及其药学上可接受的盐选择性地作用于大麻素受体,特别是外周型大麻素受体,对中枢神经系统的副作用较小,具有很好的免疫抑制作用、抗炎作用或抗过敏作用。因此,这些化合物可用作大麻素受体(特别是外周型大麻素受体)调节剂、免疫抑制剂、抗炎剂和抗过敏剂。
  • ANTIPRURITICS
    申请人:SHIONOGI & CO., LTD.
    公开号:EP1477186A1
    公开(公告)日:2004-11-17
    It is intended to provide antipruritics (drugs to control itching, antiitch agents and drugs to stop itching). It is found out that a compound having an agonistic activity to the cannabinoid receptor shows an antipruritics effect.
    其目的是提供止痒药(控制瘙痒的药物、止痒剂和止痒药)。研究发现,一种对大麻素受体具有激动活性的化合物具有止痒效果。
  • US6509352B1
    申请人:——
    公开号:US6509352B1
    公开(公告)日:2003-01-21
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