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(2-Methyl-2H-pyrazol-3-yl)acrylic acid

中文名称
——
中文别名
——
英文名称
(2-Methyl-2H-pyrazol-3-yl)acrylic acid
英文别名
3-(2-methylpyrazol-3-yl)prop-2-enoic acid
(2-Methyl-2H-pyrazol-3-yl)acrylic acid化学式
CAS
——
化学式
C7H8N2O2
mdl
MFCD08559038
分子量
152.15
InChiKey
FLMCGVRZSZMFDQ-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:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    55.1
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • ANTI-HIV COMPOUNDS
    申请人:Prosetta Antiviral, Inc.
    公开号:US20160168100A1
    公开(公告)日:2016-06-16
    This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
    这项发明提供了用于治疗病毒感染的四氢异喹啉等化合物,含有这类化合物的药物配方,以及抑制病毒(如HIV)复制或治疗疾病(如艾滋病)的方法。
  • [EN] CEPHEM COMPOUNDS<br/>[FR] COMPOSES CEPHEMES
    申请人:FUJISAWA PHARMACEUTICAL CO
    公开号:WO2004101571A1
    公开(公告)日:2004-11-25
    The present invention relates to a compound of the formula [I]: wherein R1 is lower alkyl which may have suitable substituent(s), R2 is amino, protected amino or guanidino, R3 is carboxy or protected carboxy, R4 is amino or protected amino, and A is lower alkylene, or a pharmaceutically acceptable salt thereof, a process for preparing a compound of the formula [I], and a pharmaceutical composition comprising a compound of the formula [I] in admixture with a pharmaceutically acceptable carrier.
    本发明涉及一种化合物,其化学式为[I]:其中R1是可能具有适当取代基的低碳烷基,R2是基、保护基或基,R3是羧基或保护羧基,R4是基或保护基,A是低碳烷基,或其在药学上可接受的盐,一种制备化合物[I]的方法,以及包含化合物[I]与药学上可接受的载体混合的药物组合物。
  • Cephem compounds
    申请人:Yamanaka Toshio
    公开号:US20050004094A1
    公开(公告)日:2005-01-06
    The present invention relates to a compound of the formula [I]: wherein R 1 is lower alkyl which may have suitable substituent(s), R 2 is amino, protected amino or guanidino, R 3 is carboxy or protected carboxy, R 4 is amino or protected amino, and A is lower alkylene, or a pharmaceutically acceptable salt thereof, a process for preparing a compound of the formula [I], and a pharmaceutical composition comprising a compound of the formula [I] in admixture with a pharmaceutically acceptable carrier.
    本发明涉及一种化合物,其化学式为[I],其中R1是较低的烷基,可以具有适当的取代基;R2是基,保护基或鸟氨酸基;R3是羧基或保护羧基;R4是基或保护基,A是较低的烷基烯,或其药学上可接受的盐,以及制备化合物[I]的方法和包含化合物[I]的药物组合物与药学上可接受的载体混合的药物组合物。
  • 2-phenethenyltetrahydro isoquinolines useful as anti-HIV compounds
    申请人:Prosetta Antiviral, Inc.
    公开号:US10195189B2
    公开(公告)日:2019-02-05
    This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
    除其他外,本发明还提供了用于治疗病毒感染的四氢异喹啉类化合物、含有此类化合物的药物制剂,以及抑制艾滋病毒等病毒复制或治疗艾滋病等疾病的方法。
  • 2-PHENETHENYLTETRAHYDRO ISOQUINOLINES USEFUL AS ANTI-HIV COMPOUNDS
    申请人:Prosetta Antiviral, Inc.
    公开号:US20170368051A1
    公开(公告)日:2017-12-28
    This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
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