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2-(pyridin-3-yl)-1,3-oxazole-4-carboxylic acid | 1014630-48-8

中文名称
——
中文别名
——
英文名称
2-(pyridin-3-yl)-1,3-oxazole-4-carboxylic acid
英文别名
2-(pyridine-3-yl)oxazole-4-carboxylic acid;2-pyridin-3-yl-1,3-oxazole-4-carboxylic acid
2-(pyridin-3-yl)-1,3-oxazole-4-carboxylic acid化学式
CAS
1014630-48-8
化学式
C9H6N2O3
mdl
——
分子量
190.158
InChiKey
WLESRXJDGURDDG-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):
    0.8
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    76.2
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    2-(pyridin-3-yl)-1,3-oxazole-4-carboxylic acidN-甲基咪唑 、 N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate 、 lithium hydroxide 作用下, 以 甲醇乙腈 为溶剂, 反应 2.0h, 生成 2-[6-Oxo-2-phenyl-5-[(2-pyridin-3-yl-1,3-oxazole-4-carbonyl)amino]pyrimidin-1-yl]acetic acid
    参考文献:
    名称:
    [EN] PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS
    [FR] COMPOSÉS PHARMACEUTIQUES POUR LE TRAITEMENT DE TROUBLES MÉDIÉS PAR LE COMPLÉMENT
    摘要:
    This disclosure provides compounds, compositions, and methods to treat medical disorders, such as complement-mediated disorders, including complement C1s-mediated disorders.
    公开号:
    WO2024035686A1
  • 作为产物:
    描述:
    3-吡啶甲醛 、 magnesium sulfate 、 三乙胺 、 lithium hydroxide 作用下, 以 四氢呋喃 为溶剂, 生成 2-(pyridin-3-yl)-1,3-oxazole-4-carboxylic acid
    参考文献:
    名称:
    [EN] PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS
    [FR] COMPOSÉS PHARMACEUTIQUES POUR LE TRAITEMENT DE TROUBLES MÉDIÉS PAR LE COMPLÉMENT
    摘要:
    This disclosure provides compounds, compositions, and methods to treat medical disorders, such as complement-mediated disorders, including complement C1s-mediated disorders.
    公开号:
    WO2024035686A1
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文献信息

  • [EN] DOPAMINE D3 RECEPTOR ANTAGONISTS COMPOUNDS<br/>[FR] COMPOSÉS ANTAGONISTES DES RÉCEPTEURS D3 À LA DOPAMINE
    申请人:INDIVIOR UK LTD
    公开号:WO2016067043A1
    公开(公告)日:2016-05-06
    The disclosure is directed to novel dopamine D3 receptor antagonists, processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them and their use in therapy, including treating drug dependency and psychosis.
    该披露涉及新型多巴胺D3受体拮抗剂,其制备方法,用于这些方法的中间体,含有它们的药物组合物以及它们在治疗中的用途,包括治疗药物依赖和精神病的用途。
  • Indazole Compounds as IRAK4 Inhibitors
    申请人:AURIGENE DISCOVERY TECHNOLOGIES LIMITED
    公开号:US20160326151A1
    公开(公告)日:2016-11-10
    The present invention provides indazole compounds of formula (I), which are therapeutically useful as kinase inhibitors, particularly IRAK4 inhibitors, wherein Z 1 , Z 2 , R 1 , R 2 , R 3 , ‘m’ and ‘n’ have the meanings given in the specification, and pharmaceutically acceptable salts or stereoisomers thereof that are useful in the treatment and prevention of diseases or disorders, in particular their use in diseases or disorders mediated by kinase enzyme, particularly IRAK4 enzyme. The present invention also provides pharmaceutical compositions comprising at least one of the compounds of the compound of formula (I) together with a pharmaceutically acceptable carrier, diluent or excipient.
    本发明提供了式(I)的吲唑化合物,作为激酶抑制剂在治疗上具有疗效,特别是IRAK4抑制剂,其中Z1、Z2、R1、R2、R3、'm'和'n'在规范中给出了含义,并且其药学上可接受的盐或立体异构体在治疗和预防疾病或疾病中有用,特别是它们在由激酶酶介导的疾病或疾病中的使用,特别是IRAK4酶。本发明还提供了包括至少一种式(I)化合物的药物组合物,以及药学上可接受的载体、稀释剂或赋形剂。
  • FAAH INHIBITORS
    申请人:Sprott Kevin
    公开号:US20090118503A1
    公开(公告)日:2009-05-07
    Indole derivatives that are useful for treating pain, inflammation and other conditions are described. Certain of the compounds are benzyl derivatives and others are benzoyl derivatives. The compounds are substituted at least at the 3 position of the indole.
    本文描述了可用于治疗疼痛、炎症和其他病症的吲哚生物。其中某些化合物是苄基衍生物,而其他化合物是苯甲酰基衍生物。这些化合物至少在吲哚的3位被取代。
  • USEFUL INDOLE COMPOUNDS
    申请人:Bartolini Wilmin
    公开号:US20090264653A1
    公开(公告)日:2009-10-22
    Indoles that have activity as inhibitors of FAAH are described as are indoles and indole derivatives that have activity as inhibitors of DAO.
    本文描述了具有FAAH抑制剂活性的吲哚化合物,以及具有DAO抑制剂活性的吲哚及其衍生物
  • INDOLE COMPOUNDS
    申请人:Talley John Jeffrey
    公开号:US20100197708A1
    公开(公告)日:2010-08-05
    Indole derivatives that are useful for treating pain, inflammation and other conditions are described. Certain of the compounds are benzyl derivatives and others are benzoyl derivatives. The compounds are substituted at least at the 3 position of the indole.
    本文介绍了用于治疗疼痛、炎症和其他疾病的吲哚生物。其中某些化合物是苄基衍生物,而其他化合物是苯甲酰基衍生物。这些化合物至少在吲哚的3位被取代。
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