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4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)phenol | 1038982-05-6

中文名称
——
中文别名
——
英文名称
4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)phenol
英文别名
——
4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)phenol化学式
CAS
1038982-05-6
化学式
C11H10N2O2
mdl
MFCD11189787
分子量
202.213
InChiKey
HNSHSGHQGRLQRJ-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):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.272
  • 拓扑面积:
    59.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)phenol 、 (2-(chloromethyl)-3-fluoroallyl)carbamic acid tert-butyl ester 在 potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 20.0h, 生成
    参考文献:
    名称:
    EP3626699
    摘要:
    公开号:
  • 作为产物:
    描述:
    4-羟基苯甲腈吡啶羟胺 作用下, 以 乙醇 为溶剂, 反应 32.0h, 生成 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)phenol
    参考文献:
    名称:
    3-Aryl-1,2,4-oxadiazole Derivatives Active Against Human Rhinovirus
    摘要:
    The human rhinovirus (hRV) is the causative agent of the common cold that often aggravates respiratory complications in patients with asthma or chronic obstructive pulmonary disease. The high rate of mutations and variety of serotypes are limiting the development of anti-hRV drugs, which emphasizes the need for the discovery of novel lead compounds. Previously, we identified antiviral compound 1 that we used here as the starting material for developing a novel compound series with high efficacy against hRV-A and -B. Improved metabolic stability was achieved by substituting an ester moiety with a 1,2,4-oxadiazole group. Specifically, compound 3k exhibited a high efficacy against hRV-B14, hRV-A21, and hRV-A71, with EC50 values of 66.0, 22.0, and 3.7 nM, respectively, and a relevant hepatic stability (59.6 and 40.7% compound remaining after 30 min in rat and human liver microsomes, respectively). An in vivo study demonstrated that 3k possessed a desirable pharmacokinetic profile with low systemic clearance (0.158 L.h(-1).Kg(-1)) and modest oral bioavailability (27.8%). Hence, 3k appears to be an interesting candidate for the development of antiviral lead compounds.
    DOI:
    10.1021/acsmedchemlett.8b00134
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文献信息

  • SSAO INHIBITOR
    申请人:Shandong Danhong Pharmaceutical Co., Ltd.
    公开号:EP3626699A1
    公开(公告)日:2020-03-25
    The present invention provides an SSAO inhibitor and an application thereof in preparing a drug for treating a disease related to SSAO. In particular, the present invention provides a compound shown in formula (IV) and a pharmaceutically acceptable salt thereof.
    本发明提供了一种SSAO抑制剂及其在制备治疗与SSAO相关疾病的药物中的应用。特别是,本发明提供了一种式(IV)所示的化合物及其药学上可接受的盐。
  • SSAO inhibitor
    申请人:SHANDONG DANHONG PHARMACEUTICAL CO., LTD.
    公开号:US11001563B2
    公开(公告)日:2021-05-11
    The present invention provides an SSAO inhibitor and an application thereof in preparing a drug for treating a disease related to SSAO. In particular, the present invention provides a compound shown in formula (IV) and a pharmaceutically acceptable salt thereof.
    本发明提供了一种SSAO抑制剂及其在制备治疗与SSAO相关疾病的药物中的应用。 特别是,本发明提供了一种式(IV)所示的化合物及其药学上可接受的盐。
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