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Ethanone, 2-((5-methyl-1,3,4-thiadiazol-2-yl)amino)-1-phenyl- | 69463-59-8

中文名称
——
中文别名
——
英文名称
Ethanone, 2-((5-methyl-1,3,4-thiadiazol-2-yl)amino)-1-phenyl-
英文别名
2-[(5-methyl-1,3,4-thiadiazol-2-yl)amino]-1-phenylethanone
Ethanone, 2-((5-methyl-1,3,4-thiadiazol-2-yl)amino)-1-phenyl-化学式
CAS
69463-59-8
化学式
C11H11N3OS
mdl
——
分子量
233.29
InChiKey
ZJHDOYROHOPXHV-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):
    2.5
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    83.1
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • THERAPEUTIC AGENTS FOR TREATING AND PREVENTING AUTOIMMUNE DISEASES AND CANCER AND A SCREENING METHOD
    申请人:KING FAISAL UNIVERSITY
    公开号:US20200338058A1
    公开(公告)日:2020-10-29
    A method for treating and preventing autoimmune diseases and cancer can include administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising an Arid5a inhibitor and a pharmaceutically acceptable carrier. A screening method can include identifying candidate Arid5a inhibitors through in silico predicted binding to Arid5a target domains (Pocket X) and confirming Arid5a inhibition through in vitro by binding and luciferase assays.
  • [EN] THERAPEUTIC AGENTS FOR TREATING AND PREVENTING AUTOIMMUNE DISEASES AND CANCER AND A SCREENING METHOD<br/>[FR] AGENTS THÉRAPEUTIQUES POUR LE TRAITEMENT ET LA PRÉVENTION DE MALADIES AUTO-IMMUNES ET DU CANCER ET MÉTHODE DE DÉPISTAGE
    申请人:KING FAISAL UNIV
    公开号:WO2022003439A1
    公开(公告)日:2022-01-06
    A method for treating and preventing autoimmune diseases and cancer can include administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising an Arid5a inhibitor and a pharmaceutically acceptable carrier. A screening method can include identifying candidate Arid5a inhibitors through in silico predicted binding to Arid5a target domains (Pocket X) and confirming AridSa inhibition through in vitro by binding and luciferase assays.
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