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5-ethyl-2-(2-hydroxyethyl)pyrazole-3-carboxylic acid | 1541931-86-5

中文名称
——
中文别名
——
英文名称
5-ethyl-2-(2-hydroxyethyl)pyrazole-3-carboxylic acid
英文别名
——
5-ethyl-2-(2-hydroxyethyl)pyrazole-3-carboxylic acid化学式
CAS
1541931-86-5
化学式
C8H12N2O3
mdl
——
分子量
184.195
InChiKey
MOTBLPDVHFJFMD-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:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    75.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    methyl (4R)-4-amino-1-(1-benzofuran-3-ylcarbonyl)-L-prolylglycinate5-ethyl-2-(2-hydroxyethyl)pyrazole-3-carboxylic acidN,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以63%的产率得到methyl 2-((2S,4R)-1-(benzofuran-3-carbonyl)-4-(3-ethyl-1-(2-hydroxyethyl)-1H-pyrazole-5-carboxamido)pyrrolidine-2-carboxamido)acetate
    参考文献:
    名称:
    Encoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA
    摘要:
    Tuberculosis (TB) is one of the world's oldest and deadliest diseases, killing a person every 20 s. InhA, the enoyl-ACP reductase from Mycobacterium tuberculosis, is the target of the frontline antitubercular drug isoniazid (INH). Compounds that directly target InhA and do not require activation by mycobacterial catalase peroxidase KatG are promising candidates for treating infections caused by INH resistant strains. The application of the encoded library technology (ELT) to the discovery of direct InhA inhibitors yielded compound 7 endowed with good enzymatic potency but with low antitubercular potency. This work reports the hit identification, the selected strategy for potency optimization, the structure-activity relationships of a hundred analogues synthesized, and the results of the in vivo efficacy studies performed with the lead compound 65.
    DOI:
    10.1021/jm401326j
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