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1-(2-Methoxy-phenyl)-3-(4-nitro-phenyl)-5-phenyl-4,5-dihydro-1H-pyrazole

中文名称
——
中文别名
——
英文名称
1-(2-Methoxy-phenyl)-3-(4-nitro-phenyl)-5-phenyl-4,5-dihydro-1H-pyrazole
英文别名
2-(2-methoxyphenyl)-5-(4-nitrophenyl)-3-phenyl-3,4-dihydropyrazole
1-(2-Methoxy-phenyl)-3-(4-nitro-phenyl)-5-phenyl-4,5-dihydro-1H-pyrazole化学式
CAS
——
化学式
C22H19N3O3
mdl
——
分子量
373.4
InChiKey
OFUOEGQNHUFNKF-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):
    4.8
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    70.6
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • MODULATORS OF MYOCYTE LIPID ACCUMULATION AND INSULIN RESISTANCE AND METHODS OF USE THEREOF
    申请人:Sanford Burnham Prebys Medical Discovery Institute
    公开号:US20180222874A1
    公开(公告)日:2018-08-09
    Formulations and methods for reducing blood glucose and/or increasing insulin signaling in a subject have been developed. The formulations include SBI-477 and compounds based on SBI-477 i.e., SBI-477 analogs (collectively, SBI-477 compounds) and/or Mondo family inhibitors, in an effective amount to inhibit intracellular lipid accumulation and/or increase cellular glucose uptake when compared to levels in a control subject not administered the composition. Also disclosed are methods of reducing intracellular lipid accumulation and/or increase glucose uptake in a subject in need thereof. The method includes administering to the subject an effective amount of SBI-477 compounds and/or Mondo family inhibitor to reducing intracellular lipid accumulation and/or increase glucose uptake in the subject. Also disclosed are method for treating one or more Myc-driven cancers, including neuroblastoma, lung squamous cell carcinoma/lung adenocarcinoma, liver hepatocellular carcinoma, colon adenocarcinoma, acute myeloid leukemia, and breast invasive carcinoma.
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