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3-Acetyl-5-hydroxy-2-methyl-1,4-naphthochinon | 92379-26-5

中文名称
——
中文别名
——
英文名称
3-Acetyl-5-hydroxy-2-methyl-1,4-naphthochinon
英文别名
3-Acetyl-5-hydroxy-2-methylnaphthalene-1,4-dione
3-Acetyl-5-hydroxy-2-methyl-1,4-naphthochinon化学式
CAS
92379-26-5
化学式
C13H10O4
mdl
——
分子量
230.22
InChiKey
CVFACISKKXPUFC-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):
    1.9
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    71.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • ANTI-CANCER LEAD MOLECULE
    申请人:King Abdullah University of Science and Technology
    公开号:EP2844237A1
    公开(公告)日:2015-03-11
  • CHOLESTERYL ESTER TRANSFER PROTEIN (CETP) INHIBITION IN THE TREATMENT OF CANCER
    申请人:King Abdullah University of Science and Technology
    公开号:EP3261628A1
    公开(公告)日:2018-01-03
  • US9890106B2
    申请人:——
    公开号:US9890106B2
    公开(公告)日:2018-02-13
  • [EN] ANTI-CANCER LEAD MOLECULE<br/>[FR] MOLÉCULE TÊTE DE SÉRIE ANTI-CANCER
    申请人:UNIV KING ABDULLAH SCI & TECH
    公开号:WO2013164683A1
    公开(公告)日:2013-11-07
    Derivatives of plumbagin can be selectively cytotoxic to breast cancer cells. Derivative 'A' (Acetyl Plumbagin) has emerged as a lead molecule for testing against estrogen positive breast cancer and has shown low hepatotoxicity as well as overall lower toxicity in nude mice model. The toxicity of derivative 'A' was determined to be even lower than vehicle control (ALT and AST markers). The possible mechanism of action identified based on the microarray experiments and pathway mapping shows that derivative 'A' could be acting by altering the cholesterol-related mechanisms. The low toxicity profile of derivative 'A' highlights its possible role'as future anti-cancer drug and/or as an adjuvant drug to reduce the toxicity of highly toxic chemotherapeutic 'drugs.
  • [EN] CHOLESTERYL ESTER TRANSFER PROTEIN (CETP) INHIBITION IN THE TREATMENT OF CANCER<br/>[FR] INHIBITION DE PROTÉINE DE TRANSFERT D'ESTER DE CHOLESTÉRYLE (CETP) DANS LE TRAITEMENT DE CANCER
    申请人:KING ABDULLAH UNIV OF SCIENCE & TECH
    公开号:WO2016135633A1
    公开(公告)日:2016-09-01
    In one embodiment, the invention provides methods of treatment which use therapeutically effective amounts of Choleste ryl Ester Transfer Protein (CETP) inhibitors to treat a variety of cancers. In certain embodiments, the inhibitor is a CETP-inhibiting small molecule, CETP-inhibiting antisense oligonucleotide, CETP-inhibiting siRNA or a CETP- inhibiting antibody. Related pharmaceutical compositions, kits, diagnostics and screens are also provided.
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