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5-(2,6-dimethyl-phenyl)-cyclohexane-1,3-dione | 87822-15-9

中文名称
——
中文别名
——
英文名称
5-(2,6-dimethyl-phenyl)-cyclohexane-1,3-dione
英文别名
5-(2,6-Dimethylphenyl)cyclohexane-1,3-dione
5-(2,6-dimethyl-phenyl)-cyclohexane-1,3-dione化学式
CAS
87822-15-9
化学式
C14H16O2
mdl
——
分子量
216.28
InChiKey
YBWQRPSSVLQIRT-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):
    2.1
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    5-(2,6-dimethyl-phenyl)-cyclohexane-1,3-dione1H-1,2,4-三唑四丁基溴化铵potassium carbonate 作用下, 以 甲苯乙腈 为溶剂, 反应 2.0h, 生成 5-(2,6-dimethylphenyl)-2-(1-((2-methoxyphenyl)amino)ethylidene)cyclohexane-1,3-dione
    参考文献:
    名称:
    Novel Colchicine-Site Binders with a Cyclohexanedione Scaffold Identified through a Ligand-Based Virtual Screening Approach
    摘要:
    Vascular disrupting agents (VDAs) constitute an innovative anticancer therapy that targets the tumor endothelium, leading to tumor necrosis. Our approach for the identification of new VDAs has relied on a ligand 3-D shape similarity virtual screening (VS) approach using the ROCS program as the VS tool and as query colchicine and TN-16, which both bind the alpha,beta-tubulin dimer. One of the hits identified, using TN-16 as query, has been explored by the synthesis of its structural analogues, leading to 2-(1-((2-methoxyphenyl)amino)ethylidene)-5-phenylcyclohexane-1,3-dione (compound 16c) with an IC50 = 0.09 +/- 0.01 mu M in HMEC-1 and BAEC, being 100-fold more potent than the initial hit. Compound 16c caused cell cycle arrest in the G2/M phase and interacted with the colchicine-binding site in tubulin, as confirmed by a competition assay with N,N'-ethylenebis(iodoacetamide) and by fluorescence spectroscopy. Moreover, 16c destroyed an established endothelial tubular network at 1 mu M and inhibited the migration and invasion of human breast carcinoma cells at 0.4 mu M. In conclusion, our approach has led to a new chemotype of promising antiproliferative compounds with antimitotic and potential VDA properties.
    DOI:
    10.1021/jm401939g
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文献信息

  • Cyclohexane-1,3-Diones for Use in the Treatment of Amyotrophic Lateral Sclerosis
    申请人:Kirsch Donald R.
    公开号:US20120264765A1
    公开(公告)日:2012-10-18
    The present invention relates to the identification of provided cyclohexane-1,3-diones (CHD compounds) and pharmaceutical compositions thereof for treating subjects with amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases. The invention also provides methods of preparing the provided CHD compounds.
    本发明涉及提供的环己烷-1,3-二酮(CHD化合物)的鉴定及其制备的药物组合物,用于治疗患有肌萎缩侧索硬化症(ALS)和其他神经退行性疾病的受试者。本发明还提供了制备所述CHD化合物的方法。
  • Substituted dihydropyridines and methods of use
    申请人:Hurt Ray Clarence
    公开号:US20070112015A1
    公开(公告)日:2007-05-17
    Compounds are provided that are modulators of the C5a receptor. The compounds are substituted dihydropyridines and are useful in pharmaceutical compositions, methods for the treatment of diseases and disorders involving the pathologic activtation of C5a receptors.
    提供了调节C5a受体的化合物。这些化合物是取代二氢吡啶,并可用于制药组合物、治疗涉及C5a受体病理性激活的疾病和障碍的方法。
  • US8722939B2
    申请人:——
    公开号:US8722939B2
    公开(公告)日:2014-05-13
  • US9162968B2
    申请人:——
    公开号:US9162968B2
    公开(公告)日:2015-10-20
  • US9593069B2
    申请人:——
    公开号:US9593069B2
    公开(公告)日:2017-03-14
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