(2-Chloro-4-methyl-phenyl)-acetyl chloride | 887140-04-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2-Chloro-4-methyl-phenyl)-acetyl chloride
• 英文别名: 2-(2-Chloro-4-methylphenyl)acetyl chloride
• CAS: 887140-04-7
• 化学式: C₉H₈Cl₂O
• 分子量: 203.068
• InChiKey: GGVFPIZQCGOFFO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (2-Chloro-4-methyl-phenyl)-acetyl chloride 在 盐酸 、 potassium carbonate 作用下， 以 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 生成 2-[2-(2-Chloro-4-methyl-phenyl)-acetyl]-4-(4-methylaminomethyl-phenyl)-2,4-dihydro-[1,2,4]triazol-3-one
  参考文献：
  名称：

  Structure-Based Optimization of Azole Antifungal Agents by CoMFA, CoMSIA, and Molecular Docking

  摘要：

  In a continuing effort to develop highly potent azole antifungal agents, the three-dimensional quantitative structure-activity relationship methods. CoMFA and CoMSIA, were applied using a set of novel azole antifungal compounds. The binding mode of the compounds at the active site of lanosterol 14 alpha-demethylase was further explored using the flexible docking method. Various hydrophobic, van der Waals,pi-pi stacking, and hydrogen bonding interactions were observed between the azoles and the enzyme. Based on results from the molecular modeling, a receptor-based pharmacophore model was established to guide the rational optimization of the azole antifungal agents. Thus, a total of 57 novel azoles were designed and synthesized by a three-step optimization process. In vitro antifungal assay revealed that the antifungal activities of these novel azoles were greatly improved, which confirmed the reliability of the model from molecular modeling.

  DOI：

  10.1021/jm051211n

文献信息

• US5622917A
  申请人：——

  公开号：US5622917A

  公开（公告）日：1997-04-22
• US5847211A
  申请人：——

  公开号：US5847211A

  公开（公告）日：1998-12-08
• Structure-Based Optimization of Azole Antifungal Agents by CoMFA, CoMSIA, and Molecular Docking
  作者：Chunquan Sheng、Wannian Zhang、Haitao Ji、Min Zhang、Yunlong Song、Hui Xu、Jie Zhu、Zhenyuan Miao、Qingfen Jiang、Jianzhong Yao、Youjun Zhou、Jü Zhu、Jiaguo Lü

  DOI：10.1021/jm051211n

  日期：2006.4.1

  In a continuing effort to develop highly potent azole antifungal agents, the three-dimensional quantitative structure-activity relationship methods. CoMFA and CoMSIA, were applied using a set of novel azole antifungal compounds. The binding mode of the compounds at the active site of lanosterol 14 alpha-demethylase was further explored using the flexible docking method. Various hydrophobic, van der Waals,pi-pi stacking, and hydrogen bonding interactions were observed between the azoles and the enzyme. Based on results from the molecular modeling, a receptor-based pharmacophore model was established to guide the rational optimization of the azole antifungal agents. Thus, a total of 57 novel azoles were designed and synthesized by a three-step optimization process. In vitro antifungal assay revealed that the antifungal activities of these novel azoles were greatly improved, which confirmed the reliability of the model from molecular modeling.