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2'-[(4-chlorophenylsulfonyl)oxy]-4'-methoxyacetophenone

中文名称
——
中文别名
——
英文名称
2'-[(4-chlorophenylsulfonyl)oxy]-4'-methoxyacetophenone
英文别名
(2-Acetyl-5-methoxy-phenyl) 4-chlorobenzenesulfonate;(2-acetyl-5-methoxyphenyl) 4-chlorobenzenesulfonate
2'-[(4-chlorophenylsulfonyl)oxy]-4'-methoxyacetophenone化学式
CAS
——
化学式
C15H13ClO5S
mdl
——
分子量
340.784
InChiKey
ICRPORGIFXVSBH-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):
    3.3
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    78
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • Low-dose paeonol derivatives alleviate lipid accumulation
    作者:Kuan-Chuan Pao、Jin-Feng Zhao、Tzong-Shyuan Lee、Ying-Pei Huang、Chien-Chung Han、Lin-Chiang Sherlock Huang、Kou-Hung Wu、Ming-Hua Hsu
    DOI:10.1039/c4ra13986k
    日期:——

    Here, we present a series of novel paeonol derivatives that prevent lipid accumulation at lower doses.

    这里,我们展示了一系列新颖的肉草酚衍生物,可以在较低剂量下防止脂质积聚。
  • Advanced generation of paeonol-phenylsufonyl derivatives as potential anti-HBV agents
    作者:Y. P. Huang、H. P. Shih、Y. C. Liang、H. H. Lin、M. C. Lin、C. W. Chen、T. J. Huang、Y. C. Kuo、C. C. Han、M. H. Hsu
    DOI:10.1039/c6ra06119b
    日期:——
    paeonol-phenylsulfonyl derivatives and found that the compound 2-acetyl-5-methoxyphenyl 4-methoxybenzenesulfonate (6f) had the most potent antiviral effect against HBV, with an IC50 value of 0.36 μM and a high selectivity index (SI; TC50/IC50) of 47.75. In this research, we modified compound 6f with a 2-aminothiazole scaffold and generated 13 novel paeonol derivatives by utilizing various benzoyl and acyl chlorides
    乙型肝炎病毒(HBV)感染会导致严重的肝脏疾病,开发可用于慢性乙型肝炎的有效药物仍然是全球消灭HBV的重要一步。最近,我们的小组设计了丹皮酚-苯磺酰基衍生物,发现化合物2-乙酰基-5-甲氧基苯基4-甲氧基苯磺酸酯(6f)对乙肝病毒具有最强的抗病毒作用,IC 50值为0.36μM,选择性指数高( SI; TC 50 / IC 50)为47.75。在本研究中,我们对化合物6f进行了改性用2-氨基噻唑骨架,利用各种苯甲酰和酰氯生成了13种新颖的pa药衍生物。在这一新一代产品中,化合物2-(2-苯甲并噻唑-4-基)-5-甲氧基苯基4-甲氧基苯磺酸盐(8a)的最高SI值为59.14,超过了化合物6f和拉米夫定(3TC)(可商购的抗病毒药物)的最高SI值。药品。因此,我们相信我们的研究可能为抗病毒药物的开发提供一些有用的信息。
  • Design, synthesis, and bioevaluation of paeonol derivatives as potential anti-HBV agents
    作者:Tsurng-Juhn Huang、Hong Chuang、Yu-Chuan Liang、Hui-Hsien Lin、Jia-Cherng Horng、Yu-Cheng Kuo、Chia-Wen Chen、Fu-Yuan Tsai、Shih-Chieh Yen、Shih-Ching Chou、Ming-Hua Hsu
    DOI:10.1016/j.ejmech.2014.11.050
    日期:2015.1
    Hepatitis B virus (HBV) is a causative reagent that frequently causes progressive liver diseases, leading to the development of acute, chronic hepatitis, cirrhosis, and eventually hepatocellular carcinoma (HCC). Despite several antiviral drugs including interferon-alpha and nucleotide derivatives are approved for clinical treatment for HBV, critical issues remain unresolved, e.g., low-to-moderate efficacy, adverse side effects, and resistant strains. In this study, novel Paeonol-phenylsulfonyl derivatives were synthesized and their antiviral effect against HBV was evaluated. The experimental results indicated that these compounds process significant antiviral potential, including the inhibition of viral antigen expression and secretion, and the suppression of HBV viral DNA replication. Among compounds synthesized in this research, compound 2-acetyl-5-methoxyphenyl 4-methoxybenzenesulfonate (7f) had the most potent inhibitory activity with IC50 value of 0.36 mu M, and high selectivity index, SI (TC50/IC50) 47.75; which exhibited an apparent inhibition effect on viral gene expression and viral propagation in cell culture model. So, we believe our compounds could serve as reservoir for antiviral drug development. (C) 2014 Elsevier Masson SAS. All rights reserved.
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