4-(3-benzyloxy-phenyl)-2,4-dioxo-butyric acid ethyl ester | 57696-13-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-(3-benzyloxy-phenyl)-2,4-dioxo-butyric acid ethyl ester
• 英文别名: Ethyl-(m-benzyloxyphenyl)-pyruvate；Ethyl 2,4-dioxo-4-(3-phenylmethoxyphenyl)butanoate
• CAS: 57696-13-6
• 化学式: C₁₉H₁₈O₅
• 分子量: 326.349
• InChiKey: NOADONVIZUCJNO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  24
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  69.7
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-(3-benzyloxy-phenyl)-2,4-dioxo-butyric acid ethyl ester 在 sodium hydroxide 作用下， 以 甲醇 为溶剂， 生成 LZP4
  参考文献：
  名称：

  Discovery of α,γ-Diketo Acids as Potent Selective and Reversible Inhibitors of Hepatitis C Virus NS5b RNA-Dependent RNA Polymerase

  摘要：

  alpha,gamma-Diketo acids (DKA) were discovered from screening as selective and reversible inhibitors of hepatitis C virus NS5b RNA-dependent RNA polymerase. The diketo acid moiety proved essential for activity, while substitution on the gamma position was necessary for selectivity and potency. Optimization led to the identification of a DKA inhibitor of NS5b polymerase with IC50 = 45 nM, one of the most potent HCV NS5b polymerase inhibitors reported.

  DOI：

  10.1021/jm0342109
• 作为产物：
  描述：

  3-苄氧基苯乙酮 、 草酸二乙酯 在 sodium ethanolate 作用下， 以 四氢呋喃 为溶剂， 生成 4-(3-benzyloxy-phenyl)-2,4-dioxo-butyric acid ethyl ester
  参考文献：
  名称：

  Discovery of α,γ-Diketo Acids as Potent Selective and Reversible Inhibitors of Hepatitis C Virus NS5b RNA-Dependent RNA Polymerase

  摘要：

  alpha,gamma-Diketo acids (DKA) were discovered from screening as selective and reversible inhibitors of hepatitis C virus NS5b RNA-dependent RNA polymerase. The diketo acid moiety proved essential for activity, while substitution on the gamma position was necessary for selectivity and potency. Optimization led to the identification of a DKA inhibitor of NS5b polymerase with IC50 = 45 nM, one of the most potent HCV NS5b polymerase inhibitors reported.

  DOI：

  10.1021/jm0342109

文献信息

• NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE
  申请人：Sundaresan Kumar

  公开号：US20090239810A1

  公开（公告）日：2009-09-24

  The present invention relates to piperidine derivatives that act as inhibitors of stearoyl-CoA desaturase. The invention also relates to methods of preparing the compounds, compositions containing the compounds, and to methods of treatment using the compounds.

  本发明涉及作为硬脂酰辅酶A脱饱和酶抑制剂的哌啶衍生物。该发明还涉及制备这些化合物的方法、含有这些化合物的组合物，以及使用这些化合物进行治疗的方法。
• Azido-Containing aryl β-Diketo acid HIV-1 integrase inhibitors
  作者：Xuechun Zhang、Godwin C.G Pais、Evguenia S Svarovskaia、Christophe Marchand、Allison A Johnson、Rajeshri G Karki、Marc C Nicklaus、Vinay K Pathak、Yves Pommier、Terrence R Burke

  DOI：10.1016/s0960-894x(03)00059-3

  日期：2003.3

  Aryl beta-diketo acids (ADK) comprise a general class of potent HIV-1 integrase (IN) inhibitors, which can exhibit selective inhibition of strand transfer reactions in extracellular recombinant IN assays and provide potent antiviral effects in HIV-infected cells. Recent studies have shown that polycyclic aryl or aryl rings bearing aryl-containing substituents are components of potent members of this class. Reported herein is the first use of azido functionality as an aryl replacement in beta-diketo acid IN inhibitors. The ability of azido-containing inhibitors to exhibit potent inhibition of IN and antiviral protection in HIV-infected cells, renders the azide group of potential value in the further development of ADK-based IN inhibitors. (C) 2003 Elsevier Science Ltd. All rights reserved.
• OKA Y.; ITOH K.; MIYAKE A.; TADA N.; OMURA K.; TOMIMOTO M.; YURUGI S., CHEM. AND PHARM. BULL.<CPBT-AL>, 1975, 23, NO 10, 2306-2317
  作者：OKA Y.、 ITOH K.、 MIYAKE A.、 TADA N.、 OMURA K.、 TOMIMOTO M.、 YURUGI S.

  DOI：——

  日期：——
• NOVEL PIPERIDINE DERIVATIVES AS INHIBITORS OF STEAROYL-COA DESATURASE
  申请人：Forest Laboratories Holdings Limited

  公开号：EP2268143A2

  公开（公告）日：2011-01-05
• US8129376B2
  申请人：——

  公开号：US8129376B2

  公开（公告）日：2012-03-06