2-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester | 163117-68-8

• 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-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester
• 英文别名: 2-Methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester；ethyl 2-(3-ethoxycarbonylphenyl)-3-methoxybenzoate
• CAS: 163117-68-8
• 化学式: C₁₉H₂₀O₅
• 分子量: 328.365
• InChiKey: XSXWCOGTJBOWPZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  24
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  61.8
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester 在 二甲基溴化硼 、 偶氮二甲酸二异丙酯 、 三苯基膦 作用下， 以 四氢呋喃 、 1,2-二氯乙烷 为溶剂， 反应 100.0h， 生成 2-[(3,4-bisdecyloxy)phenyl]methoxy-[1,1'-biphenyl]-6,3'-dicarboxylic acid, diethyl ester
  参考文献：
  名称：

  Biaryl diacid inhibitors of human s-PLA 2 with anti-inflammatory activity

  摘要：

  Twenty-four hydrophobic dicarboxylic acids are described which were evaluated as inhibitors of 14 kDa human platelet phospholipase A(2) (HP-PLA(2)). In general, biarylacetic acid derivatives were found to be more active than biaryl acids or biaryl-propanoic acids. More potent inhibitors were obtained when hydrophobic groups were attached to the biaryl acid nucleus using an olefin linkage as compared to an ether linkage. Compounds with larger hydrophobic groups were usually more potent inhibitors of HP-PLA(2). Five of the compounds disclosed in this report (2, 4, 28, 36b and 36i) were found to possess significant anti-inflammatory activity in a phorbol ester induced mouse ear edema model of chronic inflammation. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(00)00047-x
• 作为产物：
  描述：

  2-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxaldehyde 在 盐酸 、 sodium chlorite 、 氨基磺酸 作用下， 以 四氢呋喃 为溶剂， 反应 24.25h， 生成 2-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester
  参考文献：
  名称：

  Biaryl diacid inhibitors of human s-PLA 2 with anti-inflammatory activity

  摘要：

  Twenty-four hydrophobic dicarboxylic acids are described which were evaluated as inhibitors of 14 kDa human platelet phospholipase A(2) (HP-PLA(2)). In general, biarylacetic acid derivatives were found to be more active than biaryl acids or biaryl-propanoic acids. More potent inhibitors were obtained when hydrophobic groups were attached to the biaryl acid nucleus using an olefin linkage as compared to an ether linkage. Compounds with larger hydrophobic groups were usually more potent inhibitors of HP-PLA(2). Five of the compounds disclosed in this report (2, 4, 28, 36b and 36i) were found to possess significant anti-inflammatory activity in a phorbol ester induced mouse ear edema model of chronic inflammation. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(00)00047-x

文献信息

• Biaryl phospholipase A.sub.2 inhibitors
  申请人：Bristol-Myers Squibb

  公开号：US05391817A1

  公开（公告）日：1995-02-21

  Certain novel biaryl compounds are effective phospholipase A.sub.2 (PLA.sub.2) inhibitors.

  某些新型联苯化合物是有效的磷脂酶A.sub.2（PLA.sub.2）抑制剂。
• Biaryl diacid inhibitors of human s-PLA 2 with anti-inflammatory activity
  作者：Dane M. Springer、Bing-Yu Luh、Joanne J. Bronson、Katharine E. McElhone、Muzammil M. Mansuri、Kurt R. Gregor、David O. Nettleton、Paul L. Stanley、Kenneth M. Tramposch

  DOI：10.1016/s0968-0896(00)00047-x

  日期：2000.5

  Twenty-four hydrophobic dicarboxylic acids are described which were evaluated as inhibitors of 14 kDa human platelet phospholipase A(2) (HP-PLA(2)). In general, biarylacetic acid derivatives were found to be more active than biaryl acids or biaryl-propanoic acids. More potent inhibitors were obtained when hydrophobic groups were attached to the biaryl acid nucleus using an olefin linkage as compared to an ether linkage. Compounds with larger hydrophobic groups were usually more potent inhibitors of HP-PLA(2). Five of the compounds disclosed in this report (2, 4, 28, 36b and 36i) were found to possess significant anti-inflammatory activity in a phorbol ester induced mouse ear edema model of chronic inflammation. (C) 2000 Elsevier Science Ltd. All rights reserved.