2-(4-(2-methoxyethoxy)phenyl)acetic acid | 1019344-55-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2-(4-(2-methoxyethoxy)phenyl)acetic acid
• 英文别名: (4-(2-methoxyethoxy)phenyl)acetic acid；2-[4-(2-Methoxyethoxy)phenyl]acetic acid
• CAS: 1019344-55-8
• 化学式: C₁₁H₁₄O₄
• mdl: MFCD11131696
• 分子量: 210.23
• InChiKey: JPXYFPAHBJSIHB-UHFFFAOYSA-N

物化性质

• 沸点：
  361.5±27.0 °C(Predicted)
• 密度：
  1.166±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-(4-(2-methoxyethoxy)phenyl)acetic acid 在 硫酸 、 叠氮磷酸二苯酯 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 作用下， 以 甲苯 、 乙腈 为溶剂， 反应 7.25h， 生成 C₂₅H₂₄N₆O₄
  参考文献：
  名称：

  Structure-based drug design and potent anti-cancer activity of tricyclic 5:7:5-fused diimidazo[4,5-d:4′,5′-f][1,3]diazepines

  摘要：

  Judicial structural modifications of 5: 7-fused ring-expanded nucleosides (RENs), based on molecular modeling studies with one of its known targets, human RNA helicase (hDDX3), led to the lead, novel, 5:7-5-fused tricyclic heterocycle (1). The latter exhibited promising broad-spectrum in vitro anti-cancer activity against a number of cancer cell lines screened. This paper describes our systematic, albeit limited, structure-activity relationship (SAR) studies on this lead compound, which produced a number of analogs with broad-spectrum in vitro anti-cancer activities against lung, breast, prostate, and ovarian cancer cell lines, in particular compounds 15i, 15j, 15m and 15n which showed IC50 values in submicromolar to micromolar range, and are worthy of further explorations. The SAR data also enabled us to propose a tentative SAR model for future SAR efforts for ultimate realization of optimally active and minimally toxic anti-cancer compounds based on the diimidazo[4,5-d:4',5'-f][1,3]diazepine structural skeleton of the lead compound 1. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.11.050
• 作为产物：
  描述：

  对羟基苯乙酸 在 lithium hydroxide monohydrate 、 硫酸 、 水 、 potassium carbonate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 16.0h， 生成 2-(4-(2-methoxyethoxy)phenyl)acetic acid
  参考文献：
  名称：

  Structure-based drug design and potent anti-cancer activity of tricyclic 5:7:5-fused diimidazo[4,5-d:4′,5′-f][1,3]diazepines

  摘要：

  Judicial structural modifications of 5: 7-fused ring-expanded nucleosides (RENs), based on molecular modeling studies with one of its known targets, human RNA helicase (hDDX3), led to the lead, novel, 5:7-5-fused tricyclic heterocycle (1). The latter exhibited promising broad-spectrum in vitro anti-cancer activity against a number of cancer cell lines screened. This paper describes our systematic, albeit limited, structure-activity relationship (SAR) studies on this lead compound, which produced a number of analogs with broad-spectrum in vitro anti-cancer activities against lung, breast, prostate, and ovarian cancer cell lines, in particular compounds 15i, 15j, 15m and 15n which showed IC50 values in submicromolar to micromolar range, and are worthy of further explorations. The SAR data also enabled us to propose a tentative SAR model for future SAR efforts for ultimate realization of optimally active and minimally toxic anti-cancer compounds based on the diimidazo[4,5-d:4',5'-f][1,3]diazepine structural skeleton of the lead compound 1. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.11.050

文献信息

• Piperazine and Piperidine MGLUR5 Potentiators
  申请人：Arora Jalaj

  公开号：US20100144710A1

  公开（公告）日：2010-06-10

  Compounds of Formula I or pharmaceutically acceptable salts or solvates thereof, wherein A, B, D, Ar1, Ar2, R2, R3, R4, a, m and n are defined in the specification, methods for the use thereof, processes for making and pharmaceutical compositions containing the same.

  公式I的化合物或其药学上可接受的盐或溶剂化物，其中A、B、D、Ar1、Ar2、R2、R3、R4、a、m和n在说明书中有定义，其使用方法、制备方法和含有它们的药物组合物。
• Biaryl compound, preparation method and use thereof
  申请人：FUDAN UNIVERSITY

  公开号：US10844017B2

  公开（公告）日：2020-11-24

  The present invention belongs to the technical field of chemical pharmaceuticals, and relates to a compound represented by general formula (I) or formula (II) and a preparation method thereof. The compounds are biaryl derivatives with RORγt activation activity. The biaryl derivatives disclosed in this invention can effectively activate the RORγt protein receptor, and thereby promote the differentiation of Th17 cells and increasing the production of IL-17, which can be used as an immune modulator for the treatment of various cancers or viral infection-related diseases.

  本发明属于化学制药技术领域，涉及一种由通式（I）或式（II）代表的化合物及其制备方法。这些化合物是具有 RORγt 活化活性的双芳基衍生物。本发明公开的双芳基衍生物能有效激活 RORγt 蛋白受体，从而促进 Th17 细胞的分化，增加 IL-17 的产生，可作为免疫调节剂用于治疗各种癌症或病毒感染相关疾病。
• [EN] PIPERAZINE AND PIPERIDINE MGLUR5 POTENTIATORS<br/>[FR] PIPÉRAZINE ET POTENTIALISATEURS MGLUR5 DE PIPÉRIDINE
  申请人：ASTRAZENECA AB

  公开号：WO2008112440A1

  公开（公告）日：2008-09-18

  [EN] Compounds of Formula I or pharmaceutically acceptable salts or solvates thereof, wherein A, B, D, Ar1, Ar2, R2, R3, R4, a, m and n are defined in the specification, methods for the use thereof, processes for making and pharmaceutical compositions containing the same.
  [FR] L'invention concerne des composés de formule I ou leurs sels ou leurs solvates pharmaceutiquement acceptables, où A, B, D, Ar1, Ar2, R2, R3, R4, a, m et n sont définis dans le mémoire, des procédés d'utilisation de ceux-ci, des procédés de fabrication et des compositions pharmaceutiques les contenant.
• Structure-based drug design and potent anti-cancer activity of tricyclic 5:7:5-fused diimidazo[4,5-d:4′,5′-f][1,3]diazepines
  作者：Atul Kondaskar、Shilpi Kondaskar、James C. Fishbein、Brandon A. Carter-Cooper、Rena G. Lapidus、Mariola Sadowska、Martin J. Edelman、Ramachandra S. Hosmane

  DOI：10.1016/j.bmc.2012.11.050

  日期：2013.2

  Judicial structural modifications of 5: 7-fused ring-expanded nucleosides (RENs), based on molecular modeling studies with one of its known targets, human RNA helicase (hDDX3), led to the lead, novel, 5:7-5-fused tricyclic heterocycle (1). The latter exhibited promising broad-spectrum in vitro anti-cancer activity against a number of cancer cell lines screened. This paper describes our systematic, albeit limited, structure-activity relationship (SAR) studies on this lead compound, which produced a number of analogs with broad-spectrum in vitro anti-cancer activities against lung, breast, prostate, and ovarian cancer cell lines, in particular compounds 15i, 15j, 15m and 15n which showed IC50 values in submicromolar to micromolar range, and are worthy of further explorations. The SAR data also enabled us to propose a tentative SAR model for future SAR efforts for ultimate realization of optimally active and minimally toxic anti-cancer compounds based on the diimidazo[4,5-d:4',5'-f][1,3]diazepine structural skeleton of the lead compound 1. (C) 2012 Elsevier Ltd. All rights reserved.