trans-2-(3-Methoxy-4-p-chlorophenylthioethoxy-5-cyanophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran | 205654-34-8

• 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: trans-2-(3-Methoxy-4-p-chlorophenylthioethoxy-5-cyanophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran
• 英文别名: 2-[2-(4-chlorophenyl)sulfanylethoxy]-3-methoxy-5-[(2S,5S)-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]benzonitrile
• CAS: 205654-34-8
• 化学式: C₂₉H₃₀ClNO₆S
• 分子量: 556.079
• InChiKey: VWFHRNWFOVZDRG-ZEQRLZLVSA-N

物化性质

• 沸点：
  678.8±55.0 °C(Predicted)
• 密度：
  1.31±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  38
• 可旋转键数：
  11
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  105
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  trans-2-(3-Methoxy-4-p-chlorophenylthioethoxy-5-cyanophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 2.5h， 以60%的产率得到[2-[2-(4-chlorophenyl)sulfanylethoxy]-3-methoxy-5-[(2S,5S)-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]phenyl]methanamine
  参考文献：
  名称：

  Ram; Balram; Ram, S. Raghu, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2003, vol. 42, # 9, p. 2063 - 2068

  摘要：

  DOI：
• 作为产物：
  描述：

  Trans-2-(3-Methoxy-4-p-chlorophenylthioethoxy-5-iodophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran 在 CuCN 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 trans-2-(3-Methoxy-4-p-chlorophenylthioethoxy-5-cyanophenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran
  参考文献：
  名称：

  PHARMACEUTICAL FORMULATIONS USEFUL TO TREAT INFLAMMATORY AND IMMUNE DISORDERS

  摘要：

  提供了一种用于治疗炎症和/或免疫紊乱的制药配方，特别是那些由血小板活化因子（“PAF”）或5-脂氧合酶产物介导的疾病。在一个实施例中，该配方是一种基本无水的软膏，含有从2,5-二芳基四氢呋喃、2,5-二芳基四氢噻吩、2,4-二芳基四氢呋喃、2,4-二芳基四氢噻吩、1,3-二芳基环戊烷、2,4-二芳基吡咯烷和2,5-二芳基吡咯烷等化合物组成的活性剂，以及一个增效剂组合，其中包含一个或多个C3-18酯，如琥珀酸二乙酯、碳酸丙二酯、己二酸二异丙酯和三乙酰甘油。在另一个实施例中，该配方是一种乳霜、凝胶、乳液、油剂等，含有晶体形式的活性剂。该发明还涵盖了该活性剂的新晶体形式，以及使用这些配方治疗患有炎症和/或免疫紊乱的个体的方法。还包括异丙醇（IPA）用于增强活性剂和制药配方的稳定性。

  公开号：

  US20030008914A1

文献信息

• Compounds and methods for the treatment of inflammatory and immune disorders
  申请人：——

  公开号：US20020177723A1

  公开（公告）日：2002-11-28

  2,5-Diaryl tetrahydrofurans, 2,5-diaryl tetrahydrothiophenes, 2,4-diaryl tetrahydrofurans, 2,4-diaryl tetrahydrothiophenes, 1,3-diaryl cyclopentanes, 2,4-diaryl pyrrolidines, and 2,5-diaryl pyrrolidines are disclosed that reduce the chemotaxis and respiratory burst leading to the formation of damaging oxygen radicals of polymorphonuclear leukocytes during an inflammatory or immune response. The compounds exhibit this biological activity by acting as PAF receptor antagonists, by inhibiting the enzyme 5-lipoxygenase, or by exhibiting dual activity, i. e., by acting as both a PAF receptor antagonist and inhibitor of 5-lipoxygenase. A method to treat disorders mediated by PAF or leukotrienes is also disclosed, that includes administering an effective amount of one or more of the above-identified compounds or a pharmaceutically acceptable salt thereof, optionally in a pharmaceutically acceptable carrier.

  本文披露了以下化合物：2,5-二芳基四氢呋喃，2,5-二芳基四氢噻吩，2,4-二芳基四氢呋喃，2,4-二芳基四氢噻吩，1,3-二芳基环戊烷，2,4-二芳基吡咯烷和2,5-二芳基吡咯烷，这些化合物可以减少多形核白细胞在炎症或免疫反应中的趋化和呼吸爆发，从而减少有害氧自由基的形成。这些化合物通过作为PAF受体拮抗剂、抑制5-脂氧合酶酶或表现出双重活性即同时作为PAF受体拮抗剂和5-脂氧合酶抑制剂来表现出这种生物活性。本文还披露了一种治疗PAF或白三烯介导的疾病的方法，包括在药学上可接受的载体中投与上述化合物或其药学上可接受的盐的有效量。
• [EN] 2,5-DIARYL TETRAHYDRO-THIOPHENES, -FURANS AND ANALOGS FOR THE TREATMENT OF INFLAMMATORY AND IMMUNE DISORDERS<br/>[FR] 2,5-DIARYLE TETRAHYDRO-THIOPHENES, -FURANES ET ANALOGUES UTILISES DANS LE TRAITEMENT DE TROUBLES INFLAMMATOIRES ET IMMUNS
  申请人：CYTOMED, INC.

  公开号：WO1994001430A1

  公开（公告）日：1994-01-20

  (EN) 2,5-Diaryl tetrahydrofurans, 2,5-diaryl tetrahydrothiophenes, 2,4-diaryl tetrahydrofurans, 2,4-diaryl tetrahydrothiophenes, 1,3-diaryl cyclopentanes, 2,4-diaryl pyrrolidines, and 2,5-diaryl pyrrolidines are disclosed that reduce the chemotaxis and respiratory burst leading to the formation of damaging oxygen radicals of polymorphonuclear leukocytes during an inflammatory or immune response. The compounds exhibit this biological activity by acting as PAF receptor antagonists, by inhibiting the enzyme 5-lipoxygenase, or by exhibiting dual acitivity, i.e., by acting as both a PAF receptor antagonist and inhibitor of 5-lipoxygenase. A method to treat disorders mediated by PAF or leukotrienes is also disclosed, that includes administering an effective amount of one or more of the above-identified compounds or a pharmaceutically acceptable salt thereof, optionally in a pharmaceutically acceptable carrier.(FR) L'invention concerne des 2,5-diaryle tétrahydrofuranes, des 2,5-diaryle tétrahydrothiophènes, des 2,4-diaryle tétrahydrofuranes, des 2,4-diaryle tétrahydrothiophènes, des 1,3-diaryle cyclopentanes, des 2,4-diaryle pyrrolidines, et des 2,5-diaryle pyrrolidines réduisant le chimiotactisme et la poussée respiratoire ayant pour effet la formation de radicaux oxygène dommageables de leucocytes polymorphonucléaires pendant une réaction inflammatoire ou immune. Les composés présentent cette activité biologique par leur action d'antagoniste de récepteur du facteur d'activation plaquettaire, par inhibition de la 5-lipoxygénase, ou par le fait qu'ils présentent une double activité, c'est-à-dire une action à la fois d'antagoniste de récepteur du facteur d'activation plaquettaire et d'inhibiteur de 5-lipoxygénase. L'invention concerne également un procédé de traitement de troubles induits par le facteur d'activation plaquettaire ou des leucotriènes, consistant à administrer une dose efficace d'un ou de plusieurs des composés précités ou d'un de leurs sels pharmaceutiquement acceptables, facultativement dans un excipient pharmaceutiquement acceptable.

  2,5-联苯呋喃-1-甲基环、2,5-联苯呋喃-1-氧基环、2,4双重苯基呋喃和呋喃-2,5双重基团的吩-1-甲基环、呋喃-2,4双重基团的吩-1-氧基环、1,3-联苯环戊烷、2,4双重苯基吡咯和2,5双重苯基吡咯的结构，这些化合物均具有通过减少多形核白细胞在炎症或免疫反应中的趋化性和呼吸性冲击波使它们产生有危害的氧自由基的作用。上述化合物具有抑制5-二酯酶或作为5-二酯酶抑制剂和抗%M 肾 экстрактора, or 抑制剂的双重活性。应用这些化合物是治疗由% M or лектоцифра所致的疾病的方法。
• (±)-<i>trans</i>-2-[3-Methoxy-4-(4-chlorophenylthioethoxy)-5-(<i>N</i>-methyl-<i>N</i>- hydroxyureidyl)methylphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (CMI-392), a Potent Dual 5-Lipoxygenase Inhibitor and Platelet-Activating Factor Receptor Antagonist
  作者：Xiong Cai、Ralph T. Scannell、David Yaeger、Md. Sajjat Hussoin、David B. Killian、Changgeng Qian、Joseph Eckman、San-Bao Hwang、Lynn Libertine-Garahan、C. Grace Yeh、Stephen H. Ip、T. Y. Shen

  DOI：10.1021/jm980046r

  日期：1998.5.1

  By incorporating an N-hydroxyurea functionality onto diaryltetrahydrofurans, a novel series of compounds was investigated as dual 5-lipoxygenese (5-LO) inhibitor and platelet-activating factor (PAF) receptor antagonist. These dual functional compounds were evaluated in vitro for 5-LO inhibition in RBL cell extracts and human whole blood, and PAF receptor antagonism in a receptor binding assay. PAF-induced hemoconcentration and arachidonic acid-and TPA-induced ear edema in mice were used to determine in vivo activities. The structure-activity relationship analysis to define a preclinical lead is presented. (+/-)-trans-2-[3-methoxy-4-(4-chlorophenylthioethoxy)-5-(N-methyl-N-hydroxyureidyl)methylphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (40, CMI-392) was selected for further study. In the arachidonic acid-induced mouse ear edema model, 40 was more potent than either zileuton (a 5-LO inhibitor) or BN 50739 (a PAF receptor antagonist), and it demonstrated the same inhibitory effect as a physical combination of the latter two agents. These results suggest that a single compound which both inhibits leukotriene synthesis and blocks PAF receptor binding may provide therapeutic advantages over single-acting agents. The clinical development of compound 40 is in progress.
• (±)-Trans-2-[3-methoxy-4-(4-chlorophenyl thioethoxy)-5-cyanophenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent PAF-receptor antagonist
  作者：B Ram、B Balram、P.K Sai Prakash

  DOI：10.1016/s0040-4020(99)00544-x

  日期：1999.8

  The synthesis of (+/-)-trans-2-[3-methoxy-4-(chlorophenylthioethoxyphenyl)-5-cyanophenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran from conmercially available acetovanillone and 3,4,5-trimethoxybenzaldehyde is described. (C) 1999 Elsevier Science Ltd. All rights reserved.
• Balram; Ram; Ram, S. Raghu, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2003, vol. 42, # 9, p. 2059 - 2062
  作者：Balram、Ram、Ram, S. Raghu

  DOI：——

  日期：——