1-[4-(methylsulfonyl)butyl]cyclobutane carboxylic acid | 220880-27-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 1-[4-(methylsulfonyl)butyl]cyclobutane carboxylic acid
• 英文别名: 1-[4-(methylsulfonyl)butyl]cyclobutanecarboxylic Acid；1-[4-(Methylsulfonyl)butyl] cyclobutanecarboxylic acid；1-(4-methylsulfonylbutyl)cyclobutane-1-carboxylic acid
• CAS: 220880-27-3
• 化学式: C₁₀H₁₈O₄S
• 分子量: 234.317
• InChiKey: XBSPEEKYFGVFNT-UHFFFAOYSA-N

物化性质

• 沸点：
  441.4±18.0 °C(Predicted)
• 密度：
  1.234±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  79.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-[4-(methylsulfonyl)butyl]cyclobutane carboxylic acid 在 sodium hydroxide 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 15.0h， 生成 (S)-3-[4-(2,6-Dichloro-benzoylamino)-phenyl]-2-{[1-(4-methanesulfonyl-butyl)-cyclobutanecarbonyl]-amino}-propionic acid
  参考文献：
  名称：

  N-Cycloalkanoyl-l-Phenylalanine Derivatives as VCAM/VLA-4 Antagonists

  摘要：

  A systematic structure-activity relationship investigation of the lead compound I resulted the identification of several N-[(substituted alkyl)cycloalkanoyl]-4-[((2,6-dichlorophenyl)carbonyl)amino]-L-phenylalanine derivatives as potent VCAM/VLA-4 antagonists. The data are consistent with a model of these compounds in which these alkanoylphenylalanines reside in a compact gauche (-) bioactive conformation. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00386-4
• 作为产物：
  描述：

  环丁基甲酸甲酯 在 sodium hydroxide 、 双氧水 、 溶剂黄146 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 60.0h， 生成 1-[4-(methylsulfonyl)butyl]cyclobutane carboxylic acid
  参考文献：
  名称：

  N-Cycloalkanoyl-l-Phenylalanine Derivatives as VCAM/VLA-4 Antagonists

  摘要：

  A systematic structure-activity relationship investigation of the lead compound I resulted the identification of several N-[(substituted alkyl)cycloalkanoyl]-4-[((2,6-dichlorophenyl)carbonyl)amino]-L-phenylalanine derivatives as potent VCAM/VLA-4 antagonists. The data are consistent with a model of these compounds in which these alkanoylphenylalanines reside in a compact gauche (-) bioactive conformation. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00386-4

文献信息

• Thioamide derivatives
  申请人：Hoffmann-La Roche Inc.

  公开号：US06288267B1

  公开（公告）日：2001-09-11

  It has been discovered that compounds of the formula: and the pharmaceutically acceptable salts and esters thereof wherein X and Y are as defined below, inhibit the binding of VCAM-1 to VLA-4 and are useful in treating inflammation associated with chronic inflammatory diseases such as rheumatoid arthritis (RA), multiple sclerosis, (MS), asthma, and inflammatory bowel disease (I BD).

  已发现以下化合物的公式： 及其药用可接受的盐和酯，其中X和Y的定义如下，抑制VCAM-1与VLA-4的结合，并且在治疗与慢性炎症性疾病如类风湿性关节炎（RA）、多发性硬化（MS）、哮喘和炎症性肠病（IBD）相关的炎症方面是有用的。
• N-alkanoylphenylalanine derivatives
  申请人：——

  公开号：US20040210051A1

  公开（公告）日：2004-10-21

  Compounds of the formula: 1 are disclosed which have activity as inhibitors of binding between VCAM-1 and cells expressing VLA-4. Such compounds are useful for treating diseases whose symptoms and/or damage are related to the binding of VCAM-1 to cells expressing VLA-4.

  公式为1的化合物被披露，其具有作为VCAM-1和表达VLA-4的细胞之间结合抑制剂的活性。这些化合物对于治疗其症状和/或损伤与VCAM-1与表达VLA-4的细胞之间的结合有关的疾病是有用的。
• Diephenyl carbocyclic thioamide derivatives
  申请人：——

  公开号：US20010041799A1

  公开（公告）日：2001-11-15

  It has been discovered that compounds of the formula: 1 and the pharmaceutically acceptable salts and esters thereof wherein X and Y are as defined below, inhibit the binding of VCAM-1 to VLA-4 and are useful in treating inflammation associated with chronic inflammatory diseases such as rheumatoid arthritis (RA), multiple sclerosis, (MS), asthma, and inflammatory bowel disease (I BD).

  已发现以下化合物的公式：1及其药学上可接受的盐和酯，其中X和Y的定义如下，能够抑制VCAM-1与VLA-4的结合，并且适用于治疗与慢性炎症性疾病相关的炎症，例如类风湿性关节炎（RA），多发性硬化症（MS），哮喘和炎症性肠病（I BD）。
• PHENYL-KETO-IMIDAZOLIDINE THIOAMIDE DERIVATIVES
  申请人：——

  公开号：US20020010338A1

  公开（公告）日：2002-01-24

  It has been discovered that compounds of the formula: 1 and the pharmaceutically acceptable salts and esters thereof wherein X and Y are as defined below, inhibit the binding of VCAM-1 to VLA-4 and are useful in treating inflammation associated with chronic inflammatory diseases such as rheumatoid arthritis (RA), multiple sclerosis, (MS), asthma, and inflammatory bowel disease (I BD).

  已经发现了以下化合物的公式1及其药学上可接受的盐和酯，其中X和Y的定义如下，可以抑制VCAM-1与VLA-4的结合，并且在治疗与慢性炎症性疾病相关的炎症方面非常有用，如类风湿性关节炎（RA），多发性硬化症（MS），哮喘和炎症性肠病（IBD）。
• Diphenyl heterocyclic thioamide derivatives
  申请人：——

  公开号：US20020040148A1

  公开（公告）日：2002-04-04

  It has been discovered that compounds of the formula: 1 and the pharmaceutically acceptable salts and esters thereof wherein X and Y are as defined below, inhibit the binding of VCAM-1 to VLA-4 and are useful in treating inflammation associated with chronic inflammatory diseases such as rheumatoid arthritis (RA), multiple sclerosis, (MS), asthma, and inflammatory bowel disease (I BD).

  已经发现以下化合物的公式：1及其药学上可接受的盐和酯，其中X和Y的定义如下，可以抑制VCAM-1与VLA-4的结合，并且在治疗与慢性炎症性疾病相关的炎症方面非常有用，例如类风湿性关节炎（RA），多发性硬化症（MS），哮喘和炎症性肠病（I BD）。