3-<4-(3-pyridylmethyl)phenyl>propionic acid | 75987-23-4

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 苯丙酸
• 英文名称: 3-<4-(3-pyridylmethyl)phenyl>propionic acid
• 英文别名: 3-[4-(pyridin-3-ylmethyl)phenyl]propionic acid；3-[4-(3-pyridylmethyl)phenyl]propionic acid；3-(4-Pyridin-3-ylmethyl-phenyl)-propionic acid; hydrochloride；3-[4-(pyridin-3-ylmethyl)phenyl]propanoic acid
• CAS: 75987-23-4
• 化学式: C₁₅H₁₅NO₂
• 分子量: 241.29
• InChiKey: KWEIRBHRWDIDAM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  50.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  3-氯甲基吡啶盐酸盐 在 palladium on activated charcoal 盐酸 、 sodium hydroxide 、 氢气 、 sodium hydride 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 15.17h， 生成 3-<4-(3-pyridylmethyl)phenyl>propionic acid
  参考文献：
  名称：

  Highly selective inhibitors of thromboxane synthetase. 2. Pyridine derivatives

  摘要：

  The enzyme thromboxane (TX) synthetase is inhibited by pyridine. The beta-substituted pyridine derivatives showed higher inhibitory potency than the gamma-substituted ones having the same side chain. Among the beta-substituted derivatives containing the omega-carboxyalkyl group, the compounds with 6-8 carbon atoms in the side chain were especially effective. The derivatives holding the phenylene group in the side chain exhibited much higher inhibitory activity than those of the alkylene type. Among them, (E)-3-[4-(3-pyridylmethyl)phenyl]-2-methylacrylic acid hydrochloride (5a) had the highest potency (IC50 = 3 x 10(-9) M). The beta-substituted pyridine derivatives and 1-substituted imidazole derivatives which had the same side chain showed almost the same potency. The beta-substituted pyridine derivatives do not inhibit arachidonic acid cyclooxygenase or prostaglandin I2 synthetase, two other enzymes of the arachidonic cascade.

  DOI：

  10.1021/jm00142a006

文献信息

• US4271170A
  申请人：——

  公开号：US4271170A

  公开（公告）日：1981-06-02
• US4317828A
  申请人：——

  公开号：US4317828A

  公开（公告）日：1982-03-02
• US4427682A
  申请人：——

  公开号：US4427682A

  公开（公告）日：1984-01-24
• Highly selective inhibitors of thromboxane synthetase. 2. Pyridine derivatives
  作者：Tadao Tanouchi、Masamori Kawamura、Isao Ohyama、Ikuo Kajiwara、Yohichi Iguchi、Takanori Okada、Tsumoru Miyamoto、Ken Taniguchi、Masaki Hayashi

  DOI：10.1021/jm00142a006

  日期：1981.10

  The enzyme thromboxane (TX) synthetase is inhibited by pyridine. The beta-substituted pyridine derivatives showed higher inhibitory potency than the gamma-substituted ones having the same side chain. Among the beta-substituted derivatives containing the omega-carboxyalkyl group, the compounds with 6-8 carbon atoms in the side chain were especially effective. The derivatives holding the phenylene group in the side chain exhibited much higher inhibitory activity than those of the alkylene type. Among them, (E)-3-[4-(3-pyridylmethyl)phenyl]-2-methylacrylic acid hydrochloride (5a) had the highest potency (IC50 = 3 x 10(-9) M). The beta-substituted pyridine derivatives and 1-substituted imidazole derivatives which had the same side chain showed almost the same potency. The beta-substituted pyridine derivatives do not inhibit arachidonic acid cyclooxygenase or prostaglandin I2 synthetase, two other enzymes of the arachidonic cascade.