3-phenoxyisonicotinic acid | 54629-99-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-phenoxyisonicotinic acid
• 英文别名: 3-Phenoxy-isonicotinsaeure；3-Phenoxypyridine-4-carboxylic acid
• CAS: 54629-99-1
• 化学式: C₁₂H₉NO₃
• mdl: MFCD24160363
• 分子量: 215.208
• InChiKey: FDQFTGXHOIXOCY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  59.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-phenoxyisonicotinic acid 在 PPA 作用下， 反应 16.0h， 生成 5-(1-methyl-piperidin-4-yl)-5H-chromeno[2,3-c]pyridin-10-ol
  参考文献：
  名称：

  Benzopyranopyridine derivatives. 1. Aminoalkyl derivatives of the azaxanthenes as bronchodilating agents

  摘要：

  The preparation of the four isomeric azaxanthones 3 and a number of their aromatic ring substituted derivatives is described. These ketones were converted into the title compounds which were examined for their biological properties. The most interesting compound in this series, the 1-methyl-4-piperidylidene derivative of 1-azaxanthene, shows the profile of an orally effective potent bronchodilating agent as well as a moderate antihistamine. Biological properties of this compound were compared to a number of antihistamines as well as known bronchodilating agents. Structure-activity relationships are also discussed.

  DOI：

  10.1021/jm00235a001
• 作为产物：
  描述：

  苯酚 在 盐酸 、 copper(l) iodide 、 caesium carbonate 作用下， 以 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 生成 3-phenoxyisonicotinic acid
  参考文献：
  名称：

  INHIBITORS OF FIBROBLAST ACTIVATION PROTEIN

  摘要：

  描述了用于调节成纤维细胞活化蛋白（FAP）的化合物和组合物。这些化合物和组合物可能被用作治疗疾病的治疗剂，包括高增殖性疾病。

  公开号：

  US20190185451A1

文献信息

• Bis Aromatic Compounds for Use as LTC4 Synthase Inhibitors
  申请人：Nilsson Peter

  公开号：US20120004244A1

  公开（公告）日：2012-01-05

  There is provided compounds of formula I, wherein E 1 , E 2a , E 2b , E 2c , E 4 , D 1 , D 2 , D 3 , L 1 , Y 1 , L 2 and Y 2 have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of leukotriene C 4 synthase is desired and/or required, and particularly in the treatment of a respiratory disorder and/or inflammation.

  提供了I式化合物，其中E1、E2a、E2b、E2c、E4、D1、D2、D3、L1、Y1、L2和Y2在说明中给出了含义，以及其药学上可接受的盐。这些化合物在治疗需要或希望抑制白三烯C4合酶的疾病，特别是呼吸道疾病和/或炎症的治疗中是有用的。
• 3-Phenoxypyridine 1-oxides as anticonvulsant agents
  作者：Michael R. Pavia、Charles P. Taylor、Fred M. Hershenson、Sandra J. Lobbestael、Donald E. Butler

  DOI：10.1021/jm00399a027

  日期：1988.4

  The anticonvulsant activity of a series of 3-phenoxypyridine 1-oxides is described. An investigation carried out to optimize the activity/side effect ratio provided 4-methyl-3-phenoxypyridine 1-oxide, 3, as the derivative of choice. Overall, 3 has a pharmacological profile that is very similar to phenytoin. It exhibited significant anticonvulsant activity at doses that did not produce ataxia or sedation but caused increased spontaneous behavioral activity not seen with most anticonvulsants. The short duration of pharmacological effect of 3 was attributed to metabolic hydroxylation at the C-4 pyridine methyl group; however, structural modifications designed to inhibit this metabolic pathway were unsuccessful.
• VILLANI F. J.; MANN T. A.; WEFER E. A.; HANNON J.; LARCA L. L.; LANDON M.+, J. MED. CHEM. <JMCM-AR>, 1975, 18, NO 1, 1-8
  作者：VILLANI F. J.、 MANN T. A.、 WEFER E. A.、 HANNON J.、 LARCA L. L.、 LANDON M.+

  DOI：——

  日期：——
• PAVIA, MICHAEL R.;TAYLOR, CHARLES P.;HERSHENSON, FRED M.;LOBBESTAEL, SAND+, J. MED. CHEM., 31,(1988) N 4, 841-847
  作者：PAVIA, MICHAEL R.、TAYLOR, CHARLES P.、HERSHENSON, FRED M.、LOBBESTAEL, SAND+

  DOI：——

  日期：——
• [EN] INHIBITORS OF FIBROBLAST ACTIVATION PROTEIN<br/>[FR] INHIBITEURS DE LA PROTÉINE D'ACTIVATION DES FIBROBLASTES
  申请人：PRAXIS BIOTECH LLC

  公开号：WO2019118932A1

  公开（公告）日：2019-06-20

  Compounds and compositions for modulating fibroblast activation protein (FAP) are described. The compounds and compositions may find use as therapeutic agents for the treatment of diseases, including hyperproliferative diseases.