4-phenylthiazole-2-carboxamide | 145261-07-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-phenylthiazole-2-carboxamide
• 英文别名: (4-phenyl-thiazol-2-yl)-amide；phenylthiazole-2-carboxamide；4-phenyl-1,3-thiazole-2-carboxamide
• CAS: 145261-07-0
• 化学式: C₁₀H₈N₂OS
• 分子量: 204.252
• InChiKey: VZYJYKJYUQHDMJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  84.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-phenylthiazole-2-carboxamide 、 2-(4-氧代-3,4-二氢-1-酞嗪)乙酰肼 在 三乙胺 作用下， 反应 48.0h， 以25%的产率得到N'-(2-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)acetyl)-4-phenylthiazole-2-carbohydrazide
  参考文献：
  名称：

  Discovery of thiazolyl-phthalazinone acetamides as potent glucose uptake activators via high-throughput screening

  摘要：

  With the aim to discover orally active small molecules that stimulate glucose uptake, high throughput screening of a library of 5000 drug-like compounds was conducted in differentiated skeletal muscle cells in presence of insulin. N-Substituted phthalazinone acetamide was identified as a potential glucose uptake modulator. Several novel derivatives were synthesized to establish structure activity relationships. Identified lead thiazolyl-phthalazinone acetamide (7114863) increased glucose uptake (EC50 of 0.07 +/- 0.02 mu M) in differentiated skeletal muscle cells in presence of insulin. Furthermore, 7114863 was superior to rosiglitazone under similar experimental conditions without inducing PPAR-gamma agonist activity thus making it a very interesting scaffold. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.07.067
• 作为产物：
  描述：

  Ethyl 5-[1-(2-methoxyethyl)-6-oxo-1,6-dihydro-3-pyridazinyl]-4-phenyl-1,3-thiazole-2-carboxylate 、 环丙胺 在 乙醇 、 异丙醚 、 N-cyclopropyl-5-l 1-(2-methoxyethyl)-6-oxo-1,6-dihydro-3-pyridazinyl 作用下， 以 1,4-二氧六环 为溶剂， 反应 40.0h， 以to give N-cyclopropyl-5-l 1-(2-methoxyethyl)-6-oxo-1,6-dihydro-3-pyridazinyl]-4-phenyl-1,3-thiazole-2-carboxamide as a solid (77 mg)的产率得到4-phenylthiazole-2-carboxamide
  参考文献：
  名称：

  Thiazole derivative and pharmaceutical use thereof

  摘要：

  一种公式为(I)的噻唑衍生物，其中R是1-可选取代的6-氧代-1,6-二氢-3-吡啶基，R'是可选取代的苯基，而R2是氢，公式(i)的基团：其中R4是氢、较低的烷基或较低的烯基，而R5是氢、可选取代的较低烷基、酰基、环(较低)烷基、较低烯基、可选取代的芳基或杂环基，或公式(ii)的基团：其中X是氧或硫，R8是氢或较低的烷基，R9是氢、可选取代的较低烷基、环(较低)烷基、较低烷氧基或单-或双-较低烷基氨基，或R8和R9可以结合形成可选取代的饱和含氮杂环，或其盐。

  公开号：

  US20050004134A1

文献信息

• Piperazine and homopiperazine compounds
  申请人：Millennium Pharmaceuticals, Inc.

  公开号：US20030153556A1

  公开（公告）日：2003-08-14

  Compounds are provided having a piperazine or homopiperazine ring which are useful in the treatment of thrombosis.

  提供了具有哌嗪或同源哌嗪环的化合物，这些化合物在治疗血栓症方面很有用。
• Compounds Which Modulate The CB2 Receptor
  申请人：Berry Angela

  公开号：US20100009964A1

  公开（公告）日：2010-01-14

  Compounds of formula (I) are disclosed. Compounds according to the and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.

  公式（I）的化合物已被披露。根据该公式的化合物对治疗炎症有用。那些是激动剂的化合物还额外适用于治疗疼痛。
• Anti-Cytokine Heterocyclic Compounds
  申请人：Goldberg Daniel

  公开号：US20060276496A1

  公开（公告）日：2006-12-07

  Heterocyclic compounds and analogues thereof and their use as inhibitors of Mitogen-Activated Protein Kinase-Activated Protein kinase-2 (MAPKAP-k2), and also to a method for preventing or treating a disease or disorder that can be treated or prevented by modulating the activity of MAPKAP-K2 in a subject and to pharmaceutical compositions and kits that include these MAPKAP-K2 inhibitors.

  杂环化合物及其类似物以及它们作为丝裂原活化蛋白激酶-2（MAPKAP-k2）抑制剂的用途，以及用于预防或治疗可以通过调节受试者中MAPKAP-K2活性来治疗或预防的疾病或紊乱的方法，以及包括这些MAPKAP-K2抑制剂的药物组合物和试剂盒。
• PYRROLE-2-CARBOXAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS, THEIR PROCESS AND PHARMACEUTICAL APPLICATION
  申请人：Bhuniya Debnath

  公开号：US20100292143A1

  公开（公告）日：2010-11-18

  Pyrrole-2-carboxamide derivatives, their polymorphs, stereoisomers, prodrugs, solvates, pharmaceutically acceptable salts and formulations thereof, beneficial for prophylaxis, management, treatment, control of progression, or adjunct treatment of diseases and/or medical conditions where the activation of glucokinase would be beneficial, are disclosed. The disclosure also provides process of preparation of these pyrrole-2-carboxamides.

  吡咯烷-2-甲酰胺衍生物，其多晶型、立体异构体、前药、溶剂合物、药用可接受的盐及其制剂，有益于预防、治疗、控制疾病和/或医疗状况的进展，或辅助治疗，在这些疾病和/或医疗状况中，激活葡萄糖激酶将是有益的。该公开还提供了这些吡咯烷-2-甲酰胺的制备方法。
• Mercaptoamides as histone deacetylase inhibitors
  申请人：Ahmed Saleh

  公开号：US20060047123A1

  公开（公告）日：2006-03-02

  Mercaptoamide compounds, represented by Formulas (IA), (IB), (IIA), and (IIB): or a pharmaceutically acceptable salt thereof, inhibit histone deacetylase enzyme and are useful for the treatment and/or prevention of various infections, cancerous diseases, and conditions.

  巯基酰胺化合物，以化学式(IA)、(IB)、(IIA)和(IIB)表示，或其药用盐，抑制组蛋白去乙酰化酶，可用于治疗和/或预防各种感染、癌症疾病和疾病。