Synthesis, preliminary structure–activity relationships, and in vitro biological evaluation of 6-aryl-3-amino-thieno[2,3-b]pyridine derivatives as potential anti-inflammatory agents
| Autor: | Li Yang, Ji-Yan Liu, Huan Liu, Mingli Xiang, Bo Wang, Jun He, Yi Li, Xiaohua Wu, Xiang-Ying Wang, Hai-Yun He |
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| Rok vydání: | 2013 |
| Předmět: |
Thienopyridines
Thienopyridine Stereochemistry medicine.drug_class Aryl Organic Chemistry Clinical Biochemistry Anti-Inflammatory Agents Pharmaceutical Science Nitric Oxide Biochemistry In vitro Anti-inflammatory Nitric oxide Structure-Activity Relationship chemistry.chemical_compound chemistry Drug Discovery Pyridine medicine Molecular Medicine No production Molecular Biology Biological evaluation |
| Zdroj: | Bioorganic & Medicinal Chemistry Letters. 23:2349-2352 |
| ISSN: | 0960-894X |
| DOI: | 10.1016/j.bmcl.2013.02.059 |
| Popis: | In our previous study, a series of 6-aryl-3-amino-thieno[2,3- b ]pyridine derivatives exhibited potent antiproliferative activities and an unique hepatocellular carcinoma (HCC)-specific anticancer activity was also observed. In further anti-inflammatory research, thienopyridine derivative 1a showed potent inhibition of nitric oxide (NO) production. So a series of thienopyridine analogues of 1a were synthesized and evaluated for anti-inflammatory activities. The structure–activity relationships (SARs) revealed that the most potent analogues 1f and 1o were identified as potent inhibitors of NO production with IC 50 values of 3.30 and 3.24 μM, respectively. These results suggest that these 6-aryl-3-amino-thieno[2,3- b ]pyridine derivatives might potentially constitute a novel class of anti-inflammatory agents, which require further studies. |
| Databáze: | OpenAIRE |
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