Benzamide and Benzamidine Compounds as New Inhibitors of Urokinase-type Plasminogen Activators
dc.contributor.author | Kus, Canan | |
dc.contributor.author | Ozer, Ezgi | |
dc.contributor.author | Korkmaz, Yesim | |
dc.contributor.author | Yurtcu, Erkan | |
dc.contributor.author | Dagalp, Rukiye | |
dc.contributor.orcID | 0000-0001-6141-6788 | en_US |
dc.contributor.orcID | 0000-0003-4930-8164 | en_US |
dc.contributor.orcID | 0000-0002-7335-8578 | en_US |
dc.contributor.pubmedID | 30112993 | en_US |
dc.contributor.researcherID | AAG-1459-2020 | en_US |
dc.contributor.researcherID | AAA-2998-2021 | en_US |
dc.contributor.researcherID | W-1812-2017 | en_US |
dc.date.accessioned | 2023-05-11T13:25:04Z | |
dc.date.available | 2023-05-11T13:25:04Z | |
dc.date.issued | 2018 | |
dc.description.abstract | Background & Method: In this ongoing research, it is aimed to investigate the synthesis, structure identification and effects on urokinase-type plasminogen activators (uPA) and its receptor levels of 4-(3H-imidazo[4,5-b] pyridin-2-yl)-N-substituted benzamide and benzamidine derivatives. uPA levels obtained from 4b and 7d administration were similar to 5-FU (5-fluorouracil) for colorectal carcinoma cells (p<0.05). 4b and 7d significantly reduced uPAR (urokinase-type plasminogen activator receptor) levels on both cell lines (p<0.05). Conclusion: uPAR levels obtaining from 4b and 7d administration were similar to 5-FU for both cell lines colorectal (Colo205, CCL-222) and hepatocellular (HepG2, CCL-23) carcinoma cells (p<0.05). | en_US |
dc.identifier.endpage | 1758 | en_US |
dc.identifier.issn | 1389-5575 | en_US |
dc.identifier.issue | 20 | en_US |
dc.identifier.scopus | 2-s2.0-85057451499 | en_US |
dc.identifier.startpage | 1753 | en_US |
dc.identifier.uri | http://hdl.handle.net/11727/9005 | |
dc.identifier.volume | 18 | en_US |
dc.identifier.wos | 000451817800005 | en_US |
dc.language.iso | eng | en_US |
dc.relation.isversionof | 10.2174/1389557518666180816110740 | en_US |
dc.relation.journal | MINI-REVIEWS IN MEDICINAL CHEMISTRY | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Imidazopyridine | en_US |
dc.subject | benzamide | en_US |
dc.subject | benzamidine | en_US |
dc.subject | urinary plasminogen activator | en_US |
dc.subject | uPAR | en_US |
dc.subject | upamostat | en_US |
dc.title | Benzamide and Benzamidine Compounds as New Inhibitors of Urokinase-type Plasminogen Activators | en_US |
dc.type | article | en_US |
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