dc.contributor.author | Coskun, Goknil Pelin | |
dc.contributor.author | Djikic, Teodora | |
dc.contributor.author | Kalayci, Sadik | |
dc.contributor.author | Yelekci, Kemal | |
dc.contributor.author | Sahin, Fikrettin | |
dc.contributor.author | Kucukguzel, S. Guniz | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T09:37:22Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T09:37:22Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1570-1808 | |
dc.identifier.issn | 1875-628X | |
dc.identifier.uri | https://dx.doi.org/10.2174/1570180815666180627130208 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/6043 | |
dc.description | WOS: 000460607700003 | en_US |
dc.description.abstract | Background: The main factor for the prolongation of the ulcer treatment in the gastrointestinal system would be Helicobacter pylori infection, which can possibly lead to gastrointestinal cancer. Triple therapy is the treatment of choice by today's standards. However, observed resistance among the bacterial strains can make the situation even worse. Therefore, there is a need to discover new targeted antibacterial therapy in order to make success in the eradication of H. pylori infections. Methods: The targeted therapy rule is to identify the related macromolecules that are responsible for the survival of the bacteria. Thus, 2-[(2',4'-difluoro-4-hydroxybiphenyl-3-yl)carbonyl]-N-( substituted)hydrazinocarbothioamide (3-13) and 5-(2',4'-difluoro-4-hydroxybiphenyl-3-yl)-4-( substituted)-2,4-dihydro-3H-1,2,4-triazole-3-thiones (14-17) were synthesized and evaluated for antibacterial activity in vitro against H. pylori. Results: All of the tested compounds showed remarkable antibacterial activity compared to the standard drugs (Ornidazole, Metronidazole, Nitrimidazin and Clarithromycin). Compounds 4 and 13 showed activity as 2 mu g/ml MIC value. Conclusion: In addition, we have investigated binding modes and energy of the compounds 4 and 13 on urease enzyme active by using the molecular docking tools. | en_US |
dc.description.sponsorship | Scientific and Technical Research Council of Turkey (TUBITAK) [114S966] | en_US |
dc.description.sponsorship | This work was supported by The Scientific and Technical Research Council of Turkey (TUBITAK), Research Fund Project Number: 114S966. The authors are grateful to Dr. Jurgen Gross from the Institute of Organic Chemistry, University of Heidelberg, for his generous help in obtaining HR-EI/FAB mass spectra of the synthesized compounds. Diflunisal was supplied by Sanovel Pharmaceutical Industry Inc. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | BENTHAM SCIENCE PUBL LTD | en_US |
dc.relation.isversionof | 10.2174/1570180815666180627130208 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Diflunisal | en_US |
dc.subject | Helicobacter pylori | en_US |
dc.subject | molecular docking | en_US |
dc.subject | thiosemicarbazide | en_US |
dc.subject | 1,2,4-triazole-3-thiones | en_US |
dc.subject | macromolecules | en_US |
dc.title | Synthesis, Molecular Modelling and Antibacterial Activity Against Helicobacter pylori of Novel Diflunisal Derivatives as Urease Enzyme Inhibitors | en_US |
dc.type | article | en_US |
dc.relation.journal | LETTERS IN DRUG DESIGN & DISCOVERY | en_US |
dc.contributor.department | [Coskun, Goknil Pelin] Cumhuriyet Univ, Dept Pharmaceut Chem, Fac Pharm, Sivas, Turkey -- [Djikic, Teodora -- Yelekci, Kemal] Kadir Has Univ, Fac Engn & Nat Sci, Dept Bioinformat & Genet, Istanbul, Turkey -- [Kalayci, Sadik -- Sahin, Fikrettin] Yeditepe Univ, Dept Genet & Bioengn, Fac Engn & Architecture, Istanbul, Turkey -- [Kucukguzel, S. Guniz] Marmara Univ, Dept Pharmaceut Chem, Fac Pharm, Istanbul, Turkey | en_US |
dc.identifier.volume | 16 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.endpage | 400 | en_US |
dc.identifier.startpage | 392 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |