Sonstiges: |
- Nachgewiesen in: MEDLINE
- Sprachen: English
- Publication Type: Journal Article
- Language: English
- [Arch Pharm (Weinheim)] 2021 Jul; Vol. 354 (7), pp. e2100037. <i>Date of Electronic Publication: </i>2021 Apr 07.
- MeSH Terms: Anti-Bacterial Agents / *pharmacology ; Antifungal Agents / *pharmacology ; Thiazolidines / *pharmacology ; Anti-Bacterial Agents / chemical synthesis ; Anti-Bacterial Agents / chemistry ; Antifungal Agents / chemical synthesis ; Antifungal Agents / chemistry ; Bacteria / drug effects ; Candida albicans / drug effects ; Cryptococcus neoformans / drug effects ; HEK293 Cells ; Humans ; Structure-Activity Relationship ; Thiazolidines / chemical synthesis ; Thiazolidines / chemistry
- References: L. Piddock , Lancet Infect. Dis. 2012, 12, 249. https://doi.org/10.1016/S1473-3099(11)70316-4. ; G. Cheng , M. Dai , S. Ahmed , H. Hao , X. Wang , Z. Yuan , Front. Microbiol. 2016, 7, 470. https://doi.org/10.3389/fmicb.2016.00470. ; N. Kerru , L. Gummidi , S. Maddila , K. Gangu , S. Jonnalagadda , Molecules 2020, 25, 1909. https://doi.org/10.3390/molecules25081909. ; T. Tomasić , L. P. Masic , Curr. Med. Chem. 2009, 16, 1596. https://doi.org/10.2174/092986709788186200. ; D. Kaminskyy , A. Kryshchyshyn , R. Lesyk , Expert Opin. Drug Discov. 2017, 12, 1233. https://doi.org/10.1080/17460441.2017.1388370. ; D. Kaminskyy , A. Kryshchyshyn , R. Lesyk , Eur. J. Med. Chem. 2017, 140, 542. https://doi.org/10.1016/j.ejmech.2017.09.031. ; A. K. Jain , A. Vaidya , V. Ravichandran , S. K. Kashawa , R. K. Agrawal , Bioorg. Med. Chem. 2012, 20, 3378. https://doi.org/10.1016/j.bmc.2012.03.069. ; N. C. Desai , K. A. Jadeja , D. J. Jadeja , V. M. Khedkar , P. C. Jha , Synth. Commun. 2021, 51, 952. https://doi.org/10.1080/00397911.2020.1861302. ; R. Suryawanshi , S. Jadhav , N. Makwana , D. Desai , D. Chaturbhuj , A. Sonawani , S. Idicula-Thomas , V. Murugesan , S. Katti , S. Tripathi , R. Paranjape , S. Kulkarni , Bioorg. Chem. 2017, 71, 211. https://doi.org/10.1016/j.bioorg.2017.02.007. ; G. Bansal , P. Thanikachalam , R. Maurya , P. Chawla , S. Ramamurthy , J. Adv. Res. 2020, 23, 163. https://doi.org/10.1016/j.jare.2020.01.008. ; M. Ramirez , N. Borja-Hart , Pharmacotherapy 2008, 28, 646. https://doi.org/10.1592/phco.28.5.646. ; N. Agrawal , Curr. Chem. Lett. 2021, 10, 119. https://doi.org/10.5267/j.ccl.2020.11.002. ; D. R. Godhania , A. A. Jogela , P. B. Dobariyaa , A. M. Sanghanib , J. Saudi Chem. Soc. 2016, 20, S523. https://doi.org/10.1016/j.jscs.2013.03.002. ; R. F. George , Eur. J. Med. Chem. 2012, 47, 377. https://doi.org/10.1016/j.ejmech.2011.11.006. ; M. M. Ghorab , M. S. Al-Said , Y. M. Nissan , Arzneimittelforschung 2012, 62, 497. https://doi.org/10.1055/s-0032-1323660. ; M. M. Hanna , R. F. George , Chem. Pharm. Bull. 2012, 60, 1195. https://doi.org/10.1248/cpb.c12-00498. ; M. A. Salem , Croat. Chem. Acta 2017, 90, 7. https://doi.org/10.5562/cca295. ; T. Nasr , S. Bondock , S. Eid , J. Enzyme Inhib. Med. Chem. 2016, 31, 236. https://doi.org/10.3109/14756366.2015.1016514. ; S. A. Rostom , I. M. El-Ashmawy , H. A. Abd El Razikm , M. H. Badr , M. A. Hayam , Bioorg. Med. Chem. 2009, 17, 882. https://doi.org/10.1016/j.bmc.2008.11.035. ; M. H. M. Helal , M. A. Salem , M. S. A. El-Gabyd , M. Aljahdali , Eur. J. Med. Chem. 2013, 65, 517. https://doi.org/10.1016/j.ejmech.2013.04.005. ; T. Chaban , V. Horishny , M. Arshad , Z. Chulovska , L. Kostyshyn , I. Drapak , V. Matiychuk , Biointerface Res. Appl. Chem. 2021, 11, 12434. https://doi.org/10.33263/BRIAC114.1243412446. ; Z. Chulovska , I. Drapak , T. Chaban , V. Ogurtsov , V. Matiychuk , Eur. Chem. Bull. 2021, 10, 147. https://doi.org/10.17628/ecb.2021.10.147-154. ; N. T. Pokhodylo , Y. O. Teslenko , V. S. Matiychuk , M. D. Obushak , Synthesis 2009, 16, 2741. https://doi.org/10.1055/s-0029-1216875. ; T. I. Chaban , Y. E. Matiichuk , O.Y.a Shyyka , I. G. Chaban , V. V. Ogurtsov , I. A. Nektegayev , V. S. Matiychuk , Acta Chim. Slov. 2020, 67, 1035. https://doi.org/10.17344/acsi.2019.5439. ; N. T. Pokhodylo , V. S. Matiychuk , M. D. Obushak , Chem. Heterocycl. Compd. 2009, 45, 121. https://doi.org/10.1007/s10593-009-0238-2. ; Y. Bazel , A. Tupys , Y. Ostapiuk , O. Tymoshuk , V. Matiychuk , J. Mol. Liq. 2017, 242, 471. https://doi.org/10.1016/j.molliq.2017.07.047. ; T. I. Chaban , Y. E. Matiichuk , V. Y. Horishny , I. G. Chaban , V. S. Matiychuk , Russ. J. Org. Chem. 2020, 56, 813. https://doi.org/10.1134/S1070428020050139. ; N. T. Pokhodylo , V. S. Matiychuk , M. D. Obushak , Chem. Heterocycl. Compd. 2009, 45, 483. https://doi.org/10.1007/s10593-009-0287-6. ; A. Tupys , J. Kalembkiewicz , Y. Ostapiuk , V. Matiichuk , O. Tymoshuk , E., Woźnicka , Ł. Byczyński , J. Therm. Anal. Calorim. 2017, 127, 2233. https://doi.org/10.1007/s10973-016-5784-0. ; Z. Chulovska , T. Chaban , I. Drapak , V. Matiychuk , I. Chaban , I. Nektegaev , Biointerface Res. Appl. Chem. 2021, 11, 8009. https://doi.org/10.33263/BRIAC111.80098017. ; N. T. Pokhodylo , V. S. Matiychuk , J. Heterocycl. Chem. 2010, 47, 415. https://doi.org/10.1002/jhet.321. ; T. Chaban , V. Ogurtsov , A. Mahlovanyy , N. Sukhodolska , I. Chaban , S. Harkov , V. Matiychuk , Pharmacia 2019, 66, 171. https://doi.org/10.3897/pharmacia.66.e36764. ; N. T. Pokhodylo , V. S. Matiychuk , M. D. Obushak , Synthesis 2009, 8, 1297. https://doi.org/10.1055/s-0028-1087992. ; O. Tymoshuk , L. Oleksiv , L. Khvalbota , T. Chaban , I. Patsay , Acta Chim. Slov. 2019, 66, 62. https://doi.org/10.17344/acsi.2018.4570. ; T. Chaban , V. Ogurtsov , I. Chaban , I. Myrko , S. Harkov , M. Leluykh , Pharmacia 2019, 66, 27. https://doi.org/10.3897/pharmacia.66.e35131. ; N. Obushak , A. Lesyuk , Y. Gorak , V. Matiichuk , Russ. J. Org. Chem. 2009, 45, 1375. https://doi.org/10.1134/S1070428009090103. ; N. Obushak , Y. Gorak , V. Matiichuk , R. Lytvyn , Russ. J. Org. Chem. 2008, 44, 1689. https://doi.org/10.1134/S1070428008110213. ; WHO, Global Antimicrobial Resistance Surveillance System. Manual for Early Implementation 2015. https://www.who.int/antimicrobial-resistance/publications/surveillance-system-manual/en/ (accessed: December 2021). ; Open-access antimicrobial screening program. https://www.co-add.org (accessed: January 2021).
- Grant Information: project 2020.01/0166 National Research Foundation of Ukraine
- Contributed Indexing: Keywords: 4-oxo-thiazolidin-2-ylidenes; antimicrobial activity; synthesis
- Substance Nomenclature: 0 (Anti-Bacterial Agents) ; 0 (Antifungal Agents) ; 0 (Thiazolidines)
- Entry Date(s): Date Created: 20210407 Date Completed: 20211209 Latest Revision: 20211214
- Update Code: 20231215
|