In vitro antimicrobial studies of new benzimidazolium salts and silver N-heterocyclic carbene complexes

References

• Gök Y, Akkoç S, Albayrak S, et al. Phenyl-substituted carbene precursors and their silver complexes: synthesis, characterization and antimicrobial activities. Appl Organometal Chem 2014;28:244–51
   Web of Science ®Google Scholar
• Ha SK, Shobha D, Moon E, et al. Anti-neuroinflammatory activity of 1,5-benzodiazepine derivatives. Bioorg Med Chem Lett 2010;20:3969–71
   PubMed Web of Science ®Google Scholar
• Haris RC, Straley JM. Cationic polymethine dyes for acrylic fibers. U.S. patent 1,537,757; 1968. [Chem Abstr 1970;73:00054w]
   Google Scholar
• Shaharyar M, Mazumder A, Salahuddin, et al. Synthesis, characterization and pharmacological screening of novel benzimidazole derivatives. Arab J Chem 2011. [Epub ahead of print]. doi: 10.1016/j.arabjc.2011.04.013
   Web of Science ®Google Scholar
• Gök Y, Akkoç S, Çelikal ÖÖ, et al. Nfunctionalized benzimidazol-2-ylidene silver complexes: synthesis, characterization, and antimicrobial studies. Turk J Chem 2013;37:1007–13
   Web of Science ®Google Scholar
• Hattori K, Yamaguchi K, Yamaguchi J, Itami K. Pd- and Cu-catalyzed C–H arylation of indazoles. Tetrahedron 2012;68:7605–12
   Web of Science ®Google Scholar
• Zulikha HZ, Haque RA, Budagumpi S, Abdul Majid AMS. Topology control in nitrile-functionalized silver(I)-N-heterocyclic carbene complexes: synthesis, molecular structures, and in vitro anticancer studies. Inorg Chim Acta 2014;411:40–7
   Web of Science ®Google Scholar
• El-Emam AA, Al-Deeb AO, Al-Omar M, Lehmann J. Synthesis, antimicrobial, and anti-HIV-1 activity of certain 5-(1-adamantyl)-2-substituted thio-1,3,4-oxadiazoles and 5-(1-adamantyl)-3-substituted aminomethyl-1,3,4-oxadiazoline-2-thiones. Bioorg Med Chem 2004;12:5107–13
   PubMed Web of Science ®Google Scholar
• Ersmark K, Nervall M, Hamelink E, et al. Synthesis of malarial plasmepsin inhibitors and prediction of binding modes by molecular dynamics simulations. J Med Chem 2005;48:6090–106
   PubMed Web of Science ®Google Scholar
• Macaev F, Rusu G, Pogrebnoi S, et al. Synthesis of novel 5-aryl-2-thio-1,3,4-oxadiazoles and the study of their structure–anti-mycobacterial activities. Bioorg Med Chem 2005;13:4842–50
   PubMed Web of Science ®Google Scholar
• Mullican MD, Wilson MW, Conner DT, et al. Design of 5-(3,5-di-tert-butyl-4-hydroxyphenyl)-l,3,4-thiadiazoles, -1,3,4-oxadiazoles, and -1,2,4-triazoles as orally-active, nonulcerogenic antiinflammatory agents. J Med Chem 1993;36:1090–9
   PubMed Web of Science ®Google Scholar
• Shingalapur RV, Hosamani KM, Keri RS, Hugar MH. Derivatives of benzimidazole pharmacophore: synthesis, anticonvulsant, antidiabetic and DNA cleavage studies. Eur J Med Chem 2010;45:1753–9
   PubMed Web of Science ®Google Scholar
• Kumar M, Narasimhan B, Kumar P, et al. 4(1-Aryl-5-chloro-2-oxo-1,2-dihydro-indol-3-ylideneamino)-N-substituted benzene sulfonamides: synthesis, antimicrobial, anticancer evaluation and QSAR studies. Arab J Chem 2014;7:436–47
   Web of Science ®Google Scholar
• Kumar M, Ramasamy K, Mani V, et al. Synthesis, antimicrobial, anticancer, antiviral evaluation and QSAR studies of 4-(1-aryl-2-oxo-1,2-dihydro-indol-3-ylideneamino)-N-substituted benzene sulfonamides. Arab J Chem 2014;7:396–408
   Web of Science ®Google Scholar
• Özkay Y, Tunalı Y, Karaca H, Işıkdağ İ. Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety. Eur J Med Chem 2010;45:3293–8
   PubMed Web of Science ®Google Scholar
• Tunçbilek M, Kiper T, Altanlar N. Synthesis and in vitro antimicrobial activity of some novel substituted benzimidazole derivatives having potent activity against MRSA. Eur J Med Chem 2009;44:1024–33
   PubMed Web of Science ®Google Scholar
• Ansari KF, Lal C. Synthesis, physicochemical properties and antimicrobial activity of some new benzimidazole derivatives. Eur J Med Chem 2009;44:4028–33
   PubMed Web of Science ®Google Scholar
• Padalkar VS, Gupta VD, Phatangare KR, et al. Synthesis of novel dipodal-benzimidazole, benzoxazole and benzothiazole from cyanuricchloride: structural, photophysical and antimicrobial studies. J Saudi Chem Soc 2014;18:262–8
   Web of Science ®Google Scholar
• Seenaiah D, Reddy PR, Reddy GM, et al. Synthesis, antimicrobial and cytotoxic activities of pyrimidinyl benzoxazole, benzothiazole and benzimidazole. Eur J Med Chem 2014;77:1–7
   PubMed Web of Science ®Google Scholar
• Güven ÖÖ, Erdoğan T, Göker H, Yıldız S. Synthesis and antimicrobial activity of some novel phenyl and benzimidazole substituted benzyl ethers. Bioorg Med Chem Lett 2007;17:2233–6
   PubMed Web of Science ®Google Scholar
• Akkoç S, Gök Y. Synthesis and characterization of 1-phenyl-3-alkylbenzimidazol-2-ylidene salts and their catalytic activities in the Heck and Suzuki cross-coupling reactions. J Coord Chem 2013;66:1396–404
   Web of Science ®Google Scholar
• Gök Y, Akkoç S, Özeroğlu Çelikal Ö, et al. In Vitro antimicrobial studies of naphthalen-1-ylmethyl substituted silver N-heterocyclic carbene complexes. Arab J Chem 2015. [Epub ahead of print]. doi: 10.1016/j.arabjc.2015.04.019
   Web of Science ®Google Scholar
• Lin IJB, Vasam CS. Preparation and application of N-heterocyclic carbene complexes of Ag(I). Coord Chem Rev 2007;251:642–70
   Web of Science ®Google Scholar
• Aktaş A, Akkoç S, Gök Y. Palladium catalyzed Mizoroki–Heck and Suzuki–Miyaura reactions using napthalenomethyl-substituted imidazolidin-2-ilidene ligands in aqueous media. J Coord Chem 2013;66:2901–9
   Web of Science ®Google Scholar
• Iqbal MA, Haque RA, Nasri SF, et al. Potential of silver against human colon cancer: synthesis, characterization and crystal structures of xylyl (ortho, meta, para) linked bis-benzimidazolium salts and Ag(I)-NHC complexes: in vitro anticancer studies. Chem Central J 2013;7:27
   PubMed Web of Science ®Google Scholar
• Iqbal MA, Umar MI, Haque RA, et al. Macrophage and colon tumor cells as targets for a binuclear silver(I) N-heterocyclic carbene complex, an anti-inflammatory and apoptosis mediator. J Inorg Biochem 2015;146:1–13
   PubMed Web of Science ®Google Scholar
• Akkurt M, Akkoç S, Gök Y, et al. Chlorido[1-phenyl-3-(2,3,5,6-tetra-methyl-benz-yl)benzimidazol-2-yl-idene]silver (I). Acta Crystallogr 2012;E68:m590–1
   Google Scholar