%0 Journal Article %1 ISI:000304802600023 %A Kharat, Ali Nemati %A Foroutannejad, Sahar %A Khavasi, Hamid Reza %C 325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA %D 2012 %I TAYLOR & FRANCIS INC %J SYNTHESIS AND REACTIVITY IN INORGANIC METAL-ORGANIC AND NANO-METAL CHEMISTRY %K activity; antimicrobial microorganism; pathogenic properties; terpyridine; tetrachloridoaurate(III)} {antifungal %N 5 %P 752-757 %R 10.1080/15533174.2011.615074 %T Biological Evaluation of 4 `-(2-Thienyl)-2, 2 `; 6 `, 2 `'-terpyridine-1,1 `'-diium Chloride Tetrachloridoaurate (III): The Effect of Countercations %V 42 %X 4'-(2-Thienyl)-2, 2'; 6', 2 `'-terpyridine (thioterpy) -1, 1 `'-diium chloride tetrachloridoaurate (III), (H(2)thioterpy) Cl(AuCl4) (1), was synthesized based on the potential pharmacophores of the 2, 2'; 6', 2 `'-terpyridine agents. Its antimicrobial and antifungal activity was tested in vitro for their growth inhibitory activities against pathogenic microorganism and fungi. The in vitro bioactivity evaluation of the similar compounds was investigated. Complex (1) had highest microbicidal and fungicidal activities against pathogenic agents rather than other same proton transfer compounds.

@article{ISI:000304802600023, abstract = {{4'-(2-Thienyl)-2, 2'; 6', 2 `'-terpyridine (thioterpy) -1, 1 `'-diium chloride tetrachloridoaurate (III), {[}(H(2)thioterpy) Cl(AuCl4)] (1), was synthesized based on the potential pharmacophores of the 2, 2'; 6', 2 `'-terpyridine agents. Its antimicrobial and antifungal activity was tested in vitro for their growth inhibitory activities against pathogenic microorganism and fungi. The in vitro bioactivity evaluation of the similar compounds was investigated. Complex (1) had highest microbicidal and fungicidal activities against pathogenic agents rather than other same proton transfer compounds.}}, added-at = {2017-05-10T15:29:29.000+0200}, address = {{325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA}}, affiliation = {{Kharat, AN (Reprint Author), POB 13145-1357, Tehran, Iran. Kharat, Ali Nemati, Univ Tehran, Sch Chem, Univ Coll Sci, Tehran, Iran. Foroutannejad, Sahar, Univ Tehran Med Sci, Dept Med Biotechnol, Fac Allied Med, Tehran, Iran. Khavasi, Hamid Reza, Shahid Beheshti Univ, Dept Chem, GC, Tehran, Iran.}}, author = {Kharat, Ali Nemati and Foroutannejad, Sahar and Khavasi, Hamid Reza}, author-email = {{alnema@khayam.ut.ac.ir}}, biburl = {https://www.bibsonomy.org/bibtex/256aa1a46d1ffa8bc4f1db5397718c70d/hkhavasi}, cited-references = {{Casini A, 2008, J INORG BIOCHEM, V102, P564, DOI 10.1016/j.jinorgbio.2007.11.003. Cave GWV, 2000, CHEM COMMUN, P2199, DOI 10.1039/b007431o. El-Tarabily KA, 2004, J APPL MICROBIOL, V96, P69, DOI 10.1046/j.1365-2672.2003.02043.x. Eryazici I, 2008, CHEM REV, V108, P1834, DOI 10.1021/cr0781059. Heller M, 2003, EUR J ORG CHEM, P947. Hofmeier H, 2004, CHEM SOC REV, V33, P373, DOI 10.1039/b400653b. JURIS A, 1988, COORDIN CHEM REV, V84, P85, DOI 10.1016/0010-8545(88)80032-8. KARMALI MA, 1989, CLIN MICROBIOL REV, V2, P15. KROHNKE F, 1976, SYNTHESIS-STUTTGART, P1, DOI 10.1055/s-1976-23941. Magaldi S, 2004, INT J INFECT DIS, V8, P39, DOI 10.1016/j.ijid.2003.03.002. Sheldrick G.M., 1997, SHELX97 PROGRAM CRYS. {[}Anonymous], 2005, X AREA VERS 1 30 PRO. {[}Anonymous], 2004, X SHAPE VERS 2 05 PR. {[}Anonymous], 2005, X RED VERS 1 28B PRO. Stoe\&Cie, 2000, X STEP 32 VERS 1 07B. WARREN JW, 1982, J INFECT DIS, V146, P719. Yildirim SO, 2009, ACTA CRYSTALLOGR E, V65, pM491, DOI 10.1107/S1600536809012264.}}, doc-delivery-number = {{952OU}}, doi = {{10.1080/15533174.2011.615074}}, funding-acknowledgement = {{University of Tehran}}, funding-text = {{The authors thank the University of Tehran for financial support.}}, interhash = {ab3cf721c15b493eeab1fd2ec86b9b8f}, intrahash = {56aa1a46d1ffa8bc4f1db5397718c70d}, issn = {{1553-3174}}, journal = {{SYNTHESIS AND REACTIVITY IN INORGANIC METAL-ORGANIC AND NANO-METAL CHEMISTRY}}, journal-iso = {{Synth. React. Inorg. Met.-Org. Nano-Metal Chem.}}, keywords = {activity; antimicrobial microorganism; pathogenic properties; terpyridine; tetrachloridoaurate(III)} {antifungal}, keywords-plus = {{COMPLEXES; PYRIDINES}}, language = {{English}}, number = {{5}}, number-of-cited-references = {{17}}, pages = {{752-757}}, publisher = {{TAYLOR \& FRANCIS INC}}, research-areas = {{Chemistry; Science \& Technology - Other Topics}}, times-cited = {{3}}, timestamp = {2017-05-10T15:29:29.000+0200}, title = {{Biological Evaluation of 4 `-(2-Thienyl)-2, 2 `; 6 `, 2 `'-terpyridine-1,1 `'-diium Chloride Tetrachloridoaurate (III): The Effect of Countercations}}, type = {{Article}}, unique-id = {{ISI:000304802600023}}, usage-count-last-180-days = {{0}}, usage-count-since-2013 = {{3}}, volume = {{42}}, web-of-science-categories = {{Chemistry, Inorganic \& Nuclear; Nanoscience \& Nanotechnology}}, year = {{2012}} }