New gold(I) and silver(I) complexes of sulfamethoxazole: Synthesis, X-ray structural characterization and microbiological activities of triphenylphosphine(sulfamethoxazolato-N2)gold(I) and (sulfamethoxazolato)silver(I)

Inorganic Chemistry Communications

Volumn 10, Issue 9, 2007, Pages 1083-1087

  Marques, Lenice L ^a   Manzoni de Oliveira, Gelson ^a   Schulz Lang, Ernesto ^a   Anraku de Campos, Marli Matiko ^a   Soccol Gris, Lara Regina ^a  

^a FEDERAL UNIVERSITY OF SANTA MARIA   (Brazil)

Author keywords

Antimicrobial activity; Au and Ag complexes; Sulfamethoxazole

Indexed keywords

EID: 34547839711     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2007.06.005     Document Type: Article

References (43)

1. Toth J.E., Grindey G.B., Ehlhardt W.J., Ray J.E., Boder G.B., Bewley J.R., Klingerman K.K., Gates S.B., Rinzel S.M., Schultz R.M., Weir L.C., and Worzalla J.F. J. Med. Chem. 40 (1997) 1018
2. Medina J.C., Roche D., Shan B., Learned R.M., Frankmoelle W.P., and Clark D.L. Bioorg. Med. Chem. Lett. 9 (1999) 1843
3. Yoshino H., Ueda N., Niijima J., Sugumi H., Kotake Y., Koyanagi N., Yoshimatsu K., Asada M., and Watanabe T. J. Med. Chem. 35 (1992) 2496
4. Owa T., Yoshino H., Okauchi T., Yoshimatsu K., Ozawa Y., Hata Sugi N., Nagasu T., Koyanagi N., and Kitoh K. J. Med. Chem. 42 (1999) 3789
5. Baenziger N.C., and Struss A.W. Inorg. Chem. 15 (1976) 1807
6. Cook D.S., and Turner M.F. J. Chem. Soc., Perkin Trans. 2 (1975) 1021
7. Baenziger N.C., Modak S.L., and Fox Jr. C.L. Acta Crystallogr. C39 (1983) 1620
8. Brown C.J., Cook D.S., and Sengier L. Acta Crystallogr. C41 (1985) 718
9. Shaw C.F. Chem. Rev. 99 (1999) 2589
10. Ahmad S., Isab A.A., Perzanowski H.P., Hussain M.S., and Akhtar M.N. Trans. Met. Chem. 27 (2002) 177
11. Bachechi F., Burini A., Galassi R., Pietroni B.R., and Severini M. J. Organomet. Chem. 575 (1999) 269
12. Best S.L., and Sadler P.J. Gold Bull. 29 (1996) 87
13. Schmidbaur H., Reber G., Schier A., Wagner F.E., and Müller G. Inorg. Chim. Acta 147 (1988) 143
14. Rawls R. Chem. Eng. News 6 October (1986) 21
15. Marques L.L., Manzoni de Oliveira G., Schulz Lang E., and Burrow R.A. Z. Naturforsch. 60b (2005) 318
16. Manzoni de Oliveira G., Soccol Gris L.R., Marques L.L., and Schulz Lang E. Z. Anorg. Allg. Chem. 633 (2007) 610
17. García-Raso A., Fiol J.J., Rigo S., López-López A., Mollins E., Espinosa E., Borrás E., Alzuet G., Borrás J., and Castiñeiras A. Polyhedron 19 (2000) 991
18. Borrás E., Alzuet G., Borrás J., Server-Carrió J., Castiñeiras A., Liu González M., and Sanz-Ruiz F. Polyhedron 19 (2000) 1859
19. Schulz Lang E., Burrow R.A., and Marques L.L. Acta Crystallogr. C59 (2003) m95
20. Schulz Lang E., Marques L.L., and Burrow R.A. Acta Crystallogr. E59 (2003) m707
21. Maury L., Rambaud J., Pauvert B., Lasserre Y., Berge G., and Audran M. Can. J. Chem. 63 (1985) 3012
22. Randhawa H.S., Sekhon B.S., Sahai H.K., and Lakhani R. J. Therm. Anal. Calorim. 57 (1999) 551
23. Kanagaraj G., and Rao G.N. Synth. React. Inorg. Met. Org. Chem. 22 (1992) 559
24. Kanagaraj G., and Rao G.N. Indian J. Chem. 32 (1993) 594
25. Karthikeyan G., Mohanraj K., Elango K.P., and Girishkumar K. Russian J. Coord. Chem. 32 (2005) 380
26. Marques L.L., Schulz Lang E., Fenner H., and Castellano E.E. Z. Anorg. Allg. Chem. 631 (2005) 745
27. Schulz Lang E., Marques L.L., and Manzoni de Oliveira G. Z. Naturforsch. 60b (2005) 1264
28. Marques L.L., Manzoni de Oliveira G., and Schulz Lang E. Z. Anorg. Allg. Chem. 632 (2006) 2310
29. Sekhon B.S., Sahai H.K., and Randhawa H.S. Proc. Nat. Acad. Sci. India 71-A (2001) 195
30. Sahai H.K., Sekhon B.S., and Randhawa H.S. S. Afr. J. Chem. 52 (1999) 20
31. Yang X.-L., Liu J., Yang L., and Zhang X.-Y. Synth. React. Inorg. Met. Org. Nano-Met. Chem. 35 (2005) 761
32. Yang L., Yang X., Liu J., Li Y., Lou Q., and Liu Q. J. Coord. Chem. 56 (2003) 1131
33. 2)].
34. -3): 0.618 and -0.427 (1), 1.001 and -1.108 (2).
35. Sheldrick G.M. shelxs-97, Program for Crystal Structure Solution (1997), University of Göttingen, Germany
36. Sheldrick G.M. shelxl-97, Program for Crystal Structure Refinement (1997), University of Göttingen, Germany
37. -1. The plate was incubated at 37 °C for 18-24 h. All tests and inoculations were performed in triplicate. MIC and MBC determination: after the incubation times and addition of the indicator to the wells, the lowest concentration of drug inhibiting microbial growth was selected as the minimal inhibitory concentration (MIC). The minimum bactericidal concentration (MBC) was determined by transferring 100 μL from the lowest growth well for subculture in agar Mueller-Hinton plates which were incubated aerobically at 37 °C for 18-24 h. The MBC was read as the lowest concentration of drug which reduces the count of viable cells by 99.9% from the initial inoculum.
38. NCCLS, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically: Approved Standard - Sixth Edition. NCCLS document M7-A6 (ISBN 1-56238-486-4). NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898 USA, 2003.
39. Bondi A. J. Phys. Chem. 68 (1964) 441
40. Gringauz A. Introduction to Medicinal Chemistry (1997), Wiley-UCH, New York pp. 61-67
41. Foye W.O., Lemke T.L., and Williams D.A. Principles of Medicinal Chemistry. fourth ed. (1995), Williams & Williams pp. 709-713
42. Mizushima E., Sato K., Hayashi T., and Tanaka M. Angew. Chem., Int. Ed. 41 (2002) 4563
43. Shaw III C.F., Beery A., and Stocco G.C. Inorg. Chim. Acta 123 (1986) 213