Syntheses, characterization and biological activity of diorganotin(IV) derivatives of 2-amino-6-hydroxypurine (guanine)

Inorganic Chemistry Communications

Volumn 12, Issue 10, 2009, Pages 1049-1052

  Nath, Mala ^a   Singh, Hitendra ^a   Eng, George ^b   Song, Xuequing ^b   Kumar, Ashok ^c  

^a INDIAN INSTITUTE OF TECHNOLOGY ROORKEE   (India)

^b UNIVERSITY OF THE DISTRICT OF COLUMBIA   (United States)

^c LLRM MEDICAL COLLEGE   (India)

Author keywords

2 Amino 6 hydroxypurine; 119Sn M ssbauer; Anti inflammatory activity; Cardiovascular activity; Organotin(IV)

Indexed keywords

EID: 70349435909     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2009.08.019     Document Type: Article

References (23)

1. In: Davis A.G., Gielen M., Pannell K.H., and Tiekink E.R.T. (Eds). Tin Chemistry: Fundamentals, Frontiers, and Applications (2008), Wiley 413-492 and references there in
2. Gielen M. Coord. Chem. Rev. 151 (1996) 41-51 and references therein
3. Yang P., and Guo M. Coord. Chem. Rev. 185-186 (1999) 189-211 and references therein
4. Nath M., Pokharia S., and Yadav R. Coord. Chem. Rev. 215 (2001) 99-149 and references therein
5. Pellerito L., and Nagy L. Coord. Chem. Rev. 224 (2002) 111-150 and references therein
6. Nath M., Pokharia S., Song X., Eng G., Gielen M., Kemmer M., Biesemans M., Williams R., and deVos D. Appl. Organomet. Chem. 17 (2003) 305-314
7. Roseberg B., Van Camp V., Trosko J.E., and Mansour V.H. Nature 222 (1969) 385
8. Barnard C.F.J. Platinum Met. Rev. 33 (1989) 162-167
9. Roberts J.J., and Pascoe J.M. Nature 235 (1972) 282-284
10. A.J. Crowe, in: M. Gielen (Ed.), Metal-Based Antitumor Drugs, vol. I, Freunel, London, 1989, pp. 103-149.
11. Clarke M.J., Zhu F., and Frasca D.R. Chem. Rev. 99 (1999) 2511-2533 and references therein
12. Barbieri R., Pellerito L., Ruisi G., LoGuidice M.T., Huber F., and Atassi G. Inorg. Chim. Acta 66 (1982) L39-L40
13. Cardin C.J., and Roy A. Inorg. Chim. Acta 107 (1985) 57-61
14. Nath M., Jairath R., Eng G., Song X., and Kumar A. Inorg. Chem. Commun. 7 (2004) 1161-1163
15. Nath M., Pokharia S., Eng G., Song X., and Kumar A. Eur. J. Med. Chem. 40 (2005) 289-298
16. 2), 7.36 s (Sn-Ph). For anti-inflammatory and cardiovascular activity, p-values (using Student's t-test) are as follows: p < 0.05; p < 0.01; p < 0.001. These activities were carried out by taking one group of five animals as control and the other of five pretreated with the synthesized complex. The mean value of each treated complex as compared to that of control was used.
17. Nath M., Singh H., Eng G., and Song X. J. Organomet. Chem. 693 (2008) 2541-2550
18. Nath M., Saini P.K., Eng G., and Song X. J. Organomet. Chem. 693 (2008) 2271-2278
19. Nath M., Pokharia S., Eng G., Song X., and Kumar A. J. Organomet. Chem. 669 (2003) 109-123
20. Barbieri R., Pellerito L., and Huber F. Inorg. Chim. Acta 30 (1978) L321-L323
21. Ho B.Y.K., and Zuckerman J.J. Inorg. Chem. 12 (1973) 1552-1561
22. 1H FTNMR Spectra vol. 3 (1993), Aldrich Chemical Company, Wisconsin
23. Barbieri R., Ruisi G., and Atassi G. J. Inorg. Biochem. 41 (1991) 25-30