Synthesis and characterization of polymer eight-coordinate (enH 2)[YIII(pdta)(H2O)]2·10H 2O as well as the interaction of [YIII(pdta)(H 2O)]22- with BSA

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 77, Issue 5, 2010, Pages 1115-1121

  Liu, Bin ^a,b   Wang, Jun ^b   Wang, Xin ^b   Liu, Bing Mi ^b   He, Ling Ling ^a,c   Xu, Shu Kun ^a  

^a NORTHEASTERN UNIVERSITY   (China)

^b LIAONING UNIVERSITY   (China)

^c SHENYANG UNIVERSITY OF CHEMICAL TECHNOLOGY   (China)

Author keywords

1,3 Propylenediamine N,N,N ,N tetraacetic acid (H4pdta); Bovine serum albumin (BSA); Ethylenediamine (en); Interaction; YIII ion

Indexed keywords

BOVINE SERUM ALBUMINS; ETHYLENEDIAMINE (EN); INTERACTION; TETRAACETIC ACID; YIII ION;

ACIDS; BINDING SITES; FLUORESCENCE; HYDROGEN; HYDROGEN BONDS; SYNTHESIS (CHEMICAL); VAN DER WAALS FORCES; X RAY DIFFRACTION;

BODY FLUIDS;

BOVINE SERUM ALBUMIN; COORDINATION COMPOUND; DRUG DERIVATIVE; EDETIC ACID; ETHYLENEDIAMINE; ETHYLENEDIAMINE DERIVATIVE; POLYMER; PROPANOLDIAMINETETRACETIC ACID; WATER; YTTRIUM;

ANIMAL; ARTICLE; BIOLOGICAL MODEL; CATTLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DRUG INTERACTION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ANIMALS; CATTLE; COORDINATION COMPLEXES; CRYSTALLOGRAPHY, X-RAY; DRUG INTERACTIONS; EDETIC ACID; ETHYLENEDIAMINES; MODELS, BIOLOGICAL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; POLYMERS; SERUM ALBUMIN, BOVINE; WATER; YTTRIUM;

EID: 78049527110     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2010.09.012     Document Type: Article

References (24)

1. S. Jurisson, D. Berning, W. Jia, and D. Ma Chem. Rev. 93 1993 1137 1156
2. G.A. Kaltsas, J.J. Mukherjee, and A.B. Grossman Ann. Oncol. 12 2001 47 50
3. R. Stein, S. Chen, L. Reed, H. Richel, and D.M. Goldenberg Cancer 94 2002 51 61
4. J. Wang, Y. Wang, and Zh. H. Zhang J. Struct. Chem. 46 2005 895 905
5. Y.S. Song, B. Yan, and Z.X. Chen J. Mol. Struct. 750 2005 101 108
6. J. Wang, X.D. Zhang, Y. Zhang, and W.G. Jia J. Struct. Chem. 45 2004 114 123
7. J. Wang, G.R. Gao, Z.H. Zhang, X.D. Zhang, and Y.J. Wang J. Coord. Chem. 60 2007 2221 2241
8. J. Wang, P. Hu, B. Liu, R. Xu, and X.D. Zhang J. Coord. Chem. 62 2009 3168 3178
9. F. Zsila, Z. Bikadi, and M. Simonyi Biochem. Pharmacol. 65 2003 447 456
10. S.M.T. Shaikh, J. Seetharamappa, P.B. Kandagal, and S. Ashoka J. Mol. Struct. 786 2006 46 52
11. D. Silva, C.M. Cortez, J. Cunha-Bastos, and S.R.W. Louro Toxicol. Lett. 147 2004 53 61
12. Z. Wang, C.M. Jin, and T. Shao Inorg. Chem. Commun. 5 2002 642 648
13. M.R. Eftink, and C.A. Ghiron J. Phys. Chem. 80 1976 486 493
14. S. Heitmeier, and G. Blaschke J. Chromatogr. B 721 1999 93 108
15. W.R. Ware J. Phys. Chem. 66 1962 455 458
16. M.R. Eftink, and C.A. Ghiron Anal. Biochem. 114 1981 199 227
17. D.A. Leckband Rev. Biophys. Biomol. Struct. 29 2000 1 26
18. I.M. Klotz, and J.M. Urquhart J. Am. Chem. Soc. 71 1949 847 851
19. D.R. Philip, and S. Subramanian Biochem. J. 20 1981 3096 3102
20. M. Alain, B. Michel, and D. Michel J. Chem. Educ. 63 1986 365 366
21. L. Stryer Annu. Rev. Biochem. 47 1978 819 846
22. P.B. Kandagal, S. Ashoka, J. Seetharamappa, V. Vani, and S.M.T. Shaikh J. Photochem. Photobiol. A 179 2006 161 166
23. J.N. Miller Proc. Anal. Div. Chem. Soc. 16 1979 203 208
24. M. Guo, W.J. Lü, M.H. Li, and W. Wang Eur. J. Med. Chem. 43 2008 2140 2144