Study of the lipophilicity of novel diquinothiazines

Journal of Planar Chromatography - Modern TLC

Volumn 19, Issue 108, 2006, Pages 157-160

  Nowak, Małgorzata ^a   Pluta, Krystian ^a  

^a MEDICAL UNIVERSITY OF SILESIA   (Poland)

Author keywords

Correlation analysis; Diquinothiazines; Lipophilicity; Phenothiazines; Reversed phase thin layer chromatography

Indexed keywords

ACETONE; CALIBRATION; CORRELATION METHODS; EXTRAPOLATION; LIPIDS;

ACETONE CONCENTRATION; DIQUINOTHIAZINES; LINEAR EXTRAPOLATION; LIPOPHILICITY; PHENOTHIAZINES; REVERSED-PHASE THIN-LAYER CHROMATOGRAPHY;

THIN LAYER CHROMATOGRAPHY;

ACETONE; ALKYLDIQUINOTHIAZINE DERIVATIVE; AMINOALKYLDIQUINOTHIAZINE DERIVATIVE; ARYLDIQUINOTHIAZINE DERIVATIVE; DIQUINOTHIAZINE DERIVATIVE; PHENOTHIAZINE DERIVATIVE; SILICON DIOXIDE; THIAZINE DERIVATIVE; TROMETAMOL; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CALIBRATION; CHEMICAL PARAMETERS; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; CORRELATION ANALYSIS; DATA ANALYSIS SOFTWARE; DRUG DETERMINATION; LIPOPHILICITY; MATHEMATICAL MODEL; PLOTS AND CURVES; QUANTITATIVE STRUCTURE ACTIVITY RELATION; STANDARD; THIN LAYER CHROMATOGRAPHY;

EID: 33744955452     PISSN: 09334173     EISSN: None     Source Type: Journal    
DOI: 10.1556/JPC.19.2006.2.13     Document Type: Article

References (21)

1. R.R. Gupta (Ed.) Phenothiazines and 1,4-Benzothiazines - Chemical and Biological Aspects, Elsevier, Amsterdam, 1988.
2. K. Pluta, Phosphorus, Sulfur, Silicon 126 (1997) 145-156.
3. K. Pluta, A. Maślankiewicz, and M. Szmielew, Phosphorus, Sulfur, Silicon 159 (2000) 79-86.
4. M. Nowak, K. Pluta, and K. Suwińska, New J. Chem. 26 (2002) 1216-1220.
5. A. Leo, C. Hansch, and D. Elkins, Chem. Rev. 71 (1971) 525-616.
6. K. Jóźwiak, H. Szumiło, and E. Soczewiński, Wiad. Chem. 55 (2001) 1047-1074.
7. R. Kaliszan, J. Chromatogr. 220 (1981) 71-83.
8. G.L. Biaggi, A.M. Barbaro, and A. Saponi, J. Chromatogr. A 662 (1994) 341-361.
9. R. Mannhold, G. Cruciani, K. Dross, and R. Rekker, J. Compt.-Aided Mol. Design 12 (1998) 573-581.
10. R. Mannhold and K. Dross, Quant. Struct.-Act. Relat. 15 (1996) 403-409.
11. U. Franke; A. Munk, and M. Wiese, J. Pharm. Sci. 88 (1999) 89-95.
12. A. Hulshoff and J.H Perrin, J. Med. Chem. 20 (1977) 430-439.
13. M.W. Goosey and N.S. Doggett, Biochem. Pharmacol. 32 (1983) 2411-2415.
14. http://www.ibmh.msk.su/PASS - a server for the on-line prediction of the range of biological activity for substances.
15. M. Nowak and K. Pluta, manuscript in preparation.
16. ClogP (CS Chem 3D Ultra 7.0, Molecular Modeling and Analysis) distributed by CambridgeSoft.
17. N. Bodor, Z. Garbany, and C.-K. Wong, J. Am. Chem. Soc. 111 (1989) 3783-3786.
18. W.L. Klotz, M.R. Schure, and J.P. Foley, J. Chromatogr. A 930 (2001) 145-153.
19. A. Leo, Chem. Rev. 93 (1993) 1281-1306.
20. K. Pluta, M. Nowak, and K. Suwińska, J. Chem. Cryst. 30 (2000) 479-482.
21. M.L. Bieganowska, A. Doraczyńska, and A. Petruczyńska, J. Planar Chromatogr. 8 (1995) 1282-1289.