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267 Testa, B; van de Waterbeemd, H; Folkers, G; Guy, R (eds), Pharmacokinetic Optimization in Drug Research, Verlag Helvetica Chimica Acta, Zurich and WileyVCH: Weinheim, 2001 268 Kramer, S D; Gautier, J-C; Saudemon, P, Considerations on the potentiometric log P determination, Pharm Res 15, 1310 1313 (1998) 269 Bouchard, G; Pagliara, A; van Balen, G P; Carrupt, P-A; Testa, B; Gobry, V; Girault, H H; Caron, G; Ermondi, G; Fruttero, R, Ionic partition diagram of the zwitterionic antihistamine cetirizine, Helv Chim Acta 84, 375 387 (2001) 270 Scherrer, R A; Howard, S M, Use of distribution coef cients in quantitative structureactivity relationships, J Med Chem 20, 53 58 (1977) 271 Schaper, K-J, Simultaneous determination of electronic and lipophilic properties [pKa, P(ion), P(neutral)] for acids and bases by nonlinear regression analysis of pH-dependent partittion measurements, J Chem Res (S) 357 (1979) 272 Taylor, P J; Cruickshank, J M, Distribution coef cients of atenolol and sotalol, J Pharm Pharmacol 36, 118 119 (1984) 273 Taylor, P J; Cruickshank, J M, Distribution coef cients of atenolol and sotalol, J Pharm Pharmacol 37, 143 144 (1985) 274 Manners, C N; Payling, D W; Smith, D A, Distribution coef cient, a convenient term for the relation of predictable physico-chemical properties to metabolic processes, Xenobiotica 18, 331 350 (1988) 275 Avdeef, A, Assessment of distribution-pH pro les, in Pliska, V; Testa, B; van de Waterbeemd, H (eds), Methods and Principles in Medicinal Chemistry, Vol 4, VCH, Weinheim, Germany, 1996, pp 109 139 276 Scherrer, R A, Biolipid pKa values in the lipophilicity of ampholytes and ion pairs, in Testa, B; van de Waterbeemd, H; Folkers, G; Guy, R (eds), Pharmacokinetic Optimization in Drug Research, Verlag Helvetica Chimica Acta, Zurich and WileyVCH, Weinheim, 2001, pp 351 381 277 Murthy K S; Zogra , G, Oil-water partitioning of chlorpromazine and other phenothiazine derivatives using dodecane and n-octanol, J Pharm Sci 59, 1281 1285 (1970) 278 Tomlinson, E; Davis, S S, Interactions between large organic ions of opposite and unequal charge II Ion pair and ion triplet formation, J Colloid Interface Sci 74, 349 357 (1980) 279 van der Giesen, W F; Janssen, L H M, Int J Pharm 12, 231 249 (1982) 280 Scherrer, R A, The treatment of ionizable compounds in quantitative structure-activity studies with special consideration of ion partitioning, in Magee, P S; Kohn, G K; Menn, J J (eds), Pesticide Syntheses through Rational Approaches, ACS Symposium Series 225, ACS (American Chemical Society), Washington, DC, 1984, pp 225 246 281 Scherrer, R A; Crooks, S L, Titrations in water-saturated octanol: A guide to partition coef cients of ion pairs and receptor-site interactions, Quant Struct-Act Relat 8, 59 62 (1989) 282 Akamatsu, M; Yoshida, Y; Nakamura, H; Asao, M; Iwamura, H; Fujita, T, Hydrophobicity of di- and tripeptides having unionizable side chains and correlation with substituent and structural parameters, Quant Struc -Act Relat 8, 195 203 (1989)
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283 Manners, C N; Payling, D W; Smith, D A, Lipophilicity of zwitterionic suphate conjugates of tiaramide, propanolol and 40 -hydroxypropranolol, Xenobiotica 19, 1387 1397 (1989) 284 Westall, J C; Johnson, C A; Zhang, W, Distribution of LiCl, NaCl, KCl, HCl, MgCl2, and CaCl2 between octanol and water, Environ Sci Technol 24, 1803 1810 (1990) 285 Chmel k, J; Hudecek, J; Putyera, K; Makovicka, J; Kalous, V; Chmel kova, J, Characterization of the hydrophobic properties of amino acids on the basis of their partition and distribution coef cients in the 1-octanol-water system, Collect Czech Chem Commum 56, 2030 2040 (1991) 286 Tsai, R-S; Testa, B; El Tayar, N; Carrupt, P-A, Structure-lipophilicity relationships of zwitterionic amino acids, J Chem Soc Perkin Trans 2, 1797 1802 (1991) 287 Akamatsu, M; Fujita, T, Quantitative analysis of hydorphobicity of di- to pentapeptides having un-ionizable side chains with substituent and structural parameters, J Pharm Sci 81, 164 174 (1992) 288 Akamatsu, M; Katayama, T; Kishimoto, D; Kurokawa, Y; Shibata, H, Quantitative analysis of the structure-hydophibicity relationships for n-acetyl di- and tripeptide amides, J Pharm Sci 83, 1026 1033 (1994) 289 Abraham, M H; Takacs-Novak, K; Mitchell, R C, On the partition of ampholytes: Application to blood-brain distribution, J Pharm Sci 86, 310 315 (1997) 290 Bierer, D E; Fort, D M; Mendez, C D; Luo, J; Imbach, P A; Dubenko, L G; Jolad, S D; Gerber, R E; Litvak, J; Lu, Q; Zhang, P; Reed, M J; Waldeck, N; Bruening, R C; Noamesi, B K; Hector, R F; Carlson, T J; King, S R, Ethnobotanical-directed discovery of the antihyperglycemic properties of cryptolepine: Its isolation from Cryptolepis sanguinolenta, synthesis, and in vitro and in vivo activities, J Med Chem 41, 894 901 (1998) 291 Takacs-Novak, K; Szasz, G, Ion-pair partition of quaternary ammonium drugs: The in uence of counter ions of different lipophilicity, size, and exibility, Pharm Res 16, 1633 1638 (1999) 292 Valko, K; Slegel, P, New chromotographic hydrophobicity index (j0) based on the slope and the intercept of the log k0 versus organic phase concentration plot, J Chromotogr 631, 49 61 (1993) 293 Valko, K; Bevan, C; Reynolds, D, Chromatographic hydrophobicity index by fastgradient RP-HPLC: A high-thorughput alternative to logP/logD, Anal Chem 69, 2022 2029 (1997) 294 Hitzel, L; Watt, A P; Locker, K L, An increased throughput method for the determination of partition coef cients, Pharm Res 17, 1389 1395 (2000) 295 Schrader, W; Andersson, J T, Fast and direct method for measuring 1-octanol-water partition coef cients exempli ed for six local anesthetics, J Pharm Sci 90, 1948 1954 (2001) 296 Lombardo, F; Shalaeva, M Y; Tupper, K A; Gao, F; Abraham, M H, E logPoct: A tool for lipophilicity determination in drug discovery, J Med Chem 43, 2922 2928 (2000) 297 Lombardo, F; Shalaeva, M Y; Tupper, K A; Gao, F, E logDoct: A tool for lipophilicity determination in drug discovery 2 Basic and neutral compounds, J Med Chem 43, 2922 2928 (2000)
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