Evaluation of the predictive power of calculation procedure for molecular hydrophobicity of some estradiol derivates

This publication has 18 references indexed in Scilit:

• Substructure and whole molecule approaches for calculating log P
  Journal of Computer-Aided Molecular Design, 2001
• Lipophilicity characterization by reversed-phase liquid chromatography of some furan derivatives
  Journal of Chromatography A, 2000
• The lipophilic behaviour of organic compounds: 1. An updating of the hydrophobic fragmental constant approach
  Quantitative Structure-Activity Relationships, 1998
• Chromatographic Hydrophobicity Index by Fast-Gradient RP-HPLC: A High-Throughput Alternative to log P/log D
  Analytical Chemistry, 1997
• Calculation Procedures for Molecular Lipophilicity: a Comparative Study
  Quantitative Structure-Activity Relationships, 1996
• Comparative Evaluation of the Predictive Power of Calculation Procedures for Molecular Lipophilicity
  Journal of Pharmaceutical Sciences, 1995
• New chromatographic hydrophobicity index (ϕ0) based on the slope and the intercept of the log k′ versus organic phase concentration plot
  Journal of Chromatography A, 1993
• Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics
  Journal of Chemical Information and Computer Sciences, 1989
• Atomic physicochemical parameters for three-dimensional-structure-directed quantitative structure-activity relationships. 2. Modeling dispersive and hydrophobic interactions
  Journal of Chemical Information and Computer Sciences, 1987
• p-σ-π Analysis. A Method for the Correlation of Biological Activity and Chemical Structure
  Journal of the American Chemical Society, 1964