K H Kim

Quantitative structure-activity relationships of the metabolism of drugs by uridine diphosphate glucuronosyltransferase.

K H Kim, K. H. Kim, 1991, Journal of pharmaceutical sciences.

Direct prediction of dissociation constants (pKa's) of clonidine-like imidazolines, 2-substituted imidazoles, and 1-methyl-2-substituted-imidazoles from 3D structures using a comparative molecular field analysis (CoMFA) approach.

Y. Martin, K H Kim, Y C Martin, 1991, Journal of medicinal chemistry.

Quantitative structure-activity relationships in 1-aryl-2-(alkylamino)ethanol antimalarials.

P. N. Craig, P. Y. Jow, E. E. Steller, 1979, Journal of medicinal chemistry.

"Aromatic" substituent constants for structure-activity correlations.

S H Unger, A. Leo, C. Hansch, 1973, Journal of medicinal chemistry.

Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis.

A. Debnath, C. Hansch, Y. Martin, 1993, Journal of medicinal chemistry.