Sung Chun Kim

β-Methanesulfonyl-L-valine as a novel, unnatural amino acid surrogate for P2 in the design of HIV protease inhibitors.

Y. Kwon, Ho-il Choi, J. Koh, 1996 .

Synthesis of irreversible HIV-1 protease inhibitors containing sulfonamide and sulfone as amide bond isosteres

Ho-il Choi, J. Koh, W. Jung, 1997 .

Synthesis of Irreversible HIV-1 Protease Inhibitors Containing Sulfonamide and Sulfone as Amide Bond Isosteres.

Ho-il Choi, J. Koh, W. Jung, 1998 .

DESIGN, SYNTHESIS, AND CHARACTERIZATION OF DIPEPTIDE ISOSTERE CONTAINING CIS-EPOXIDE FOR THE IRREVERSIBLE INACTIVATION OF HIV PROTEASE

Sangsoo Kim, J. Ok, Ho-il Choi, 1996 .

Rational design of irreversible, pseudo-C2-symmetric hiv-1 protease inhibitors

Ho-il Choi, K. Moon, J. Koh, 1995 .

The x-ray crystallographic study of covalently modified carboxypeptidase A by 2-benzyl-3,4-epoxybutanoic acid, a pseudomechanism-based inactivator

Sangsoo Kim, D. H. Kim, Mikyung Yun, 1992 .