A. Kaplan

发表

Synthesis and evaluation of an inhibitor of carboxypeptidase A with a Ki value in the femtomolar range.

P. Bartlett, A. Kaplan, Paul A. Bartlett, 1991, Biochemistry.

A concise and efficient solid-phase synthesis of 2-amino-4(3H)-quinazolinones

Rui Yang, A. Kaplan, 2000 .

Phosphonate analogues of carboxypeptidase A substrates are potent transition-state analogue inhibitors.

J. Hanson, P. Bartlett, A. Kaplan, 1989, Biochemistry.

Transition-state characterization: a new approach combining inhibitor analogues and variation in enzyme structure.

W. Rutter, P. Bartlett, M. A. Phillips, 1992, Biochemistry.

Reaction of isothiourea with 2,3-diaza-3-pentenedioic anhydride. A solid-phase synthesis of 3-amino-1,2,4-triazin-5(4H)-ones

Rui Yang, A. Kaplan, 2001 .

A search for conformational change on ligand binding in a human M macroglobulin. I. Circular dichroism and hydrogen exchange.

H. Metzger, R. Ashman, A. Kaplan, 1971, Immunochemistry.

Partial sequences of six macroglobulin light chains. Absence of sequence correlates to functional activity.

H. Metzger, A. Kaplan, 1969, Biochemistry.

Azetidine-based selective glycine transporter-1 (GlyT1) inhibitors with memory enhancing properties.

Michael R. Kennedy, Kiev S. Ly, Marco Peters, 2020, Bioorganic & medicinal chemistry letters.

A new class of HIV-1 protease inhibitor: the crystallographic structure, inhibition and chemical synthesis of an aminimide peptide isostere.

R M Stroud, R. Stroud, C. Craik, 1996, Bioorganic & medicinal chemistry.

Amino terminal sequences of human immunoglobulin heavy chains.

L. Hood, H. Metzger, W. Terry, 1971, Immunochemistry.

Design and Synthesis of Novel and Selective Glycine Transporter-1 (GlyT1) Inhibitors with Memory Enhancing Properties.

Michael R. Kennedy, Kiev S. Ly, D. M. Chung, 2018, Journal of medicinal chemistry.