R. Craig

发表

Rational design of diflunisal analogues with reduced affinity for human serum albumin.

P. Hajduk, S. Fesik, R. Bell, 2001, Journal of the American Chemical Society.

(R)-(+)-N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl- 2-propynyl]-N-hydroxyurea (ABT-761), a second-generation 5-lipoxygenase inhibitor.

J. Bouska, G. Carter, P. Bhatia, 1995, Journal of medicinal chemistry.

Behavioral effects of A71623, a highly selective CCK-A agonist tetrapeptide.

L. Bednarz, M. Cullen, P. A. Gore, 1992, The American journal of physiology.

Lysyl 4-aminobenzoic acid derivatives as potent small molecule mimetics of plasminogen kringle 5.

J. Henkin, D. Davidson, G. Sheppard, 2004, Bioorganic & medicinal chemistry letters.

3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2.

Scott A. Erickson, Jyoti R. Patel, Chang H. Park, 2004, Bioorganic & medicinal chemistry letters.

Characterization of two novel cholecystokinin tetrapeptide (30-33) analogues, A-71623 and A-70874, that exhibit high potency and selectivity for cholecystokinin-A receptors.

B. Bianchi, A. Nadzan, K. Shiosaki, 1991, Molecular pharmacology.

Development of CCK-tetrapeptide analogues as potent and selective CCK-A receptor agonists.

B. Bianchi, A. Nadzan, K. Shiosaki, 1990, Journal of medicinal chemistry.

Design of inhibitors of leukotriene biosynthesis and their therapeutic potential

J. Bouska, G. Carter, R. Harris, 1998 .

Structure-activity relationships of N-hydroxyurea 5-lipoxygenase inhibitors.

R. Maki, P. Young, J. Summers, 1997, Journal of medicinal chemistry.

Alkylation of tricarbonyl(diene)iron complexes: Model studies for the preparation of protomycinolide IV ☆

W. A. Donaldson, R. Henry, J. Wasicak, 1997 .

Symmetrical bis(heteroarylmethoxyphenyl)alkylcarboxylic acids as inhibitors of leukotriene biosynthesis.

J. Bouska, G. Carter, K. Hulkower, 2000, Journal of medicinal chemistry.

Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N epsilon)-amide residues.

B. Bianchi, M. Stashko, A. Nadzan, 1992, Journal of medicinal chemistry.

Diastereoselective alkylation of tricarbonyl(methyl 3,5-hexadienoate)iron

W. A. Donaldson, S. Spanton, R. Craig, 1992 .

Development of non-sulfated tetrapeptides as potent and selective CCK-A receptor agonists

B. Bianchi, A. Nadzan, K. Shiosaki, 1991 .

NMR-based modification of matrix metalloproteinase inhibitors with improved bioavailability.

Yan Guo, Michael Michaelides, Richard Craig, 2002, Journal of medicinal chemistry.