C. G. Caldwell

发表

Fluoropyrrolidine amides as dipeptidyl peptidase IV inhibitors.

Ping Chen, N. Thornberry, B. Leiting, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of optically active 3-diazoacetylretinals with triisopropylphenylsulfonylhydrazone

Anil Kumar Singh, K. Nakanishi, C. G. Caldwell, 1988 .

Photoisomerization mechanism of the rhodopsin chromophore: picosecond photolysis of pigment containing 11-cis-locked eight-membered ring retinal.

K. Nakanishi, H. Kandori, T. Yoshizawa, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Comparison of the structure of human recombinant short form stromelysin by multidimensional heteronuclear NMR and X-ray crystallography

Paul R. Gooley, Melinda G. Axel, J. W. Becker, 1996, Journal of biomolecular NMR.

Novel tetrahydropyran analogs as dipeptidyl peptidase IV inhibitors: Profile of clinical candidate (2R,3S,5R)-2- (2,5-difluorophenyl)-5-(4,6-dihydropyrrolo [3,4-c]pyrazol-5-(1H)-yl)tetrahydro-2H-pyran-3-amine (23) [corrected].

Ping Chen, G. Scapin, R. S. Roy, 2013, Bioorganic & medicinal chemistry letters.

2,3-Dihydro-5-benzofuranols as antioxidant-based inhibitors of leukotriene biosynthesis.

F. Baker, D. Macintyre, J. Boger, 1989, Journal of medicinal chemistry.

Fluoropyrrolidine amides as dipeptidyl peptidase IV inhibitors.

Ping Chen, N. Thornberry, B. Leiting, 2004, Bioorganic & medicinal chemistry letters.

Orally active inhibitors of stromelysin-1 (MMP-3)

M. Maccoss, W. Hagmann, K. Chapman, 1996 .

Phosphinic acid inhibitors of matrix metalloproteinases

W. Hagmann, R. Stein, S. Mills, 1996 .

Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-pentylsulfones as CCR5 antagonists.

D. Hazuda, Ping Chen, W. Schleif, 2004, Bioorganic & medicinal chemistry letters.

Confirmation of the secondary deuterium isotope effect for the peptidyl prolyl cis-trans isomerase activity of cyclophilin by a competitive, double-label technique

D. Melillo, R. Stein, C. G. Caldwell, 1990 .

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists: modifications of the arylpropylpiperidine side chains.

D. Hazuda, Ping Chen, W. Schleif, 2003, Bioorganic & medicinal chemistry letters.

Inhibition of matrix metalloproteinases by N-carboxyalkyl dipeptides: Enhanced potency and selectivity with substituted P1′ homophenylalanines

M. Maccoss, W. Hagmann, K. Chapman, 1995 .

Imidazopiperidine amides as dipeptidyl peptidase IV inhibitors for the treatment of diabetes.

Ping Chen, N. Thornberry, B. Leiting, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of [(1R)-1-amino-2-(2,5-difluorophenyl)ethyl]cyclohexanes and 4-[(1R)-1-amino-2-(2,5-difluorophenyl)ethyl]piperidines as DPP-4 inhibitors.

Ping Chen, N. Thornberry, Huaibing He, 2011, Bioorganic & medicinal chemistry letters.

The inhibition of C5a receptor binding by analogs of L-156,602, a cyclic hexadepsipeptide antibiotic

Sumire V. Kobayashi, W. Hagmann, J. Boger, 1992 .

Substituted 2-aminopyridines as inhibitors of nitric oxide synthases.

W. F. Hoffman, Kenny K. Wong, M. Maccoss, 2000, Bioorganic & medicinal chemistry letters.

Substituted 4,6-diaminoquinolines as inhibitors of C5a receptor binding.

W. Hagmann, S. Kobayashi, M. Springer, 1992, Journal of medicinal chemistry.

Synthesis of analogs of (1,4)-3- and 5-imino oxazepane, thiazepane, and diazepane as inhibitors of nitric oxide synthases.

Kenny K. Wong, Ping Chen, M. Maccoss, 2004, Bioorganic & medicinal chemistry letters.

L-156,602, a C5a antagonist with a novel cyclic hexadepsipeptide structure from Streptomyces sp. MA6348. Fermentation, isolation and structure determination.

O. Hensens, C. Schwartz, S. Currie, 1991 .

Isoform-Selective and Stereoselective Inhibition of Hypoxia Inducible Factor-2.

Thomas H Scheuermann, John B MacMillan, Liela Bayeh, 2015, Journal of medicinal chemistry.

The di--butylsilylene protecting group for diols

B. Trost, C. G. Caldwell, C. Caldwell, 1981 .

Total synthesis of 1-156,602, a novel cyclic hexadepsipeptide antibiotic

F. Baker, J. Boger, S. Bondy, 1990 .

A convenient synthesis of 4-tert-butyl-5-benzofuranols and dihydrobenzofuranols

R. Zambias, C. G. Caldwell, M. Hammond, 1988 .

Binding of 2-aryl-4-(piperidin-1-yl)butanamines and 1,3,4-trisubstituted pyrrolidines to human CCR5: a molecular modeling-guided mutagenesis study of the binding pocket.

M. Maccoss, J. Demartino, C. L. Lynch, 2003, Biochemistry.

Synthesis of the lipophilic side chain of the cyclic hexadepsipeptide antibiotic L-156,602

S. Bondy, C. G. Caldwell, K. Rupprecht, 1990 .

Synthesis of retinals with eight- and nine-membered rings in the side chain. Models for rhodopsin photobleaching intermediates

K. Nakanishi, J. Wang, C. Bigge, 1993 .

Additions and Corrections - Bacteriorhodopsins Containing Cyanine Dye Chromophores. Support for the External Point-Charge Model

K. Nakanishi, M. Motto, C. G. Caldwell, 1983 .

Synthesis of Retinals with Eight- and Nine-Membered Rings in the Side Chain. Models for Rhodopsin Photobleaching Intermediates.

K. Nakanishi, J. Wang, C. Bigge, 1993 .

Sulfur-substituted dienes and the silylene protecting group in synthesis. Deoxypillaromycinone

B. Trost, D. Heissler, C. G. Caldwell, 1983 .

Inhibition of stromelysin-1 (MMP-3) by P1'-biphenylylethyl carboxyalkyl dipeptides.

M. Maccoss, J. W. Becker, W. Hagmann, 1997, Journal of medicinal chemistry.