J. Bauman

发表

The identification of a small molecule inhibitor that specifically reduces T cell-mediated adaptive but not LPS-mediated innate immunity by T cell membrane-monocyte contact bioassay.

T. Zollner, M. Bao, Yi-Yang Yvonne Li, 2008, Immunology letters.

An Aspirin-Triggered Lipoxin A4 Stable Analog Displays a Unique Topical Anti-Inflammatory Profile

K. Asadullah, A. Schottelius, S. Colgan, 2002, The Journal of Immunology.

Identification and Characterization of a Potent, Selective, and Orally Active Antagonist of the CC Chemokine Receptor-1*

D. Taub, S. Harvey, R. Horuk, 2000, The Journal of Biological Chemistry.

Species selectivity of a small molecule antagonist for the CCR1 chemokine receptor.

R. Horuk, P. Kretschmer, M. Morrissey, 2000, European journal of pharmacology.

Novel 3-oxa lipoxin A4 analogues with enhanced chemical and metabolic stability have anti-inflammatory activity in vivo.

A. Schottelius, D. Davey, C. Mallari, 2004, Journal of medicinal chemistry.

Anti-Inflammatory Profile Analog Displays a Unique Topical Stable 4 An Aspirin-Triggered Lipoxin A

K. Asadullah, A. Schottelius, S. Colgan, 2002 .

Discovery of novel and potent aryl diamines as leukotriene A4 hydrolase inhibitors.

H. Ye, J. Parkinson, G. Phillips, 2008, Bioorganic & medicinal chemistry letters.

Synthesis of N-alkyl glycine amides as potent inhibitors of leukotriene A4 hydrolase.

H. Ye, D. Davey, J. Parkinson, 2008, Bioorganic & Medicinal Chemistry Letters.

A Non-peptide Functional Antagonist of the CCR1 Chemokine Receptor Is Effective in Rat Heart Transplant Rejection*

C. Weber, A. Krensky, H. Gröne, 2001, The Journal of Biological Chemistry.

CCR1-specific non-peptide antagonist: efficacy in a rabbit allograft rejection model.

R. Horuk, M. Morrissey, H. Perez, 2001, Immunology letters.

Detection of neutrophil-activating peptide NAP/IL-8 and NAP/IL-8 mRNA in human recombinant IL-1 alpha- and human recombinant tumor necrosis factor-alpha-stimulated human dermal fibroblasts. An immunocytochemical and fluorescent in situ hybridization study.

M. Sticherling, W. Sterry, J. Schröder, 1990, Journal of immunology.

The vinylketene acetal route to aklavinone and 11-deoxydaunomycinone

H. Rapoport, J. Bauman, R. Gless, 1981 .

AN EFFICIENT SYNTHESIS OF AKLAVINONE AND RELATED 11-DEOXYANTHRACYCLINONES

R. C. Hawley, H. Rapoport, J. Bauman, 1985 .

Lipoxins and novel 15‐epi‐lipoxin analogs display potent anti‐inflammatory actions after oral administration

C. Serhan, K. Gronert, P. Devchand, 2004, British journal of pharmacology.

Identification and Characterization of Small Molecule Functional Antagonists of the CCR1 Chemokine Receptor*

D. Taub, Wei Zheng, R. Horuk, 1998, The Journal of Biological Chemistry.

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase.

J. Haeggström, M. Adler, M. Whitlow, 2008, Bioorganic & medicinal chemistry.

Synthesis of a cyclohexadiene monoepoxide by intramolecular darzens condensation efficient synthesis of an a ring anthracyclinone precursor

R. C. Hawley, H. Rapoport, J. Bauman, 1984 .

Practical Synthesis of AZT and AZDU from Xylose: Efficient Deoxygenation via Nucleoside 2′-Xanthates

C. K. Chu, J. Bauman, Yaoquan Chen, 1992 .

Discovery of novel non-peptide CCR1 receptor antagonists.

R. Horuk, M. Morrissey, H. Perez, 1999, Journal of medicinal chemistry.

Identification of Morpholino-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-ones as Nonsteroidal Mineralocorticoid Antagonists.

S. Wright, P. Loria, A. Casimiro-Garcia, 2018, Journal of medicinal chemistry.