W. Schilling

发表

Intermediates of rifamycin polyketide synthase produced by an Amycolatopsis mediterranei mutant with inactivated rifF gene.

R. Traber, L. Oberer, T. Schupp, 1999, Microbiology.

Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. I. Taxonomy, fermentation, isolation and biological activity.

K. Memmert, H. Hofmann, J. Sanglier, 1999, The Journal of antibiotics.

Cymbimicin A and B, two novel cyclophilin-binding structures isolated from actinomycetes.

A. Enz, J. Sanglier, V. Quesniaux, 1997, The Journal of antibiotics.

Sanglifehrins A, B, C and D, novel cyclophilin-binding compounds isolated from Streptomyces sp. A92-308110. II. Structure elucidation, stereochemistry and physico-chemical properties.

J. Kallen, J. Sanglier, L. Oberer, 1999, The Journal of antibiotics.

SAR of 2-benzyl-4-aminopiperidines: CGP 49823, an orally and centrally active non-peptide NK1 antagonist

S. Ofner, A. Vassout, S. Veenstra, 1996 .

Antascomicins A, B, C, D and E. Novel FKBP12 binding compounds from a Micromonospora strain.

J. Sanglier, W. Schuler, W. Schilling, 1996, The Journal of antibiotics.

New insights into rifamycin B biosynthesis: isolation of proansamycin B and 34a-deoxy-rifamycin W as early macrocyclic intermediates indicating two separated biosynthetic pathways.

R. Traber, L. Oberer, T. Schupp, 2002, The Journal of antibiotics.

Food intake in free-feeding and energy-deprived lean rats is mediated by the neuropeptide Y5 receptor.

S. Whitebread, C. Gerald, L. Criscione, 1998, The Journal of clinical investigation.

Design, synthesis and SAR of a series of 2-substituted 4-amino-quinazoline neuropeptide Y Y5 receptor antagonists.

S. Whitebread, I. Islam, J. Zhang, 2000, Bioorganic & medicinal chemistry letters.

CGP 49823, a novel, non-peptidic NK-1 receptor antagonist: in vitro pharmacology

J. Heid, S. Ofner, L. Criscione, 1994, Neuropeptides.

Endothelium-dependent relaxant effect of neurokinins on rabbit aorta is mediated by the NK1 receptor.

L. Criscione, J. Henlin, W. Schilling, 1992, European journal of pharmacology.