S. Aster

发表

A new class of angiotensin-converting enzyme inhibitors

C. A. Stone, W. Greenlee, E. Thorsett, 1980, Nature.

Dipeptide mimics. Conformationally restricted inhibitors of angiotensin-converting enzyme.

E. Thorsett, A. Patchett, E. Harris, 1983, Biochemical and biophysical research communications.

Benzolactams. A new class of converting enzyme inhibitors.

E. Thorsett, A. Patchett, D. Taub, 1983, Biochemical and biophysical research communications.

Selective inhibitors of biosynthesis of aminergic neurotransmitters

A. Patchett, S. Aster, A. Maycock, 1978, Nature.

Discovery and Pharmacology of a Novel Somatostatin Subtype 5 (SSTR5) Antagonist: Synergy with DPP-4 Inhibition.

Margaret S. Wu, Yun-ping Zhou, A. Howard, 2018, ACS medicinal chemistry letters.

Adamantyl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type 1.

R. Thieringer, S. Wright, J. Schaeffer, 2005, Bioorganic & medicinal chemistry letters.

Both coactivator LXXLL motif-dependent and -independent interactions are required for peroxisome proliferator-activated receptor gamma (PPARgamma) function.

Y. Li, G. Zhou, D. Moller, 2000, The Journal of biological chemistry.

Conformationally restricted inhibitors of angiotensin converting enzyme: synthesis and computations.

J. Snyder, J. Springer, J. Hirshfield, 1986, Journal of medicinal chemistry.

Design and synthesis of novel antibacterial agents with inhibitory activity against DNA polymerase III.

R. Painter, K. Ellsworth, W. Geissler, 2001, Bioorganic & Medicinal Chemistry Letters.

Both Coactivator LXXLL Motif-dependent and -independent Interactions Are Required for Peroxisome Proliferator-activated Receptor γ (PPARγ) Function*

Bruce A. Johnson, D. Moller, Gaochao Zhou, 2000, The Journal of Biological Chemistry.

Inactivation of 3-(3,4-dihydroxyphenyl)alanine decarboxylase by 2-(fluoromethyl)-3-(3,4-dihydroxyphenyl)alanine.

A. Patchett, S. Aster, A. Maycock, 1980, Biochemistry.