J. Leber

发表

Inhibition of 3-hydroxy-3-methylglutaryl coenzyme A synthase by antibiotic 1233A and other beta-lactones.

J. D. Elliott, R. Mayer, M. Fisher, 1990, Biochemical and biophysical research communications.

Nonpeptide endothelin receptor antagonists. VII: Binding characteristics of [3H]SB 209670, a novel nonpeptide antagonist of endothelin receptors.

N. Aiyar, H. Wu, R. Ruffolo, 1996, Journal of Pharmacology and Experimental Therapeutics.

SB 209670, a rationally designed potent nonpeptide endothelin receptor antagonist.

S. Douglas, E. Ohlstein, P. Nambi, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Identification of 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-7-{[(3S)-3-piperidinylmethyl]oxy}-1H-imidazo[4,5-c]pyridin-4-yl)-2-methyl-3-butyn-2-ol (GSK690693), a novel inhibitor of AKT kinase.

G. Warren, R. Copeland, T. J. Lansing, 2008, Journal of medicinal chemistry.

1,3-Diarylindan-2-carboxylic acids, potent and selective non-peptide endothelin receptor antagonists.

J. D. Elliott, N. Elshourbagy, K. Erhard, 1994, Journal of medicinal chemistry.

Correction: Slow binding inhibition of 3-hydroxy-3-methylglutaryl-coenzyme A reductase [Erratum to document cited in CA112(23):212921g]

J. D. Elliott, C. E. Peishoff, R. Mayer, 1990 .

Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity.

Robert A Copeland, Anthony E Choudhry, T. Gilmer, 2008, Cancer research.

Discovery of aminofurazan-azabenzimidazoles as inhibitors of Rho-kinase with high kinase selectivity and antihypertensive activity.

S. Semus, M. Head, D. Behm, 2007, Journal of medicinal chemistry.

Tetrasubstituted pyridines as potent and selective AKT inhibitors: Reduced CYP450 and hERG inhibition of aminopyridines.

Sharad Verma, Kristin K. Brown, Anthony E Choudhry, 2010, Bioorganic & medicinal chemistry letters.

A revised structure for sibiromycin

J. R. Hoover, S. Hecht, Randall K. Johnson, 1988 .

Aminofurazans as potent inhibitors of AKT kinase.

D. Heerding, E. Minthorn, N. Concha, 2009, Bioorganic & medicinal chemistry letters.

Lysine 182 of endothelin B receptor modulates agonist selectivity and antagonist affinity: evidence for the overlap of peptide and non-peptide ligand binding sites.

C. E. Peishoff, J. Stadel, R. D. Cousins, 1994, Biochemistry.

Slow binding inhibition of 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

J. D. Elliott, C. E. Peishoff, R. Mayer, 1990, Biochemistry.

The preparation of 9-alkylthiofluorenes from biphenyl-2-carboxaldehydes

J. D. Elliott, J. Leber, 1989 .

Advances in development of Pb-free piezoelectric materials for transducer applications

A. Safari, Qifa Zhou, Yushun Zeng, 2023, Japanese Journal of Applied Physics.