J. Moliterni

发表

Design and synthesis of potent, selective inhibitors of endothelin-converting enzyme.

A. Jeng, P. Savage, E. Wallace, 1998, Journal of medicinal chemistry.

Benzazepinones and benzoxazepinones as antagonists of inhibitor of apoptosis proteins (IAPs) selective for the second baculovirus IAP repeat (BIR2) domain.

Robert T. Taylor, A. Polonskaia, M. Weisel, 2013, Journal of medicinal chemistry.

Optimization of benzodiazepinones as selective inhibitors of the X-linked inhibitor of apoptosis protein (XIAP) second baculovirus IAP repeat (BIR2) domain.

A. Polonskaia, M. Weisel, C. Lukacs, 2013, Journal of medicinal chemistry.

Potent and selective non-peptidic inhibitors of endothelin-converting enzyme-1 with sustained duration of action.

D. Hoyer, Y. Satoh, D. Hoyer, 2000, Journal of medicinal chemistry.

Synthesis of tetrazole analogs of α-amino acids by alkylation of a Schiff base of α-aminomethyltetrazole

Y. Satoh, E. Wallace, N. Marcopulos, 1998 .

The scope and limitations of the Suzuki–Miyaura cross-coupling reactions of 6- and 8-substituted 1,2,3,4-tetrahydroisoquinoline-3-carboxylates

J. Mckenna, Y. Qiao, J. Moliterni, 2001 .

CGS 27830, a potent nonpeptide endothelin receptor antagonist

C. Cioffi, R. Webb, K. Lipson, 1993 .

Discovery of [4-Amino-2-(1-methanesulfonylpiperidin-4-ylamino)pyrimidin-5-yl](2,3-difluoro-6- methoxyphenyl)methanone (R547), a potent and selective cyclin-dependent kinase inhibitor with significant in vivo antitumor activity.

Nader Fotouhi, Sung-Sau So, S. So, 2006, Journal of medicinal chemistry.

Preclinical In vivo Evaluation of Efficacy, Pharmacokinetics, and Pharmacodynamics of a Novel MEK1/2 Kinase Inhibitor RO5068760 in Multiple Tumor Models

N. Fotouhi, A. Railkar, D. Heimbrook, 2010, Molecular Cancer Therapeutics.

HOMOLOGATION OF 1-(BENZYLOXYMETHYL)-1H-TETRAZOLE VIA LITHIATION

Y. Satoh, J. Moliterni, 1998 .

Homologation of 1-(Benzyloxymethyl)-1H-tetrazole via Lithiation.

Y. Satoh, J. Moliterni, 1998 .

Synthesis and pharmacological evaluation of a series of new 3-methyl-1,4-disubstituted-piperidine analgesics.

M. Ossipov, F. Rudo, J. Moliterni, 1990, Journal of medicinal chemistry.