M. Jetter

发表

Synthesis and structure--activity relationships of aroylpyrrole alkylamide bradykinin (B2) antagonists.

Sui-Po Zhang, R. Colburn, D. Stone, 2003, Bioorganic & medicinal chemistry letters.

Chapter 2. Centrally Acting Analgesics

R. Raffa, A. Reitz, K. Wild, 1995 .

Synthesis of 4-Substituted Imidazoles via Palladium-Catalyzed Cross-Coupling Reactions

A. Reitz, M. Jetter, 1998 .

Design and synthesis of novel pyrrolidine-containing bradykinin antagonists.

C. Reynolds, Sui-Po Zhang, D. Hlasta, 2003, Bioorganic & medicinal chemistry letters.

Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1

A. Dubin, M. McDonnell, Sui-Po Zhang, 2007 .

Novel thiazole based heterocycles as inhibitors of LFA-1/ICAM-1 mediated cell adhesion.

P J Sanfilippo, R A Noe, M C Jetter, 1995, Journal of medicinal chemistry.

7,8-Dihydro-8-oxoadenine as a replacement for cytosine in the third strand of triple helices. Triplex formation without hypochromicity.

F. Hobbs, M. Jetter, 1993, Biochemistry.

EXPEDIENT SYNTHESIS OF N 1-TRITYLIMIDAZOLE-4-CARBOXALDEHYDE

A. Reitz, R. E. Boyd, M. Jetter, 1996 .

Identification and biological evaluation of 4-(3-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid (5-trifluoromethylpyridin-2-yl)amide, a high affinity TRPV1 (VR1) vanilloid receptor antagonist.

N. Carruthers, A. Dubin, Sui-Po Zhang, 2005, Journal of medicinal chemistry.

N-isoquinolin-5-yl-N'-aralkyl-urea and -amide antagonists of human vanilloid receptor 1.

A. Dubin, Sui-Po Zhang, N. Nasser, 2004, Bioorganic & medicinal chemistry letters.

N-pyridin-3-yl- and N-quinolin-3-yl-benzamides: modulators of human vanilloid receptor 1 (TRPV1).

A. Dubin, M. McDonnell, Sui-Po Zhang, 2008, Bioorganic & medicinal chemistry letters.

N‐Isoquinolin‐5‐yl‐N′‐aralkyl‐urea and ‐amide Antagonists of Human Vanilloid Receptor 1.

A. Dubin, Sui-Po Zhang, N. Nasser, 2004 .