Jenny Tan

发表

Discovery of benzothiazole-based adenosine A2B receptor antagonists with improved A2A selectivity.

R. Hamid, Yang Wen, J. Grimsby, 2011, Bioorganic & medicinal chemistry letters.

4-Substituted-7-N-alkyl-N-acetyl 2-aminobenzothiazole amides: drug-like and non-xanthine based A2B adenosine receptor antagonists.

A. Flohr, R. Hamid, Yang Wen, 2010, Bioorganic & medicinal chemistry letters.

Discovery of orally active carboxylic acid derivatives of 2-phenyl-5-trifluoromethyloxazole-4-carboxamide as potent diacylglycerol acyltransferase-1 inhibitors for the potential treatment of obesity and diabetes.

C. Rondinone, Yingsi Chen, Y. Qian, 2011, Journal of medicinal chemistry.

Potent non-peptidic dual inhibitors of endothelin-converting enzyme and neutral endopeptidase 24.11

A. Jeng, P. Savage, M. WallaceEli, 1997 .

Suppression of Substance P Biosynthesis in Sensory Neurons of Dorsal Root Ganglion by Prodrug Esters of Potent Peptidylglycine α-Amidating Monooxygenase Inhibitors*

M. Erion, A. Jeng, R. Fujimoto, 1997, The Journal of Biological Chemistry.

Non-peptidic inhibitors of neutral endopeptidase 24.11 1. Discovery and optimization of potency

R. Ghai, C. Berry, Y. Sakane, 1995 .

Non‐Peptidic Inhibitos of Neutral Endopeptidase 24.11. Part 1. Discovery and Optimization of Potency.

R. Ghai, C. Berry, Y. Sakane, 1995 .

Mitigation of reactive metabolite formation for a series of 3-amino-2-pyridone inhibitors of Bruton's tyrosine kinase (BTK).

P. Wovkulich, P. Di Lello, D. Fry, 2017, Bioorganic & medicinal chemistry letters.

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

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

Dual inhibition of neutral endopeptidase and angiotensin-converting enzyme by N-phosphonomethyl and N-carboxyalkyl dipeptides

Stéphane De Lombaert, Jenny Tan, Lisa J. Stamford, 1994 .

Perhydroquinolylbenzamides as novel inhibitors of 11beta-hydroxysteroid dehydrogenase type 1.

A. Jeng, P. Kukkola, J. Stanton, 2005, 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 and biological activity of potent heterocyclic thiol-based inhibitors of endothelin-converting enzyme-1.

A. Jeng, P. Savage, C. Fink, 2002, Bioorganic & medicinal chemistry letters.