Weixing Li

发表

Identification of GS 4104 as an Orally Bioavailable Prodrug of the Influenza Virus Neuraminidase Inhibitor GS 4071

Norbert Bischofberger, Matt Williams, C. Sweet, 1998, Antimicrobial Agents and Chemotherapy.

Post-treatment with a novel PARG inhibitor reduces infarct in cerebral ischemia in the rat

Jie Zhang, Weixing Li, Xi-Chun M. Lu, 2003, Brain Research.

Poly(ADP-ribose) glycohydrolase inhibitor as chemosensitiser of malignant melanoma for temozolomide.

C. Leonetti, M. Scarsella, L. Tentori, 2005, European journal of cancer.

PARG activity mediates intestinal injury induced by splanchnic artery occlusion and reperfusion

E. Mazzon, S. Cuzzocrea, Zhao-Qi Wang, 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

GS 4071 is a potent and selective inhibitor of the growth and neuraminidase activity of influenza A and B viruses in vitro

R. Sidwell, J. Huffman, Matthew A. Williams, 1997 .

Synthesis and biological evaluation of thiol-based inhibitors of glutamate carboxypeptidase II: discovery of an orally active GCP II inhibitor.

Qun Liu, T. Tsukamoto, B. Slusher, 2003, Journal of medicinal chemistry.

Azetidine-based inhibitors of dipeptidyl peptidase IV (DPP IV).

D. Ferraris, C. Rojas, B. Thomas, 2007, Current Topics in Medicinal Chemistry.

Inhibition of native hepatitis C virus replicase by nucleotide and non-nucleoside inhibitors.

N. Cammack, K. Klumpp, Weixing Li, 2005, Virology.

Oral Administration of a Prodrug of the Influenza Virus Neuraminidase Inhibitor GS 4071 Protects Mice and Ferrets against Influenza Infection

R. Sidwell, C. Sweet, J. Huffman, 1998, Antimicrobial Agents and Chemotherapy.

Accumulation of Free ADP-ribose from Mitochondria Mediates Oxidative Stress-induced Gating of TRPM2 Cation Channels*

B. Stoddard, A. Perraud, A. Scharenberg, 2005, Journal of Biological Chemistry.

Structure of glutamate carboxypeptidase II, a drug target in neuronal damage and prostate cancer

J. Konvalinka, R. Hilgenfeld, J. Mesters, 2006, The EMBO journal.

Proteolytic Inhibition in Regulating the Insulin-Like Growth Factor-Binding Proteins in Prostate Cancer

Barry S. Cooperman, B. Cooperman, Catherine Yang, 2012 .

Synthesis of substituted 5[H]phenanthridin-6-ones as potent poly(ADP-ribose)polymerase-1 (PARP1) inhibitors.

J. Zhang, V. Kalish, D. Ferraris, 2001, Bioorganic & medicinal chemistry letters.