Bo Liu

发表

Discovery and characterization of non-ATP site inhibitors of the mitogen activated protein (MAP) kinases.

Hua Tang, Bo Liu, Gang Liu, 2011, ACS chemical biology.

A Novel Multi-Component Reaction to Imidazo[4,5-g]-quinazolines

Li Li, Bo Liu, Qianqian Zhang, 2013, Molecules.

Aminopyridine-based c-Jun N-terminal kinase inhibitors with cellular activity and minimal cross-kinase activity.

Chaohong Sun, E. Olejniczak, Eric F. Johnson, 2006, Journal of medicinal chemistry.

Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors.

Eric F. Johnson, C. Abad-Zapatero, H. Sham, 2006, Journal of Medicinal Chemistry.

The prospects of antagonizing the growth hormone secretagogue receptor to treat obesity

Bo Liu, Hongyu Zhao, Michael D. Serby, 2008 .

Aminopyridine carboxamides as c-Jun N-terminal kinase inhibitors: targeting the gatekeeper residue and beyond.

H. Sham, R. Gum, D. Haasch, 2006, Bioorganic & medicinal chemistry letters.

Optimization of 2,4-diaminopyrimidines as GHS-R antagonists: side chain exploration.

H. Sham, C. Collins, Gang Liu, 2006, Bioorganic & medicinal chemistry letters.

Hemodynamic effects of potent and selective JNK inhibitors in anesthetized rats: implication for targeting protein kinases in metabolic diseases.

H. Sham, D. Beno, J. Trevillyan, 2007, Bioorganic & medicinal chemistry letters.

Discovery and pharmacological evaluation of growth hormone secretagogue receptor antagonists.

E. Bush, H. Sham, D. Beno, 2006, Journal of medicinal chemistry.

2,4-diaminopyrimidine derivatives as potent growth hormone secretagogue receptor antagonists.

E. Bush, H. Sham, D. Beno, 2006, Journal of medicinal chemistry.

Synthesis and Structure—Activity Relationships of Isoxazole Carboxamides as Growth Hormone Secretagogue Receptor Antagonists.

H. Sham, Gang Liu, W. Kaszubska, 2005 .

Structure-activity relationship studies on tetralin carboxamide growth hormone secretagogue receptor antagonists.

Jyoti R. Patel, H. Sham, C. Collins, 2005, Bioorganic & medicinal chemistry letters.

Novel isoxazole carboxamides as growth hormone secretagogue receptor (GHS-R) antagonists.

H. Sham, C. Collins, Gang Liu, 2004, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of isoxazole carboxamides as growth hormone secretagogue receptor antagonists.

H. Sham, Gang Liu, W. Kaszubska, 2005, Bioorganic & medicinal chemistry letters.

A Natural Lipotrisaccharide and Its Derivatives Selectively Lyse Streptococcus pneumoniae via Interaction with Cell Membrane.

Bo Liu, Gang Liu, Jing-Ren Zhang, 2017, ACS infectious diseases.

Discovery of piperidine-aryl urea-based stearoyl-CoA desaturase 1 inhibitors.

H. Sham, T. Surowy, C. Collins, 2008, Bioorganic & medicinal chemistry letters.

A new approach for the synthesis of O-glycopeptides through a combination of solid-phase glycosylation and fluorous tagging chemistry (SHGPFT).

Yan Zhang, Bo Liu, Gang Liu, 2014, Organic & biomolecular chemistry.

Discovery of potent, selective, orally bioavailable stearoyl-CoA desaturase 1 inhibitors.

Bo Liu, Gang Liu, Hongyu Zhao, 2007, Journal of medicinal chemistry.

Facile synthesis of tetrasaccharide aided by fluorous chemistry toward a dengue virus vaccine

Bo Liu, Gang Liu, Yan zhang, 2013, Molecular Diversity.