Chao Li

发表

Synthesis and biological evaluation of dihydrotriazine derivatives as potential antibacterial agents

Changji Zheng, Liangpeng Sun, H. Piao, 2017 .

Novel monobactams utilizing a siderophore uptake mechanism for the treatment of gram-negative infections.

V. Shanmugasundaram, M. Huband, T. Harris, 2012, Bioorganic & medicinal chemistry letters.

5-Heteroatom-substituted pyrazoles as canine COX-2 inhibitors: Part 2. Structure-activity relationship studies of 5-alkylethers and 5-thioethers.

M. P. Lynch, S. Sakya, Jin Li, 2006, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of heteroaryl-phenyl-substituted pyrazole derivatives as highly selective and potent canine COX-2 inhibitors.

S. Sakya, Jin Li, Hengmiao Cheng, 2006, Bioorganic & medicinal chemistry letters.

Pyridone-conjugated monobactam antibiotics with gram-negative activity.

V. Shanmugasundaram, M. Huband, T. Harris, 2013, Journal of medicinal chemistry.

Synthesis and biological evaluation of 1,3-diaryl pyrazole derivatives as potential antibacterial and anti-inflammatory agents.

Changji Zheng, Liangpeng Sun, H. Piao, 2015, Bioorganic & medicinal chemistry letters.

Tetraethyl 1,1′-(ethane-1,2-diyl)bis(2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate)

Shih-fan Wang, Chao Li, Shuai Chen, 2010, Acta crystallographica. Section E, Structure reports online.

Design, synthesis and molecular modeling of aloe-emodin derivatives as potent xanthine oxidase inhibitors.

Yu-Wei Liu, Wei Huang, D. Shi, 2014, European journal of medicinal chemistry.

Synthesis, biological evaluation and molecular modeling of aloe-emodin derivatives as new acetylcholinesterase inhibitors.

Wei Huang, D. Shi, Chao Li, 2013, Bioorganic & medicinal chemistry.

Siderophore receptor-mediated uptake of lactivicin analogues in gram-negative bacteria.

V. Shanmugasundaram, M. Huband, Ye Che, 2014, Journal of medicinal chemistry.

Synthesis and structure based optimization of novel Akt inhibitors.

Tracey Clark, Blaise Lippa, J. Pandit, 2008, Bioorganic & medicinal chemistry letters.

Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitors.

G. S. Walker, V. Shanmugasundaram, R. Obach, 2014, Journal of medicinal chemistry.

Comparative structure-activity relationship studies of 1-(5-methylsulfonylpyrid-2-yl)-5-alkyl and (hetero)aryl triazoles and pyrazoles in canine COX inhibition.

M. P. Lynch, S. Sakya, Jin Li, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and antimicrobial evaluation of 5-aryl-1,2,4-triazole-3-thione derivatives containing a rhodanine moiety.

Changji Zheng, H. Piao, Hong-yan Liu, 2015, Bioorganic & medicinal chemistry letters.

Stereospecific Synthesis and Biological Evaluation of Monodesmethyl Metabolites of (+)-13a-(S)-Deoxytylophorinine as Potential Antitumor Agents

P. Yu, H. Lv, Jinhong Ren, 2012 .

Synthesis and Antimicrobial Evaluation of Aminoguanidine and 3-amino- 1,2,4-triazole Derivatives as Potential Antibacterial Agents

Changji Zheng, Liangpeng Sun, H. Piao, 2016 .

Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitors.

G. S. Walker, V. Shanmugasundaram, M. Hayward, 2014, Journal of medicinal chemistry.

Discovery of a potent, selective and orally active canine COX-2 inhibitor, 2-(3-difluoromethyl-5-phenyl-pyrazol-1-yl)-5-methanesulfonyl-pyridine.

M. P. Lynch, S. Sakya, Jin Li, 2004, Bioorganic & medicinal chemistry letters.

Design, synthesis and molecular modeling of aloe-emodin derivatives as potent xanthine oxidase inhibitors.

Yu-Wei Liu, Wei Huang, D. Shi, 2014, European journal of medicinal chemistry.