Qingqing Huang

Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives.

F. Nan, Q. Ye, Jia Li, 2005, Bioorganic & medicinal chemistry letters.

Facilely tuning the intrinsic catalytic sites of the spinel oxide for peroxymonosulfate activation: From fundamental investigation to pilot-scale demonstration

Mingjie Huang, Z. Qiang, Xiaohui Wu, 2022, Proceedings of the National Academy of Sciences of the United States of America.

RCM-mediated stereoselective synthesis of three novel tetrahydroisoquinoline tetracyclic core frameworks

F. Nan, Qingqing Huang, Chen Lin-hai, 2008 .

Metalloform-selective inhibition: synthesis and structure-activity analysis of Mn(II)-form-selective inhibitors of Escherichia coli methionine aminopeptidase.

F. Nan, Q. Ye, Min Huang, 2005, Bioorganic & medicinal chemistry letters.

Metalloform-Selective Inhibition: Synthesis and Structure—Activity Analysis of Mn(II)-Form-Selective Inhibitors of Escherichia coli Methionine Aminopeptidase.

F. Nan, Q. Ye, Min Huang, 2006 .

Inhibition of monometalated methionine aminopeptidase: inhibitor discovery and crystallographic analysis.

F. Nan, S. Xie, Q. Ye, 2007, Journal of medicinal chemistry.

Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives.

F. Nan, Q. Ye, L. Chen, 2005, Bioorganic & medicinal chemistry letters.

Structural analysis of inhibition of E. coli methionine aminopeptidase: implication of loop adaptability in selective inhibition of bacterial enzymes

F. Nan, S. Xie, Q. Ye, 2007 .