Qingping Wang

发表

Development of a time-resolved fluorescent assay for measuring tyrosine-phosphorylated proteins in cells.

D. Waddleton, C. Ramachandran, Qingping Wang, 2002, Analytical biochemistry.

A β-tryptase inhibitor with a tropanylamide scaffold to improve in vitro stability and to lower hERG channel binding affinity.

Xin Chen, Qingping Wang, Jiesheng Kang, 2012, Bioorganic & medicinal chemistry letters.

Structure-based design, synthesis, and profiling of a β-tryptase inhibitor with a spiro-piperidineamide scaffold, benzylamine P1 group, and a substituted indole P4 group

Roy J. Vaz, Xin Chen, Qingping Wang, 2011 .

The identification of potent, selective, and bioavailable cathepsin S inhibitors.

M. Percival, W. Cromlish, J. Gauthier, 2007, Bioorganic & medicinal chemistry letters.

3,6-Fluorescein Diphosphate: A Sensitive Fluorogenic and Chromogenic Substrate for Protein Tyrosine Phosphatases

R. Zamboni, C. Ramachandran, Qingping Wang, 1999, Journal of biomolecular screening.

Glycosynthases: Mutant Glycosidases for Oligosaccharide Synthesis

S. Withers, Qingping Wang, L. Mackenzie, 1998 .

A spectroscopic study of the interaction of octacarboxylic metal phthalocyanine with bovine serum albumin

Qingping Wang, Baoquan Huang, Yi-ru Peng, 2008 .

The development of potent non-peptidic PTP-1B inhibitors.

E. Asante-Appiah, Y. Boie, B. Kennedy, 2004, Bioorganic & medicinal chemistry letters.

Changing Enzymic Reaction Mechanisms by Mutagenesis: Conversion of a Retaining Glucosidase to an Inverting Enzyme

S. Withers, Qingping Wang, R. Graham, 1994 .

A conformationally constrained inhibitor with an enhanced potency for β-tryptase and stability against semicarbazide-sensitive amine oxidase (SSAO).

Roy J. Vaz, Xin Chen, Qingping Wang, 2010, Bioorganic & medicinal chemistry letters.

Chemical bonds in precursors regulate g-C3N4 structure and its photocatalytic performance

Qingping Wang, Qingbo Yu, X. Ren, 2022, Journal of Alloys and Compounds.

Substrate-Assisted Catalysis in Glycosidases.

S. Withers, Qingping Wang, 1996 .

Structure based design of a series of potent and selective non peptidic PTP-1B inhibitors.

C. Bayly, E. Asante-Appiah, Y. Boie, 2004, Bioorganic & medicinal chemistry letters.

Naphthalenebis[α,α-difluoromethylenephosphonates] as potent inhibitors of protein tyrosine phosphatases

Scott D. Taylor, C. Ramachandran, Qingping Wang, 1998 .

A Stereoselective Process for the Manufacture of a 2′-Deoxy-β-d-Ribonucleoside Using the Vorbrüggen Glycosylation

Qingping Wang, Guo-Dong Zhu, Kun Hu, 2013 .

The structural basis for the selectivity of benzotriazole inhibitors of PTP1B.

C. Bayly, C. Desponts, E. Asante-Appiah, 2003, Biochemistry.

Investigation of ketone warheads as alternatives to the nitrile for preparation of potent and selective cathepsin K inhibitors.

R. Oballa, Qingping Wang, F. Massé, 2009, Bioorganic & medicinal chemistry letters.

Presystemic and First‐Pass Metabolism

Qingping Wang, Meng Li, 2016 .

Transcriptional repression of the dnaA gene of Escherichia coli by dnaA protein

Qingping Wang, J. Kaguni, 1987, Molecular and General Genetics MGG.

Identification of a nonbasic, nitrile-containing cathepsin K inhibitor (MK-1256) that is efficacious in a monkey model of osteoporosis.

C. Bayly, J. Falgueyret, M. Percival, 2008, Journal of Medicinal Chemistry.

Novel caged fluorescein diphosphates as photoactivatable substrates for protein tyrosine phosphatases.

M. Gresser, C. Ramachandran, Qingping Wang, 2002, Biochimica et biophysica acta.

Mechanism of Staggered Multiple Seedling Production from Amorphophallus bulbifer and Amorphophallus muelleri and its Application to Cultivation in Southeast Asia

Qingping Wang, Donghua Zhang, S. George, 2010 .

Distorted amides as models for activated peptide N-C=O units. 2. The synthesis, hydrolytic profile, and molecular structure of 3,4-dihydro-2-oxo-1,4-propanoquinoline

B. Santarsiero, Qingping Wang, A. J. Bennet, 1990 .

The structure of PTP-1B in complex with a peptide inhibitor reveals an alternative binding mode for bisphosphonates.

Claude Dufresne, Yves Leblanc, E. Asante-Appiah, 2002, Biochemistry.

How Does Alendronate Inhibit Protein-tyrosine Phosphatases?*

M. Gresser, C. Ramachandran, Qingping Wang, 1997, The Journal of Biological Chemistry.

Glu280 is the nucleophile in the active site of Clostridium thermocellum CelC, a family A endo-beta-1,4-glucanase.

S. Withers, R. Aebersold, N. Gilkes, 1993, The Journal of biological chemistry.

Liquid Chromatography‐Mass Spectrometry (LC‐MS) Quantification of Reactive Metabolites

Qingping Wang, Chuang Lu, 2021, Transporters and Drug‐Metabolizing Enzymes in Drug Toxicity.

Catalytic inactivation of protein tyrosine phosphatase CD45 and protein tyrosine phosphatase 1B by polyaromatic quinones.

M. Gresser, C. Ramachandran, Qingping Wang, 2004, Biochemistry.

Identification of the acid/base catalyst in Agrobacterium faecalis beta-glucosidase by kinetic analysis of mutants.

S. Withers, Qingping Wang, R. Graham, 1995, Biochemistry.

A high-throughput glutathione trapping assay with combined high sensitivity and specificity in high-resolution mass spectrometry by applying product ion extraction and data-dependent neutral loss.

Qingping Wang, Chuang Lu, M. Fitzgerald, 2019, Journal of mass spectrometry : JMS.