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Weidong Ding

Observed names: W.‐D. DING, WEI-DONG DING, WEIDONG DING, Wei-Dong Ding, Wei-dong Ding, WeiDong Ding, Wei‐Dong Ding
OpenAlex ID: A5113872243
Delineating the role of cooperativity in the design of potent PROTACs for BTK
2018 · Adelajda Zorba, Chuong Nguyen, et al. · Proceedings of the National Academy of Sciences · 419
Lomaiviticins A and B, Potent Antitumor Antibiotics from Micromonospora lomaivitiensis
2001 · Haiyin He, Wei-Dong Ding, et al. · Journal of the American Chemical Society · 247
Kinetic Mechanism of Staphylococcus aureus Sortase SrtA
2003 · Xinyi Huang, Ann Aulabaugh, et al. · Biochemistry · 165
Discovery of novel inhibitors of the ZipA/FtsZ complex by NMR fragment screening coupled with structure-based design
2006 · Désirée H.H. Tsao, Alan G. Sutherland, et al. · Bioorganic & Medicinal Chemistry · 93
Namenamicin, a New Enediyne Antitumor Antibiotic from the Marine Ascidian Polysyncraton lithostrotum
1996 · Leonard A. McDonald, Todd L. Capson, et al. · Journal of the American Chemical Society · 78
Pyranonaphthoquinone Lactones: A New Class of AKT Selective Kinase Inhibitors Alkylate a Regulatory Loop Cysteine
2009 · Edward J. Salaski, Girija Krishnamurthy, et al. · Journal of Medicinal Chemistry · 76
Development of a fluorescence polarization assay to screen for inhibitors of the FtsZ/ZipA interaction
2003 · Cynthia Hess Kenny, Weidong Ding, et al. · Analytical Biochemistry · 76
Discovery of lactoquinomycin and related pyranonaphthoquinones as potent and allosteric inhibitors of AKT/PKB: mechanistic involvement of AKT catalytic activation loop cysteines
2007 · Lourdes Toral-Barza, Wei-Guo Zhang, et al. · Molecular Cancer Therapeutics · 61
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Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus sp. LL-42D005. I. Isolation and structure determination.
1994 · WEIDONG DING, DAVID R. WILLIAMS, et al. · The Journal of Antibiotics · 61
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Design and synthesis of indolo[2,3-a]quinolizin-7-one inhibitors of the ZipA–FtsZ interaction
2004 · Lee D. Jennings, Ken W. Foreman, et al. · Bioorganic & Medicinal Chemistry Letters · 60
Combinatorial synthesis of substituted 3-(2-indolyl)piperidines and 2-phenyl indoles as inhibitors of ZipA–FtsZ interaction
2004 · Lee D. Jennings, Kenneth W. Foreman, et al. · Bioorganic & Medicinal Chemistry · 56
Structure-based design of carboxybiphenylindole inhibitors of the ZipA–FtsZ interaction
2003 · Alan G. Sutherland, Juan Alvarez, et al. · Organic & Biomolecular Chemistry · 54
Novel and Specific Respiratory Syncytial Virus Inhibitors That Target Virus Fusion
1998 · Wei-dong Ding, Boris Mitsner, et al. · Journal of Medicinal Chemistry · 42
Theoretical simulation of the electronic circular dichroism spectrum of calicheamicin
2005 · Egidio Giorgio, Katsunori Tanaka, et al. · Bioorganic & Medicinal Chemistry · 40
CL387626 exhibits marked and unusual antiviral activity against respiratory syncytial virus in tissue culture and in cotton rats
1998 · Philip R Wyde, Donna K Moore-Poveda, et al. · Antiviral Research · 38
Flavins Inhibit Human Cytomegalovirus UL80 Protease via Disulfide Bond Formation
1996 · Ellen Z. Baum, Wei-Dong Ding, et al. · Biochemistry · 33
Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitors
2017 · Frank Lovering, Paul Morgan, et al. · European Journal of Medicinal Chemistry · 26
Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors
2014 · Seungil Han, Robert M. Czerwinski, et al. · Biochemical Journal · 26
Biophysical Characterization of the Interactions of HTI-286 with Tubulin Heterodimer and Microtubules
2003 · Girija Krishnamurthy, Wendy Cheng, et al. · Biochemistry · 26
Circular dichroism studies of calicheamicin-DNA interaction: Evidence for calicheamicin-induced DNA conformational change
1994 · Girija Krishnamurthy, Wei-dong Ding, et al. · Tetrahedron · 26
Inhibiting peptidylarginine deiminases (PAD1-4) by targeting a Ca2+ dependent allosteric binding site
2025 · Leslie A. Dakin, Li Xing, et al. · Nature Communications · 22
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Natural Product Bis-Intercalator Depsipeptides as a New Class of Payloads for Antibody–Drug Conjugates
2018 · Anokha S. Ratnayake, Li-ping Chang, et al. · Bioconjugate Chemistry · 21
Development of an HPLC assay for Staphylococcus aureus sortase: Evidence for the formation of the kinetically competent acyl enzyme intermediate
2006 · Ann Aulabaugh, Weidong Ding, et al. · Analytical Biochemistry · 21
Pyrimido[1,2-b]-1,2,4,5-tetrazin-6-ones as HCMV protease inhibitors: a new class of heterocycles with flavin-like redox properties
2003 · Martin J. Di Grandi, Kevin J. Curran, et al. · Bioorganic & Medicinal Chemistry Letters · 21
Biological and Mechanistic Activities of Phenazine Antibiotics Produced by Culture LL-14I352.
1997 · MAYA P. SINGH, ANA T. MENENDEZ, et al. · The Journal of Antibiotics · 19
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Works count: 36
Citation count: 1,838
H-index: 21
I10-index: 26
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