mindong@tju.edu.cn
天津市青年****
长聘教授

Organometallic and radical intermediates reveal mechanism of diphthamide biosynthesis

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Substrate-Dependent Cleavage Site Selection by Unconventional Radical S-Adenosylmethionine Enzymes in Diphthamide Biosynthesi

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An organometallic complex formed by an unconventional radical SAM enzyme.

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Dph3 is an electron donor for Dph1-Dph2 in the first step of eukaryotic diphthamide biosynthesis

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Noncanonical Radical SAM Enzyme Chemistry Learned from Diphthamide Biosynthesis

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Methods for Studying the Radical SAM Enzymes in Diphthamide Biosynthesis

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Cytochrome B5 reductase is a Dph3 reductase required for the tRNA wobble uridine modification.

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Revealing CD38 cellular localization using a cell permeable, mechanism-based fluorescent small molecule probe.

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Direct Access to Tetrahydro[1,2]diazepinones from α,β-Epoxy-N- aziridinylimines via Anionic Rearrangement

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Design, synthesis and biological characterization of novel inhibitors of CD38

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Trifluoromethylated Cyclic-ADP- Ribose Mimic: Synthesis of 8-trifluoromethyl-N1-[(5′′-O-Phosphorylethoxy)methyl]-5′-O-phospho

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Catalyzation of 1,4-additions of arylboronic acids to a,b-unsaturated substrates using nickel(I) complexes

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Concise syntheses of trifluoromethylated cyclic and acyclic analogues of cADPR