Hening Lin to Molecular Structure
This is a "connection" page, showing publications Hening Lin has written about Molecular Structure.
Connection Strength
0.935
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A Glycoconjugated SIRT2 Inhibitor with Aqueous Solubility Allows Structure-Based Design of SIRT2 Inhibitors. ACS Chem Biol. 2019 08 16; 14(8):1802-1810.
Score: 0.142
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Direct Comparison of SIRT2 Inhibitors: Potency, Specificity, Activity-Dependent Inhibition, and On-Target Anticancer Activities. ChemMedChem. 2018 09 19; 13(18):1890-1894.
Score: 0.133
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Substrate-Dependent Cleavage Site Selection by Unconventional Radical S-Adenosylmethionine Enzymes in Diphthamide Biosynthesis. J Am Chem Soc. 2017 04 26; 139(16):5680-5683.
Score: 0.121
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An improved fluorogenic assay for SIRT1, SIRT2, and SIRT3. Org Biomol Chem. 2016 Feb 21; 14(7):2186-90.
Score: 0.111
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Chemogenomic approach identified yeast YLR143W as diphthamide synthetase. Proc Natl Acad Sci U S A. 2012 Dec 04; 109(49):19983-7.
Score: 0.089
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Thiosuccinyl peptides as Sirt5-specific inhibitors. J Am Chem Soc. 2012 Feb 01; 134(4):1922-5.
Score: 0.084
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Mechanistic understanding of Pyrococcus horikoshii Dph2, a [4Fe-4S] enzyme required for diphthamide biosynthesis. Mol Biosyst. 2011 Jan; 7(1):74-81.
Score: 0.077
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Indirubin Derivatives as Dual Inhibitors Targeting Cyclin-Dependent Kinase and Histone Deacetylase for Treating Cancer. J Med Chem. 2021 10 28; 64(20):15280-15296.
Score: 0.041
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High-Throughput Screening Identifies Ascorbyl Palmitate as a SIRT2 Deacetylase and Defatty-Acylase Inhibitor. ChemMedChem. 2021 11 19; 16(22):3484-3494.
Score: 0.041
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Cysteine derivatives as acetyl lysine mimics to inhibit zinc-dependent histone deacetylases for treating cancer. Eur J Med Chem. 2021 Dec 05; 225:113799.
Score: 0.041
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Structural Basis of the Substrate Selectivity of Viperin. Biochemistry. 2020 02 11; 59(5):652-662.
Score: 0.037
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Covalent and noncovalent intermediates of an NAD utilizing enzyme, human CD38. Chem Biol. 2008 Oct 20; 15(10):1068-78.
Score: 0.017