Dong H. Shin

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 32 publications

A study of flavonoid inhibitors against Monkeypox H1 phosphatase.

A study of flavonoid inhibitors against Monkeypox H1 phosphatase.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: August 12, 2025

Targeting the Cell Wall Salvage Pathway: Dual-Enzyme Inhibition of AmgK and MurU as a Strategy Against Antibiotic Resistance.

Targeting the Cell Wall Salvage Pathway: Dual-Enzyme Inhibition of AmgK and MurU as a Strategy Against Antibiotic Resistance.

Journal: International journal of molecular sciences

Published: May 12, 2025

Everolimus exerts anticancer effects through inhibiting the interaction of matrix metalloproteinase-7 with syndecan-2 in colon cancer cells.

Everolimus exerts anticancer effects through inhibiting the interaction of matrix metalloproteinase-7 with syndecan-2 in colon cancer cells.

Journal: American journal of physiology. Cell physiology

Published: February 05, 2024

Amentoflavone, a potent natural matrix metalloproteinase 2 inhibitor.

Amentoflavone, a potent natural matrix metalloproteinase 2 inhibitor.

Journal: Natural product research

Published: December 19, 2023

5-aminosalicylic acid suppresses osteoarthritis through the OSCAR-PPARγ axis.

5-aminosalicylic acid suppresses osteoarthritis through the OSCAR-PPARγ axis.

Journal: Nature communications

Published: April 20, 2023

Meclizine, a piperazine-derivative antihistamine, binds to dimerized translationally controlled tumor protein and attenuates allergic reactions in a mouse model.

Meclizine, a piperazine-derivative antihistamine, binds to dimerized translationally controlled tumor protein and attenuates allergic reactions in a mouse model.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: October 30, 2022

A Study of Drug Repurposing to Identify SARS-CoV-2 Main Protease (3CLpro) Inhibitors.

A Study of Drug Repurposing to Identify SARS-CoV-2 Main Protease (3CLpro) Inhibitors.

Journal: International journal of molecular sciences

Published: April 21, 2022

Dimerization Tendency of 3CLpros of Human Coronaviruses Based on the X-ray Crystal Structure of the Catalytic Domain of SARS-CoV-2 3CLpro.

Dimerization Tendency of 3CLpros of Human Coronaviruses Based on the X-ray Crystal Structure of the Catalytic Domain of SARS-CoV-2 3CLpro.

Journal: International journal of molecular sciences

Published: April 05, 2022

A study of inhibitors of d-glycero-β-d-manno-heptose-1-phosphate adenylyltransferase from Burkholderia pseudomallei as a potential antibiotic target.

A study of inhibitors of d-glycero-β-d-manno-heptose-1-phosphate adenylyltransferase from Burkholderia pseudomallei as a potential antibiotic target.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: March 18, 2021

A Study of 3CLpros as Promising Targets against SARS-CoV and SARS-CoV-2.

A Study of 3CLpros as Promising Targets against SARS-CoV and SARS-CoV-2.

Journal: Microorganisms

Published: March 04, 2021

A triple-targeting inhibitory activity of Rose Bengal on polysaccharide biosynthesis of Burkholderia pseudomallei.

A triple-targeting inhibitory activity of Rose Bengal on polysaccharide biosynthesis of Burkholderia pseudomallei.

Journal: Archiv der Pharmazie

Published: September 22, 2020

Inhibition of d-glycero-β-d-manno-heptose 1-phosphate adenylyltransferase from Burkholderia pseudomallei by epigallocatechin gallate and myricetin.

Inhibition of d-glycero-β-d-manno-heptose 1-phosphate adenylyltransferase from Burkholderia pseudomallei by epigallocatechin gallate and myricetin.

Journal: The Biochemical journal

Published: September 03, 2020

Showing 1-12 of 32

Last Updated: 09/26/2026