Eidarus Salah

12 Mansfield Road
Oxford, ENG OX13TA, United Kingdom

Last Updated: 09/26/2026

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Found 55 publications

Cephalosporins are potent SARS-CoV-2 main protease inhibitors.

Cephalosporins are potent SARS-CoV-2 main protease inhibitors.

Journal: European journal of medicinal chemistry

Published: March 30, 2026

Substrate-Selective Inhibition of the SARS-CoV-2 Papain-Like Protease: Inhibition of Hydrolysis of Human Over Viral Substrates.

Substrate-Selective Inhibition of the SARS-CoV-2 Papain-Like Protease: Inhibition of Hydrolysis of Human Over Viral Substrates.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: January 15, 2026

C6-Alkoxy substituted penicillins are potent non-covalently binding inhibitors of the SARS-CoV-2 main protease.

C6-Alkoxy substituted penicillins are potent non-covalently binding inhibitors of the SARS-CoV-2 main protease.

Journal: RSC medicinal chemistry

Published: September 07, 2025

Profiling Inhibitor Scaffolds for the Cancer Target Jumonji-C Domain-Containing Protein 6.

Profiling Inhibitor Scaffolds for the Cancer Target Jumonji-C Domain-Containing Protein 6.

Journal: ChemMedChem

Published: August 07, 2025

Derivatives of the Clinically Used HIF Prolyl Hydroxylase Inhibitor Desidustat Are Efficient Inhibitors of Human γ-Butyrobetaine Hydroxylase.

Derivatives of the Clinically Used HIF Prolyl Hydroxylase Inhibitor Desidustat Are Efficient Inhibitors of Human γ-Butyrobetaine Hydroxylase.

Journal: Journal of medicinal chemistry

Published: April 23, 2025

Investigating the N-terminal linker histone H1 subtypes as substrates for JmjC lysine demethylases.

Investigating the N-terminal linker histone H1 subtypes as substrates for JmjC lysine demethylases.

Journal: RSC chemical biology

Published: April 08, 2025

Evidence human FTO catalyses hydroxylation of N6-methyladenosine without direct formation of a demethylated product contrasting with ALKBH5/2/3 and bacterial AlkB.

Evidence human FTO catalyses hydroxylation of N6-methyladenosine without direct formation of a demethylated product contrasting with ALKBH5/2/3 and bacterial AlkB.

Journal: Nucleic acids research

Published: March 17, 2025

RaPID discovery of cell-permeable helical peptide inhibitors con-taining cyclic β-amino acids against SARS-CoV-2 main protease.

RaPID discovery of cell-permeable helical peptide inhibitors con-taining cyclic β-amino acids against SARS-CoV-2 main protease.

Journal: RSC chemical biology

Published: February 02, 2025

Biochemical investigations using mass spectrometry to monitor JMJD6-catalysed hydroxylation of multi-lysine containing bromodomain-derived substrates.

Biochemical investigations using mass spectrometry to monitor JMJD6-catalysed hydroxylation of multi-lysine containing bromodomain-derived substrates.

Journal: RSC chemical biology

Published: December 15, 2024

Silaproline-bearing nirmatrelvir derivatives are potent inhibitors of the SARS-CoV-2 main protease highlighting the value of silicon-derivatives in structure-activity-relationship studies.

Silaproline-bearing nirmatrelvir derivatives are potent inhibitors of the SARS-CoV-2 main protease highlighting the value of silicon-derivatives in structure-activity-relationship studies.

Journal: European journal of medicinal chemistry

Published: December 12, 2024

KDM3A catalyses the oxidation of acetyl-lysine to hydroxyacetyl-lysine on histone H3K9.

KDM3A catalyses the oxidation of acetyl-lysine to hydroxyacetyl-lysine on histone H3K9.

Journal: Nature chemistry

Published: December 02, 2024

Crystallographic and Selectivity Studies on the Approved HIF Prolyl Hydroxylase Inhibitors Desidustat and Enarodustat.

Crystallographic and Selectivity Studies on the Approved HIF Prolyl Hydroxylase Inhibitors Desidustat and Enarodustat.

Journal: ChemMedChem

Published: July 03, 2024

Showing 1-12 of 55

Last Updated: 09/26/2026