Bisubstrate Strategies to Target Methyltransferases - Archive ouverte HAL Access content directly
Journal Articles European Journal of Organic Chemistry Year : 2022

Bisubstrate Strategies to Target Methyltransferases

(1) , (1) , (1)
1

Abstract

Bisubstrate strategies address the lack of specificity encountered with S-adenosyl-L-methionine (SAM) analogues targeting methyltransferases (MTases). Specifically, a bisubstrate inhibitor mimics the transition state complex associating a substrate and the SAM methyl group donor to a particular methyltransferase. These potential inhibitors contain both parts of the substrate and the methyl group donor. In this review, bisubstrate inhibitors of several MTases including DNA, RNA, protein, catechol or nicotinamide MTases are discussed in order to evaluate the interest of these promising molecules for the development of selective therapeutics against cancers, neuropsychiatric disorders and viral infections.
Fichier principal
Vignette du fichier
European J Organic Chem - 2022 - Bisubstrate Strategies to Target Methyltransferases.pdf (1.6 Mo) Télécharger le fichier
Origin : Publication funded by an institution

Dates and versions

hal-03727961 , version 1 (19-07-2022)

Identifiers

Cite

Rostom Ahmed‐belkacem, Françoise Debart, Jean‐jacques Vasseur. Bisubstrate Strategies to Target Methyltransferases. European Journal of Organic Chemistry, 2022, 2022 (21), pp.e202101481. ⟨10.1002/ejoc.202101481⟩. ⟨hal-03727961⟩
68 View
13 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More