TY - JOUR
T1 - De-Novo Design of pre-miR-21 Maturation Inhibitors
T2 - Synthesis and Activity Assessment
AU - Shcheholeva, Iryna
AU - Fernández-Remacha, Daniel
AU - Estrada-Tejedor, Roger
AU - Duca, Maria
AU - Michelet, Véronique
N1 - This research received funding from the French government through the UCAJEDI Investments in the Future project with the reference number ANR-15-IDEX-01, Region PACA and BoostUrCareer project European Union's Horizon 2020 research and innovation program under grant agreement no. 847581. M.A. and V.M. also acknowledge Université Côte d'Azur and Centre National de la Recherche Scientifique (CNRS). This study was partly supported by research funding from the Canceropôle PACA, Institut National du Cancer and Région Sud. We are grateful to Dr Marc Gaysinski (Université Côte d'Azur) for help with the STD NMR.
Publisher Copyright:
© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.
PY - 2023/7/14
Y1 - 2023/7/14
N2 - Targeting RNA with small molecules is a major challenge of current medicinal chemistry, and the identification and design of original scaffolds able to selectively interact with an RNA target remains difficult. Various approaches have been developed based on classical medicinal chemistry strategies (fragment-based drug design, dynamic combinatorial chemistry, HTS or DNA-encoded libraries) as well as on advanced structural biology and biochemistry methodologies (such as X-ray, cryo-EM, NMR, or SHAPE). Here, we report the de novo design, synthesis, and biological evaluation of RNA ligands by using a straightforward and sustainable chemistry combined with molecular docking and biochemical and biophysical studies that allowed us to identify a novel pharmacophore for RNA binding. Specifically, we focused on targeting the biogenesis of microRNA-21, the well-known oncogene. This led us not only to promising inhibitors but also to a better understanding of the interactions between the small-molecule compounds and the RNA target paving the way for the rational design of efficient inhibitors with potential anticancer activity.
AB - Targeting RNA with small molecules is a major challenge of current medicinal chemistry, and the identification and design of original scaffolds able to selectively interact with an RNA target remains difficult. Various approaches have been developed based on classical medicinal chemistry strategies (fragment-based drug design, dynamic combinatorial chemistry, HTS or DNA-encoded libraries) as well as on advanced structural biology and biochemistry methodologies (such as X-ray, cryo-EM, NMR, or SHAPE). Here, we report the de novo design, synthesis, and biological evaluation of RNA ligands by using a straightforward and sustainable chemistry combined with molecular docking and biochemical and biophysical studies that allowed us to identify a novel pharmacophore for RNA binding. Specifically, we focused on targeting the biogenesis of microRNA-21, the well-known oncogene. This led us not only to promising inhibitors but also to a better understanding of the interactions between the small-molecule compounds and the RNA target paving the way for the rational design of efficient inhibitors with potential anticancer activity.
KW - binding mechanisms
KW - drug discovery
KW - inhibitors
KW - oncogenes
KW - RNA
UR - http://www.scopus.com/inward/record.url?scp=85160780922&partnerID=8YFLogxK
UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Alerting&SrcApp=Alerting&DestApp=WOS&DestLinkType=FullRecord;KeyUT=000998779100001
U2 - 10.1002/chem.202300825
DO - 10.1002/chem.202300825
M3 - Article
AN - SCOPUS:85160780922
SN - 0947-6539
VL - 29
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 40
M1 - e202300825
ER -