» Articles » PMID: 25262941

Design, Synthesis and Biological Activity of Flavonoid Derivatives As Selective Agonists for Neuromedin U 2 Receptor

Overview
Journal Bioorg Med Chem
Specialties Biochemistry
Chemistry
Date 2014 Sep 30
PMID 25262941
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Central neuromedin U 2 receptor (NMU2R) plays important roles in the regulation of food intake and body weight. Identification of NMU2R agonists may lead to the development of pharmaceutical agents to treat obesity. Based on the structure of rutin, a typical flavonoid and one of the NMU2R agonists we previously identified from an in-house made natural product library, 30 flavonoid derivatives have been synthesized and screened on a cell-based reporter gene assay. A number of compounds were found to be selective and highly potent to NMU2R. For example, the EC50 value of compound NRA 4 is very close to that of NMU, the endogenous peptide ligand of NMU2R. Structure-activity relationship analysis revealed that a 3-hydroxyl group in ring C and a 2'-fluoride group in ring B were essential for this class of compounds to be active against NMU2R.

Citing Articles

Iodine-PEG as a unique combination for the metal-free synthesis of flavonoids through iodonium-triiodide ion-pair complexation.

Kumar N, Sharma N, Kumar V, Kumar V, Jangid K, Devi B RSC Adv. 2024; 14(9):6225-6233.

PMID: 38375003 PMC: 10875328. DOI: 10.1039/d3ra08810c.


DNA methylation in blood is associated with metabolic and inflammatory indices: results from the Moli-sani study.

Marotta A, Noro F, Parisi R, Gialluisi A, Tirozzi A, De Curtis A Epigenetics. 2021; 16(12):1347-1360.

PMID: 33393847 PMC: 8813069. DOI: 10.1080/15592294.2020.1864167.