Recent advances in methylation: a guide for selecting methylation reagents

Y Chen - Chemistry–A European Journal, 2019 - Wiley Online Library
Methylation is a well‐known structural modification in organic and medicinal chemistry. This
review summarizes recent advances in methylation by categorizing specific methylation …

Recent advances in indazole-containing derivatives: synthesis and biological perspectives

SG Zhang, CG Liang, WH Zhang - Molecules, 2018 - mdpi.com
Indazole-containing derivatives represent one of the most important heterocycles in drug
molecules. Diversely substituted indazole derivatives bear a variety of functional groups and …

GPR120/FFAR4 pharmacology: focus on agonists in type 2 diabetes mellitus drug discovery

G Carullo, S Mazzotta, M Vega-Holm… - Journal of Medicinal …, 2021 - ACS Publications
The G-protein coupled receptors (GPCRs) activated by free fatty acids (FFAs) have emerged
as new and exciting drug targets, due to their plausible translation from pharmacology to …

Free fatty acid receptors (FFARs): emerging therapeutic targets for the management of diabetes Mellitus

DPS Loona, B Das, R Kaur, R Kumar… - Current Medicinal …, 2023 - ingentaconnect.com
Free fatty acids (FFAs) present in our dietary fats not only act as vital nutrients but also
function as signalling molecules and modulate key biological functions through their active …

FFA4 (GPR120) as a fatty acid sensor involved in appetite control, insulin sensitivity and inflammation regulation

DS Im - Molecular aspects of medicine, 2018 - Elsevier
Unsaturated long-chain fatty acids have been suggested to be beneficial in the context of
cardiovascular disorders based in epidemiologic studies conducted in Greenland and …

The discovery of water-soluble indazole derivatives as potent microtubule polymerization inhibitors

YJ Cui, Y Zhou, X Zhang, B Dou, CC Ma… - European Journal of …, 2023 - Elsevier
Taking a previously discovered indazole derivative 1 as a lead, systematic structural
modifications were performed with an indazole core at the 1-and 6-positions to improve its …

Design, synthesis, and bioevaluation of 1h-pyrrolo[3,2-c]pyridine derivatives as colchicine-binding site inhibitors with potent anticancer activities

C Wang, Y Zhang, S Yang, L Shi, R Rong… - Journal of Enzyme …, 2024 - Taylor & Francis
A new series of 1 H-pyrrolo [3, 2-c] pyridine derivatives were designed and synthesised as
colchicine-binding site inhibitors. Preliminary biological evaluations showed that most of the …

Identification and target-pathway deconvolution of FFA4 agonists with anti-diabetic activity from Arnebia euchroma (Royle) Johnst

F Xu, P Wang, X Zhang, T Hou, L Qu, C Wang… - Pharmacological …, 2021 - Elsevier
FFA4 is a novel therapeutic target for the treatment of metabolic diseases, such as type II
diabetes. However, there are still few ligands with structural diversity, selectivity and high …

Novel GPR120 agonists with improved pharmacokinetic profiles for the treatment of type 2 diabetes

G Ji, Q Guo, Q Xue, R Kong, S Wang, K Lei, R Liu… - Molecules, 2021 - mdpi.com
GPR120 is a promising target for the treatment of type 2 diabetes (T2DM), which is activated
by free fatty acids (FFAs) and stimulates the release of glucagon-like peptide-1 (GLP-1). GLP …

Surprising reactivity in NiXantphos/palladium-catalyzed α-arylation of substituted cyclopropyl nitriles

BA Wright, MJ Ardolino - The Journal of Organic Chemistry, 2018 - ACS Publications
α-Arylations of cyclopropyl and related nitriles provide access to important synthetic
intermediates and pharmacophores for biologically active molecules. However, robust …