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Depression is a complex mental disorder, and consequently, the successful treatment of the depressive disorder remains challenging. The available medications often show limitations in terms of both safety and efficacy. In this case, the presence of the prenyl motif in pharmaceutical compounds has resulted in a broad spectrum of biological activities. Various studies have highlighted that the potent antidepressant activity of many natural compounds is associated with the presence of the prenyl motif. Thus, some studies have attempted to prepare prenyl fragment derivatives with the aim of enhancing their hydrophobicity and developing promising antidepressant compounds. Prenyl motif-containing compounds exhibit antidepressant action multiple mechanisms, including selective serotonin/norepinephrine reuptake inhibition, blocking of NMDA receptors, 5-HT antagonism, TREK-1 inhibition, MAO-A inhibition, and anti-inflammatory and antioxidant properties. This review presents synthetic derivatives of xanthones, flavonoids, and chalcones bearing prenyl groups. It also covers polyprenylated benzoyl phloroglucinols/acylphloroglucinols, naphthoquinones, volatile oils, tricyclic products, and steroidal saponins containing prenyl motifs. This study aims to further guide and support medicinal chemists in directing the synthesis of more potent compounds possessing prenyl fragments as antidepressants, thus advancing treatment options for depression.
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http://dx.doi.org/10.1039/d5md00473j | DOI Listing |
Nat Prod Res
September 2025
Key Laboratory of Plant Resources and Chemistry in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, P. R. China.
Chemical investigations of the -butanol extract of the roots of were carried out using column chromatography, flash, semi-preparative HPLC, and chiral HPLC. Five unidentified compounds, including two prenylated coumarin glucosides, two prenylated furanocoumarin glucosides, and a benzofuran glucoside, together with twelve known compounds, were isolated from the -butanol fraction of extract. The structures of these compounds were identified by HRMS, NMR, UV, ECD in combination with quantum chemical calculations, and comparison with the literature.
View Article and Find Full Text PDFEur J Pharmacol
September 2025
Department of Cardiology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China. Electronic address:
Protein prenylation is an evolutionarily conserved post-translational modification encompassing farnesylation and geranylgeranylation. This modification is fundamental to the precise regulation of protein localization, activity, and stability, thereby underpinning critical cellular functions. Aberrant prenylation is closely associated with cardiovascular diseases and influences a spectrum of pathological mechanisms in a complex manner.
View Article and Find Full Text PDFJ Nat Prod
September 2025
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, People's Republic of China.
Moralbaflavone D () is a newly identified natural diprenylated flavonoid demonstrating cytotoxic activity. Herein, we report its first total synthesis, accomplished in only six steps with an overall yield of 5.1%.
View Article and Find Full Text PDFPharmacol Res
August 2025
Dr. Neher's Biophysics Laboratory for Innovative Drug Discovery, State Key Laboratory of Quality Research in Chinese Medicine, Faculty of Chinese Medicine, Macau University of Science and Technology, Macau, China; Macau University of Science and Technology Zhuhai MUST Science and Technology Research
Kawasaki disease (KD) is an acute systemic vasculitis affecting children and leads to severe coronary artery complications, such as aneurysms. The cause of KD remains elusive, with infections suspected as potential triggers. Diagnosis is largely dependent on clinical symptoms due to the lack of specific laboratory molecular markers.
View Article and Find Full Text PDFAnalyst
August 2025
Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Padualaan 8, Utrecht 3584 CH, The Netherlands.
Long-chain -acylation is the addition of long-chain fatty acids to cysteine residues on proteins. This lipid modification is essential for protein membrane association and signalling but presents analytical challenges due to both its hydrophobicity and the labile nature of thioester bonds. We developed and optimised a bottom-up mass spectrometry workflow tailored for the detection of long-chain -acylated peptides.
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