Year: 2025
Type: article
Abstract: -rich five-membered ring scaffolds. Through systematic SAR analysis, we found that γ-lactam derivatives act as inhibitors, while butenolide and cyclopentanone derivatives serve as enzyme activators. Structure-activity relationship analysis revealed that the identity of the atom at the β-position and the nature of the substituents at the γ-position, both relative to the ring carbonyl, play a critical role in modulating 15-LOX-1 activity. Selectivity studies demonstrated that the compounds display species- and substrate-specific modulation of lipoxygenase activity. Enzyme kinetic analysis confirmed a competitive mechanism for both inhibition and activation. Molecular modeling provided structural insights, highlighting key interactions with the active site iron and surrounding residues. Overall, our findings expand the chemical space for 15-LOX-1 modulation and offer promising leads for the development of selective enzyme regulators.
Source: Organic & Biomolecular Chemistry
DOI: 10.1039/d5ob00820d
Institution: University of Crete
Language: English
Topic: Bioactive natural compounds
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W4411661073
