15-LOX

15-Lipoxygenase-1 (15-LOX-1, ALOX15) is a non-heme iron-containing dioxygenase that catalyzes the oxygenation of polyunsaturated fatty acids and contributes to the generation of bioactive lipid mediators involved in lipid metabolism, inflammation, and cellular homeostasis[1]. Mechanistically, 15-LOX-1 participates in the lipoxygenase pathway by converting arachidonic acid and other polyunsaturated fatty acids into oxygenated lipid products that regulate inflammatory signaling and membrane remodeling processes[1]. Through these activities, ALOX15 has been implicated in multiple physiological and pathological settings, and its functions have been investigated extensively in cellular systems and animal disease models associated with inflammatory, hyperproliferative, and neurodegenerative conditions[1]. Compared with the closely related isoform ALOX15B (15-LOX-2), which primarily catalyzes oxygenation at carbon 15 and has limited capacity to generate alternative products, 15-LOX-1 exhibits broader substrate utilization and distinct reaction specificity, highlighting important functional differences among lipoxygenase isoforms[2]. This distinction is particularly relevant when interpreting lipid mediator profiles and designing mechanistic studies targeting specific LOX pathways[2]. For experimental applications, selective pharmacological inhibition of 15-LOX-1 has emerged as a valuable strategy for dissecting enzyme-dependent signaling networks; a potent 15-LOX-1 inhibitor was reported to protect macrophages from regulated cell death, supporting the use of 15-LOX-1 inhibitors as research tools for investigating inflammatory mechanisms and lipid-peroxidation-driven cellular responses[3].