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Widely referenced in preclinical literature for its interaction with VEGF, FAK-paxillin, and nitric oxide pathways

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Notably, studies have systematically evaluated the compounds efficacy following oral, intraperitoneal, and intragastric administration, often within the same pathological model [3,4,5,6,7,8,9,10,11,12,13,14,16,17,18,19,20,21,22,23,24,27,28,29,30,31,32,34,37,39,40]

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Its exceptional biochemical stability makes it a foundational, indispensable compound for systemic recovery models in peptide-focused laboratory studies