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Analogues 1 and 2 exhibited superior potency (IC 50 = 0.30 and 0.94 M, respectively), up to 90 times more selective for AKR1C3 over AKR1C2, and demonstrated higher efficacy than indomethacin without off-target effects on AKR1C2 and COX1/2 ( 6.1.3 N-phenylanthranilic acids Among the compounds explored as AKR1C3 inhibitors, Flufenamic acid (FLU), a sort of NSAIDs, has demonstrated potent inhibition of AKR1C3 activity (IC 50 = 8.63 M)

The p38 MAPK pathway allows response to external stimuli and can affect levels of apoptosis as well as gene expression and skin differentiation, while the activation of NFB p65 has shown a correlation to the development of various types of cancer as well as diseases related to aging such as cardiovascular disease, osteoporosis, and Alzheimers ( In order to reduce peptide breakdown, keep peptides refrigerated at all times but DO NOT FREEZE