Chemical Structure : AA520
Catalog No.: PC-23590Not For Human Use, Lab Use Only.
AA520 is a potent, dual inhibitor of cyclooxygenase-2 (COX-2) and PPARα with IC50 of 0.1 uM (inhibition of LPS-induced PGE2).
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AA520 is a potent, dual inhibitor of cyclooxygenase-2 (COX-2) and PPARα with IC50 of 0.1 uM (inhibition of LPS-induced PGE2).
AA520 dispays exquisite selectivity on PPARα concerning PPARγ, and 697-fold selective over COX-1.
AA520 does not affect LPS-induced monocyte COX-2 expression, and other eicosanoids generated by enzymatic and nonenzymatic pathways.
AA520 inhibited COX-2-dependent PGE2 generation in the colon cancer cell line HCA7. AA520 (1 μM) significantly reduced MTT in HCA7 cells.
M.Wt | 500.99 | |
Formula | C25H25ClN2O5S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Ammazzalorso A, et al. Front Pharmacol. 2024 Nov 26;15:1488722.
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