Size: | Price | Quantity | |
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$50.00 | |||
$195.00 |
SC-560 (188817-13-2) is a highly selective (700-fold selective over COX-2) and potent (IC50 = 9 nM) inhibitor of cyclooxygenase-1(COX-1).1 SC-560 inhibited TNF α-induced PGE2 synthesis in neurons and, PGE2 and thromboxane A2 synthesis in human monocytes and platelets (IC50’s = 1.8 nM and 2.5 nM respectively) indicating non-selective COX inhibition. SC-560 was able to inhibit PGE2 synthesis in COX-1-deficient neurons indicating a COX-1 independent mechanism. This unselective COX inhibition was only observed in whole cells – it remained COX-1 specific in cell lysates.2
References/Citations:
1) Smith et al. (1998), Pharmacological analysis of cyclooxygenase-1 in inflammation; Proc. Natl. Acad. Sci. USA 95 13313
2) Brenneis et al. (2006), Inhibition of prostaglandin E2 synthesis by SC-560 is independent of cyclooxygenase 1 inhibition; FASEB J. 20 1352
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SC-560 (188817-13-2) is a highly selective (700-fold selective over COX-2) and potent (IC50 = 9 nM) inhibitor of cyclooxygenase-1(COX-1).1 SC-560 inhibited TNF α-induced PGE2 synthesis in neurons and, PGE2 and thromboxane A2 synthesis in human monocytes and platelets (IC50’s = 1.8 nM and 2.5 nM respectively) indicating non-selective COX inhibition. SC-560 was able to inhibit PGE2 synthesis in COX-1-deficient neurons indicating a COX-1 independent mechanism. This unselective COX inhibition was only observed in whole cells – it remained COX-1 specific in cell lysates.2
References/Citations:
1) Smith et al. (1998), Pharmacological analysis of cyclooxygenase-1 in inflammation; Proc. Natl. Acad. Sci. USA 95 13313
2) Brenneis et al. (2006), Inhibition of prostaglandin E2 synthesis by SC-560 is independent of cyclooxygenase 1 inhibition; FASEB J. 20 1352
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