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COX Cyclooxygenase

Cat.No.  Name Information
M3264 Pravadoline Pravadoline (WIN 48098) is a cyclooxygesase inhibitor and inhibits prostaglandin synthesis with IC50 of 4.9 μM, also a cannabinoid agonist.
M2495 Carprofen Carprofen inhibits canine COX2 with IC50 of 0.03 mM.
M3359 Ibuprofen Ibuprofen (Dolgesic) is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50 of 13 μM and 370 μM, respectively.
M3936 Saikosaponin D Saikosaponin D is a COX-2 and iNOS inhibitor,a Saikosaponin A epimer, which Inhibits NF-κB, TNF-α, IL-1β and IL-6 and Inhibits apoptosis.
M1965 Celecoxib Celecoxib is a selective cyclooxygenase-2 (COX-2) inhibitor (IC50 values are 15 and 0.04 μM for COX-1 and COX-2 respectively).
M3471 Ketorolac Ketorolac (Ketorolac tromethamine) is a non-selective COX inhibitor of COX-1 and COX-2 with IC50 of 1.23 μM and 3.50 μM, respectively.
M20423 Etoricoxib Etoricoxib is a new COX-2 selective inhibitor with anti-inflammatory, antipyretic, analgesic, and potential antineoplastic properties.
M2824 Lumiracoxib Lumiracoxib is a novel, selective COX-2 inhibitor with IC50 and Ki of 0.14 μM and 0.06 μM, exhibits 515-fold selectivity over COX-1.
M4547 Roburic-acid Roburic acid is a tetracyclic triterpenoid in Gentiana macrophylla. As an inhibitor of COX, the IC50 values of COX-1 and COX-2 are 5 and 9 μM, respectively.
M4445 Prim-o-glucosylcimifugin Prim-o-glucosylcimifugin has a potent anti-inflammatory effect. INOS and COX-2 expression could be inhibited by regulating JAK2/STAT3 signal transduction.
M4437 Rutaecarpine Rutaecarpine is a delayed rectifier K+ channel blocker, inhibits platelet aggregation.
M4284 Harpagoside Harpagoside was separated from Harpagophytum procumbens (Hp). Harpagoside inhibited COX-1 and COX-2 activity and NO production.
M4212 CG (-) -catechin gallate is a microcomponent of green tea Catechin. (-) -catechin gallate inhibited COX-1 and COX-2 activities.
M4209 ECG ECG
M4207 (-)Epicatechin Epicatechin inhibited coX-1 with IC50 of 3.2 μM. (-)Epicatechin inhibits il-1 β -induced iNOS expression by blocking nuclear localization of NF-κB p65 subunit.
M4125 8-Shogaol [8]-Shogaol, an irritant phenolic compound from ginger, has antiplatelet activity (IC50=5 μM) and inhibition of COX-2 (IC50=17.5 μM). [8]-Shogaol induces apoptosis of human leukemia cells.
M4088 Ginsenoside Compound-K Ginsenoside Compound-K is a bacterial metabolite of G-Rb1, exhibits anti-inflammatory effects by reducing iNOS and COX-2.
M3994 Hederagenin Hederagenin is a derivative of oleanolic acid isolated from the leaves of ivy (Hedera helix L.) that has been shown to have potential anti-tumor activity. Hederagenin can inhibit LPS-stimulated expression of iNOS, COX-2, and NF-κB.
M3809 Isofraxidin Isofraxidin is an anti-bacterial, anti-oxidant, and anti-inflammatory agent, it acts by reducing the levels of tumor necrosis factor-a (TNF-a), interleukin-6 (IL-6), and prostaglandin E2 (PGE2), inhibiting cyclooxygenase-2 (COX-2) protein expression.
M3614 FK-3311 Fk3311 is a selective inhibitor of COX-2. Anti-inflammatory compounds.
M3608 Naproxen sodium Naproxen is a COX inhibitor for COX-1 and COX-2 with IC50 of 8.7 μM and 5.2 μM, respectively.
M3554 Fenoprofen Calcium Fenoprofen Calcium is a nonsteroidal, anti-inflammatory antiarthritic agent.
M3439 Licofelone Licofelone is a dual COX/LOX inhibitor being considered as a treatment for osteoarthritis.
M3430 Phenylbutazone Phenylbutazone is used as a non-steroidal anti-inflammatory agent for the treatment of chronic pain, including the symptoms of arthritis.
M3429 Piroxicam Piroxicam is a non-selective COX inhibitor with an IC50 of 6 mM.
M3420 Diclofenac Sodium Diclofenac Sodium is a non-selective COX inhibitor with IC50 of 60 and 220 nM for ovine COX-1 and -2, respectively.
M3398 Nimesulide Nimesulide is a relatively COX-2 selective inhibitor with IC50 of 26 μM.
M3391 Ketoprofen Ketoprofen is a non-selective NSAID with IC50 of 0.5 μM and 2.33 μM for human recombinant COX-1 and COX-2, respectively.




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