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. |
M10099 | CAY10404 | CAY10404 is one of the most selective inhibitors of COX-2 (IC50 = 1 nM) over COX-1. |
M9682 | TFAP | TFAP is a selective cyclooxygenase-1 (COX-1) inhibitor with IC50 of 0.8 μM. |
M8277 | 680C91 | 680C91 is a potent inhibitor of the enzyme tryptophan 2,3-dioxygenase (TDO), which directs the conversion of trypophan to kynurenin. |
M8040 | SC-236 | Sc-236 is a COX-2 specific inhibitor with an IC50 value of 10 nM for COX-1 and a PPARγ agonist with oral activity. Sc-236 inhibits activator protein-1 (AP-1) activity by c-Jun amino terminus. Sc-236 exerts anti-inflammatory effects by inhibiting ERK phosphorylation in mouse models. |
M7274 | SC 560 | SC 560 is a cyclooxygenase-1 (COX-1) inhibitor. |
M7051 | NS 398 | NS 398 is a cyclooxygenase-2 (COX-2) inhibitor. |
M6693 | DuP 697 | DuP 697 is a cyclooxygenase-2 (COX-2) inhibitor. |
M6057 | Vitamin E (D-alpha-Tocopherol) | Vitamin E (D-alpha-Tocopherol) is a naturally occurring form of Vitamin E that is a potent antioxidant. |
M5996 | Tenoxicam | Tenoxicam is a good HO. radicals scavenger with an IC50 of 56.7 μM. |
M5985 | Suprofen | Suprofen is a dual COX-1/COX-2 inhibitor, used as a non-steroidal anti-inflammatory analgesic and antipyretic. |
M5945 | Salicylic acid | Salicylic acid is a beta hydroxy acid that occurs as a natural compound in plants which is an inhibitor of ethylene biosynthesis and cyclooxygenase activity. |
M5923 | Rebamipide | Rebamipide (OPC12759) is a cholecystokinin-1 (CCK1) receptor inhibitor that inhibits [125I]BH-CCK-8S with an IC50 of 37.7 μM. Rebamipide is an orally effective gastroprotective agent. Rebamipide enhances the production of endogenous PGs (particularly intragastric PGE2) by inducing COX-2 expression, thereby protecting the gastric mucosa from injury. Rebamipide also has anti-proliferative activity against gastric cancer cells. |
M5907 | Propyphenazone | Propyphenazone is a pyrazolone derivative with anti-inflammatory, analgesic and antipyretic activity, Propyphenazone-based analogues as prodrugs and selective cyclooxygenase-2 inhibitors. |
M5893 | Pranoprofen | Pranoprofen is a non-steroidal COX inhibitor, used as an anti-inflammatory drug in ophthalmology. |
M5874 | Phenacetin | Phenacetin is a non-opioid analgesic without anti-inflammatory properties. |
M5859 | Parecoxib Sodium | Parecoxib is a potent and selective COX-2 inhibitor. |
M5858 | Parecoxib | Parecoxib is a selective COX2 inhibitor. |
M5814 | Niflumic acid | Niflumic acid is an inhibitor of cyclooxygenase-2 used for joint and muscular pain. |
M5755 | Loxoprofen | Loxoprofen is a non-steroidal anti-inflammatory drug in the propionic acid derivatives group. |
M5716 | Isoxicam | Isoxicam is a new non-steroidal anti-inflammatory benzothiazine derivative. |
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