COX

COX

The enzyme cyclooxygenase (COX), also referred to as prostaglandin-endoperoxide synthase (PTGS), is in charge of producing the vital biological mediators known as prostanoids, such as prostaglandins, prostacyclin, and thromboxane. Pain and inflammation symptoms can be reduced by pharmacologically inhibiting COX. The general public has had access to cyclooxygenase activity-inhibiting medications for about 100 years, including aspirin. The two cyclooxygenase isoforms, COX-1 and COX-2, have been identified. The COX-1 enzyme is frequently produced constitutively (i.e., in the gastric mucosa), whereas the COX-2 enzyme is induced (i.e., at sites of inflammation). Aspirin and ibuprofen are examples of NSAIDs that work by inhibiting COX to produce their desired effects. The non-steroidal anti-inflammatory drugs (NSAIDs) are the primary COX inhibitors.

COX related products

Structure Cat No. Product Name CAS No. Product Description
V74822 Piroxicam cinnamate (Cinnoxicam; SPA-S-510; Sinartol) 87234-24-0 Piroxicam cinnamate (Cinnoxicam) is a cyclooxygenase (COX) inhibitor (antagonist) with anti-inflammatory activity.
V74853 Plantanone B (Kaempferol 3-O-rhamnosylgentiobioside) 55780-30-8 Plantanone B is a moderate antioxidant with IC50 of 169.8±5.2 μM.
V73940 PPOH 206052-01-9 PPOH, a fatty acid analogue, is a selective cyclooxygenase (COX) inhibitor that can suppress arachidonic acid cyclooxygenase activity in renal cortical microsomes.
V1056 Pranoprofen (Pyranoprofen) 52549-17-4 Pranoprofen (also known as Pyranoprofen), a potent and approved non-steroidal anti-inflammatory drugs (NSAIDs), is a COX inhibitor that has been used as an anti-inflammatory drug in ophthalmology.
V74842 Propyphenazone-d3 (Propyphenazone-d3) 162935-29-7 Propyphenazone-d3 is the deuterium labelled form of Propyphenazone.
V74805 Regaloside B (regaloside B) 114420-67-6 Regaloside B is a phenylpropanoid extracted from Lilium longiflorum.
V75116 Rehmapicrogenin (rehmapicrogenin) 135447-39-1 Rehmapicrogenin can be extracted from the roots of Rehmannia glutinosa and displays potent anti-inflammatory effects by inhibiting iNOS, COX-2 and IL-6.
V1045 Rofecoxib (MK 966) 162011-90-7 Rofecoxib (formerly MK-0966; MK0966; MK-966; MK966; Vioxx; Ceoxx; Ceeoxx.), an NSAID drug, is a potent and selective COX-2 inhibitor with potential anti-inflammatory activity.
V74813 Sinapyl alcohol 537-33-7 Sinapyl alcohol is an orally bioactive anti-inflammatory and anti-injury agent.
V60122 Sphondin 483-66-9 Sphondin has an inhibitory activity against IL-1β-induced increases in COX-2 protein and PGE2 release levels in A549 cells.
V1042 Sulindac (MK-231) 38194-50-2 Sulindac(Aflodac; Algocetil; MK231; MK 231;MK-231), belonging to the arylalkanoic acid class of non-steroidal antiinflammatory drugs (NSAIDs), isa non-steroidal COX inhibitor, which potently inhibits prostaglandin synthesis.
V1077 Suprofen (TN-762) 40828-46-4 Suprofen(R25061;TN762;R-25061;TN-762;Suprofen; Suprofenum; Profenal), a nonsteroid anti-inflammatory drug (NSAID), is a potent and nonselective dual inhibitor of COX-1/COX-2 enzymeswith potential anti-inflammatory and antipyretic activity.
V74804 Tazofelone (LY 213829) 107902-67-0 Tazofelone (LY 213829) is a cyclooxygenase-II (COX-II) inhibitor.
V73505 Tebufelone (NE-11740) 112018-00-5 Tebufelone (NE-11740) is a nonsteroidal anti-inflammatory agent (NSAID) and a selective dual COX-2/5-lipoxygenase inhibitor.
V74815 Tenidap-d3 (CP-66248-d3) 142741-60-4 Tenidap-d3 is the deuterium labelled form of Tenidap.
V74851 Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) 1011244-72-6 Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) is a selective COX-1 inhibitor (antagonist) with IC50 of 30 µM and low activity against COX-2 (IC50>100 µM).
V60123 Tetrahydrocoptisine (Stylopine) 4312-32-7 (±)-Stylopine (Tetrahydrocoptisine) is an alkaloid compound extracted from plant tubers of the genus Corydalis.
V74847 Tinoridine (Y-3642) 24237-54-5 Tinoridine (Y-3642) is an orally bioactive non-steroidal anti-inflammatory agent with potent antioxidant capacity and free radical scavenging activity.
V1059 Tolfenamic Acid (GEA 6414) 13710-19-5 Tolfenamic Acid (formerly GEA 6414;GEA6414;GEA-6414;Clotam), a non-steroidal anti-inflammatory drugs (NSAIDs), is a potent and selective COX-2 inhibitor with potential anti-inflammatory activity.
V74824 Tolfenamic acid-d4 (Tolfenamic acid d4) 1246820-82-5 Tolfenamic acid-d4 is the deuterated form of Tolfenamic Acid.
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