Cox 1 Suppliers USA
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Product | Description | |
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COX-1 Inhibitor IV, TFAP - CAS 1011244-68-0 Quick inquiry Where to buy Suppliers range | The COX-1 Inhibitor IV, TFAP, also referenced under CAS 1011244-68-0, controls the biological activity of COX-1. This small molecule/inhibitor is primarily used for Cell Signaling applications. Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. CAS No. 1011244-68-0. Pack Sizes: 10MG. Mole weight: 281.23. Catalog: AP1011244680. Assay: ≥97% (HPLC). | |
1, 3-Bis (methoxymethoxy) -5-[ (1E) -2-[4- (methoxymethoxy) phenyl]ethenyl]-benzene Quick inquiry Where to buy Suppliers range | 1, 3-Bis (methoxymethoxy) -5-[ (1E) -2-[4- (methoxymethoxy) phenyl]ethenyl]-benzene is a useful synthetic intermediate in the synthesis of Resveratrol Impurity B (H950990); an impurity of Resveratrol (R150000) which is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1 and also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Grades: Highly Purified. CAS No. 1414361-09-3. Pack Sizes: 1g, 10g. Molecular Formula: C20H24O6, Molecular Weight: 360.4. US Biological Life Sciences. | Worldwide |
1-Propyl Etodolac Quick inquiry Where to buy Suppliers range | 1-Propyl Etodolac is an impurity in the synthesis of Etodolac (E933100), may have use in the treatment of myeloma. COX-1/COX-2/ β-catenin inhibitors, or anti-inflammatory agent. Group: Biochemicals. Alternative Names: 1-Ethyl-1,3,4,9-tetrahydro-8-(1-methylethyl)-Pyrano[3,4-b]indole-1-acetic Acid. Grades: Highly Purified. CAS No. 57816-83-8. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
2,4,6-trichloro-N-phenylaniline Quick inquiry Where to buy Suppliers range | A Diclofenac impurity which is a non-selective COX inhibitor with IC50 of 60 and 220 nM for ovine COX-1 and -2, respectively. Synonyms: 2,4,6-Trichlorodiphenylamine; Diphenylamine, 2,4,6-trichloro; Diclofenac Impurity 10. CAS No. 15362-44-4. Molecular formula: C12H8Cl3N. Mole weight: 272.56. | |
2-Phenoxylaniline Quick inquiry Where to buy Suppliers range | 2-Phenoxylaniline (Nimesulide EP Impurity C) is an impurity of Nimesulide (N477500) which is an antiinflammatory agent that preferentially inhibits COX-2 over COX-1. Group: Biochemicals. Grades: Highly Purified. CAS No. 2688-84-8. Pack Sizes: 5g, 25g. Molecular Formula: C12H11NO. US Biological Life Sciences. | Worldwide |
2'-Phenoxymethane sulfonanilide Quick inquiry Where to buy Suppliers range | 2'-Phenoxymethane sulfonanilide is a metabolite of nimesulide (N477500), which is an antiinflammatory agent. It preferentially inhibits COX-2 over COX-1 and suppresses chemical-induced carcinogenesis in mice and rats. Nimesulide also nhibits LPS-induced TNF-alpha production. Group: Biochemicals. Grades: Highly Purified. CAS No. 51765-51-6. Pack Sizes: 100mg, 1g. Molecular Formula: C13H13NO3S, Molecular Weight: 263.31. US Biological Life Sciences. | Worldwide |
2-Phenylthio-5-propionylphenylacetic Acid Quick inquiry Where to buy Suppliers range | 2-Phenylthio-5-propionylphenylacetic Acid is a useful synthetic intermediate in the synthesis of Zaltoprofen (Z146000); an inhibitor of Cox-1 and Cox-2. Zaltoprofen preferentially inhibits Cox-2. Group: Biochemicals. Grades: Highly Purified. CAS No. 103918-73-6. Pack Sizes: 1g, 10g. Molecular Formula: C17H16O3S. US Biological Life Sciences. | Worldwide |
3-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-5-(phenylmethoxy)-phenol Quick inquiry Where to buy Suppliers range | 3-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-5-(phenylmethoxy)-phenol is the impurity C of Resveratrol (R150000); a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1 and also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Grades: Highly Purified. CAS No. 678149-02-5. Pack Sizes: 5mg, 50mg. Molecular Formula: C21H18O3, Molecular Weight: 318.37. US Biological Life Sciences. | Worldwide |
3-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-5-(phenylmethoxy)-phenol-d7 Quick inquiry Where to buy Suppliers range | 3-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-5-(phenylmethoxy)-phenol-d7 is the isotope labelled analog of 3-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-5-(phenylmethoxy)-phenol (H950995); the impurity C of Resveratrol (R150000) which is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1 and also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C21H11D7O3, Molecular Weight: 325.41. US Biological Life Sciences. | Worldwide |
3-(7-Ethyl-1H-indol-3-yl)-3-(7-Ethyl-3-(2-Hydroxyethyl)-1H-indol-2-yl)Pentanoic Acid (Etodolac Impurity) Quick inquiry Where to buy Suppliers range | 3-(7-Ethyl-1H-indol-3-yl)-3-(7-ethyl-3-(2-Hydroxyethyl)-1H-indol-2-yl)Pentanoic Acid is an impurity in the synthesis of Etodolac (E933100). Like other Etodolac impurities (P835255) may have use in the treatment of myeloma. COX-1/COX-2/ β-catenin inhibitors. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H32N2O3, Molecular Weight: 432.55. US Biological Life Sciences. | Worldwide |
4-Methoxy Lornoxicam Quick inquiry Where to buy Suppliers range | 4-Methoxy Lornoxicam is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Grades: 98%. Molecular formula: C14H12ClN3O4S2. Mole weight: 385.85. | |
5-Hydroxy Lornoxicam Quick inquiry Where to buy Suppliers range | 5-Hydroxy Lornoxicam is one of lornoxicam metabolites. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 6-Chloro-4-hydroxy-N-(5-hydroxy-2-pyridinyl)-2-methyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-Dioxide; 2H-Thieno(2,3-e)-1,2-thiazine-3-carboxamide, 6-chloro-4-hydroxy-N-(5-hydroxy-2-pyridinyl)-2-methyl-, 1,1-dioxide. Grades: 98%. CAS No. 123252-96-0. Molecular formula: C13H10ClN3O5S2. Mole weight: 387.82. | |
7-(Trifluoromethyl)1H-indole-2,3-dione Quick inquiry Where to buy Suppliers range | An indole derivative as inhibitor of COX-1, COX-2, and β-catenin. Useful in the treatment of diseases such as: lung cancer, diabetes and Alzheimer's disease. Group: Biochemicals. Alternative Names: 7- (Trifluoromethyl) isatin. Grades: Highly Purified. CAS No. 391-12-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
7-(Trifluoromethyl)-1H-indole-2,3-dione-d2 Quick inquiry Where to buy Suppliers range | 7-(Trifluoromethyl)1H-indole-2,3-dione-d2 is a labelled 7-(Trifluoromethyl)1H-indole-2,3-dione (T791300), an inhibitor of COX-1, COX-2, and β-catenin. Useful in the treatment of diseases such as: lung cancer, diabetes and Alzheimer's disease. Group: Biochemicals. Alternative Names: 7- (Trifluoromethyl) isatin-d2. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
Allyl Bromide (Stabilized with Propylene Oxide) Quick inquiry Where to buy Suppliers range | Allyl Bromide is used as a reagent in the synthesis of Resveratrol derivatives. Resveratrol (R150000) is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Alternative Names: 3-Bromo-1-propene; 1-Bromo-2-propene; 2-Propenyl Bromide; 3-Bromo-1-propene; 3-Bromopropene; 3-Bromopropylene; Allyl Bromide; NSC 7596. Grades: Highly Purified. CAS No. 106-95-6. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
Allyl-d5 Bromide Quick inquiry Where to buy Suppliers range | Isotope labelled Allyl Bromide is used as a reagent in the synthesis of Resveratrol derivatives. Resveratrol (R150000) is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Alternative Names: 3-Bromo-1-propene-d5; 1-Bromo-2-propene-d5; 2-Propenyl Bromide-d5; 3-Bromo-1-propene-d5; 3-Bromopropene-d5; 3-Bromopropylene-d5; Allyl Bromide-d5; NSC 7596-d5. Grades: Highly Purified. CAS No. 102910-37-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
Bromfenac Sodium Salt Quick inquiry Where to buy Suppliers range | Bromfenac Sodium Salt is a potent inhibitor of both COX-1 and COX-2. Uses: Anti-inflammatory agents, non-steroidal. Synonyms: AHR 10282R; AHR10282R; AHR-10282R. Grades: > 95%. CAS No. 91714-93-1. Molecular formula: C15H11BrNO3.Na. Mole weight: 356.15. | |
BW 755C Quick inquiry Where to buy Suppliers range | Constitutive cyclooxygenase (COX-1) is present in cells under physiological conditions, whereas COX-2 is induced by some cytokines, mitogens, and endotoxin in pathological conditions, such as inflammation. Since 5-lipoxygenase (5-LO) oxidizes arachidonic acid to 5-hydroperoxyeicosatetraenoic acid. BW 755C is a dual inhibitor of 5-lipoxygenase (5-LO) and cyclooxygenase (COX) pathways. It inhibits 5-LO with IC50s of 0.75 μM, COX-1 with IC50s of 0.65 μg/ml, and COX-2 with IC50s of 1.2 μg/ml. BW 755C may also inhibit other LO pathways in vivo. Uses: Anti-inflammatory agents, non-steroidal. Synonyms: BW755C; BW-755C; 1H-Pyrazol-3-amine, 4,5-dihydro-1-[3-(trifluoromethyl)phenyl]-; 4,5-Dihydro-1-[3-(trifluoromethyl)phenyl]-1H-pyrazol-3-amine; 1-(3-Trifluoromethylphenyl)-4,5-dihydro-1H-pyrazol-3-amine; 3-Amino-1-[3-(trifluoromethyl)phenyl]-2-pyrazoline; 3-Amino-1-[3-(trifluoromethyl)phenyl]pyrazoline; 3-Amino-1-[m-(trifluoromethyl)phenyl]-2-pyrazoline; Compound BW 755C. Grades: ≥95%. CAS No. 66000-40-6. Molecular formula: C10H10F3N3. Mole weight: 229.20. | |
CAY10589 Quick inquiry Where to buy Suppliers range | CAY10589 is a dual inhibitor of mPGES-1 with IC50 of 1.3 μM and 5-LO with IC50 of 1.0 μM. It effectively inhibits PGE2 and LT synthesis in both cell free and intact cell assays. CAY10589 has minor effects on COX-1 and COX-2, inhibiting these enzymes 34% and 38.8%, respectively. Synonyms: CAY 10589; CAY-10589. Grades: ≥98%. CAS No. 1077626-52-8. Molecular formula: C25H28ClN3O2S. Mole weight: 470. | |
Celecoxib (Celebrex, 4-[5-(4-Methylphenyl)-3-trifluoromethyl)-1H-pyrazol-yl]benzenesulfonamide) Quick inquiry Where to buy Suppliers range | Celecoxib is a highly selective COX-2 inhibitor and primarily inhibits prostaglandin production. Celecoxib is approximately 7.6-fold more selective for COX-2 inhibition over COX-1. This specificity allows celecoxib to reduce inflammation and pain while minimizing gastrointestinal adverse drug reactions (e.g. stomach ulcers) that are common with non-selective non-steroidal anti-inflammatory drugs (NSAIDs). Group: Biochemicals. Alternative Names: Celecoxib, 4-[5-(4-Methylphenyl)-3-trifluoromethyl)-1H-pyrazol-yl]benzenesulfonamide. Grades: Highly Purified. CAS No. 169590-42-5. Pack Sizes: 300mg, 500mg, 1g, 5g. Molecular Formula: C17H14F3N3O2S, Molecular Weight: 381.37. US Biological Life Sciences. | Worldwide |
Chebulagic acid Quick inquiry Where to buy Suppliers range | Chebulagic acid is a polyphenol and tannin that has been found in T. chebula and has diverse biological activities. It is an inhibitor of COX-1, COX-2, and 5-lipoxygenase (5-LO; IC50s = 15, 0.92, and 2.1 μM, respectively) as well as α-glucosidase and 15-LO (IC50s = 0.05 and 24.9 μM, respectively). Chebulagic acid inhibit the LPS-induced upregulation of TNF-α and IL-1β in a dose- and time-dependent manner. And it can also inhibit the production of NO, prostaglandin E2 (PGE2), and reactive oxygen species (ROS), and nuclear translocation of NF-κB in RAW 264.7 macrophages in a concentration-dependent manner. Chebulagic acid also show a protective effect against 1-methyl-4-phenylpyridinium (MPP+) - induce cytotoxicity which mimics the pathological symptom of Parkinson's disease. Uses: Topoisomerase i inhibitors. Synonyms: β-D-glucopyranose; Cyclic 3,6-[(1R)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1-(3,4,5-trihydroxybenzoate); Cyclic 2?2:4?1-ester with (2S)-2-[(3S,4S)-5-carboxy-3,4-dihydro-3,7,8-trihydroxy-2-oxo-2H-1-benzopyran-4-yl]butanedioic acid. Grades: ≥98%. CAS No. 23094-71-5. Molecular formula: C41H30O27. Mole weight: 954.66. | |
cis-Resveratrol Quick inquiry Where to buy Suppliers range | Minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Alternative Names: 5-[(1Z)-2-(4-Hydroxyphenyl)ethenyl]-1,3-benzenediol; cis-3,4',5-Trihydroxystilbene; Z-5-[2-(4-Hydroxyphenyl)ethenyl]-1,3-benzenediol; (Z)-Resveratrol. Grades: Highly Purified. CAS No. 61434-67-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
Diclofenac Quick inquiry Where to buy Suppliers range | A non-selective COX inhibitor with IC50 of 60 and 220 nM for ovine COX-1 and -2, respectively. Synonyms: Voltaren; Ecofenac; Solaraze. Grades: > 95%. CAS No. 15307-86-5. Molecular formula: C14H11Cl2NO2. Mole weight: 296.15. | |
Dipyrone Quick inquiry Where to buy Suppliers range | Dipyrone is a non-steroidal anti-inflammatory drug that, when coadministered with morphine, potentiates its antinociceptive action and delays the development of tolerance. Dipyrone is a relatively selective inhibitor of cyclooxygenase-3 (COX-3), with lower activity against COX-1 and no activity against COX-2. Dipyrone blocks PGE2-induced hyperalgesia in several models. Group: Biochemicals. Alternative Names: 1- [ (2, 3-Dihydro-1, 5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl) methylamino] methanesulfonic Acid Sodium Salt; (Antipyrinyl methyl amino) methanesulfonic Acid Sodium Salt; ARPF; Algocalmin; Algopyrin; Anador; Analgin; Analgine; Andolor; Conmel; Diprofarn; Gifaril; Lisador; Metamizol; Metamizole; Metamizole Sodium; Metamizole Sodium Salt; Metapyrin; Methamizole Sodium; Methampyrone; Methylmelubrin; Metilon; Narone; Sulpin; Sulpyrin; Sulpyrine. Grades: Highly Purified. CAS No. 68-89-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
(-)-Epicatechin Gallate Quick inquiry Where to buy Suppliers range | (-)-Epicatechin gallate (Epicatechin gallate) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 7.5 μM. Group: Biobased Products. Alternative Names: (2R)-2α-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3β,5,7-triol 3-(3,4,5-trihydroxybenzoate). Grades: 98%. CAS No. 1257-08-5. Product ID: BBC1257085. Molecular formula: C22H18O10. Mole weight: 442.37. IUPAC Name: [(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate. Appearance: White powder. Density: 1.80±0.1 g/ml. SMILES: C1[C@H] ([C@H] (OC2=CC (=CC (=C21)O)O)C3=CC (=C (C=C3)O)O)OC (=O)C4=CC (=C (C (=C4)O)O)O. | |
FR 122047 hydrochloride Quick inquiry Where to buy Suppliers range | FR-122047 is a selective cyclooxygenase-1 (COX-1) inhibitor with IC50 values is 0.028μM for COX-1 and 65 μM for COX-2. FR-122047 displays 2300 fold greater selectivity towards inhibition of COX-1 over COX-2. It shows analgesic, anti-platelet and anti-inflammatory properties. No development was reported for the treatment of Pain, Rheumatoid arthritis and Thrombosis. Uses: Pain; rheumatoid arthritis; thrombosis. Synonyms: FR 122047 hydrochloride;1-[[4,5-bis-(4-Methoxyphenyl)-2-thiazolyl]carbonyl]-4-methylpiperazine hydrochloride. Grades: >98 %. CAS No. 130717-51-0. Molecular formula: C23H25N3O3S.HCl. Mole weight: 459.99. | |
FR122047 hydrochloride hydrate Quick inquiry Where to buy Suppliers range | FR122047 is a selective inhibitor of COX-1 with an IC50 value of 0.028 μM. Synonyms: 1-[[4,5-bis(4-methoxyphenyl)-2-thiazolyl]carbonyl]-4-methyl-piperazine, monohydrochloride, monohydrate. Grades: ≥98%. Molecular formula: C23H25N3O3S·HCl·H2O. Mole weight: 478. | |
Guaiacin Quick inquiry Where to buy Suppliers range | Guaiacin is a lignan isolated from the leaves of Guaiacum officinale. Guaiacin inhibits COX-1 and COX-2 leading to the reduction of inflammations. Synonyms: (6R,7S,8S)-8-(4-hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol. Grades: >98%. CAS No. 36531-08-5. Molecular formula: C20H24O4. Mole weight: 328.408. | |
Ibuprofen Quick inquiry Where to buy Suppliers range | Ibuprofen is an inhibitor of COX-1 and COX-2 with IC50 of 13 μM and 370 μM, respectively. Synonyms: α-methyl-4-(2-methylpropyl)?-benzeneacetic acid. CAS No. 15687-27-1. Molecular formula: C13H18O2. Mole weight: 206.28. | |
Indometacin sodium Quick inquiry Where to buy Suppliers range | Indomethacin sodium is the sodium salt of indomethacin, a non-selective, reversible, and competitive inhibitor of COX-1 and -2 with anti-inflammatory, analgesic-antipyretic and tocolytic effects. Synonyms: 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid sodium salt. Grades: ≥98% (HPLC). CAS No. 74252-25-8. Molecular formula: C19H21ClNNaO7. Mole weight: 433.82. | |
Indomethacin, 2'-Trifluoromethyl (Indomethacin, 2'-Trifluoromethyl, Indomethacin, 2-CF3, CF3-Indomethacin, CF3-INDO) Quick inquiry Where to buy Suppliers range | A cell-permeable, bioavailable 2-trifluoromethyl analog of Indomethacin that acts as a highly potent, time-dependent inhibitor of cyclooxygenase -2 (COX-2; IC50 = 267 and 388nM for mouse and human COX-2, respectively) and its several mutant forms. Does not affect COX-1 activity even at high concentrations (IC50 >100uM). Interacts with human COX-2 with much greater affinity than indomethacin (KI = 1.5 vs 13uM) and blocks COX-2 dependent arachidonic acid oxygenation (IC50 = 150nM in 1483 human head and neck squamous cell carcinoma cells). Further, minimizes swelling in carrageenan-induced rat paw edema model (EC50 = 1.7mg/kg, p.o.) with no gastrointestinal bleeding at higher doses (10mg/kg). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
Indomethacin N-octyl amide Quick inquiry Where to buy Suppliers range | Indomethacin N-octyl amide is a derivative of indomethacin, a non-selective, reversible, and competitive inhibitor of COX-1 and -2 with anti-inflammatory, analgesic-antipyretic and tocolytic effects. Synonyms: 2-(1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)-N-octylacetamide. Grades: ≥98%. CAS No. 282728-65-8. Molecular formula: C27H33ClN2O3. Mole weight: 469. | |
Ketorolac Quick inquiry Where to buy Suppliers range | Ketorolac, a non-selective COX inhibitor, is a non-steroidal anti-inflammatory drug. It shows inhibition of eicosanoid formation in HEL cells (COX-1) and LPS-stimulated Mono Mac 6 cells (COX-2), but does not significantly inhibit NO accumulation in supernatants of LPS-stimulated RAW 264.7 cells. It significantly inhibits thymidine incorporation of human osteoblasts (hOBs) upon 24 hours treatment in a dose-dependent manner, and inhibits proliferation and arrests cell cycle at G0/G1 phase in hOBs. Uses: Cyclooxygenase inhibitors. Synonyms: Acular LS; RS37619; RS 37619; RS-37619; Sprix; Toradol. Grades: >98%. CAS No. 74103-06-3. Molecular formula: C15H13NO3. Mole weight: 255.27. | |
Ketorolac Tromethamine Quick inquiry Where to buy Suppliers range | 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. Synonyms: 5-benzoyl-2,?3-dihydro-1H-pyrrolizine-1-carboxylic acid,compd. with 2-amino-2-(hydroxymethyl)?-1,?3-propanediol (1:1). CAS No. 74103-07-4. Molecular formula: C19H24N2O6. Mole weight: 376.4. | |
Licofelone Quick inquiry Where to buy Suppliers range | Licofelone is a dual inhibitor of COX-1/COX-2 and 5-lipoxygenase. Uses: Lipoxygenase inhibitors. Synonyms: ML 3000; ML3000; ML-3000; 6-(4-chlorophenyl)-2,3-dihydro-2,2-dimethyl-7-phenyl-1H-pyrrolizine-5-acetic acid. CAS No. 156897-06-2. Molecular formula: C23H22ClNO2. Mole weight: 379.9. | |
Lornoxicam Quick inquiry Where to buy Suppliers range | Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor used as an anti-inflammatory drug. Uses: Anti-inflammatory agents, non-steroidal. Synonyms: Chlortenoxicam; Xefocam; Xefo. Grades: > 95%. CAS No. 70374-39-9. Molecular formula: C13H10ClN3O4S2. Mole weight: 371.82. | |
Lornoxicam Impurity 1 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 1 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: N-Des(2-pyridinyl)-N-(5-carboxy-2-thiazolyl) Lornoxicam; 6-Chloro-4-hydroxy-2-methyl-N-(5-carboxy-2-thiazolyl)-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-Dioxide; MTB-2. Grades: > 98%. CAS No. 1246819-40-8. Molecular formula: C12H8ClN3O6S3. Mole weight: 421.86. | |
Lornoxicam Impurity 13 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 13 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Molecular formula: C6H6ClNO4S2. Mole weight: 255.70. | |
Lornoxicam Impurity 14 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 14 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Grades: 98%. Molecular formula: C14H12ClN3O4S2. Mole weight: 385.85. | |
Lornoxicam Impurity 15 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 15 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Molecular formula: C9H10ClNO4S2. Mole weight: 295.76. | |
Lornoxicam Impurity 16 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 16 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 2-methyl-2,3-dihydro-4H-thieno[2,3-e][1,2]thiazin-4-one 1,1-dioxide; 2-Methyl-2H-thieno[2,3-e][1,2]thiazin-4(3H)-one 1,1-dioxide; 2-methyl-3H-thiopheno[2,3-e]1,2-thiazine-1,1,4-trione; 4H-Thieno[2,3-e]-1,2-thiazin-4-one, 2,3-dihydro-2-methyl-, 1,1-dioxide. Grades: 98%. CAS No. 72975-44-1. Molecular formula: C7H7NO3S2. Mole weight: 217.27. | |
Lornoxicam Impurity 2 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 2 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: N-Des(2-pyridinyl)-N-(5-hydroxymethyl-2-thiazolyl) Lornoxicam; 6-chloro-4-hydroxy-N-(5-(hydroxymethyl)thiazol-2-yl)-2-methyl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide; MTB-1. Grades: > 98%. CAS No. 1246818-50-7. Molecular formula: C12H10ClN3O5S3. Mole weight: 407.87. | |
Lornoxicam Impurity 3 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 3 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 2-Thiophenecarboxylic acid, 5-chloro-3-sulfino-; 5-Chloro-3-sulfino-2-thiophenecarboxylic acid. Grades: ≥95%. CAS No. 187746-97-0. Molecular formula: C5H3ClO4S2. Mole weight: 226.66. | |
Lornoxicam Impurity 8 Sodium Salt Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 8 Sodium Salt is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 2-carboxy-5-chlorothiophene-3-sulfonate, sodium salt (1:1). Molecular formula: C5H2ClO5S2.Na. Mole weight: 264.64. | |
Lornoxicam Impurity 9 Quick inquiry Where to buy Suppliers range | Lornoxicam Impurity 9 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 5-chloro-3-sulfamoylthiophene-2-carboxylic acid; 3-(aminosulfonyl)-5-chlorothiophene-2-carboxylic acid. Grades: 98%. CAS No. 1017791-22-8. Molecular formula: C5H4ClNO4S2. Mole weight: 241.67. | |
Lumiracoxib Quick inquiry Where to buy Suppliers range | Lumiracoxib is a novel, selective COX-2 inhibitor. Uses: Cyclooxygenase 2 inhibitors. Synonyms: CGS-35189; CGS 35189; CGS35189; COX-189; COX189; COX 189; Lumiracoxib; trade name: Prexige. Grades: > 95%. CAS No. 220991-20-8. Molecular formula: C15H13ClFNO2. Mole weight: 293.72. | |
Meclofenamate Sodium Quick inquiry Where to buy Suppliers range | A dual COX-1/COX-2 inhibitor with IC50 of 40 nM and 50 nM, respectively. Uses: Anti-inflammatory agents, non-steroidal. Synonyms: 2-[(2,6-dichloro-3-methylphenyl)amino]-benzoic acid, sodium salt (1:1). CAS No. 6385-02-0. Molecular formula: C14H11Cl2NO2.Na. Mole weight: 318.13. | |
N-acetyl-2-carboxy Benzenesulfonamide Quick inquiry Where to buy Suppliers range | N-acetyl-2-carboxy Benzenesulfonamide is a COX-1/COX-2 inhibitor. Synonyms: 2-[(acetylamino)sulfonyl]-benzoic acid. CAS No. 849067-18-1. Molecular formula: C9H9NO5S. Mole weight: 243.2. | |
Naproxen Quick inquiry Where to buy Suppliers range | (S)-Naproxen is a non-selective COX inhibitor. The IC50 values for human recombinant COX-1 and -2 are 0.6-4.8 μM and 2.0-28.4 μM, respectively. It is an anti-inflammatory agent with analgesic and antipyretic activities, which is commonly used for the treatment of rheumatoid arthritis and gout. Uses: The treatment of rheumatoid arthritis and gout. Synonyms: (S)-6-Methoxy-α-methyl-2-naphthaleneacetic Acid; po-Naproxen; Aproxen; Bonyl; CG 3117; CG3117; CG-3117; Diocodal; Dysmenalgit; Equiproxen; Floginax; Laraflex; Laser; MNPA; Naixan; Napren; Naprium; Naprius; Naprosyn; Naprosyne; Naproxen; Naprux; Naxen; Nycopren; Panoxen; Prexan; Proxen; Proxine; RS 3540; RS3540; RS-3540; Reuxen; Veradol; Xenar; Xenar-CR; d-2-(6-Methoxy-2-naphthyl)propionic Acid; d-Naproxen. Grades: >98%. CAS No. 22204-53-1. Molecular formula: C14H14O3. Mole weight: 230.26. | |
NCX 466 ((aS)-6-Methoxy-a-methyl-2-naphthalene acetic acid (5S)-5,6-bis(nitrooxy)hexyl ester) Quick inquiry Where to buy Suppliers range | Cyclooxygenase (COX)-inhibiting nitric oxide (NO) donor (CINOD). Inhibits COX-1 and COX-2 while releasing NO. Demonstrates higher efficacy than naproxen, its congener drug, in reducing levels of profibrotic cytokine transforming growth factor-beta and oxidative stress in a mouse model of bleomycin-induced lung fibrosis. Orally available. Group: Biochemicals. Grades: Highly Purified. CAS No. 1262956-64-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
Nepafenac Quick inquiry Where to buy Suppliers range | Nepafenac is an inhibitor of COX-1 and COX-2. Synonyms: AL 6515; AL6515; AL-6515; AHR 9434; AHR9434; AHR-9434; Nevanac; Nepafenac; Nevanac. 2-(2-amino-3-benzoylphenyl)acetamide. CAS No. 78281-72-8. Molecular formula: C15H14N2O2. Mole weight: 254.28. | |
Niflumic Acid Quick inquiry Where to buy Suppliers range | Niflumic Acid is a selective COX-2 inhibitor and GPR35 activator. Cox-2: IC50 = 918 nM (human); Cox-1: IC50 = 1.06 μM (human); GPR35: IC50 = 1.28 μM (human). Uses: Anti-inflammatory agents, non-steroidal. Synonyms: 2-[[3-(trifluoromethyl)phenyl]amino]-3-pyridinecarboxylic acid; Actol; Donalgin; Nifluril; UP83. CAS No. 4394-00-7. Molecular formula: C13H9F3N2O2. Mole weight: 282.2. | |
Nimesulide (N- (4-Nitro-2-phenoxyphenyl) methanesulfonamide) Quick inquiry Where to buy Suppliers range | Antiinflammatory agent. Preferentially inhibits COX-2 over COX-1. Suppresses chemical-induced carcinogenesis in mice and rats. Inhibits LPS-induced TNF-alpha production. Group: Biochemicals. Alternative Names: N- (4-Nitro-2-phenoxyphenyl) methanesulfonamide. Grades: Highly Purified. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
O-Acetyl Salicylhydroxamic Acid Quick inquiry Where to buy Suppliers range | An irreversible, non-selective inhibitor of COX-1 and COX-2. Synonyms: N-(acetyloxy)-2-hydroxy benzamide; AcSHA; O-ASHA. CAS No. 199854-00-7. Molecular formula: C9H9NO4. Mole weight: 195.2. | |
O-Acetylsalicyl hydroxamic Acid (AcSHA, O-ASHA) Quick inquiry Where to buy Suppliers range | An irreversible, non-selective inhibitor of COX-1 and COX-2. Group: Biochemicals. Alternative Names: AcSHA, O-ASHA. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
Oxaprozin Impurity 1 (4,5-Diphenylimidazole-2-propionic acid) Quick inquiry Where to buy Suppliers range | An impurity of Oxaprozin, which is a inhibitor of both COX-1 and COX-2. Synonyms: 4,5-Diphenyl-1H-imidazole-2-propanoic Acid; Wy 23120; 3-(4,5-Diphenyl-1H-imidazol-2-yl)propanoic Acid. Grades: > 95%. CAS No. 55217-15-7. Molecular formula: C18H16N2O2. Mole weight: 292.34. | |
Oxaprozin Impurity 2 Quick inquiry Where to buy Suppliers range | An impurity of Oxaprozin, which is a inhibitor of both COX-1 and COX-2. Synonyms: 4,5-Diphenyl-2-oxazolepropanamide; 3-(4,5-Diphenyloxazol-2-yl)propanamide; β-(4,5-Diphenyloxazol-2-yl)propionamide. Grades: > 95%. CAS No. 24248-49-5. Molecular formula: C18H16N2O2. Mole weight: 292.34. | |
para-(2-Thenoyl) hydratropic acid Quick inquiry Where to buy Suppliers range | A dual COX-1/COX-2 inhibitor. Uses: Anti-inflammatory agents, non-steroidal. Synonyms: R-25061; R25061; R 25061; α-methyl-4-(2-thienylcarbonyl)?-benzeneacetic acid. CAS No. 40828-46-4. Molecular formula: C14H12O3S. Mole weight: 260.31. | |
PD 146176 Quick inquiry Where to buy Suppliers range | PD 146176 is a specific, non-competitve 15-lipoxygenase (15-LOX) inhibitor (Ki = 197nM), without effect on 5-LOX, 12-LOX, COX-1 or COX-2 (IC50 = 0.54 μM for 15-LOX in rabbit reticulocytes). It is known that PD-146176 acts as a noncompetitive inhibitor towards 15-LO, displaying a Ki=197 nM. Furthermore, PD-146176 reduces monocyte macrophage enrichment of atherosclerotic lesions and development of fibrofoamy and fibrous plaque. Synonyms: 6,11-Dihydro[1]benzothiopyrano[4,3-b]indole; PD 146176; PD-146176; PD146176; NSC 168807; NSC-168807; NSC168807. Grades: ≥98% by HPLC. CAS No. 4079-26-9. Molecular formula: C15H11NS. Mole weight: 237.32. | |
PF 9184 Quick inquiry Where to buy Suppliers range | This active molecular is selective mPGES-1 (microsomal prostaglandin E synthase-1 inhibitor. mPGES-1 is an enzyme induced during the inflammatory response and it is for developing anti-inflammatory drugs. PF-9184 inhibited recombinant human mPGES-1 with IC50 value of 16.5nM. PF-9184 had no effect against COX-1 and COX-2 with more than 6500-fold selectivity. PF-9184 inhibited PGE(2) synthesis with IC50 value in the range of 0.5-5 mM in serum-free cell and human whole blood cultures. Uses: Anti-inflammatory agent. Synonyms: N-(3',4'-Dichloro[1,1'-biphenyl]-4-yl)-4-hydroxy-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide. Grades: 98%. CAS No. 1221971-47-6. Molecular formula: C21H14Cl2N2O4S. Mole weight: 461.31. | |
Pirinixic acid aminothiazole Quick inquiry Where to buy Suppliers range | Pirinixic acid aminothiazole is a dual inhibitor of 5-lipoxygenase (5-LO) and microsomal prostaglandin E2 synthase 1 (mPGES-1) with IC50 values of 0.4 and 0.2 μM, respectively. It also weakly inhibits COX-1 and -2. Synonyms: 2-[4-Chloro-6-[4-(2-naphthyl)-2-thiazolylamino]-2-pyrimidinylthio]octanoic acid. Grades: ≥98%. CAS No. 1492060-44-2. Molecular formula: C25H25ClN4O2S2. Mole weight: 513.1. | |
p-Phenetidine Quick inquiry Where to buy Suppliers range | A toxic metabolite of Phenacetin which exhibits high renal toxicity. p-Phenetidine also reduced COX-1 and COX-2 expression in neutrophils. Group: Biochemicals. Alternative Names: 4-Ethoxybenzenamine; 1-Amino-4-ethoxybenzene; 4-Aminophenetole; 4-Ethoxyaniline; 4-Ethoxybenzenamine; 4-Ethoxyphenylamine; NSC 3116; p-Aminophenetole; p-Ethoxyaniline; p-Ethoxyphenylamine; p-Phenetidin. Grades: Highly Purified. CAS No. 156-43-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
p-Phenetidine-d5 Hydrochloride Quick inquiry Where to buy Suppliers range | Labeled p-Phenetidine. A toxic metabolite of Phenacetin which exhibits high renal toxicity. p-Phenetidine also reduced COX-1 and COX-2 expression in neutrophils. Group: Biochemicals. Alternative Names: 4-(Ethoxy-d5)benzenamine Hydrochloride; 1-Amino-4-(ethoxy-d5)benzene Hydrochloride; 4-Aminophenetole-d5 Hydrochloride; 4-Ethoxyaniline-d5 Hydrochloride; 4-(Ethoxy-d5)benzenamine Hydrochloride; 4-(Ethoxy-d5)phenylamine Hydrochloride; NSC 3116-d5 Hydrochloride; p-Aminophenetole-d5 Hydrochloride; p-Ethoxyaniline-d5 Hydrochloride; p-(Ethoxy-d5)phenylamine Hydrochloride; p-Phenetidin-d5 Hydrochloride. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
Radicicol Quick inquiry Where to buy Suppliers range | Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1 expression in LPS-stimulated macrophages. Induces the differentiation of HL-60 cells into macrophages. Potent HSP90 inhibitor. Anticancer compound. In vivo Rad/Raf interaction inhibitor. Inhibitor of AP-1-, NF-kappaB- and serum response factor (SRF)-mediated transcription. Suppresses expression of iNOS (NOS II). Non-competitive inhibitor of ATP citrate lyase. DNA topoisomerase VI and type II DNA topoisomerase inhibitor. Protects against LPS/IFN-gamma-induced neuronal cell death. Apoptosis inducer. Group: Biochemicals. Grades: Highly Purified. CAS No. 12772-57-5. Pack Sizes: 1mg, 5mg. Molecular Formula: C18H17ClO6. US Biological Life Sciences. | Worldwide |
Resveratrol Quick inquiry Where to buy Suppliers range | Potent phenolic antioxidant found in grapes and red wine. Eicosanoid synthesis and platelet aggregation inhibitor. Estrogen receptor agonist. Chemopreventive. Specific inhibitor of cyclooxygenase-1 (COX-1). Anti-inflammatory. Ribonucleotide reductase and DNA synthesis. Arrests cell cycle at S/G2 phase. Anticancer and antiproliferative compound. Apoptosis inducer. Protein kinase D inhibitor. Does not inhibit PKC. Autophagy inducer. Potent SIRT1 (sirtuin 1) activator. Neuroprotective. Adipogenesis inhibitor. PGC-1alpha activator. Sonic hedgehog (Shh) signaling pathway modulator. Gli1 mRNA expression inhibitor. Downregulates Gli transcriptional activity. Cardioprotective. Anti-diabetic. Senescence modulator. Extends lifespan. Group: Biochemicals. Alternative Names: 3,4,5-Trihydroxy-trans-stilbene; 5-[(1E)-2-(4-Hydroxyphenyl)ethenyl]-1,3-benzenediol. Grades: Highly Purified. CAS No. 501-36-0. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C14H12O3, Molecular Weight: 228.24. US Biological Life Sciences. | Worldwide |
Resveratrol-13C6 Quick inquiry Where to buy Suppliers range | Minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
R-Ibuprofen Quick inquiry Where to buy Suppliers range | R-Ibuprofen is an inhibitor of Cox-1 and Cox-2 used as a nonsteroidal anti-inflammatory drug. Synonyms: l-Ibuprofen; Levibuprofen; (R)-(-)-Ibuprofen; (R)-Ibuprofen. Grades: > 95%. CAS No. 51146-57-7. Molecular formula: C13H18O2. Mole weight: 206.28. | |
Salicin Quick inquiry Where to buy Suppliers range | Salicin is a phenol β-glycosid produced from willow bark that shows an anti-inflammatory effect. It acts as a non-selective COX inhibitor (IC50 values > 100 μM for COX-1 and COX-2). Salicin is a natural compound used in cosmetics material. Uses: Ingredient of health care products. Synonyms: 2-(Hydroxymethyl)phenyl b-D-glucopyranoside. Grades: ≥ 98%. CAS No. 138-52-3. Molecular formula: C13H18O7. Mole weight: 286.28. | |
Salsalate-d4 Quick inquiry Where to buy Suppliers range | Nonacetylated salicylate. Non-steroidal anti-inflammatory drug (NSAID). Reduces pain and inflammation caused by conditions such as rheumatoid arthritis, osteoarthritis and related rheumatic conditions. Prostaglandin synthesis inhibitor in vivo. Inactivates cyclooxygenase-1 (COX-1) and -2 (COX-2). IKKbeta/NF-kappaB inhibitor (at significantly higher concentrations than required for COX inhibition). Used to target inflammation in the treatment of insulin resistance, type 2 diabetes, or rheumatic pain. Group: Biochemicals. Alternative Names: 2-Hydroxybenzoic Acid 2-Carboxyphenyl Ester-d4; Salicylic Acid Salicylate-d4; 2-Hydroxybenzoic Acid 2-Carboxyphenyl Ester-d4; Diacesal-d4; Diplosal-d4; Disalcid-d4; Disalgesic-d4; Disalicylic-d4 Acid; Disalyl-d4; Mono-Gesic-d4; NSC 49171-d4; Nobacid-d4; Salflex-d4; Salical-d4; Salicyl Salicylate-d4; Salicyloxysalicylic Acid-d4; Salicyloylsalicylic-d4 Acid; Salicylsalicylic-d4 Acid; Salina-d4; Salsalate-d4; Salysal-d4; Sasapirin-d4; Sasapyrine-d4; Sasapyrinum-d4; o-Salicylsalicylic-d4 Acid. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
Salsalate (NSC 49171) Quick inquiry Where to buy Suppliers range | Nonacetylated salicylate. Non-steroidal anti-inflammatory drug (NSAID). Reduces pain and inflammation caused by conditions such as rheumatoid arthritis, osteoarthritis and related rheumatic conditions. Prostaglandin synthesis inhibitor in vivo. Inactivates cyclooxygenase-1 (COX-1) and -2 (COX-2). IKKbeta/NF-kappaB inhibitor (at significantly higher concentrations than required for COX inhibition). Used to target inflammation in the treatment of insulin resistance, type 2 diabetes, or rheumatic pain.Salsalate reduces blood glucose concentrations in patients with type 2 diabetes, as well as in insulin-resistant patients without diabetes. Reduces blood glucose, triglyceride, free fatty acid and C-reactive protein concentrations, improves glucose utilization and increases circulating insulin and adiponectin concentrations in obese adults at risk for the development of type 2 diabetes as well as for patients with type 2 diabetes. Dimeric prodrug comprising two esterified salicylate moieties. It is advantageous over sodium salicylate because it is insoluble at the acid pH of the stomach and passes suspended but undissolved into the small intestine, sparing the gastric mucosa direct contact. Group: Biochemicals. Alternative Names: Salicylsalicylic acid, NSC 49171, BRN 2590908, 2-Hydroxy-2-carboxyphenyl ester-benzoic acid. Grades: Highly Purified. CAS No. 552-94-3. Pack Sizes: 1g, 5g, 10g, 25g, 50g. Molecular Formula: C??H??O?, Molecular Weight: 258.23. US Biological Life Sciences. | Worldwide |