226 Results for "

NSAIDs

" in MedChemExpress (MCE) Product Catalog:
Products (226)

226 Results for "NSAIDs" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-118189
CAS No.: 112137-89-0
Research Areas:  

Inflammation/Immunology

Misoprostol acid is an active metabolite of Misoprostol. Misoprostol is a synthetic analogue of prostaglandin E1 (PGE1), extensively absorbed, and undergoes rapid de-esterification to Misoprostol acid in the gastrointestinal tract after oral administration. Misoprostol can be used for non-steroidal anti-inflammatory drug-induced (NSAID) gastric ulcers . Misoprostol is an oral agent used to induce labor .
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1
1 Cited Publications
Cat. No.: HY-B0270
CAS No.: 40828-46-4
Synonyms: TN-762
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

Suprofen (TN-762) is a non-steroidal anti-inflammatory drug (NSAID).
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1
1 Cited Publications
Cat. No.: HY-17485
CAS No.: 39718-89-3
Synonyms: EB-382
Target:  

Phospholipase COX

Research Areas:  

Inflammation/Immunology

Alminoprofen (EB-382) is a nonsteroidal anti-inflammatory agent (NSAID) of the phenylpropionic acid class. Alminoprofen possesses a dual anti-inflammatory action, by inhibiting both secretory phospholipase A2 (sPLA2) and COX-2 .
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1 Cited Publications
Cat. No.: HY-B1489
CAS No.: 64490-92-2
Target:  

COX

Research Areas:  

Inflammation/Immunology Cancer

Tolmetin sodium dihydrate is an orally active and potent COX inhibitor with IC50s of 0.35 μM and 0.82 μM human COX-1 and COX-2, respectively. Tolmetin sodium dihydrate is a non-steroidal anti-inflammatory drug (NSAID) .
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1
1 Cited Publications
Cat. No.: HY-B0580C
CAS No.: 167105-81-9
Synonyms: RS37619 hemicalcium
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Ketorolac (RS37619) hemicalcium is a non-steroidal anti-inflammatory drug (NSAID), acting as a nonselective COX inhibitor, with IC50s of 20 nM for COX-1 and 120 nM for COX-2. Ketorolac tromethamine is used as 0.5% ophthalmic solution for the research of allergic conjunctivitis, cystoid macular edema, intraoperative miosis, and postoperative ocular inflammation and pain. Ketorola chemicalcium is also a DDX3 inhibitor that can be used for cancer research .
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1 Cited Publications
Cat. No.: HY-106907
CAS No.: 66318-17-0
Purity:  98.90%
Target:  

PGE synthase

Furprofen is an non-steroidal anti-inflammatory drug (NSAID) with analgesic properties . Furprofen acts via the inhibition of prostaglandin (PGE) synthesis. Furprofen can be treated orally for the relief of pain .
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1
1 Cited Publications
Cat. No.: HY-106579
CAS No.: 33005-95-7
Purity:  98.74%
Target:  

COX

Research Areas:  

Inflammation/Immunology

Tiaprofenic acid is an orally active nonsteroidal anti-inflammatory agent (NSAID) with anti-inflammatory and analgesic potency. Tiaprofenic acid inhibits prostaglandin synthesis by suppressing cyclo-oxygenase (COX). Tiaprofenic acid can be used in the treatment of rheumatic diseases .
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1
1 Cited Publications
Cat. No.: HY-B1355A
CAS No.: 129-20-4
Target:  

COX Bacterial

Research Areas:  

Infection Inflammation/Immunology

Oxyphenbutazone is a Phenylbutazone (HY-B0230) metabolite, with anti-inflammatory effect. Oxyphenbutazone is an orally active non-selective COX inhibitor. Oxyphenbutazone selectively kills non-replicating Mycobaterium tuberculosis .
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1 Cited Publications
Cat. No.: HY-13507
CAS No.: 220991-20-8
Purity:  99.56%
Synonyms: COX-189
Target:  

COX

Lumiracoxib is a potent,selective and orally active COX-2 inhibitor with a Ki value of 0.06?μM . Lumiracoxib acts as a nonselective NSAID with?anti-inflammatory, analgesic and antipyretic activities. Lumiracoxib can be used for osteoarthritis and bone cancer research .
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1
1 Cited Publications
Cat. No.: HY-B0578
CAS No.: 68767-14-6
Target:  

COX

Loxoprofen is a non-steroidal, orally active anti-inflammatory agent with analgesic and anti-pyretic properties. Loxoprofen is a nonselective COX inhibitor with IC50s of 6.5 and 13.5 μM for COX-1 and COX-2, respectively. Loxoprofen can reduce atherosclerosis and shows antitumor activity .
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1
1 Cited Publications
Cat. No.: HY-B0578A
CAS No.: 80382-23-6
Target:  

COX

Loxoprofen sodium is a non-steroidal, orally active anti-inflammatory agent with analgesic and anti-pyretic properties. Loxoprofen sodium is a nonselective COX inhibitor with IC50s of 6.5 and 13.5 μM for COX-1 and COX-2, respectively. Loxoprofen sodium can reduce atherosclerosis and shows antitumor activity .
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1
1 Cited Publications
Cat. No.: HY-B1138
CAS No.: 36330-85-5
Synonyms: CL-82204
Fenbufen (CL-82204) is an orally active non-steroidal anti-inflammatory drug (NSAID), with analgetic and antipyretic effects. Fenbufen has potent activity in a variety of animal model, including carageenin edema, UV erythema and adjuvant arthritis. Fenbufen has inhibitory activities against COX-1 and COX-2 with IC50s of 3.9 μM and 8.1 μM, respectively. Fenbufen is a caspases (caspase-1, 3, 4, 5, 9) inhibitor .
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1
1 Cited Publications
Cat. No.: HY-B0008
CAS No.: 38194-50-2
Synonyms: MK-231
Target:  

NF-κB PD-1/PD-L1

Research Areas:  

Inflammation/Immunology Cancer

Sulindac (MK-231) is an orally active nonsteroidal anti-inflammatory agent. Sulindac also is an immunomodulatory agent. Sulindac can be used for the research of arthritis of the spine, gouty arthritis and kinds of cancer including colorectal cancer (CRC) and lung cancer .
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Cat. No.: HY-B0808
CAS No.: 21256-18-8
Synonyms: Oxaprozinum; Wy21743
Target:  

COX NF-κB Akt IKK Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Oxaprozin is an orally active and potent COX inhibitor, with IC50 values of 2.2 μM for human platelet COX-1 and and 36 μM for IL-1-stimulated human synovial cell COX-2, respectively. Oxaprozin also inhibits the activation of NF-κB. Oxaprozin induces cell apoptosis. Oxaprozin shows anti-inflammatory activity. Oxaprozin-mediated inhibition of the Akt/IKK/NF-κB pathway contributes to its anti-inflammatory properties .
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Cat. No.: HY-118827
CAS No.: 71109-09-6
Purity:  99.81%
Synonyms: Quadrisol; CERM 10202; PM 150
Target:  

COX

Research Areas:  

Inflammation/Immunology

Vedaprofen (Quadrisol) is a COX-1 selective nonsteroidal anti-inflammatory agent (NSAID) for serum TxB2 and exudate PGE2 inhibition . Vedaprofen is a Escherichia coli (E. coli) sliding clamp (SC) inhibitor with the IC50 of 222 μM .
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Cat. No.: HY-135731
CAS No.: 519-98-2
Purity:  99.80%
Target:  

COX Drug Metabolite

Research Areas:  

Inflammation/Immunology

4-Methylamino antipyrine is an active metabolite of Metamizole. Metamizole is a pyrazolone non-steroidal anti-inflammatory drug (NSAID) and inhibits COX. Metamizole is an nonopioid analgesic agent and can be used for pain and fever . 4-Methylamino antipyrine has analgesic, antipyretic, and relatively weak antiinflammatory properties .
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Cat. No.: HY-17361
CAS No.: 30544-47-9
Target:  

COX

Research Areas:  

Inflammation/Immunology

Etofenamate, a non-steroid anti-inflammatory agent (NSAID) and a non-selective COX inhibitor, possesses analgesic, anti-rheumatic, antipyretic and anti-inflammatory properties. Etofenamate is used in the research for osteoarthritis, arthritis and other inflammatory diseases .
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Cat. No.: HY-108596
CAS No.: 18200-13-0
Purity:  99.81%
Target:  

Potassium Channel

Research Areas:  

Inflammation/Immunology

BL-1249 is a nonsteroidal anti-inflammatory agent (NSAID) and a potassium channel activator. BL-1249 potently activates K2P2.1 (TREK-1) and K2P10.1 (TREK-2) with EC50 values of 5.5 μM and 8.0 μM, respectively. BL-1249 extracellular application activates all TREK subfamily members but has no effect on other K2P subfamilies. BL-1249 exhibits more selective for the bladder (EC50 of 1.26 μM) than vascular tissue (EC50 of 21.0 μM) .
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Cat. No.: HY-16726
CAS No.: 301692-76-2
Synonyms: CG100649
Target:  

COX Carbonic Anhydrase

Research Areas:  

Cancer

Polmacoxib (CG100649) is a first-in-class, orally active nonsteroidal anti-inflammatory agent (NSAID) which is a dual inhibitor of COX-2 (IC50 around 0.1 μg/ml) and carbonic anhydrase . Polmacoxib inhibits colorectal adenoma and tumor growth in mouse models .
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Cat. No.: HY-N7133
CAS No.: 537-67-7
Synonyms: N-Phenylaniline hydrochloride
Diphenylamine hydrochloride (N-Phenylaniline hydrochloride) is an antihyperglycemic agent with oral activity and a common structure in non-steroidal anti-inflammatory drugs (NSAIDs) that uncouples oxidative phosphorylation in mitochondria, leading to a decrease in hepatic cell ATP levels and causing liver cell damage. Diphenylamine hydrochloride is also an industrial antioxidant, a dyeing mordant, and is used in agriculture as an antifungal and antibacterial agent .
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