Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H13NO7 |
Molecular Weight | 331.2769 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)OC1=CC=CC=C1C(=O)OC2=CC(CO[N+]([O-])=O)=CC=C2
InChI
InChIKey=IOJUJUOXKXMJNF-UHFFFAOYSA-N
InChI=1S/C16H13NO7/c1-11(18)23-15-8-3-2-7-14(15)16(19)24-13-6-4-5-12(9-13)10-22-17(20)21/h2-9H,10H2,1H3
NCX-4016, a nitric oxide non-steroidal anti-inflammatory drug (NO-NSAID) which can inhibit cyclooxygenase as well as release nitric oxide, is under development by NicOx as a potential treatment for thrombosis, inflammation and rheumatoid arthritis. NCX-4016 possesses a broad spectrum of antithrombotic and antiinflammatory activities. NCX-4016 has been shown to inhibit platelet activation in vitro more effectively than aspirin, to inhibit smooth muscle cell proliferation, to exert an endothelial cell protective activity and to suppress the function of several inflammatory cells potentially involved in atherothrombosis. In animal models, NCX-4016 protected from platelet thromboembolism, prevented restenosis in atherosclerosis-prone animals, protected the heart from ischemia/reperfusion injury, and induced neoangiogenesis in critically ischemic limbs. Moreover, it displayed little or no gastric toxicity and appeared to protect stomach from noxious stimuli, including aspirin. NCX-4016 has been evaluated in healthy volunteers and found to inhibit platelet cyclo-oxygenase-1 (COX-1) similarly to or slightly less than aspirin, to raise the circulating levels of NO-degradation products, and to have little or no gastric toxicity in short term studies. NCX-4016 was in Phase II clinical trials for the treatment of vascular disorders such as peripheral vascular disease and other cardiovascular diseases including thrombosis, complications of endothelium-related diseases such as diabetes and other. But this research was discontinued.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL221 |
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Target ID: GO:0070527 |
39.0 µM [IC50] | ||
Target ID: GO:0038193 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8950792 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
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161.94 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15063462 |
1600 mg single, oral dose: 1600 mg route of administration: Oral experiment type: SINGLE co-administered: |
NCX 4015 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
784.85 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15063462 |
1600 mg single, oral dose: 1600 mg route of administration: Oral experiment type: SINGLE co-administered: |
NCX 4015 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
3.1 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15063462 |
1600 mg single, oral dose: 1600 mg route of administration: Oral experiment type: SINGLE co-administered: |
NCX 4015 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
PubMed
Title | Date | PubMed |
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Nitric oxide-releasing aspirin inhibits vasoconstriction in perfused tail artery of normotensive and spontaneously hypertensive rats. | 2003 Sep 5 |
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NO-releasing aspirin exerts stronger growth inhibitory effect on Barrett's adenocarcinoma cells than traditional aspirin. | 2006 Dec |
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Nitric oxide-donating aspirin inhibits colon cancer cell growth via mitogen-activated protein kinase activation. | 2006 Jan |
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Nitric oxide-releasing aspirin and indomethacin are potent inhibitors against colon cancer in azoxymethane-treated rats: effects on molecular targets. | 2006 Jun |
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Cardioprotective effects of nitric oxide-aspirin in myocardial ischemia-reperfused rats. | 2007 Sep |
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Hyperglycemia-induced platelet activation in type 2 diabetes is resistant to aspirin but not to a nitric oxide-donating agent. | 2010 Jun |
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NO-donating aspirin and aspirin partially inhibit age-related atherosclerosis but not radiation-induced atherosclerosis in ApoE null mice. | 2010 Sep 21 |
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Nitric oxide (NO)-releasing aspirin exhibits a potent esophagoprotection in experimental model of acute reflux esophagitis. Role of nitric oxide and proinflammatory cytokines. | 2011 Feb |
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Nitro-aspirin is a potential therapy for non alcoholic fatty liver disease. | 2011 Jun 1 |
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Nitric oxide-releasing aspirin but not conventional aspirin improves healing of experimental colitis. | 2011 Sep 28 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01256775
NCX-4016 800 mg b.i.d. for 6 months on top of aspirin 100 mg o.d.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12738997
Cytostatic activity was observed after a 24-h NCX-4016 exposure and 50% growth inhibition was reached at concentrations ranging from 165 to 250 uM in all human colon adenocarcinoma cell lines.
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ACTIVE MOIETY
METABOLITE (PARENT)