U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of NCX-4016

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

HIDE SMILES / InChI
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

Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
161.94 ng/mL
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

AUC

ValueDoseCo-administeredAnalytePopulation
784.85 ng × h/mL
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

T1/2

ValueDoseCo-administeredAnalytePopulation
3.1 h
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

PubMed

TitleDatePubMed
Nitric oxide-releasing aspirin inhibits vasoconstriction in perfused tail artery of normotensive and spontaneously hypertensive rats.
2003 Sep 5
Nitric oxide-releasing aspirin derivative, NCX 4016, promotes reparative angiogenesis and prevents apoptosis and oxidative stress in a mouse model of peripheral ischemia.
2004 Nov
Nitroaspirin plus clopidogrel versus aspirin plus clopidogrel against platelet thromboembolism and intimal thickening in mice.
2005 Mar
NO-donating aspirin inhibits both the expression and catalytic activity of inducible nitric oxide synthase in HT-29 human colon cancer cells.
2005 Oct 1
NO-releasing aspirin exerts stronger growth inhibitory effect on Barrett's adenocarcinoma cells than traditional aspirin.
2006 Dec
Nitric oxide-releasing aspirin and indomethacin are potent inhibitors against colon cancer in azoxymethane-treated rats: effects on molecular targets.
2006 Jun
Nitro-aspirin inhibits MCF-7 breast cancer cell growth: effects on COX-2 expression and Wnt/beta-catenin/TCF-4 signaling.
2009 Nov 15
Hyperglycemia-induced platelet activation in type 2 diabetes is resistant to aspirin but not to a nitric oxide-donating agent.
2010 Jun
NCX-1000, a nitric oxide-releasing derivative of UDCA, does not decrease portal pressure in patients with cirrhosis: results of a randomized, double-blind, dose-escalating study.
2010 May
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
Nitro-aspirin is a potential therapy for non alcoholic fatty liver disease.
2011 Jun 1
Nitric oxide-releasing aspirin but not conventional aspirin improves healing of experimental colitis.
2011 Sep 28
Patents

Sample Use Guides

NCX-4016 800 mg b.i.d. for 6 months on top of aspirin 100 mg o.d.
Route of Administration: Oral
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.
Name Type Language
NCX-4016
Common Name English
2-(ACETYLOXY)-(3-(NITROXYMETHYL)PHENYL)BENZOIC ACID
Common Name English
BENZOIC ACID, 2-(ACETYLOXY)-, 3-((NITROOXY)METHYL)PHENYL ESTER
Common Name English
NITROASPIRIN
Common Name English
Code System Code Type Description
DRUG BANK
DB12445
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY
NCI_THESAURUS
C61499
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID60938618
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY
PUBCHEM
119032
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY
FDA UNII
EH04H13L6B
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY
CAS
175033-36-0
Created by admin on Fri Dec 15 15:59:50 GMT 2023 , Edited by admin on Fri Dec 15 15:59:50 GMT 2023
PRIMARY