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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

Description

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.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
39.0 µM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown
Primary
Unknown
Primary
Unknown

Cmax

ValueDoseCo-administeredAnalytePopulation
161.94 ng/mL
1600 mg single, oral
NCX-4015 plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
784.85 ng × h/mL
1600 mg single, oral
NCX-4015 plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
3.1 h
1600 mg single, oral
NCX-4015 plasma
Homo sapiens

PubMed

Sample Use Guides

In Vivo Use Guide
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
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.