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

Details

Stereochemistry ACHIRAL
Molecular Formula C21H21ClN4O3.C4H4O4
Molecular Weight 528.942
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NIZOFENONE FUMARATE

SMILES

OC(=O)\C=C\C(O)=O.CCN(CC)CC1=NC=CN1C2=C(C=C(C=C2)[N+]([O-])=O)C(=O)C3=C(Cl)C=CC=C3

InChI

InChIKey=JDQAUUIBFFFOOV-WLHGVMLRSA-N
InChI=1S/C21H21ClN4O3.C4H4O4/c1-3-24(4-2)14-20-23-11-12-25(20)19-10-9-15(26(28)29)13-17(19)21(27)16-7-5-6-8-18(16)22;5-3(6)1-2-4(7)8/h5-13H,3-4,14H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1+

HIDE SMILES / InChI

Molecular Formula C21H21ClN4O3
Molecular Weight 412.869
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including

Nizofenone (Ekonal, Midafenone) is a neuroprotective drug which protects neurons from death following cerebral anoxia (interruption of oxygen supply to the brain). It might thus be useful in the treatment of acute neurological conditions such as stroke. Nizofenone ameliorates various pathophysiologic events during ischemia, such as ATP depletion, lactate accumulation, glutamate release, free fatty acid liberation, edema, and neuronal degeneration; in particular, ischemia-induced excessive glutamate release has been completely blocked by this drug. This drug has also radical-scavenging action, comparable to vitamin E, and inhibits oxygen radical-induced lipid peroxidation. The potent cerebroprotective effect of nizofenone has been demonstrated in various experimental models of cerebral hypoxia, ischemia (focal and global), ischemia-reperfusion, and infarction. The clinical efficacy of nizofenone has been proved by pioneering double-blind studies in acute subarachnoid hemorrhage patients. Nizofenone is clinically used for preventing the delayed ischemic neurologic deficits due to late vasospasm following subarachnoid hemorrhage.

Originator

Curator's Comment: Eli Lilly launched nizofenone in 1995 # Eli Lilly

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Prostacyclin synthesis
Target ID: Peroxidative disintegration of mitochondria
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Effect of nizofenone on pyramidal response, electrocorticogram and regional cerebral blood flow following recirculation after complete global brain ischemia in cats].
1984 Dec
[An experimental study on the protective effect of nizofenone in cerebral ischemia].
1984 Nov
Biphasic liberation of arachidonic and stearic acids during cerebral ischemia.
1985 Jul
[Effects of nizofenone on the action potential of guinea-pig papillary muscle and S-A node and dog Purkinje fibers].
1985 Mar
Nizofenone, a neuroprotective drug, suppresses glutamate release and lactate accumulation.
1994 Sep 1
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: In humans: two ampules of the test drug were given three times a day for 2 weeks beginning on the day of admission. Drug administration was either by intravenous drip infusion with I00 ml of an electrolytic solution or by slow intravenous injection with 20 ml of the same solution. https://www.ncbi.nlm.nih.gov/pubmed/3512795
Nizofenone (1 mg/kg, i.v.) - to treat brain ischemia in cats
Route of Administration: Intravenous
In Vitro Use Guide
In spontaneously firing pacemaker cells, nizofenone (above 1 uM) decreased the heart rate. Above 3 uM, nizofenone reduced the maximum upstroke velocity, the amplitude of the action potential and the slope of the phase 4 depolarization, and prolonged the action potential duration at 50% repolarization in rabbit sino-atrial node.
Substance Class Chemical
Created
by admin
on Sat Dec 16 00:44:04 GMT 2023
Edited
by admin
on Sat Dec 16 00:44:04 GMT 2023
Record UNII
1I1Z517Z3Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NIZOFENONE FUMARATE
MI   WHO-DD  
Common Name English
Y-9179
Code English
NIZOFENONE FUMARATE [JAN]
Common Name English
1-(2-(2-CHLOROBENZOYL)-4-NITROPHENYL)-2-(DIETHYLAMINOMETHYL)IMIDAZOLE FUMARATE
Systematic Name English
Nizofenone fumarate [WHO-DD]
Common Name English
NSC-315856
Code English
METHANONE, (2-CHLOROPHENYL)(2-(2-((DIETHYLAMINO)METHYL)-1H-IMIDAZOL-1-YL)-5-NITROPHENYL)-, (2E)-2-BUTENEDIOATE (1:1)
Systematic Name English
EKONAL
Brand Name English
NIZOFENONE FUMARATE [MI]
Common Name English
MIDAFENONE
Brand Name English
Code System Code Type Description
ChEMBL
CHEMBL2106822
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
SMS_ID
100000085720
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
CAS
54533-86-7
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
FDA UNII
1I1Z517Z3Y
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
PUBCHEM
5282422
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID5048637
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
EVMPD
SUB03448MIG
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
NSC
315856
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY
MERCK INDEX
m8018
Created by admin on Sat Dec 16 00:44:04 GMT 2023 , Edited by admin on Sat Dec 16 00:44:04 GMT 2023
PRIMARY Merck Index
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY