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Details

Stereochemistry ACHIRAL
Molecular Formula C21H21ClN4O3
Molecular Weight 412.869
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NIZOFENONE

SMILES

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

InChI

InChIKey=WZGBZLHGOVJDET-UHFFFAOYSA-N
InChI=1S/C21H21ClN4O3/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/h5-13H,3-4,14H2,1-2H3

HIDE SMILES / InChI

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
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
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.
Name Type Language
NIZOFENONE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
NIZOFENONE [MART.]
Common Name English
Nizofenone [WHO-DD]
Common Name English
NIZOFENONE [JAN]
Common Name English
nizofenone [INN]
Common Name English
2'-CHLORO-2-(2-((DIETHYLAMINO)METHYL)IMIDAZOL-1-YL)-5-NITROBENZOPHENONE
Systematic Name English
NIZOFENONE [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QN06BX10
Created by admin on Fri Dec 15 16:20:08 GMT 2023 , Edited by admin on Fri Dec 15 16:20:08 GMT 2023
WHO-ATC N06BX10
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NCI_THESAURUS C1509
Created by admin on Fri Dec 15 16:20:08 GMT 2023 , Edited by admin on Fri Dec 15 16:20:08 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2106822
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PRIMARY
MERCK INDEX
m8018
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PRIMARY Merck Index
INN
4940
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WIKIPEDIA
NIZOFENONE
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DRUG BANK
DB13546
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FDA UNII
7A2NOC3R88
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SMS_ID
100000083582
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NCI_THESAURUS
C76783
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DRUG CENTRAL
1956
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EPA CompTox
DTXSID401014745
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PUBCHEM
4514
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MESH
C016910
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EVMPD
SUB09336MIG
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CAS
54533-85-6
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