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
SMILES
OC(=O)\C=C\C(O)=O.CCN(CC)CC1=NC=CN1C2=CC=C(C=C2C(=O)C3=CC=CC=C3Cl)[N+]([O-])=O
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+
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/8110594Curator's Comment: Description was created based on several sources, including
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8110594
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.
CNS Activity
Originator
Sources: http://docslide.us/documents/pp8launch19951997.html
Curator's Comment: Eli Lilly launched nizofenone in 1995 # Eli Lilly
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Prostacyclin synthesis Sources: https://www.ncbi.nlm.nih.gov/pubmed/6431991 |
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Target ID: Peroxidative disintegration of mitochondria Sources: https://www.ncbi.nlm.nih.gov/pubmed/7320731 |
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Target ID: Thromboxane A2 biosynthesis Sources: http://www.genome.jp/dbget-bin/www_bget?D01465 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nizofenone, a neuroprotective drug, suppresses glutamate release and lactate accumulation. | 1994-09-01 |
|
| Biphasic liberation of arachidonic and stearic acids during cerebral ischemia. | 1985-07 |
|
| [Effects of nizofenone on the action potential of guinea-pig papillary muscle and S-A node and dog Purkinje fibers]. | 1985-03 |
|
| [Effect of nizofenone on pyramidal response, electrocorticogram and regional cerebral blood flow following recirculation after complete global brain ischemia in cats]. | 1984-12 |
|
| [An experimental study on the protective effect of nizofenone in cerebral ischemia]. | 1984-11 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6519584
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3219485
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.
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CHEMBL2106822
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100000085720
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SUB03448MIG
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315856
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m8018
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PRIMARY | Merck Index |
ACTIVE MOIETY
SUBSTANCE RECORD