Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H15N3O2 |
| Molecular Weight | 365.3841 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC(C#N)=C(C=C1)C2=CC(=CN(C3=CC=CC=C3)C2=O)C4=NC=CC=C4
InChI
InChIKey=LTKVPVLPRNJRJD-UHFFFAOYSA-N
InChI=1S/C23H15N3O2/c24-14-16-12-19(27)9-10-20(16)21-13-17(22-8-4-5-11-25-22)15-26(23(21)28)18-6-2-1-3-7-18/h1-13,15,27H
| Molecular Formula | C23H15N3O2 |
| Molecular Weight | 365.3841 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:39:35 GMT 2025
by
admin
on
Mon Mar 31 22:39:35 GMT 2025
|
| Record UNII |
X376H44R70
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
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X376H44R70
Created by
admin on Mon Mar 31 22:39:35 GMT 2025 , Edited by admin on Mon Mar 31 22:39:35 GMT 2025
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PRIMARY | |||
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91800174
Created by
admin on Mon Mar 31 22:39:35 GMT 2025 , Edited by admin on Mon Mar 31 22:39:35 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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PARENT -> METABOLITE INACTIVE |
In vitro studies show that the primary oxidative metabolic route of perampanel is via cytochrome P450 (CYP)3A4 and/or CYP3A5, based on the results of metabolism by recombinant human CYPs, and inhibition studies using anti-CYP3A4 and ketoconazole in human liver microsomes.
FECAL; URINE
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