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=C1)C2=CN(C3=CC=CC=C3)C(=O)C(=C2)C4=CC=CC=C4C#N
InChI
InChIKey=ANABGQBVYPBTIS-UHFFFAOYSA-N
InChI=1S/C23H15N3O2/c24-13-16-6-4-5-9-20(16)21-12-17(22-11-10-19(27)14-25-22)15-26(23(21)28)18-7-2-1-3-8-18/h1-12,14-15,27H
| 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
Sat Dec 16 09:22:20 UTC 2023
by
admin
on
Sat Dec 16 09:22:20 UTC 2023
|
| Record UNII |
3A2H7791I2
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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380919-57-3
Created by
admin on Sat Dec 16 09:22:20 UTC 2023 , Edited by admin on Sat Dec 16 09:22:20 UTC 2023
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22319219
Created by
admin on Sat Dec 16 09:22:20 UTC 2023 , Edited by admin on Sat Dec 16 09:22:20 UTC 2023
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3A2H7791I2
Created by
admin on Sat Dec 16 09:22:20 UTC 2023 , Edited by admin on Sat Dec 16 09:22:20 UTC 2023
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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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