Details
| Stereochemistry | MIXED |
| Molecular Formula | C15H12N2O2 |
| Molecular Weight | 252.268 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)N1C2=CC=CC=C2C3OC3C4=CC=CC=C14
InChI
InChIKey=ZRWWEEVEIOGMMT-UHFFFAOYSA-N
InChI=1S/C15H12N2O2/c16-15(18)17-11-7-3-1-5-9(11)13-14(19-13)10-6-2-4-8-12(10)17/h1-8,13-14H,(H2,16,18)
| Molecular Formula | C15H12N2O2 |
| Molecular Weight | 252.268 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The influence of food on the bioavailability of a twice-daily controlled release carbamazepine formulation. | 2001 Feb |
|
| Reanalysis of carbamazepine and carbamazepine-epoxide pharmacokinetics after multiple dosing of extended release formulation. | 2002 May-Aug |
|
| Administration of Carbatrol to children with feeding tubes. | 2002 Sep |
|
| Haplotype structures of EPHX1 and their effects on the metabolism of carbamazepine-10,11-epoxide in Japanese epileptic patients. | 2005 Mar |
|
| Transitional polytherapy: tricks of the trade for monotherapy to monotherapy AED conversions. | 2009 Jun |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Oct 22 15:04:17 UTC 2019
by
admin
on
Tue Oct 22 15:04:17 UTC 2019
|
| Record UNII |
QC9505F279
|
| Record Status |
Validated (UNII)
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| Record Version |
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Created by
admin on Tue Oct 22 15:04:18 UTC 2019 , Edited by admin on Tue Oct 22 15:04:18 UTC 2019
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2555
Created by
admin on Tue Oct 22 15:04:18 UTC 2019 , Edited by admin on Tue Oct 22 15:04:18 UTC 2019
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| Related Record | Type | Details | ||
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BINDER->LIGAND |
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PARENT -> METABOLITE ACTIVE |
