Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H13N |
| Molecular Weight | 195.2597 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CC2=CC=CC=C2NC3=CC=CC=C13
InChI
InChIKey=ZSMRRZONCYIFNB-UHFFFAOYSA-N
InChI=1S/C14H13N/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)15-13/h1-8,15H,9-10H2
| Molecular Formula | C14H13N |
| Molecular Weight | 195.2597 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Iminodibenzyl is an impurity in commercial preparations of Carbamazepine. It is the final product of antidepressant imipramine oxidation. Iminodibenzyl is a building block of many antipsychotic drugs. Iminodibenzyl derivatives demonstrated anti-leishmanial activity. Iminodibenzyl, in combination with 3-methyl-2-benzothiazolinonehydrazone hydrochloride are used as chromogenic co-substrates for quantification of hydrogen peroxide and glucose.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| New iminodibenzyl derivatives with anti-leishmanial activity. | 2017-07 |
|
| Iminodibenzyl class antipsychotics for schizophrenia: a systematic review and meta-analysis of carpipramine, clocapramine, and mosapramine. | 2014 |
|
| In vitro studies of DNA damage caused by tricyclic antidepressants: a role of peroxidase in the side effects of the drugs. | 2010-09-20 |
|
| Quantification of hydrogen peroxide and glucose using 3-methyl-2-benzothiazolinonehydrazone hydrochloride with 10,11-dihydro-5H-benz(b,f)azepine as chromogenic probe. | 2009-12-15 |
|
| A TRIAL OF FOUR ANTI-DEPRESSANT DRUGS. | 1963-02-22 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:07:26 GMT 2025
by
admin
on
Mon Mar 31 18:07:26 GMT 2025
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| Record UNII |
262BX7OE3U
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| Record Status |
Validated (UNII)
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| Record Version |
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262BX7OE3U
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207-787-1
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1337004
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DTXSID8049414
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