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=C(NC3=C1C=CC=C3)C=CC=C2
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 |
---|---|---|
In vitro studies of DNA damage caused by tricyclic antidepressants: a role of peroxidase in the side effects of the drugs. | 2010 Sep 20 |
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Iminodibenzyl class antipsychotics for schizophrenia: a systematic review and meta-analysis of carpipramine, clocapramine, and mosapramine. | 2014 |
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New iminodibenzyl derivatives with anti-leishmanial activity. | 2017 Jul |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:45:08 GMT 2023
by
admin
on
Fri Dec 15 15:45:08 GMT 2023
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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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