Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H20ClN3O.ClH |
Molecular Weight | 366.285 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(C)CCCN1C(=O)N(C2=CC(Cl)=CC=C12)C3=CC=CC=C3
InChI
InChIKey=NQRQQRMSSZZIFE-UHFFFAOYSA-N
InChI=1S/C18H20ClN3O.ClH/c1-20(2)11-6-12-21-16-10-9-14(19)13-17(16)22(18(21)23)15-7-4-3-5-8-15;/h3-5,7-10,13H,6,11-12H2,1-2H3;1H
Molecular Formula | C18H20ClN3O |
Molecular Weight | 329.824 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Clodazon (AW 142446) is an antidepressant drug investigated in Germany in the 1960s. In animal models, clodazon inhibits the catalepsy induced by tetrabenazine and it potentiates the effect of catecholamines, both effects being of the order experienced with imipramine. In clinical trials, about 2/3 of the patients showed a positive antidepressive effect with few side effects.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:42:04 GMT 2023
by
admin
on
Fri Dec 15 17:42:04 GMT 2023
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Record UNII |
N0FW29BP3C
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Common Name | English |
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NCI_THESAURUS |
C265
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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Code System | Code | Type | Description | ||
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N0FW29BP3C
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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DTXSID70197698
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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C78675
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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4913-61-5
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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56841979
Created by
admin on Fri Dec 15 17:42:05 GMT 2023 , Edited by admin on Fri Dec 15 17:42:05 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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SOLVATE->ANHYDROUS | |||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |