Details
Stereochemistry | UNKNOWN |
Molecular Formula | C17H23NO.ClH |
Molecular Weight | 293.832 |
Optical Activity | ( - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(C)CCC1(C)OCCC2=C1CC3=C2C=CC=C3
InChI
InChIKey=OZWMTVPSSFWHIM-UHFFFAOYSA-N
InChI=1S/C17H23NO.ClH/c1-17(9-10-18(2)3)16-12-13-6-4-5-7-14(13)15(16)8-11-19-17;/h4-7H,8-12H2,1-3H3;1H
Molecular Formula | C17H23NO |
Molecular Weight | 257.3706 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
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 |
Pirandamine is the potential antidepressant drug. It is a relatively selective inhibitor of the serotonin uptake mechanism and does not exhibit appreciable norepinephrine uptake blocking activity in contrast to the tricyclic antidepressant drugs imipramine and amitriptyline. Pirandamine is equivalent to amitriptyline and greater than imipramine in potency as a serotonin uptake blocker and a potentiator of central serotonin pharmacological actions, and in contrast, does not exhibit appreciable central anticholinergic effects. Pirandamine potentiated the behavioral effects of 5-hydroxytryptophan in mice. Pirandamine, in contrast to desimipramine and imipramine, did not prevent reserpine-induced hypothermia. The (-)-enantiomer of pirandamine retained the activity of the racemate; the (+I-enantiomer was much less effective.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 18:27:50 GMT 2023
by
admin
on
Sat Dec 16 18:27:50 GMT 2023
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Record UNII |
6F67BUX3Z2
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Record Status |
Validated (UNII)
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Record Version |
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-
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Systematic Name | English |
Code System | Code | Type | Description | ||
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6F67BUX3Z2
Created by
admin on Sat Dec 16 18:27:50 GMT 2023 , Edited by admin on Sat Dec 16 18:27:50 GMT 2023
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60218-35-1
Created by
admin on Sat Dec 16 18:27:50 GMT 2023 , Edited by admin on Sat Dec 16 18:27:50 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |