Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10ClN3S |
| Molecular Weight | 227.714 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC(Cl)=CC=C1N2CCSC2=N
InChI
InChIKey=YYPCUGJKDYEIHT-UHFFFAOYSA-N
InChI=1S/C9H10ClN3S/c10-6-1-2-8(7(11)5-6)13-3-4-14-9(13)12/h1-2,5,12H,3-4,11H2
| Molecular Formula | C9H10ClN3S |
| Molecular Weight | 227.714 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Timirdine (also known as EGY-4201) is an iminothiazolidine derivative patented by EGIS Gyogyszergyar as an antidepressant. In the behavioral despair model and in antagonizing the effect of tetrabenazine, Timirdine efficacy was considerably higher than that of several tricyclic and second-generation antidepressant drugs. Timirdine was also active in inhibiting the hypothermic effect of apomorphine. It potentiated the lethal effect of yohimbine, the hypermotility provoked by L-dopa, and the stereotypy induced by D-amphetamine. In contrast to amitriptyline and nomifensine, Timirdine showed neither sedative nor stimulant actions on spontaneous and conditioned behavior.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:07:55 GMT 2025
by
admin
on
Mon Mar 31 18:07:55 GMT 2025
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| Record UNII |
3I3H31VAS6
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English |
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NCI_THESAURUS |
C29710
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DTXSID40869350
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CHEMBL2107484
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100417-09-2
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3I3H31VAS6
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100000077204
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3063289
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SUB11066MIG
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C76452
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6532
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |