Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H22N2OS.ClH |
| Molecular Weight | 362.917 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(C)CCN1C2=CC=CC=C2SC(CC1=O)C3=CC=CC=C3
InChI
InChIKey=IUZXQGCIJLIGLS-UHFFFAOYSA-N
InChI=1S/C19H22N2OS.ClH/c1-20(2)12-13-21-16-10-6-7-11-17(16)23-18(14-19(21)22)15-8-4-3-5-9-15;/h3-11,18H,12-14H2,1-2H3;1H
| Molecular Formula | C19H22N2OS |
| Molecular Weight | 326.456 |
| 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 |
Thiazesim (also known as ) is a benzothiazepine derivative patented by Olin Mathieson Chemical Corp. as an oral anti-depressant and tranquilizer useful in the treatment of Parkinsonism. Thiazesim is chemically related to the tranquilizing drugs chlordiazepoxide and diazepam but possesses a unique action on the limbic system, namely a selective depression of the lateral amygdaloid nucleus in experimental animals. Thiazesim shows potent anti-depressant activity in clinical trials.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4867805
100 mg. t.d.s., and increased after one week if no clinical effects had been noted
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:59:39 GMT 2025
by
admin
on
Mon Mar 31 18:59:39 GMT 2025
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| Record UNII |
4CIH6N1U25
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C265
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m10727
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169509
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3122-01-8
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4CIH6N1U25
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66263
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CHEMBL2111123
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C152586
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ACTIVE MOIETY |