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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
Structure of THIAZESIM HYDROCHLORIDE

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

HIDE SMILES / InChI

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

PubMed

PubMed

TitleDatePubMed
The pathology of a cross-over trial: (thiazesim--a new anti-depressant drug).
1968-02
The effects of thiazesim, LSD-25, and bilateral lesions of the amygdalae on the release of a suppressed response.
1966
Patents

Patents

Sample Use Guides

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 Mon Mar 31 18:59:39 GMT 2025
Edited
by admin
on Mon Mar 31 18:59:39 GMT 2025
Record UNII
4CIH6N1U25
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIAZESIM HYDROCHLORIDE
MI   USAN  
USAN  
Official Name English
ALTINIL
Preferred Name English
NSC-169509
Code English
THIAZESIM HYDROCHLORIDE [MI]
Common Name English
SQ-10496
Code English
5-[2-(Dimethylamino)ethyl]-2,3-dihydro-2-phenyl-1,5-benzothiazepin-4(5H)-one monohydrochloride
Systematic Name English
1,5-BENZOTHIAZEPIN-4(5H)-ONE, 5-(2-(DIMETHYLAMINO)ETHYL)-2,3-DIHYDRO-2-PHENYL-, MONOHYDROCHLORIDE
Common Name English
THIAZESIM HYDROCHLORIDE [USAN]
Common Name English
SQ 10,496
Code English
TIAZESIM HYDROCHLORIDE
Common Name English
THIAZESIM HCL
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
Code System Code Type Description
MERCK INDEX
m10727
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY Merck Index
NSC
169509
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
SMS_ID
300000055350
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
CAS
3122-01-8
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
FDA UNII
4CIH6N1U25
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
PUBCHEM
66263
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
ChEMBL
CHEMBL2111123
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
NCI_THESAURUS
C152586
Created by admin on Mon Mar 31 18:59:39 GMT 2025 , Edited by admin on Mon Mar 31 18:59:39 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY