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Details

Stereochemistry RACEMIC
Molecular Formula C11H12N2S
Molecular Weight 204.291
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRAMISOLE

SMILES

C1CN2CC(N=C2S1)C3=CC=CC=C3

InChI

InChIKey=HLFSDGLLUJUHTE-UHFFFAOYSA-N
InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2

HIDE SMILES / InChI

Molecular Formula C11H12N2S
Molecular Weight 204.291
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:59:00 UTC 2023
Edited
by admin
on Fri Dec 15 17:59:00 UTC 2023
Record UNII
C8M7RFE4NO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TETRAMISOLE
INN   WHO-DD  
INN  
Official Name English
ASCAVERM
Brand Name English
Tetramisole [WHO-DD]
Common Name English
TETRAMIZOLE
Common Name English
(±)-2,3,5,6-TETRAHYDRO-6-PHENYLIMIDAZO(2,1-B)THIAZOLE
Systematic Name English
LEVAMISOLE DL-FORM
MI  
Common Name English
R-8299
Code English
tetramisole [INN]
Common Name English
LEVAMISOLE DL-FORM [MI]
Common Name English
NSC-102063
Code English
Classification Tree Code System Code
WHO-VATC QP52AE52
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
WHO-VATC QP52AE02
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
NCI_THESAURUS C2141
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
Code System Code Type Description
MESH
D013773
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
CHEBI
77289
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
PUBCHEM
3913
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
FDA UNII
C8M7RFE4NO
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
ChEMBL
CHEMBL277775
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
INN
1973
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
CAS
5036-02-2
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
MERCK INDEX
m6781
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY Merck Index
EVMPD
SUB10945MIG
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
SMS_ID
100000082718
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
ECHA (EC/EINECS)
225-729-3
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
EPA CompTox
DTXSID20860143
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
NSC
102063
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
NCI_THESAURUS
C95050
Created by admin on Fri Dec 15 17:59:00 UTC 2023 , Edited by admin on Fri Dec 15 17:59:00 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY