U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry RACEMIC
Molecular Formula C13H16N2O2S
Molecular Weight 264.343
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIALBARBITAL

SMILES

C=CCC2(C1CCCC=C1)C(=O)NC(=S)NC2=O

InChI

InChIKey=PXLVRFQEBVNJOH-UHFFFAOYSA-N
InChI=1S/C13H16N2O2S/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2,4,6,9H,1,3,5,7-8H2,(H2,14,15,16,17,18)

HIDE SMILES / InChI

Molecular Formula C13H16N2O2S
Molecular Weight 264.343
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

THIALBARBITAL is a barbiturate derivative with sedative effects. Barbiturates have hypnotic properties and are used as active moiety on central nervous system. Thialbarbital was synthesized in the 1960s. It was used primarily as a surgical anesthesia. Thialbarbital causes marked depression of the activity of the reticular formation and only slight depression of cortical activity. Thialbarbital is short acting and has less of a tendency to induce respiratory depression than other barbiturate derivatives such as pentobarbital.

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:42:21 GMT 2025
Edited
by admin
on Wed Apr 02 09:42:21 GMT 2025
Record UNII
ENV72C33QD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIALBARBITAL [MI]
Preferred Name English
THIALBARBITAL
INN   MI   WHO-DD  
INN  
Official Name English
THIALBARBITONE
Common Name English
Thialbarbital [WHO-DD]
Common Name English
5-ALLYL-5-(2-CYCLOHEXEN-1-YL)-2-THIOBARBITURIC ACID
Systematic Name English
thialbarbital [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67084
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
Code System Code Type Description
CAS
467-36-7
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104657
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
SMS_ID
100000082396
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
INN
14
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
EVMPD
SUB10966MIG
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
DRUG CENTRAL
3595
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
FDA UNII
ENV72C33QD
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID90861960
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
NCI_THESAURUS
C77631
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
PUBCHEM
3032306
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-390-3
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY
MERCK INDEX
m10714
Created by admin on Wed Apr 02 09:42:21 GMT 2025 , Edited by admin on Wed Apr 02 09:42:21 GMT 2025
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY