U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C11H18N2O3
Molecular Weight 226.2722
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMOBARBITAL

SMILES

CCC1(CCC(C)C)C(=O)NC(=O)NC1=O

InChI

InChIKey=VIROVYVQCGLCII-UHFFFAOYSA-N
InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)

HIDE SMILES / InChI
Molecular Formula C11H18N2O3
Molecular Weight 226.2722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:04 UTC 2023
Edited
by admin
on Fri Dec 15 15:01:04 UTC 2023
Record UNII
GWH6IJ239E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMOBARBITAL
EP   HSDB   INN   MART.   MI   VANDF   WHO-DD  
INN  
Official Name English
amobarbital [INN]
Common Name English
ISOMYTAL
Brand Name English
AMOBARBITAL [VANDF]
Common Name English
AMOBARBITAL [MART.]
Common Name English
AMOBARBITAL [JAN]
Common Name English
AMOBARBITAL CII [USP-RS]
Common Name English
5-Ethyl-5-isopentylbarbituric acid
Systematic Name English
Amobarbital [WHO-DD]
Common Name English
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-ETHYL-5-(3-METHYLBUTYL)-
Systematic Name English
AMOBARBITAL [EP IMPURITY]
Common Name English
NSC-10815
Code English
AMOBARBITAL CII
USP-RS  
Common Name English
AMYTAL
Brand Name English
AMOBARBITAL [HSDB]
Common Name English
AMOBARBITAL [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QN05CA02
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
NCI_THESAURUS C67084
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
WHO-ATC N05CA02
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
DEA NO. 2125
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
LIVERTOX 46
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
Code System Code Type Description
FDA UNII
GWH6IJ239E
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
RXCUI
719
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY RxNorm
MESH
D000654
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
DRUG BANK
DB01351
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-330-7
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
DRUG CENTRAL
184
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
DAILYMED
GWH6IJ239E
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
INN
1111
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
CAS
57-43-2
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
SMS_ID
100000087425
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
PUBCHEM
2164
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
CHEBI
2673
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
EPA CompTox
DTXSID9020081
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
HSDB
3286
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
EVMPD
SUB05468MIG
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
RS_ITEM_NUM
1030001
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
WIKIPEDIA
AMOBARBITAL
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
ChEMBL
CHEMBL267894
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
NSC
10815
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
MERCK INDEX
m1837
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C76523
Created by admin on Fri Dec 15 15:01:04 UTC 2023 , Edited by admin on Fri Dec 15 15:01:04 UTC 2023
PRIMARY
Related Record Type Details
Structure of AMOBARBITAL SODIUM
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of AMOBARBITAL
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966