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

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H12N2O3.C10H21N
Molecular Weight 387.5157
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BARBEXACLONE

SMILES

CN[C@@H](C)CC1CCCCC1.CCC2(C(=O)NC(=O)NC2=O)C3=CC=CC=C3

InChI

InChIKey=MJCBWPMBFCUHBP-NPULLEENSA-N
InChI=1S/C12H12N2O3.C10H21N/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16;1-9(11-2)8-10-6-4-3-5-7-10/h3-7H,2H2,1H3,(H2,13,14,15,16,17);9-11H,3-8H2,1-2H3/t;9-/m.0/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
BARBEXACLONE
INN   MART.   WHO-DD  
INN  
Official Name English
BARBEXACLONE [MART.]
Common Name English
PROPYLHEXEDRINE L-FORM ETHYLPHENYLBARBITURATE [MI]
Common Name English
MALIASIN
Brand Name English
(-)-N,A-DIMETHYLCYCLOHEXANEETHYLAMINE COMPOUND WITH 5-ETHYL-5-PHENYLBARBITURIC ACID
Common Name English
barbexaclone [INN]
Common Name English
Barbexaclone [WHO-DD]
Common Name English
PROPYLHEXEDRINE L-FORM ETHYLPHENYLBARBITURATE
MI  
Common Name English
Classification Tree Code System Code
WHO-ATC N03AA04
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
WHO-VATC QN03AA04
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
NCI_THESAURUS C264
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
Code System Code Type Description
EVMPD
SUB06101MIG
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
MERCK INDEX
m9242
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY Merck Index
PUBCHEM
71196
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
WIKIPEDIA
BARBEXACLONE
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
EPA CompTox
DTXSID90195974
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
ECHA (EC/EINECS)
224-504-7
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
NCI_THESAURUS
C77998
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
FDA UNII
291GX1YB65
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
DRUG BANK
DB09001
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
DRUG CENTRAL
4345
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
MESH
C011019
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
RXCUI
46795
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY RxNorm
SMS_ID
100000088428
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
CAS
4388-82-3
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
INN
1982
Created by admin on Fri Dec 15 15:29:02 UTC 2023 , Edited by admin on Fri Dec 15 15:29:02 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of PHENOBARBITAL
PARENT (SALT/SOLVATE)
Structure of LEVOPROPYLHEXEDRINE
SUBSTANCE RECORD
Structure of BARBEXACLONE
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