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

Details

Stereochemistry ACHIRAL
Molecular Formula C17H16N2O
Molecular Weight 264.3217
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETAQUALONE

SMILES

CCC1=CC=CC=C1N2C(C)=NC3=CC=CC=C3C2=O

InChI

InChIKey=UVTJKLLUVOTSOB-UHFFFAOYSA-N
InChI=1S/C17H16N2O/c1-3-13-8-4-7-11-16(13)19-12(2)18-15-10-6-5-9-14(15)17(19)20/h4-11H,3H2,1-2H3

HIDE SMILES / InChI
Etaqualone (Aolan, Athinazone) is an analog of the hypnotic methaqualone, a non-barbiturate sedative it was developed and marked in France. Etaqualone possesses sedative and hypnotic properties and was used to treat insomnia resulting from its agonist activity at the β subtype of the GABAa receptor.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: β subtype of the GABAa receptor
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[EFFECTIVE SEDATION IN MEDICAL PRACTICE. EXPERIENCES WITH THE NEW DAYTIME SEDATIVE AOLAN].
1965 Mar 31
[On the polarography of 2-methyl-3-(2-methylphenyl)-3,4-dihydroquinazolinone-(4) methaqualone, Dormutil) and 2-methyl-3-(2-ethylphenyl-3,4-dihydroquinazolinone-(4) (ethinazone, Aolan). 5. Polarography of heterocyclic compounds].
1967 Nov

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
ETAQUALONE
INN   MI  
INN  
Official Name English
etaqualone [INN]
Common Name English
3-(O-ETHYLPHENYL)-2-METHYL-4(3H)-QUINAZOLINONE
Common Name English
ETAQUALONE [MI]
Common Name English
NSC-96163
Code English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Etaqualone
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
Code System Code Type Description
INN
2256
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
FDA UNII
HFS3HB32J7
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104633
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
SMS_ID
100000082370
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
CAS
7432-25-9
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
EVMPD
SUB07263MIG
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
MERCK INDEX
m5039
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY Merck Index
PUBCHEM
23914
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
NSC
96163
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
NCI_THESAURUS
C65554
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID60225333
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
WIKIPEDIA
Etaqualone
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY
DRUG CENTRAL
3192
Created by admin on Fri Dec 15 16:36:50 GMT 2023 , Edited by admin on Fri Dec 15 16:36:50 GMT 2023
PRIMARY