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Details

Stereochemistry RACEMIC
Molecular Formula C14H19NO2
Molecular Weight 233.3062
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Hydroxetamine

SMILES

CCNC1(CCCCC1=O)C2=CC(O)=CC=C2

InChI

InChIKey=CQERUJSORROCGH-UHFFFAOYSA-N
InChI=1S/C14H19NO2/c1-2-15-14(9-4-3-8-13(14)17)11-6-5-7-12(16)10-11/h5-7,10,15-16H,2-4,8-9H2,1H3

HIDE SMILES / InChI

Molecular Formula C14H19NO2
Molecular Weight 233.3062
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 Sat Dec 16 19:56:22 GMT 2023
Edited
by admin
on Sat Dec 16 19:56:22 GMT 2023
Record UNII
JQ2YE6NTZ8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Hydroxetamine
Common Name English
Cyclohexanone, 2-(ethylamino)-2-(3-hydroxyphenyl)-
Systematic Name English
O-Desmethylmethoxetamine
Common Name English
3'-Hydroxy-2-oxo-PCE
Common Name English
HXE
Common Name English
2-(Ethylamino)-2-(3-hydroxyphenyl)cyclohexan-1-one
Systematic Name English
Code System Code Type Description
FDA UNII
JQ2YE6NTZ8
Created by admin on Sat Dec 16 19:56:22 GMT 2023 , Edited by admin on Sat Dec 16 19:56:22 GMT 2023
PRIMARY
CAS
1620054-73-0
Created by admin on Sat Dec 16 19:56:22 GMT 2023 , Edited by admin on Sat Dec 16 19:56:22 GMT 2023
PRIMARY
PUBCHEM
163192347
Created by admin on Sat Dec 16 19:56:22 GMT 2023 , Edited by admin on Sat Dec 16 19:56:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID001336931
Created by admin on Sat Dec 16 19:56:22 GMT 2023 , Edited by admin on Sat Dec 16 19:56:22 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
TARGET -> INHIBITOR
Related Record Type Details
PARENT -> METABOLITE ACTIVE
Related Record Type Details
ACTIVE MOIETY