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Details

Stereochemistry RACEMIC
Molecular Formula C14H18F3NO
Molecular Weight 273.294
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXAFLOZANE

SMILES

CC(C)N1CCOC(C1)C2=CC(=CC=C2)C(F)(F)F

InChI

InChIKey=FVYUQFQCEOZYHZ-UHFFFAOYSA-N
InChI=1S/C14H18F3NO/c1-10(2)18-6-7-19-13(9-18)11-4-3-5-12(8-11)14(15,16)17/h3-5,8,10,13H,6-7,9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H18F3NO
Molecular Weight 273.294
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Oxaflozane is non-tricyclic antidepressant with serotoninergic action. In animals, oxaflozane has anti-cataleptic and anti-aggressive action with weak potentiation of stereotypes provoked by amphetamine. Oxaflozane was developed by Solvay Pharma and marketed in France under tradename Conflictan. The drug was discontinued in 2004.

Approval Year

PubMed

PubMed

TitleDatePubMed
Oxaflozane overdose in a child.
1992
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:00:31 UTC 2023
Edited
by admin
on Fri Dec 15 19:00:31 UTC 2023
Record UNII
V4WLW77V5Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXAFLOZANE
INN   MI   WHO-DD  
INN  
Official Name English
Oxaflozane [WHO-DD]
Common Name English
MORPHOLINE, 4-(1-METHYLETHYL)-2-(3-(TRIFLUOROMETHYL)PHENYL)-
Systematic Name English
oxaflozane [INN]
Common Name English
OXAFLOZANE [MI]
Common Name English
4-ISOPROPYL-2-(.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-M-TOLYL)MORPHOLINE
Systematic Name English
Classification Tree Code System Code
WHO-ATC N06AX10
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
NCI_THESAURUS C265
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
WHO-VATC QN06AX10
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
Code System Code Type Description
CAS
26629-87-8
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
INN
3044
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
MERCK INDEX
m861
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C75175
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
DRUG CENTRAL
2007
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106996
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
MESH
C005357
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
EVMPD
SUB09486MIG
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
FDA UNII
V4WLW77V5Q
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
ECHA (EC/EINECS)
247-855-8
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
SMS_ID
100000083559
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
DRUG BANK
DB13457
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
PUBCHEM
432824
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID50865308
Created by admin on Fri Dec 15 19:00:31 UTC 2023 , Edited by admin on Fri Dec 15 19:00:31 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY