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Details

Stereochemistry RACEMIC
Molecular Formula C14H18F3NO.ClH
Molecular Weight 309.755
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXAFLOZANE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=XYYSVSLSSDHEGA-UHFFFAOYSA-N
InChI=1S/C14H18F3NO.ClH/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;1H

HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
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 ( + / - )

Description

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

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Oxaflozane overdose in a child.
1992
Patents

Patents

JP2011526251A
112
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:06:11 GMT 2025
Edited
by admin
on Mon Mar 31 20:06:11 GMT 2025
Record UNII
E10FW59D1I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CONFLICTAN
Preferred Name English
OXAFLOZANE HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
1766CERM
Code English
((3-TRIFLUOROMETHYL)PHENYL)-4-ISOPROPYLTETRAHYDRO-1,4-OXAZINE HYDROCHLORIDE
Common Name English
OXAFLOZANE HYDROCHLORIDE [MI]
Common Name English
OXAFLOZANE HYDROCHLORIDE [MART.]
Common Name English
MORPHOLINE, 4-(1-METHYLETHYL)-2-(3-(TRIFLUOROMETHYL)PHENYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
CERM-1766
Code English
Oxaflozane hydrochloride [WHO-DD]
Common Name English
NSC-315281
Code English
Code System Code Type Description
ECHA (EC/EINECS)
247-854-2
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
NSC
315281
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
MERCK INDEX
m861
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY Merck Index
FDA UNII
E10FW59D1I
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
SMS_ID
100000085504
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
CAS
26629-86-7
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
EVMPD
SUB03560MIG
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
MESH
C005357
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
PUBCHEM
21124624
Created by admin on Mon Mar 31 20:06:11 GMT 2025 , Edited by admin on Mon Mar 31 20:06:11 GMT 2025
PRIMARY
Related Record Type Details
Structure of OXAFLOZANE HYDROCHLORIDE, (R)-
ENANTIOMER -> RACEMATE
Structure of OXAFLOZANE HYDROCHLORIDE, (S)-
ENANTIOMER -> RACEMATE
Structure of OXAFLOZANE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of OXAFLOZANE
ACTIVE MOIETY
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