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Details

Stereochemistry RACEMIC
Molecular Formula C16H25NO2
Molecular Weight 263.3752
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-DESMETHYLVENLAFAXINE

SMILES

CNCC(C1=CC=C(OC)C=C1)C2(O)CCCCC2

InChI

InChIKey=MKAFOJAJJMUXLW-UHFFFAOYSA-N
InChI=1S/C16H25NO2/c1-17-12-15(16(18)10-4-3-5-11-16)13-6-8-14(19-2)9-7-13/h6-9,15,17-18H,3-5,10-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H25NO2
Molecular Weight 263.3752
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
4700.0 nM [IC50]
1600.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Influence of CYP2D6 genotype on the disposition of the enantiomers of venlafaxine and its major metabolites in postmortem femoral blood.
2012-01-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:30:25 GMT 2025
Edited
by admin
on Mon Mar 31 21:30:25 GMT 2025
Record UNII
19V5EX4E8B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-DESMETHYLVENLAFAXINE
Common Name English
VENLAFAXINE RELATED COMPOUND A
USP  
Preferred Name English
VENLAFAXINE RELATED COMPOUND A [USP IMPURITY]
Common Name English
CYCLOHEXANOL, 1-(1-(4-METHOXYPHENYL)-2-(METHYLAMINO)ETHYL)-
Systematic Name English
VENLAFAXINE HYDROCHLORIDE IMPURITY D [EP IMPURITY]
Common Name English
VENLAFAXINE RELATED COMPOUND A [USP-RS]
Common Name English
NORVENLAFAXINE
Common Name English
1-((1RS)-1-(4-METHOXYPHENYL)-2-(METHYLAMINO)ETHYL)CYCLOHEXANOL
Systematic Name English
Code System Code Type Description
RS_ITEM_NUM
1711279
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
PUBCHEM
3501942
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID20881050
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
FDA UNII
19V5EX4E8B
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
CAS
149289-30-5
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
EVMPD
SUB25380
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
CHEBI
83525
Created by admin on Mon Mar 31 21:30:25 GMT 2025 , Edited by admin on Mon Mar 31 21:30:25 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY