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Details

Stereochemistry RACEMIC
Molecular Formula C9H14N2O
Molecular Weight 166.2203
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENOXYPROPAZINE

SMILES

CC(COC1=CC=CC=C1)NN

InChI

InChIKey=QNEXFJFTGQBXBJ-UHFFFAOYSA-N
InChI=1S/C9H14N2O/c1-8(11-10)7-12-9-5-3-2-4-6-9/h2-6,8,11H,7,10H2,1H3

HIDE SMILES / InChI

Molecular Formula C9H14N2O
Molecular Weight 166.2203
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Phenoxypropazine is a monoamine oxidase inhibitor. It was used in the treatment of depression. Phenoxypropazine was introduced in 1961 and withdrawn after 5 years on the market due to dose- and time-unrelated liver damage not identified in animal experiments.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.01 mM [Ki]
PubMed

PubMed

TitleDatePubMed
A preliminary study of phenoxypropazine in the treatment of depression.
1963 Apr
Preliminary report on phenoxypropazine.
1963 May
A COMPARISON OF PHENOXYPROPAZINE AND AMYTRYPTILINE IN DEPRESSION.
1963 Oct

Sample Use Guides

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:26:49 UTC 2023
Edited
by admin
on Fri Dec 15 16:26:49 UTC 2023
Record UNII
8E92V52324
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENOXYPROPAZINE
INN  
INN  
Official Name English
PHENOXYPROPAZINE [MI]
Common Name English
(1-METHYL-2-PHENOXYETHYL)HYDRAZINE
Systematic Name English
PHENOXYPROPAZINE
MI  
Common Name English
fenoxypropazine [INN]
Common Name English
HYDRAZINE, (1-METHYL-2-PHENOXYETHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C667
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
Code System Code Type Description
CAS
3818-37-9
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID1048837
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
NCI_THESAURUS
C72827
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
ChEMBL
CHEMBL1909286
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
PUBCHEM
71467
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
SMS_ID
100000081284
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
DRUG BANK
DB09251
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
EVMPD
SUB07583MIG
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
MERCK INDEX
m885
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY Merck Index
FDA UNII
8E92V52324
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
WIKIPEDIA
Phenoxypropazine
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
INN
1235
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
DRUG CENTRAL
3814
Created by admin on Fri Dec 15 16:26:49 UTC 2023 , Edited by admin on Fri Dec 15 16:26:49 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY