U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C23H29NO3
Molecular Weight 367.4813
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENOPERIDINE

SMILES

CCOC(=O)C1(CCN(CCC(O)C2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=IPOPQVVNCFQFRK-UHFFFAOYSA-N
InChI=1S/C23H29NO3/c1-2-27-22(26)23(20-11-7-4-8-12-20)14-17-24(18-15-23)16-13-21(25)19-9-5-3-6-10-19/h3-12,21,25H,2,13-18H2,1H3

HIDE SMILES / InChI
PHENOPERIDINE is an opioid analgesic partly metabolized to meperidine in the liver. It is derived from pethidine by replacing the N methyl by a phenyl propanol chain. It is reputed to be a typical morphine-like analgesic characterized by its high potency, rapid onset of action, the intensity of its peak effect and the short duration of its pharmacological effects. It is used in general anesthesia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Name Type Language
PHENOPERIDINE
INN   MI   WHO-DD  
INN  
Official Name English
phenoperidine [INN]
Common Name English
DL-PHENOPERIDINE
Common Name English
R 1406
Code English
IDS-NP-010
Code English
ISONIPECOTIC ACID, 1-(3-HYDROXY-3-PHENYLPROPYL)-4-PHENYL-, ETHYL ESTER
Systematic Name English
FENOPERIDINA
Common Name English
PHENOPERIDINE [MI]
Common Name English
NIH 7591
Code English
Phenoperidine [WHO-DD]
Common Name English
FENOPERIDINE
Common Name English
NIH-7591
Code English
R-1406
Code English
1-(3-HYDROXY-3-PHENYLPROPYL)-4-PHENYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER
Systematic Name English
Classification Tree Code System Code
WHO-ATC N01AH04
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
WHO-VATC QN01AH04
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
NCI_THESAURUS C1506
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
NCI_THESAURUS C241
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
DEA NO. 9641
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C72123
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
DRUG BANK
DB13605
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
SMS_ID
100000082259
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105385
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID90862199
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-229-2
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
RXCUI
8143
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY RxNorm
MESH
D010638
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
FDA UNII
G9BH09J4JW
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
CAS
562-26-5
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
PUBCHEM
11226
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
WIKIPEDIA
PHENOPERIDINE
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
INN
1062
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
MERCK INDEX
m8632
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
3441
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
EVMPD
SUB09775MIG
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
PRIMARY
CAS
66584-15-4
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
SUPERSEDED
CAS
55125-88-7
Created by admin on Sat Dec 16 16:50:46 GMT 2023 , Edited by admin on Sat Dec 16 16:50:46 GMT 2023
SUPERSEDED