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Details

Stereochemistry RACEMIC
Molecular Formula C21H31NO4.ClH
Molecular Weight 397.936
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FURETHIDINE HYDROCHLORIDE

SMILES

Cl.CCOC(=O)C1(CCN(CCOCC2CCCO2)CC1)C3=CC=CC=C3

InChI

InChIKey=RNKWGTCIHDAZMV-UHFFFAOYSA-N
InChI=1S/C21H31NO4.ClH/c1-2-25-20(23)21(18-7-4-3-5-8-18)10-12-22(13-11-21)14-16-24-17-19-9-6-15-26-19;/h3-5,7-8,19H,2,6,9-17H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C21H31NO4
Molecular Weight 361.4751
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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

Furethidine, a pethidine analog was studied as an analgesic agent. This compound is not currently used in medicine and is listed in schedules of the single convention on narcotic drugs of 1961 as amended by the 1972 protocol.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological actions of two new pethidine analogues.
1960-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:43:29 GMT 2025
Edited
by admin
on Mon Mar 31 23:43:29 GMT 2025
Record UNII
13Z0BH46GL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-PIPERIDINECARBOXYLIC ACID, 4-PHENYL-1-(2-((TETRAHYDRO-2-FURANYL)METHOXY)ETHYL)-, ETHYL ESTER, HYDROCHLORIDE (1:1)
Preferred Name English
FURETHIDINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
FDA UNII
13Z0BH46GL
Created by admin on Mon Mar 31 23:43:29 GMT 2025 , Edited by admin on Mon Mar 31 23:43:29 GMT 2025
PRIMARY
CAS
1177501-27-7
Created by admin on Mon Mar 31 23:43:29 GMT 2025 , Edited by admin on Mon Mar 31 23:43:29 GMT 2025
PRIMARY
PUBCHEM
11971873
Created by admin on Mon Mar 31 23:43:29 GMT 2025 , Edited by admin on Mon Mar 31 23:43:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID10474955
Created by admin on Mon Mar 31 23:43:29 GMT 2025 , Edited by admin on Mon Mar 31 23:43:29 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE