FURETHIDINE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C21H31NO4
Molecular Weight	361.4751
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of FURETHIDINE

Structure Search

SMILES

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

InChI

InChIKey=NNCOZXNZFLUYGG-UHFFFAOYSA-N

InChI=1S/C21H31NO4/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

HIDE SMILES / InChI

Description
Sources: https://caricom.org/documents/15297-st_cnd1_add1_rev2_e_v1603027.pdf | https://www.ncbi.nlm.nih.gov/pubmed/14417496

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

Title	Date	PubMed
Pharmacological actions of two new pethidine analogues.	1960 Jun	14417496

Name

Type

Language

FURETHIDINE

Official Name

English

furethidine [INN]

Common Name

English

1-(2-TETRAHYDROFURFURYLOXYETHYL)-4-PHENYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER

Systematic Name

English

IDS-NF-002

Code

English

FURETHIDINE [MI]

Common Name

English

Furethidine [WHO-DD]

Common Name

English

Classification Tree Code System Code

DEA NO.

9626

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

NCI_THESAURUS

C29702

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

Code System Code Type Description

EVMPD

SUB07839MIG

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

NCI_THESAURUS

C65785

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

INN

925

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

FDA UNII

6U9XA4JOD4

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

ECHA (EC/EINECS)

219-195-0

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

MERCK INDEX

m5602

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

Merck Index

DRUG BANK

DB01464

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

SMS_ID

100000080679

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

WIKIPEDIA

FURETHIDINE

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

EPA CompTox

DTXSID10862914

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

CAS

2385-81-1

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

PUBCHEM

61306

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

ChEMBL

CHEMBL2105078

Created by admin on Sat Dec 16 17:19:20 UTC 2023 , Edited by admin on Sat Dec 16 17:19:20 UTC 2023

PRIMARY

ACTIVE MOIETY


					6U9XA4JOD4

PARENT (SALT/SOLVATE)


					3MJW1KBQ9Z

FURETHIDINE METHYLIODIDE

PARENT (SALT/SOLVATE)


					5MLE50YVZN

FURETHIDINE PICRATE

PARENT (SALT/SOLVATE)


					X8ZF5B5HF0

FURETHIDINE HYDROBROMIDE