RACEMORAMIDE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C25H32N2O2
Molecular Weight	392.5338
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RACEMORAMIDE

Structure Search

SMILES

CC(CN1CCOCC1)C(C(=O)N2CCCC2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=INUNXTSAACVKJS-UHFFFAOYSA-N

InChI=1S/C25H32N2O2/c1-21(20-26-16-18-29-19-17-26)25(22-10-4-2-5-11-22,23-12-6-3-7-13-23)24(28)27-14-8-9-15-27/h2-7,10-13,21H,8-9,14-20H2,1H3

HIDE SMILES / InChI

Molecular Formula	C25H32N2O2
Molecular Weight	392.5338
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13664758 | https://www.ncbi.nlm.nih.gov/pubmed/13988011 | https://www.ncbi.nlm.nih.gov/pubmed/13537952 | https://www.ncbi.nlm.nih.gov/pubmed/13546267 | Anesthesie, Analgesie, Reanimation (1957), 14, 51-63.

Racemoramide (also known as Moramide) is an opioid analgesic with a central structural action. In clinical trials, Racemoramide shows a strong analgesic action and low toxicity.

Approval Year

PubMed

PubMed

Title	Date	PubMed
An evaluation of two new analgesics (dextromoramide and racemoramide) in healthy subjects and in patients with chronic pain.	1959 Jul	13664758

Patents

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 15:48:39 GMT 2023` Edited by `admin` on `Sat Dec 16 15:48:39 GMT 2023`
Record UNII	L3J8QT828G
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

RACEMORAMIDE

Official Name

English

PYRROLIDINE, 1-(3-METHYL-4-(4-MORPHOLINYL)-1-OXO-2,2-DIPHENYLBUTYL)-, (±)-

Systematic Name

English

R 610

Code

English

IDS-NR-002

Code

English

racemoramide [INN]

Common Name

English

R-610

Code

English

Classification Tree Code System Code

NCI_THESAURUS

C67413

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

DEA NO.

9645

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

Code System Code Type Description

CAS

13013-15-5

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

SUPERSEDED

CHEBI

35702

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

PUBCHEM

9648

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

FDA UNII

L3J8QT828G

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

NCI_THESAURUS

C76845

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

ECHA (EC/EINECS)

208-893-0

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

ChEMBL

CHEMBL431928

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

INN

734

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

EPA CompTox

DTXSID50859343

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

SMS_ID

100000080307

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

CAS

545-59-5

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

EVMPD

SUB10235MIG

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

WIKIPEDIA

Racemoramide

Created by admin on Sat Dec 16 15:48:40 GMT 2023 , Edited by admin on Sat Dec 16 15:48:40 GMT 2023

PRIMARY

Related Record Type Details


					7M86YFN15D

ENANTIOMER -> RACEMATE


					9S4S6CIY83

ENANTIOMER -> RACEMATE

Related Record Type Details


					L3J8QT828G

ACTIVE MOIETY