RACEFEMINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C18H23NO
Molecular Weight	269.3813
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RACEFEMINE

Structure Search

SMILES

C[C@@H](COC1=CC=CC=C1)N[C@@H](C)CC2=CC=CC=C2

InChI

InChIKey=URCIJDUOBBSMII-HOTGVXAUSA-N

InChI=1S/C18H23NO/c1-15(13-17-9-5-3-6-10-17)19-16(2)14-20-18-11-7-4-8-12-18/h3-12,15-16,19H,13-14H2,1-2H3/t15-,16-/m0/s1

HIDE SMILES / InChI

Description
Sources: https://www.drugfuture.com/chemdata/racefemine.html | Elks, J. (2014) The Dictionary of Drugs, page 804, retrieved from: https://books.google.ru/books?id=0vXTBwAAQBAJ

Dextrofemine is the (+)-form of racefemine. It is antispasmodic agent. Dextrofemine was used as utrine spasmolytic or muscle relaxant.

Approval Year

Name

Type

Language

CB 3697

Preferred Name

English

RACEFEMINE

Official Name

English

CB-3697

Code

English

RACEFEMINE [MI]

Common Name

English

racefemine [INN]

Common Name

English

BENZENEETHANAMINE, .ALPHA.-METHYL-N-((1R)-1-METHYL-2-PHENOXYETHYL)-,(.ALPHA.R)-

Systematic Name

English

(±)-.ALPHA.-METHYL-N-(1-METHYL-2-PHENOXYETHYL)PHENETHYLAMINE.

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29698

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

Code System Code Type Description

SMS_ID

100000080285

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

INN

2068

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

CAS

22232-57-1

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

NCI_THESAURUS

C76463

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

MERCK INDEX

m449

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

Merck Index

EVMPD

SUB10230MIG

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

ChEMBL

CHEMBL2106250

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

FDA UNII

GFK50B8Y78

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

ECHA (EC/EINECS)

244-856-5

Created by admin on Mon Mar 31 18:20:13 GMT 2025 , Edited by admin on Mon Mar 31 18:20:13 GMT 2025

PRIMARY

ACTIVE MOIETY


					GFK50B8Y78