BUTOPIPRINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H29NO3
Molecular Weight	319.4385
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BUTOPIPRINE

Structure Search

SMILES

CCCCOCCOC(=O)C(N1CCCCC1)C2=CC=CC=C2

InChI

InChIKey=MNBLDUWBHRTWEP-UHFFFAOYSA-N

InChI=1S/C19H29NO3/c1-2-3-14-22-15-16-23-19(21)18(17-10-6-4-7-11-17)20-12-8-5-9-13-20/h4,6-7,10-11,18H,2-3,5,8-9,12-16H2,1H3

HIDE SMILES / InChI

Molecular Formula	C19H29NO3
Molecular Weight	319.4385
Charge	0
Count

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

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19590203&CC=FR&NR=1171916A&KC=A | https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19601206&CC=US&NR=2963485A&KC=A | Bulletin de la Societe Chimique de France (1959), 1895-6.

Butopiprine is alkoxyethyl α-phenyl-α-piperidinoacetate possessing spasmolytic, local anesthetic, and antitussive activity.

Originator

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:17:45 GMT 2025` Edited by `admin` on `Mon Mar 31 18:17:45 GMT 2025`
Record UNII	EHX04MU69R
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

BUTOPIPRINE

Official Name

English

LD 2351 FREE BASE

Preferred Name

English

LD-2351 FREE BASE

Code

English

Butopiprine [WHO-DD]

Common Name

English

butopiprine [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C66917

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

Code System Code Type Description

PUBCHEM

71735

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

ECHA (EC/EINECS)

259-848-7

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

NCI_THESAURUS

C78104

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

FDA UNII

EHX04MU69R

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

ChEMBL

CHEMBL2104630

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

EVMPD

SUB06032MIG

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

EPA CompTox

DTXSID40866506

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

CAS

55837-15-5

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

SMS_ID

100000081585

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

INN

1442

Created by admin on Mon Mar 31 18:17:45 GMT 2025 , Edited by admin on Mon Mar 31 18:17:45 GMT 2025

PRIMARY

Related Record Type Details


					3A54RW6OZ2

BUTOPIPRINE HYDROBROMIDE

SALT/SOLVATE -> PARENT


					2H1P4K9C0I

BUTOPIPRINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					W6N8HGX854

BUTOPIPRINE, (S)-

ENANTIOMER -> RACEMATE


					ZE0IPS1EWN

BUTOPIPRINE, (R)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					EHX04MU69R

ACTIVE MOIETY