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Details

Stereochemistry RACEMIC
Molecular Formula C18H27NO2.ClH
Molecular Weight 325.873
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTAVERINE HYDROCHLORIDE

SMILES

Cl.CCCCOC(=O)CC(N1CCCCC1)C2=CC=CC=C2

InChI

InChIKey=JARLFDVYUFHWQL-UHFFFAOYSA-N
InChI=1S/C18H27NO2.ClH/c1-2-3-14-21-18(20)15-17(16-10-6-4-7-11-16)19-12-8-5-9-13-19;/h4,6-7,10-11,17H,2-3,5,8-9,12-15H2,1H3;1H

HIDE SMILES / InChI

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

Molecular Formula C18H27NO2
Molecular Weight 289.4125
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Butaverine is a fatty acid ester with antispasmodic activity which was under development for treatment urinary incontinence

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:32:22 GMT 2023
Edited
by admin
on Sat Dec 16 10:32:22 GMT 2023
Record UNII
12244O98K2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTAVERINE HYDROCHLORIDE
MI  
Common Name English
NSC-88582
Code English
1-PIPERIDINEPROPANOIC ACID, .BETA.-PHENYL-, BUTYL ESTER, HYDROCHLORIDE (1:1)
Systematic Name English
BUTAVERINE HYDROCHLORIDE [MI]
Common Name English
GEMORA
Brand Name English
BUTAVERINE HYDROCHLORIDE, (±)-
Common Name English
ESPASMO-GEMORA
Brand Name English
Code System Code Type Description
PUBCHEM
24189377
Created by admin on Sat Dec 16 10:32:22 GMT 2023 , Edited by admin on Sat Dec 16 10:32:22 GMT 2023
PRIMARY
MERCK INDEX
m601
Created by admin on Sat Dec 16 10:32:22 GMT 2023 , Edited by admin on Sat Dec 16 10:32:22 GMT 2023
PRIMARY Merck Index
NSC
88582
Created by admin on Sat Dec 16 10:32:22 GMT 2023 , Edited by admin on Sat Dec 16 10:32:22 GMT 2023
PRIMARY
CAS
17824-89-4
Created by admin on Sat Dec 16 10:32:22 GMT 2023 , Edited by admin on Sat Dec 16 10:32:22 GMT 2023
PRIMARY
FDA UNII
12244O98K2
Created by admin on Sat Dec 16 10:32:22 GMT 2023 , Edited by admin on Sat Dec 16 10:32:22 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE