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Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO2.C4H6O4
Molecular Weight 327.3728
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BAMETHAN SUCCINATE

SMILES

OC(=O)CCC(O)=O.CCCCNCC(O)C1=CC=C(O)C=C1

InChI

InChIKey=NDGDFKFGBZCILN-UHFFFAOYSA-N
InChI=1S/C12H19NO2.C4H6O4/c1-2-3-8-13-9-12(15)10-4-6-11(14)7-5-10;5-3(6)1-2-4(7)8/h4-7,12-15H,2-3,8-9H2,1H3;1-2H2,(H,5,6)(H,7,8)

HIDE SMILES / InChI
Bamethan (butyl-sympatol or vasculat) is an adrenaline derivative developed by C. H. Boehringer Sohn. Bamethan shows a depressor action on peripheral blood vessels as a result of the peripheral vasodilating action caused by stimulation of adrenergic beta-receptor. Bamethan has been used abroad in the treatment of certain peripheral vascular and circulatory disturbances, such as vasospastic conditions, arteriosclerotic peripheral vascular disease, Raynaud's syndrome, occlusive vascular disease of the legs, the post-thrombotic syndrome, degenerative muscular disorders, and other conditions involving peripheral vascular insuffciency.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
VASCULAT

Approved Use

Bamethan has been used abroad in the treatment of certain peripheral vascular and circulatory disturbances, such as vasospastic conditions, arteriosclerotic peripheral vascular disease, Raynaud's syndrome, occlusive vascular disease of the legs, the post-thrombotic syndrome, degenerative muscular disorders, and other conditions involving peripheral vascular insuffciency.
Doses

Doses

DosePopulationAdverse events​
100 mg single, oral
Studied dose
Dose: 100 mg
Route: oral
Route: single
Dose: 100 mg
Sources:
healthy
Health Status: healthy
Sex: M+F
Sources:
PubMed

PubMed

TitleDatePubMed
Tandem mass spectrometry with online high-flow reversed-phase extraction and normal-phase chromatography on silica columns with aqueous-organic mobile phase for quantitation of polar compounds in biological fluids.
2005
Development and validation of a liquid chromatography/tandem mass spectrometry (LC/MS/MS) method for the determination of ribavirin in human plasma and serum.
2002-06-20
The effect of bamethan on cardiovascular response.
1966-01-01

Sample Use Guides

75-100 mg
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
LARGOPHERIN
Preferred Name English
BAMETHAN SUCCINATE
WHO-DD  
Common Name English
Bamethan succinate [WHO-DD]
Common Name English
PROVASCUL
Brand Name English
BENZENEMETHANOL, .ALPHA.-((BUTYLAMINO)METHYL)-4-HYDROXY-, BUTANEDIOATE (SALT)
Common Name English
Code System Code Type Description
FDA UNII
2GLO6IOP6Y
Created by admin on Mon Mar 31 22:08:54 GMT 2025 , Edited by admin on Mon Mar 31 22:08:54 GMT 2025
PRIMARY
PUBCHEM
133065418
Created by admin on Mon Mar 31 22:08:54 GMT 2025 , Edited by admin on Mon Mar 31 22:08:54 GMT 2025
PRIMARY
RXCUI
235933
Created by admin on Mon Mar 31 22:08:54 GMT 2025 , Edited by admin on Mon Mar 31 22:08:54 GMT 2025
PRIMARY RxNorm
CAS
59547-50-1
Created by admin on Mon Mar 31 22:08:54 GMT 2025 , Edited by admin on Mon Mar 31 22:08:54 GMT 2025
PRIMARY