U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H23NO4.ClH
Molecular Weight 353.84
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ARBUTAMINE HYDROCHLORIDE

SMILES

Cl.O[C@@H](CNCCCCC1=CC=C(O)C=C1)C2=CC=C(O)C(O)=C2

InChI

InChIKey=ATBUNPBAFFCFKY-FERBBOLQSA-N
InChI=1S/C18H23NO4.ClH/c20-15-7-4-13(5-8-15)3-1-2-10-19-12-18(23)14-6-9-16(21)17(22)11-14;/h4-9,11,18-23H,1-3,10,12H2;1H/t18-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C18H23NO4
Molecular Weight 317.3795
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

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

Arbutamine was indicated to elicit acute cardiovascular responses in order to aid in diagnosing the presence or absence of coronary artery disease in patients who cannot exercise adequately. Arbutamine is a synthetic catecholamine with positive chronotropic and inotropic properties. The chronotropic (increase in heart rate [HR]) and inotropic (increase in force of contraction) effects of arbutamine serve to mimic exercise by increasing cardiac work (producing stress) and provoke myocardial ischemia in patients with compromised coronary arteries. In functional assays, arbutamine is more selective for beta-adrenergic receptors than for alpha-adrenergic receptors. The beta-agonist activity of arbutamine provides cardiac stress by increasing HR, cardiac contractility, and systolic blood pressure.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P08588
Gene ID: 153.0
Gene Symbol: ADRB1
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
GENESA

Approved Use

Unknown

Launch Date

1997
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
5 min
10 μg/kg single, intravenous
dose: 10 μg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
ARBUTAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
42%
10 μg/kg single, intravenous
dose: 10 μg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
ARBUTAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
4.62 mg/kg single, oral (mean)
Recommended
Dose: 4.62 mg/kg
Route: oral
Route: single
Dose: 4.62 mg/kg
Sources:
healthy, 20-70
n = 53
Health Status: healthy
Condition: diagnostic test
Age Group: 20-70
Sex: M+F
Population Size: 53
Sources:
Disc. AE: Arrhythmia, Hypotension...
Other AEs: Arrhythmia...
AEs leading to
discontinuation/dose reduction:
Arrhythmia (2%)
Hypotension (9%)
Other AEs:
Arrhythmia (29 patients)
Sources:
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Disc. AE: Angina, Arrhythmia...
Other AEs: Arrhythmia...
AEs leading to
discontinuation/dose reduction:
Angina (21%)
Arrhythmia (4%)
Hypotension (4%)
Dyspnea (4%)
Other AEs:
Arrhythmia (103 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Arrhythmia 2%
Disc. AE
4.62 mg/kg single, oral (mean)
Recommended
Dose: 4.62 mg/kg
Route: oral
Route: single
Dose: 4.62 mg/kg
Sources:
healthy, 20-70
n = 53
Health Status: healthy
Condition: diagnostic test
Age Group: 20-70
Sex: M+F
Population Size: 53
Sources:
Arrhythmia 29 patients
4.62 mg/kg single, oral (mean)
Recommended
Dose: 4.62 mg/kg
Route: oral
Route: single
Dose: 4.62 mg/kg
Sources:
healthy, 20-70
n = 53
Health Status: healthy
Condition: diagnostic test
Age Group: 20-70
Sex: M+F
Population Size: 53
Sources:
Hypotension 9%
Disc. AE
4.62 mg/kg single, oral (mean)
Recommended
Dose: 4.62 mg/kg
Route: oral
Route: single
Dose: 4.62 mg/kg
Sources:
healthy, 20-70
n = 53
Health Status: healthy
Condition: diagnostic test
Age Group: 20-70
Sex: M+F
Population Size: 53
Sources:
Arrhythmia 103 patients
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Angina 21%
Disc. AE
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Arrhythmia 4%
Disc. AE
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Dyspnea 4%
Disc. AE
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Hypotension 4%
Disc. AE
3.58 mg/kg single, oral (mean)
Recommended
Dose: 3.58 mg/kg
Route: oral
Route: single
Dose: 3.58 mg/kg
Sources:
healthy, 37 - 79 years
n = 134
Health Status: healthy
Condition: diagnostic test
Age Group: 37 - 79 years
Sex: M+F
Population Size: 134
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer


Drug as victim

Drug as victim

PubMed

PubMed

TitleDatePubMed
Identification of viable myocardium early after acute myocardial infarction using closed-loop arbutamine echocardiography: comparison with positron emission tomography.
2001 Dec
Effect of ligand structure on the zinc-catalyzed Henry reaction. Asymmetric syntheses of (-)-denopamine and (-)-arbutamine.
2002 Aug 8
Feasibility, safety and tolerability of accelerated dobutamine stress echocardiography.
2007 Nov 21

Sample Use Guides

Intravenous infusion, up to a maximum of 10 mcg per kg of body weight as administered by the drug delivery device
Route of Administration: Intravenous
In Vitro Use Guide
It was characterized the interactions of arbutamine with different adrenergic receptor subtypes in vitro. In the electrically stimulated left atria of rats, arbutamine increased contractile force. The pD2 values (- log of the dose that produces 50% of the maximal responses) for arbutamine and isoproterenol were 8.45 +/- 0.15 and 8.55 +/- 0.02, respectively. Both arbutamine and isoproterenol increased the rate of spontaneously beating rat right atria with pD2 values of 9.0 +/- 0.19 and 8.82 +/- 0.18, respectively. The affinity constants (KA) of arbutamine and isoproterenol for cardiac beta1-adrenergic receptors, as determined by competition binding assays, were found to be 7.32 and 6.04, respectively. In guinea pig trachea, arbutamine and isoproterenol produced a concentration-dependent relaxation that was blocked by propranolol. Their pD2 values were 7.9 +/- 0.1 and 8.2 +/- 0.1, respectively. Arbutamine contracted isolated rat aortic rings with a maximal increase of 38.1 +/- 6.7% that of 10 microM of norepinephrine. In rat white adipocytes, arbutamine, isoproterenol, and BRL-37344 stimulated glycerol release, with the order of potency being BRL-37344 > arbutamine > isoproterenol. In hamster brown adipocytes, the order was arbutamine > isoproterenol > BRL-37344. Moreover, arbutamine stimulated beta3-adrenergic receptors in guinea pig ileum. Arbutamine does not stimulate alpha-adrenergic receptors at concentrations that were high enough to maximally activate the beta-adrenergic receptors.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:37:37 GMT 2023
Edited
by admin
on Fri Dec 15 15:37:37 GMT 2023
Record UNII
K0NF2CPJ7F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ARBUTAMINE HYDROCHLORIDE
MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN  
Official Name English
1,2-BENZENEDIOL, 4-(1-HYDROXY-2-((4-(4-HYDROXYPHENYL)BUTYL)AMINO)ETHYL)-, (R) HYDROCHLORIDE
Common Name English
GP-2-121-3
Code English
ARBUTAMINE HYDROCHLORIDE [MART.]
Common Name English
GENESA
Brand Name English
Arbutamine hydrochloride [WHO-DD]
Common Name English
ARBUTAMINE HYDROCHLORIDE [USAN]
Common Name English
ARBUTAMINE HCL
Common Name English
ARBUTAMINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
ARBUTAMINE HYDROCHLORIDE [MI]
Common Name English
ARBUTAMINE HYDROCHLORIDE [VANDF]
Common Name English
(R)-3,4-DIHYDROXY-.ALPHA.-(((4-(P-HYDROXYPHENYL)BUTYL)AMINO)METHYL)BENZYL ALCOHOL HYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
Code System Code Type Description
CAS
125251-66-3
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
DRUG BANK
DBSALT001445
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
FDA UNII
K0NF2CPJ7F
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
PUBCHEM
166551
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
USAN
EE-20
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
MERCK INDEX
m2032
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID40154718
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
RXCUI
236829
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY RxNorm
SMS_ID
100000085186
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
ChEMBL
CHEMBL1201251
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
EVMPD
SUB00570MIG
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
NCI_THESAURUS
C65239
Created by admin on Fri Dec 15 15:37:37 GMT 2023 , Edited by admin on Fri Dec 15 15:37:37 GMT 2023
PRIMARY
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