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Details

Stereochemistry RACEMIC
Molecular Formula C14H20N2O2
Molecular Weight 248.3208
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUNITROLOL

SMILES

CC(C)(C)NCC(O)COC1=C(C=CC=C1)C#N

InChI

InChIKey=VCVQSRCYSKKPBA-UHFFFAOYSA-N
InChI=1S/C14H20N2O2/c1-14(2,3)16-9-12(17)10-18-13-7-5-4-6-11(13)8-15/h4-7,12,16-17H,9-10H2,1-3H3

HIDE SMILES / InChI
Bunitrolol is a beta-adrenergic antagonist that can be used for treatment of coronary heart disease. It improves cardiac performance after beta-blockade in patients with coronary artery disease. Bunitrolol was found to have a greater beta 1 than beta 2 adrenergic activity and a weak alpha 1 blocking action.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P08588
Gene ID: 153.0
Gene Symbol: ADRB1
Target Organism: Homo sapiens (Human)
42.0 nM [Ki]
Target ID: P07550|||Q53GA6|||Q9UCZ3
Gene ID: 154.0
Gene Symbol: ADRB2
Target Organism: Homo sapiens (Human)
3.55 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Plasma catecholamines, plasma renin activity and haemodynamics during sodium nitroprusside-induced hypotension and additional beta-blockage with bunitrolol.
1981
Inactivation of rat cytochrome P450 2D enzyme by a further metabolite of 4-hydroxypropranolol, the major and active metabolite of propranolol.
2001 Sep
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Bunitrolol 10 mg administered to patients with coronary artery disease
Route of Administration: Intravenous
In Vitro Use Guide
For assessments of pharmacological activities of bunitrolol the guinea pig trachea, left and right atria and aorta, and the rat aorta were used. Dose-response curves were obtained in the absence or presence of bunitrolol of the following concentrations: trachea, left and right atria 10(-8) M, guinea pig aorta 10(-4) M; rat aorta, 3x10(-6) M.
Name Type Language
BUNITROLOL
INN   MI   WHO-DD  
INN  
Official Name English
Bunitrolol [WHO-DD]
Common Name English
bunitrolol [INN]
Common Name English
KO 1366
Code English
BUNITROLOL [MI]
Common Name English
KO-1366
Code English
(±)-1-(2-CYANOPHENOXY)-2-HYDROXY-3-TERT-BUTYLAMINOPROPANE
Systematic Name English
1-(2-CYANOPHENOXY)-2-HYDROXY-3-TERT-BUTYLAMINOPROPANE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
Code System Code Type Description
DRUG CENTRAL
430
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
FDA UNII
F2613LO055
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL418134
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
PUBCHEM
2473
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID2022701
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
EVMPD
SUB05978MIG
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
CAS
34915-68-9
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
WIKIPEDIA
BUNITROLOL
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
MERCK INDEX
m2763
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY Merck Index
SMS_ID
100000088464
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
INN
3266
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY
NCI_THESAURUS
C72614
Created by admin on Sat Dec 16 16:31:42 GMT 2023 , Edited by admin on Sat Dec 16 16:31:42 GMT 2023
PRIMARY