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Details

Stereochemistry RACEMIC
Molecular Formula C23H28N2O3
Molecular Weight 380.48
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BOPINDOLOL

SMILES

CC1=CC2=C(N1)C=CC=C2OCC(CNC(C)(C)C)OC(=O)C3=CC=CC=C3

InChI

InChIKey=UUOJIACWOAYWEZ-UHFFFAOYSA-N
InChI=1S/C23H28N2O3/c1-16-13-19-20(25-16)11-8-12-21(19)27-15-18(14-24-23(2,3)4)28-22(26)17-9-6-5-7-10-17/h5-13,18,24-25H,14-15H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C23H28N2O3
Molecular Weight 380.48
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/11314603 | https://www.ncbi.nlm.nih.gov/pubmed/1706984

Bopindolol (4-[benzoyloxy-3-tertbutylaminopropoxy]-2-methylindole hydrogen malonate) is an indole beta-adrenoceptor antagonist bearing a benzoyl ester residue on the beta-carbon atom of the propanolamine side chain. Bopindolol is metabolized by esterase to benzoic acid and an active metabolite, 18-502 [4-(3-t-butylamino-2-hydroxypropoxy)-2-methyl indole], which is further metabolized to 20-785 [4-(3-t-butylaminopropoxy)-2-carboxyl indole]. Bopindolol produces sustained blockade of beta 1- and beta 2-adrenoceptors, has intrinsic sympathomimetic as well as membrane stabilizing actions, inhibits renin secretion, and interacts with 5-HT receptors. Bopindolol is used in the treatment of hypertension. In limited trials bopindolol has also successfully reduced symptoms in patients with angina pectoris, anxiety and essential tremor.

Originator

Curator's Comment: Berthold R, Waite R, Weber H (1981) Pharmacological studies with Bopindolol: a new long acting beta-adrenoceptor antagonist (Abstract). Br J Pharmacol 74:829 DOI: 10.1111/j.1476-5381.1981.tb10708.x

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
BOPINDOLOL

Approved Use

Bopindolol is a nonselective beta-adrenoceptor antagonist with partial agonist activity which is used in the treatment of hypertension.
PubMed

PubMed

TitleDatePubMed
Beta-blockers and psychic stress: a double-blind, placebo-controlled study of bopindolol vs lorazepam and butalbital in surgical patients.
1985 Sep
Bopindolol. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy.
1991 Jan
[Multicenter study of isradipine in the treatment of hypertension].
1992 Apr
Hypotensive effect of bopindolol in pithed rats.
1993 Mar
Comparison of chlorthalidone, propranolol and bopindolol in six-month treatment of arterial hypertension.
1998
Effect of vasodilatory beta-adrenoceptor blockers on cardiovascular haemodynamics in anaesthetized rats.
2002 Mar
Determination of bopindolol by sequential injection technique with spectrophotometric detection.
2003 Oct
Role of chemical structure in stereoselective recognition of beta-blockers by cyclodextrins in capillary zone electrophoresis.
2008 Apr 24
Chiral separations of some beta-adrenergic agonists and antagonists on AmyCoat column by HPLC.
2010 Jan
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2.
2011 Jul 14
Patents

Sample Use Guides

antihypertensive effects of bopindolol 0.5 to 4 mg are sustained for more than 24 hours after once daily dosing
Route of Administration: Oral
In guinea-pig isolated atria bopindolol at concentrations between 3.2 nM and 2 uM produced an inhibition of the positive chronotropic and inotropic effects of adrenaline
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:27:18 GMT 2023
Edited
by admin
on Fri Dec 15 17:27:18 GMT 2023
Record UNII
KT304VZO57
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BOPINDOLOL
INN   MI   WHO-DD  
INN  
Official Name English
(±)-1-(TERT-BUTYLAMINO)-3-((2-METHYLINDOL-4-YL)OXY)-2-PROPANOL BENZOATE (ESTER)
Common Name English
bopindolol [INN]
Common Name English
BOPINDOLOL [MI]
Common Name English
Bopindolol [WHO-DD]
Common Name English
1-((1,1-DIMETHYLETHYL)AMINO)-3-((2-METHYL-1H-INDOL-4-YL)OXY)-2-PROPANOL BENZOATE ESTER
Common Name English
Classification Tree Code System Code
WHO-ATC C07AA17
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
WHO-VATC QC07AA17
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
WHO-ATC C07CA17
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
Code System Code Type Description
EVMPD
SUB05873MIG
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
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SMS_ID
100000088637
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INN
4695
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PRIMARY
RXCUI
19605
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PRIMARY RxNorm
CAS
62658-63-3
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
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NCI_THESAURUS
C169813
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DRUG BANK
DB08807
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CHEBI
76749
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EPA CompTox
DTXSID6022684
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FDA UNII
KT304VZO57
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
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PUBCHEM
44112
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PRIMARY
MERCK INDEX
m2605
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PRIMARY Merck Index
DRUG CENTRAL
389
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
PRIMARY
WIKIPEDIA
BOPINDOLOL
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL357995
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
PRIMARY
MESH
C036007
Created by admin on Fri Dec 15 17:27:18 GMT 2023 , Edited by admin on Fri Dec 15 17:27:18 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY