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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
Comparison of chlorthalidone, propranolol and bopindolol in six-month treatment of arterial hypertension.
1998
Transdermal delivery of beta-blockers.
2006 May
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 UTC 2023
Edited
by admin
on Fri Dec 15 17:27:18 UTC 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 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
WHO-VATC QC07AA17
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
WHO-ATC C07CA17
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
Code System Code Type Description
EVMPD
SUB05873MIG
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
SMS_ID
100000088637
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
INN
4695
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
RXCUI
19605
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY RxNorm
CAS
62658-63-3
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
NCI_THESAURUS
C169813
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
DRUG BANK
DB08807
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
CHEBI
76749
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID6022684
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
FDA UNII
KT304VZO57
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
PUBCHEM
44112
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
MERCK INDEX
m2605
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY Merck Index
DRUG CENTRAL
389
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
WIKIPEDIA
BOPINDOLOL
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
ChEMBL
CHEMBL357995
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
MESH
C036007
Created by admin on Fri Dec 15 17:27:18 UTC 2023 , Edited by admin on Fri Dec 15 17:27:18 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY