LEVOBUNOLOL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C17H25NO3
Molecular Weight	291.3853
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEVOBUNOLOL

Structure Search

SMILES

CC(C)(C)NC[C@H](O)COC1=CC=CC2=C1CCCC2=O

InChI

InChIKey=IXHBTMCLRNMKHZ-LBPRGKRZSA-N

InChI=1S/C17H25NO3/c1-17(2,3)18-10-12(19)11-21-16-9-5-6-13-14(16)7-4-8-15(13)20/h5-6,9,12,18-19H,4,7-8,10-11H2,1-3H3/t12-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C17H25NO3
Molecular Weight	291.3853
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 16:52:15 UTC 2023` Edited by `admin` on `Sat Dec 16 16:52:15 UTC 2023`
Record UNII	G6317AOI7K
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LEVOBUNOLOL

Official Name

English

LEVOBUNOLOL [MI]

Common Name

English

LEVOBUNOLOL [VANDF]

Common Name

English

BUNOLOL, (S)-

Common Name

English

(-)-(S)-5-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)-3,4-DIHYDRO-1(2H)-NAPHTHALENONE

Systematic Name

English

levobunolol [INN]

Common Name

English

BUNOLOL, (-)-

Common Name

English

Levobunolol [WHO-DD]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000175556

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

WHO-VATC

QS01ED03

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

NDF-RT

N0000000161

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

NCI_THESAURUS

C29705

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

NCI_THESAURUS

C29576

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

WHO-ATC

S01ED03

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

Code System Code Type Description

INN

4706

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

DRUG CENTRAL

431

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

DAILYMED

G6317AOI7K

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

DRUG BANK

DB01210

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

CHEBI

6438

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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EPA CompTox

DTXSID1043833

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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RXCUI

1813

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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RxNorm

IUPHAR

570

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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MERCK INDEX

m6784

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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Merck Index

SMS_ID

100000082825

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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ChEMBL

CHEMBL1201237

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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WIKIPEDIA

LEVOBUNOLOL

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

EVMPD

SUB08463MIG

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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MESH

D002040

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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NCI_THESAURUS

C62043

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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CAS

47141-42-4

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

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LACTMED

Levobunolol

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

PUBCHEM

39468

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

FDA UNII

G6317AOI7K

Created by admin on Sat Dec 16 16:52:16 UTC 2023 , Edited by admin on Sat Dec 16 16:52:16 UTC 2023

PRIMARY

Related Record Type Details


					4A4MK4KIB5

BETA-1 ADRENERGIC RECEPTOR

TARGET->ANTAGONIST

Comments:

Levobunolol (LB) is the levo-rotatory isomer of bunolol, a potent, nonselective antagonist of beta-adrenergic receptors.


					VZX139UJO5

BETA-2 ADRENERGIC RECEPTOR

TARGET->ANTAGONIST

Comments:

Levobunolol (LB) is the levo-rotatory isomer of bunolol, a potent, nonselective antagonist of beta-adrenergic receptors.

Amount:


					O90S49LDHH

LEVOBUNOLOL HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					71QSY2UT3G

BUNOLOL

RACEMATE -> ENANTIOMER

Related Record Type Details


					9TH2XJ45MW

5-((2S)-3-(TERT-BUTYLAMINO)-2-HYDROXY-PROPOXY)-4H-NAPHTHALEN-1-ONE

METABOLITE -> PARENT

Comments:

IN VITRO


					G26FV3LS5J

5-((2S)-3-(TERT-BUTYLAMINO)-2-HYDROXY-PROPOXY)TETRALIN-1-OL

METABOLITE -> PARENT

Comments:

IN VITRO

Related Record Type Details


					G6317AOI7K

ACTIVE MOIETY