LEVALBUTEROL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C13H21NO3
Molecular Weight	239.3107
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEVALBUTEROL

Structure Search

SMILES

CC(C)(C)NC[C@H](O)C1=CC=C(O)C(CO)=C1

InChI

InChIKey=NDAUXUAQIAJITI-LBPRGKRZSA-N

InChI=1S/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3/t12-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C13H21NO3
Molecular Weight	239.3107
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 `Fri Dec 15 15:45:21 UTC 2023` Edited by `admin` on `Fri Dec 15 15:45:21 UTC 2023`
Record UNII	EDN2NBH5SS
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LEVALBUTEROL

Common Name

English

Levosalbutamol [WHO-DD]

Common Name

English

LEVALBUTEROL [VANDF]

Common Name

English

ALBUTEROL (R)-FORM [MI]

Common Name

English

ASF-1096

Code

English

LEVOSALBUTAMOL

Official Name

English

R-SALBUTAMOL

Common Name

English

levosalbutamol [INN]

Common Name

English

(R)-.ALPHA.(SUP 1)-((TERT-BUTYLAMINO)METHYL)-4-HYDROXY-M-XYLENE-.ALPHA.,.ALPHA.'-DIOL

Common Name

English

LEVOSALBUTAMOL [MART.]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000175779

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

NCI_THESAURUS

C48149

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

NCI_THESAURUS

C319

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

NDF-RT

N0000009922

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

Code System Code Type Description

FDA UNII

EDN2NBH5SS

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

EVMPD

SUB08491MIG

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

DRUG CENTRAL

1575

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

DAILYMED

EDN2NBH5SS

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

ChEMBL

CHEMBL1002

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

EPA CompTox

DTXSID80187964

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

PUBCHEM

123600

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

MERCK INDEX

m1480

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

Merck Index

WIKIPEDIA

LEVOSALBUTAMOL

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

INN

7681

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

DRUG BANK

DB13139

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

CHEBI

8746

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

RXCUI

237159

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

RxNorm

SMS_ID

100000082284

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

NCI_THESAURUS

C74196

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

LACTMED

Levalbuterol

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

CAS

34391-04-3

Created by admin on Fri Dec 15 15:45:21 UTC 2023 , Edited by admin on Fri Dec 15 15:45:21 UTC 2023

PRIMARY

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ALBUTEROL

RACEMATE -> ACTIVE ENANTIOMER

Amount:


					VZX139UJO5

BETA-2 ADRENERGIC RECEPTOR

TARGET -> AGONIST

Interaction Type:

SHORT-ACTING

Amount:


					71TH42O2CQ

LEVALBUTEROL SULFATE

SALT/SOLVATE -> PARENT

Amount:


					ADS4I3E22M

LEVALBUTEROL TARTRATE

SALT/SOLVATE -> PARENT

Amount:


					WDQ1526QJM

LEVALBUTEROL HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:

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					38DWL97D64

LEVALBUTEROL-4-O-SULPHATE

METABOLITE INACTIVE -> PARENT

Comments:

catalysed almost exclusively by sulphotransferase (SULT) 1A3

Interaction Type:

MAJOR

Qualification:

PLASMA

Amount:

Related Record Type Details


					EDN2NBH5SS

ACTIVE MOIETY

Amount:

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Biological Half-life	PHARMACOKINETIC