CLENBUTEROL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C12H18Cl2N2O
Molecular Weight	277.19
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CLENBUTEROL

Structure Search

SMILES

CC(C)(C)NCC(O)C1=CC(Cl)=C(N)C(Cl)=C1

InChI

InChIKey=STJMRWALKKWQGH-UHFFFAOYSA-N

InChI=1S/C12H18Cl2N2O/c1-12(2,3)16-6-10(17)7-4-8(13)11(15)9(14)5-7/h4-5,10,16-17H,6,15H2,1-3H3

HIDE SMILES / InChI

Molecular Formula	C12H18Cl2N2O
Molecular Weight	277.19
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:40:55 UTC 2023` Edited by `admin` on `Fri Dec 15 15:40:55 UTC 2023`
Record UNII	XTZ6AXU7KN
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CLENBUTEROL

Official Name

English

CLENBUTEROL [MI]

Common Name

English

Clenbuterol [WHO-DD]

Common Name

English

clenbuterol [INN]

Common Name

English

PLANIPART

Brand Name

English

NAB 365

Code

English

CONTRASPASMIN

Brand Name

English

NSC-758633

Code

English

Classification Tree Code System Code

WHO-VATC

QR03CC13

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-VATC

QR03AC14

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-VATC

QR03CC90

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-ATC

R03CC13

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

CFR

21 CFR 530.41

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

CFR

21 CFR 520.452

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

FDA ORPHAN DRUG

451614

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

NCI_THESAURUS

C319

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

FDA ORPHAN DRUG

546316

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-ATC

R03CC63

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-ATC

R03AC14

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

FDA ORPHAN DRUG

653918

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

WHO-VATC

QG02CA91

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

NCI_THESAURUS

C48149

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

Code System Code Type Description

DRUG CENTRAL

673

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

EVMPD

SUB06651MIG

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

DAILYMED

XTZ6AXU7KN

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

CAS

37148-27-9

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

SMS_ID

100000080213

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

MESH

D002976

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

FDA UNII

XTZ6AXU7KN

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

EPA CompTox

DTXSID7022833

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

PUBCHEM

2783

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

INN

3264

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

WIKIPEDIA

CLENBUTEROL

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

DRUG BANK

DB01407

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

CHEBI

174690

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

RXCUI

2580

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

RxNorm

MERCK INDEX

m3615

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

Merck Index

ECHA (EC/EINECS)

253-366-0

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

NSC

758633

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

ChEMBL

CHEMBL49080

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

NCI_THESAURUS

C65335

Created by admin on Fri Dec 15 15:40:55 UTC 2023 , Edited by admin on Fri Dec 15 15:40:55 UTC 2023

PRIMARY

Related Record Type Details


					GOR5747GWU

CLENBUTEROL HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					32SXB5VH2O

CLENBUTEROL, (S)-

ENANTIOMER -> RACEMATE


					VZX139UJO5

BETA-2 ADRENERGIC RECEPTOR

TARGET -> AGONIST

Interaction Type:

SHORT-ACTING

Amount:


					95Q3052YP1

CLENBUTEROL, (R)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					BIK7NS3B2F

4-AMINO-3,5-DICHLOROBENZOIC ACID

METABOLITE -> PARENT

Amount:

Related Record Type Details


					XTZ6AXU7KN

ACTIVE MOIETY