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Merck

F1016

Fenoterol hydrobromide

adrenoceptor agonist

Synonym(s):

2-(3,5-Dihydroxyphenyl)-2-hydroxy-2′-(4-hydroxyphenyl)-1′-methyldiethylamine hydrobromide

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About This Item

Empirical Formula (Hill Notation):
C17H21NO4 · HBr
CAS Number:
1944-12-3
Molecular Weight:
384.26
NACRES:
NA.77
PubChem Substance ID:
24278431
UNSPSC Code:
41116107
EC Number:
217-742-8
MDL number:
MFCD00079288
Quality level:
100

Key Documents

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Product Name

Fenoterol hydrobromide,

InChI key

SGZRQMALQBXAIQ-UHFFFAOYSA-N

InChI

1S/C17H21NO4.BrH/c1-11(6-12-2-4-14(19)5-3-12)18-10-17(22)13-7-15(20)9-16(21)8-13;/h2-5,7-9,11,17-22H,6,10H2,1H3;1H

SMILES string

Br[H].CC(Cc1ccc(O)cc1)NCC(O)c2cc(O)cc(O)c2

originator

Boehringer Ingelheim

Quality Level

100

Gene Information

human ... ADRB2(154)

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General description

Fenoterol hydrobromide is a sympathomimetic drug. It is used to treat asthma, bronchitis and emphysema. Fenoterol administration might be linked to liver damage. It has anti-inflammatory effects on eosinophil function.

Application

Fenoterol hydrobromide has been used in chromatography-tandem mass spectrometry (LC&-MS-MS) for specific and sensitive detection of β-agonists (BAG).

Biochem/physiol Actions

β2-adrenoceptor agonist; bronchodilator.

Features and Benefits

This compound was developed by Boehringer Ingelheim. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9615
BCCK4967
BCCD4605
BCBQ9398V
020M1606V

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Dorota Latek et al.
Journal of molecular modeling, 17(9), 2353-2366 (2011-03-03)
Cannabinoid and adrenergic receptors belong to the class A (similar to rhodopsin) G protein coupled receptors. Docking of agonists and antagonists to CB(1) and CB(2) cannabinoid receptors revealed the importance of a centrally located rotamer toggle switch and its possible
Thiago Duarte et al.
The Journal of pharmacology and experimental therapeutics, 341(3), 820-828 (2012-03-23)
β(2)-Adrenoceptor (β(2)-AR) agonists increase skeletal muscle contractile force via activation of G(s) protein/adenylyl cyclases (AC) and increased generation of cAMP. Herein, we evaluated the possible dual coupling of β(2)-AR to G(s) and G(i) proteins and the influence of the β(2)-AR/G(s)-G(i)/cAMP
J M Preuss et al.
Naunyn-Schmiedeberg's archives of pharmacology, 360(2), 171-178 (1999-09-24)
We examined the influence of animal age on the functional response of guinea-pig (0-156 weeks) and rat (4-136 weeks) isolated tracheal tissue to beta-adrenoceptor agonists. In addition, the binding density and affinity of [125I]iodocyanopindolol ([125I]CYP) binding to tracheal tissue was
Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions (2015)
Hegui Wang et al.
PloS one, 7(9), e46186-e46186 (2012-10-03)
Increasing evidence indicates that the rapid component of delayed rectifier potassium current (I(Kr)) is modulated by α- and β-adrenergic stimulation. However, the role and mechanism regulating I(Kr) through β(2)-adrenoreceptor (β-AR) stimulation in heart failure (HF) are unclear. In the present
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