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Formoterol hemifumarate_Molecular_structure_CAS_43229-80-7)
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Formoterol hemifumarate

Catalog No. S2020 Name Selleck Chemicals
CAS Number 43229-80-7 Website http://www.selleckchem.com
M. F. C42H52N4O12 Telephone (877) 796-6397
M. W. 804.88188 Fax (832) 582-8590
Purity Email sales@selleckchem.com
Storage -20°C Chembase ID: 73232

SYNONYMS

IUPAC name
(2E)-but-2-enedioic acid; bis(N-{2-hydroxy-5-[(1S)-1-hydroxy-2-{[(2S)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]phenyl}formamide)
IUPAC Traditional name
bis(N-{2-hydroxy-5-[(1S)-1-hydroxy-2-{[(2S)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]phenyl}formamide); fumaric acid

DATABASE IDS

CAS Number 43229-80-7

PROPERTIES

Target adrenergic receptor
Salt Data fumarate
Storage Condition -20°C

DETAILS

Description (English)
Research Area: Cancer
Biological Activity:
Formoterol hemifumarate is a potent, selective and long-acting β2-adrenoceptor agonist to β2 and β1 receptors with pKd of 8.12 and 5.58, respectively. Formoterol hemifumarate reveals 330-fold selectivity forβ2 over β1 receptors. Formoterol hemifumarate potently relaxes guinea pig trachea (pD2 = 9.29), and is longer-acting and 100-fold more potent than salbutamol. [1] Formoterol hemifumarate works like other β2-agonists, causing bronchodilation by relaxing the smooth muscle in the airway so as to treat the exacerbation of asthma. The long duration of formoterol action occurs because the formoterol molecules initially diffuse into the plasma membrane of the lung cells, and then are slowly released back outside, where they can come into contact with β2 adrenergic receptors. [2]References on Formoterol hemifumarate[1] Life Sci. , 1993, 52(26):2145-60[2] http://en.wikipedia.org/wiki/Formoterol, ,

REFERENCES

  • http://en.wikipedia.org/wiki/Formoterol