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bitolterol

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EntityQ4918914· pop 10· linked from 631 articles

bitolterol

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Also known as Bitolterol Mesylate, Bitolterolum, 4-[2-(tert-butylamino)-1-hydroxyethyl]-o-phenylene di-p-toluate, bis(4-methylbenzoic acid) 4-[2-(tert-butylamino)-1-hydroxyethyl]-1,2-phenylene ester, 4-(2-(tert-butylamino)-1-hydroxyethyl)-o-phenylene di-p-toluate

Bitolterol mesylate, formerly sold under the brand name Tornalate, is a short-acting β2-adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and chronic obstructive pulmonary disease (COPD). Bitolterol relaxes the smooth muscles present continuously around the bronchi and bronchioles facilitating the flow of air through them.

Chemical data

Formula
C28H31NO5
Molecular weight
461.5 g/mol
IUPAC name
[4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate
SMILES
CC1=CC=C(C=C1)C(=O)OC2=C(C=C(C=C2)C(CNC(C)(C)C)O)OC(=O)C3=CC=C(C=C3)C
InChIKey
FZGVEKPRDOIXJY-UHFFFAOYSA-N
XLogP
5.2
Polar surface area
84.9 Ų
H-bond donors
2
H-bond acceptors
6
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1984
Admin. routes
topical
Indications
Airway obstruction

via ChEMBL · EBI

Wikidata facts

Mass
461.220223
Has use
medication
Show 6 more facts
chemical formula
C₂₈H₃₁NO₅
medical condition treated
asthma
canonical SMILES
CC1=CC=C(C=C1)C(=O)OC2=C(C=C(C=C2)C(CNC(C)(C)C)O)OC(=O)C3=CC=C(C=C3)C
World Health Organisation international non-proprietary name
bitolterol
subject has role
bronchodilator
Commons category
Bitolterol
Sources (2)

via Wikidata · CC0

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Encyclopedic overview

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Contents
  • References

Bitolterol mesylate, formerly sold under the brand name Tornalate, is a short-acting β2-adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and chronic obstructive pulmonary disease (COPD). Bitolterol relaxes the smooth muscles present continuously around the bronchi and bronchioles facilitating the flow of air through them.

225px|thumb|left|class=skin-invert-image|Colterol

Excerpted from Wikipedia’s “bitolterol” article, available under the CC BY-SA 4.0 licence.

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