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Indacaterol

Indacaterol Structure
CAS No.
312753-06-3
Chemical Name:
Indacaterol
Synonyms
CS-272;Arcapta;Indaterol;Indacaterol;Indacaterol-d3;Indacaterol (Onbrez;Indacaterol USP/EP/BP;Indacaterol acetate salt;Indacaterol and its intermediates;Procaterol Impurity 17 ammonium salt
CBNumber:
CB82512068
Molecular Formula:
C24H28N2O3
Molecular Weight:
392.49
MOL File:
312753-06-3.mol
MSDS File:
SDS
Modify Date:
2023/11/7 17:33:14

Indacaterol Properties

Melting point >165°C (dec.)
Boiling point 660.3±55.0 °C(Predicted)
Density 1.27
storage temp. -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
pka 8.68±0.20(Predicted)
form Solid
color Off-White to Light Yellow
InChIKey QZZUEBNBZAPZLX-QFIPXVFZSA-N
SMILES N1C2=C(C([C@@H](O)CNC3CC4=C(C3)C=C(CC)C(CC)=C4)=CC=C2O)C=CC1=O

Indacaterol Chemical Properties,Uses,Production

Description

Inhaled β2 adrenoceptor agonists are effective in the management of asthma and COPD, primarily through their bronchodilating properties. These drugs induce bronchodilation by causing direct relaxation of airway smooth muscle through activation of adenylate cyclase, which in turn increases intracellular cAMP levels. Indacaterol is the newest β2 agonist to reach the market. It is an ultra-long-acting agent with a duration of action suitable for once-a-day dosing. Indacaterol is supplied as an aerosol formulation of its maleate salt and is administered via a dry powder inhaler device. It is specifically approved for once-daily maintenance treatment of airflow obstruction in adult patients with COPD. In preclinical models, indacaterol is close to a full agonist at the human b2 adrenoceptor (Emax = 73 ± 1% of isoprenaline′s maximal effect, pEC50 = 8.06 ±0.02) while salmeterol displays only partial efficacy (38 ±1%). The functional selectivity profile of indacaterol over β1 human adrenoceptors is similar to that of formoterol, whereas its β3 adrenoceptor selectivity profile is similar to that of formoterol and salbutamol.

Uses

Indacaterol is a β-adrenoreceptor agonists for treatment of asthma and bronchodilator treatment for patients with chronic obstructive pulmonary diseases.

Definition

ChEBI: A monohydroxyquinoline that consists of 5-[(1R)-2-amino-1-hydroxyethyl]-8-hydroxyquinolin-2-one having a 5,6-diethylindan-2-yl group attached to the amino function. Used as the maleate salt for treatment of chronic obstructive pulmonary di ease.

Side effects

The most commonly reported adverse events associated with indacaterol treatment were nasopharyngitis, upper respiratory tract infection, and headache and cough following inhalation. Adverse events were mild or moderate in most cases, and became less frequent with continued treatment.

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Indacaterol Spectrum

Indacaterol 5-[(1R)-2-[(5,6-Diethyl-2,3-dihydro-1H-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxyquinolin-2(1H)-one (R)-5-(2-(5,6-diethyl-2,3-dihydro-1H-inden-2-ylaMino)-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one, Maleate salt Arcapta 5-[2-(5,6-Diethyl-2,3-dihydro-1H-inden-2-ylaMino)-(1R)-hydroxyethyl]-8-hydroxyquinolin-2(1H)-one (R)-5-(2-(5,6-Diethyl-2,3-dihydro-1H-inden-2-ylamino)-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)- 2(1H)-Quinolinone,5-[(1R)-2-[(5,6-diethyl-2,3-dihydro-1H-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy- Indacaterol-d3 CS-272 Indacaterol and its intermediates Indacaterol USP/EP/BP Indacaterol acetate salt 5-[2-(5,6-Diethyl-2,3-dihydro-1H-inden-2-ylamino)-(1R)-hydro... IndacaterolQ: What is Indacaterol Q: What is the CAS Number of Indacaterol Q: What is the storage condition of Indacaterol Q: What are the applications of Indacaterol asthma,Beta Receptor,HT1080 cells,myocardial infarction,Adrenergic Receptor,NF-κB,β-arrestin2,Indacaterol,Inhibitor,COPD,inhibit,heart failure Indacaterol /5-[(1R)-2-[(5,6-Diethyl-2,3-dihydro-1H-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxyquinolin-2(1H)-one Procaterol Impurity 17 ammonium salt Indaterol Indacaterol (Onbrez (R) -5-[2- (5, 6-diethyldihydroindene-2-amino) -1-hydroxyethyl] -8-hydroxy-1H-quinolin-2-one 312753-06-3 Intermediates & Fine Chemicals Pharmaceuticals Inhibitors Agonist Amines Aromatics Heterocycles