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Postion:Product Catalog >Biochemical Engineering>Inhibitors>Neuronal Signaling>Adrenergic Receptor agonists>Indacaterol maleate
Indacaterol maleate
  • Indacaterol maleate

Indacaterol maleate NEW

Price $30 $30 $30 $30 $48 $48 $48 $48 $68 $68 $68 $68
Package 10mg 10mg 10mg 10mg 25mg 25mg 25mg 25mg 50mg 50mg 50mg 50mg
Min. Order:
Supply Ability: 10g
Update Time: 2024-11-19

Product Details

Product Name: Indacaterol maleate CAS No.: 753498-25-8
Purity: 99.67% Supply Ability: 10g
Release date: 2024/11/19

Product Introduction

Bioactivity

NameIndacaterol maleate
DescriptionIndacaterol maleate (QAB149) is an ultra-long-acting β-adrenoceptor agonist.
In vitroIndacaterol inhibits cAMP production in Chinese hamster ovary cells stably transfected with human β2 adrenoceptors with pEC50 of 8.06. Indacaterol inhibits electrically induced contraction on the electrically stimulated guinea pig trachea in a concentration-dependent manner with pEC50 of 8.23. Indacaterol induces a concentration-dependent inotropic effect with maximal efficacy of 75% in the isolated guinea pig left atrium. [1] Indacaterol reverses the carbachol-induced contraction in a concentration-dependent manner with IC50 of 37 nM in human small airways. Indacaterol concentration dependently reverses the serotonin-induced contraction with IC50 of 10.5 nM in rat small airways. Indacaterol has the highest intrinsic efficacy of 53% in rat small airways and 73% in human small airways. [2] Indacaterol (10 μM) induces close to full inhibition of the EFS-induced contraction of isolated human bronchi and the effect lasts 12 hours. [3] Indacaterol inhibits the IgE-dependent release of histamine from mast cells with the intrinsic activity (Emax of a long-acting Indacaterol/Emax of Isoprenaline) of 1.03. [4] Indacaterol inihbits cAMP release from human airway smooth muscle with pEC50 of 8.53 and Emax of 48%. Indacaterol appears to have a reduced efficacy compared with the CHO-K1 data in the primary ASM cells. [5]
In vivoIndacaterol (6.7 μg/kg) inhibits 5-HT-induced bronchoconstriction with a maximal effect of 85% in the conscious guinea pig. Indacaterol (12.5 μg/kg) dose-dependently inhibits methacholine-induced bronchoconstriction with a maximal effect of 85% in the anesthetized rhesus monkey. [1]
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 94 mg/mL (184.8 mM)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
KeywordsInhibitor | NF-κB | heart failure | Indacaterol maleate | myocardial infarction | Adrenergic Receptor | Indacaterol Maleate | asthma | QAB-149 | HT1080 cells | QAB 149 | inhibit | Indacaterol | COPD | β-arrestin2 | Beta Receptor
Inhibitors RelatedOctopamine hydrochloride | Trazodone hydrochloride | Mianserin hydrochloride
Related Compound LibrariesAnti-Neurodegenerative Disease Compound Library | Bioactive Compound Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | FDA-Approved Drug Library | Anti-Cancer Approved Drug Library | Anti-Cancer Drug Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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  • Since: 2011-01-07
  • Address: 36?Washington?Street, Wellesley?Hills
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