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Indacaterol

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Catalog No. T2320Cas No. 312753-06-3

Indacaterol (Onbrez; Arcapta) is a β2-Adrenergic Agonist. The mechanism of action of indacaterol is as an Adrenergic beta2-Agonist.

Indacaterol

Indacaterol

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Purity: 99.96%
Catalog No. T2320Cas No. 312753-06-3
Indacaterol (Onbrez; Arcapta) is a β2-Adrenergic Agonist. The mechanism of action of indacaterol is as an Adrenergic beta2-Agonist.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$43In StockIn Stock
50 mg$62-In Stock
1 mL x 10 mM (in DMSO)$98In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.96%
Appearance:Solid
Color:Yellow
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Product Introduction

Indacaterol AI Summary
Indacaterol exhibits significant agonist activity at the human beta2 adrenergic receptor, showing a high potency with an EC50 of 11.0 nM for increasing cAMP levels. It effectively inhibits bronchoconstriction in guinea pig tracheal strips, evidenced by an IC50 of 7.9 nM against electrically-induced conditions and an ED80 of 14.0 ug/kg against histamine-induced constriction. The compound also demonstrates a strong binding affinity for the beta2 adrenoceptor (Ki = 76.0 nM) and a moderate affinity for the beta1 adrenoceptor (IC50 = 316.23 nM), indicating a selective beta2 activity profile (selectivity ratio of 21.0). Pharmacokinetics data reveal a high plasma protein binding percentage (PPB = 95.1%), a terminal half-life of 7.6 hours in rats, and notable metabolism in rat liver microsomes. Additionally, Indacaterol shows efficacy in inhibiting serotonin and acetylcholine-induced bronchoconstriction as well as minor activity against SARS-CoV-2, human HDAC6 (15.57% inhibition), and human CYP1B1 inhibition (IC50 = 59200.0 nM). The compound also involves in GPCR beta-arrestin recruitment assays, exhibiting activation and inhibition across various receptors. However, it displays moderate lipophilicity with a log P value of 3.05 and shows cytotoxicity against human HepG2 cells with an IC50 of 9100.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Indacaterol (Onbrez; Arcapta) is a β2-Adrenergic Agonist. The mechanism of action of indacaterol is as an Adrenergic beta2-Agonist.
Targets&IC50
β1-adrenoceptor:7.36(pKi), β2-adrenoceptor:5.48(pKi)
Chemical Properties
Molecular Weight392.49
FormulaC24H28N2O3
Cas No.312753-06-3
SmilesCCc1cc2CC(Cc2cc1CC)NC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12
Relative Density.1.27 g/cm3
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 49.59 mg/mL (126.35 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.1 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5478 mL12.7392 mL25.4784 mL127.3918 mL
5 mM0.5096 mL2.5478 mL5.0957 mL25.4784 mL
10 mM0.2548 mL1.2739 mL2.5478 mL12.7392 mL
20 mM0.1274 mL0.6370 mL1.2739 mL6.3696 mL
50 mM0.0510 mL0.2548 mL0.5096 mL2.5478 mL
100 mM0.0255 mL0.1274 mL0.2548 mL1.2739 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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