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PF-03635659

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Catalog No. T33941Cas No. 931409-24-4
Alias PF03635659, PF 03635659

PF-03635659 is a potent and long dissociative half-life muscarinic M3 antagonist (Ki: 0.2 nM) that shows potential for the treatment of chronic obstructive pulmonary disease (COPD).

PF-03635659

PF-03635659

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Purity: 99.85%
Catalog No. T33941Alias PF03635659, PF 03635659Cas No. 931409-24-4
PF-03635659 is a potent and long dissociative half-life muscarinic M3 antagonist (Ki: 0.2 nM) that shows potential for the treatment of chronic obstructive pulmonary disease (COPD).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$240In StockIn Stock
5 mg$590In StockIn Stock
10 mg$843In StockIn Stock
25 mg$1,280In StockIn Stock
50 mg$1,730In StockIn Stock
100 mg$2,330-In Stock
500 mg$4,6706-8weeks6-8weeks
1 mL x 10 mM (in DMSO)$673In 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.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.85%
Appearance:Solid
Color:White
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Product Introduction

PF-03635659 AI Summary
PF-03635659 exhibits a range of bioactivities, mainly as an antagonist at the human recombinant M3 receptor. It inhibits carbamoyl choline-induced calcium currents and displaces [3H]-NMS. The compound has shown efficacy in several models, including CHO cells, Dunkin-Hartley guinea pig tracheal strips, human bronchial rings, and Beagle dogs. In terms of bronchodilator activity, PF-03635659 reduces lung resistance induced by acetylcholine and methacholine. Additionally, it demonstrates metabolic stability in human hepatocytes and significant unbound clearance in intravenously dosed rats..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
PF-03635659 is a potent and long dissociative half-life muscarinic M3 antagonist (Ki: 0.2 nM) that shows potential for the treatment of chronic obstructive pulmonary disease (COPD).
SynonymsPF03635659, PF 03635659
Chemical Properties
Molecular Weight444.57
FormulaC28H32N2O3
Cas No.931409-24-4
SmilesC(CCC(C)(C)N1CC(OC2=CC(O)=CC=C2)C1)(C(N)=O)(C3=CC=CC=C3)C4=CC=CC=C4
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 4.45 mg/mL (10.01 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2494 mL11.2468 mL22.4936 mL112.4682 mL
5 mM0.4499 mL2.2494 mL4.4987 mL22.4936 mL
10 mM0.2249 mL1.1247 mL2.2494 mL11.2468 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:
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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