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CS-003 Free base
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Catalog No. T10892Cas No. 191672-52-3
CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on neurokinin-related respiratory diseases.
CS-003 Free base
Copy Product Info😃Good
Catalog No. T10892Cas No. 191672-52-3
CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on neurokinin-related respiratory diseases.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $3,420 | 3-6 months | 3-6 months | |
| 50 mg | $4,280 | 3-6 months | 3-6 months | |
| 100 mg | $5,600 | 3-6 months | 3-6 months |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on neurokinin-related respiratory diseases. |
| Targets&IC50 | NK1:2.3 nM (ki), NK2:0.54 nM (ki), NK3:0.74 nM (ki) |
| In vitro | CS-003 (0.01-10 μM; 24 hours) inhibits inositol phosphate formation induced by NK1, NK2, or NK3 in a concentration-dependent manner, with pA2 values of 8.7, 9.4, and 9.5 μM, respectively. |
| In vivo | CS-003 (intravenous injection; 0.01-3.0 mg/kg; neurokinin A/B/C 5 minutes before injection) inhibits substance P-induced increases in tracheal vascular permeability and neurokinin A and B-induced bronchial contraction, with ID50 values of 0.13, 0.040, and 0.063 mg/kg, respectively. |
| Molecular Weight | 673.65 |
| Formula | C34H38Cl2N2O6S |
| Cas No. | 191672-52-3 |
| Smiles | O=S1C2(C=3C(C1)=CC=CC3)CCN(CC[C@]4(CN(C(=O)C5=CC(OC)=C(OC)C(OC)=C5)CCO4)C6=CC(Cl)=C(Cl)C=C6)CC2 |
| Relative Density. | 1.41 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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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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