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M3 mAChR agonist 1
Catalog No. T214018 Copy Product Info
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M3mAChRagonist 1 is a dual positive allosteric modulator (PAM) that primarily targets the M3 subtype of M3/M5 mAChRs. It demonstrates high subtype selectivity over other mAChR subtypes, including M1, M2, and M4. By modulating the M3 muscarinic acetylcholine receptor, M3mAChRagonist 1 enhances the signaling pathway, leading to increased contraction of isolated rat bladder strips.
M3 mAChR agonist 1
Copy Product Info🥰Excellent
Catalog No. T214018
M3mAChRagonist 1 is a dual positive allosteric modulator (PAM) that primarily targets the M3 subtype of M3/M5 mAChRs. It demonstrates high subtype selectivity over other mAChR subtypes, including M1, M2, and M4. By modulating the M3 muscarinic acetylcholine receptor, M3mAChRagonist 1 enhances the signaling pathway, leading to increased contraction of isolated rat bladder strips.
M3 mAChR agonist 1
Cas No. 1624297-26-2
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | M3mAChRagonist 1 is a dual positive allosteric modulator (PAM) that primarily targets the M3 subtype of M3/M5 mAChRs. It demonstrates high subtype selectivity over other mAChR subtypes, including M1, M2, and M4. By modulating the M3 muscarinic acetylcholine receptor, M3mAChRagonist 1 enhances the signaling pathway, leading to increased contraction of isolated rat bladder strips. |
| In vitro | M3 mAChR agonist 1 (compound 9; 1-10 µM) can enhance the effects of ACh released from nerves under electrical field stimulation (EFS), leading to increased contraction of isolated rat bladder strips. |
| Molecular Weight | 618.68 |
| Formula | C29H33F3N6O4S |
| Cas No. | 1624297-26-2 |
| Smiles | C(C1=C(N=C(NC(=O)C=2C=NC(=CN2)N3CCC(C(O)=O)CC3)S1)C4=CC(C(F)(F)F)=C(OC)C=C4)N5[C@H](CC)CCC5 |
| 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.
Dose Conversion
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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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