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DS39201083
Catalog No. T213756 Copy Product Info
🥰Excellent
DS39201083, a Conolidine derivative, is a potent oral analgesic. It does not exhibit agonistic activity at the μ-opioid receptor. DS39201083 is applicable in the study of neurological disorders.
DS39201083
Copy Product Info🥰Excellent
Catalog No. T213756
DS39201083, a Conolidine derivative, is a potent oral analgesic. It does not exhibit agonistic activity at the μ-opioid receptor. DS39201083 is applicable in the study of neurological disorders.
DS39201083
Cas No. 2361560-81-6
| 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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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 | DS39201083, a Conolidine derivative, is a potent oral analgesic. It does not exhibit agonistic activity at the μ-opioid receptor. DS39201083 is applicable in the study of neurological disorders. |
| In vitro | DS39201083 exhibits an IC50 of 71 μM in μ-opioid receptor (MOR) binding assays; in functional MOR cAMP assays, it shows an EC50 greater than 100 μM and an Emax of 12%. |
| In vivo | DS39201083 (Compound 17a) (30 mg/kg, oral, single dose) effectively inhibits acute pain induced by formalin in mice through a non-opioid mechanism. In the acetic acid-induced writhing test with Slc:ddY mice, DS39201083 demonstrates excellent dose-dependent activity (ED50=7.8 mg/kg; inhibition rates are 23%, 52%, and 94% at 3, 10, and 30 mg/kg, respectively). |
| Molecular Weight | 254.33 |
| Formula | C16H18N2O |
| Cas No. | 2361560-81-6 |
| Smiles | O=C1C=2NC=3C=CC=CC3C2CN4CCC1(C)CC4 |
| 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
You can also refer to dose conversion for different animals. More Dose Conversion
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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