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Dibucaine
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Catalog No. T0364Cas No. 85-79-0
Alias Cinchocaine
Dibucaine (Cinchocaine), a local anesthetic of the amide type, is now usually used for surface anesthesia.
Dibucaine
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Purity: 99.88%
Catalog No. T0364Alias CinchocaineCas No. 85-79-0
Dibucaine (Cinchocaine), a local anesthetic of the amide type, is now usually used for surface anesthesia.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 200 mg | $30 | In Stock | In Stock | |
| 500 mg | $44 | In Stock | In Stock | |
| 1 g | $52 | In Stock | In Stock | |
| 1 mL x 10 mM (in DMSO) | $48 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Batch Information
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Purity:99.88%
Appearance:Solid
Color:White
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Product Introduction
Dibucaine AI Summary
Dibucaine is a multifaceted bioactive compound that inhibits the binding of Batrachotoxinin to high affinity sites on voltage-dependent sodium channels in guinea pig cerebral cortex, with an IC50 value of 1400.0 nM and an inhibition of 77.4% at 10 uM. It exhibits distinct partitioning behaviors, with a logD value of 2.906 at pH 7.4 and log P values ranging from 3.77 to 4.4, indicating substantial lipophilicity and potential cellular membrane permeability. It also inhibits the apamin-sensitive SKCa channel in guinea-pig hepatocytes, with an IC50 value of 470,000.0 nM. Dibucaine demonstrates broad bioactivity, including antiviral efficacy against Enterovirus D68 and SARS-CoV-2, inhibition of human BSEP activity with an IC50 of 41650.0 nM, and various enzymatic inhibitions such as HDAC6. It also inhibits SARS-CoV-2 3CL-Pro protease by 31.42% at a concentration of 20µM and shows a dissociation constant pKa of 8.85. The azithromycin derivative has a significant inhibitory effect against SARS-CoV-2-induced cytotoxicity in human cells, making it a potential antiviral therapeutic. Additionally, it exhibits binding affinities to a range of receptors and modulatory activity on Lamin A Splicing, SMN2 splice variant expression, and several other targets, indicating its diverse pharmacological potential..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Dibucaine (Cinchocaine), a local anesthetic of the amide type, is now usually used for surface anesthesia. |
| Synonyms | Cinchocaine |
| Molecular Weight | 343.46 |
| Formula | C20H29N3O2 |
| Cas No. | 85-79-0 |
| Smiles | CCCCOc1cc(C(=O)NCCN(CC)CC)c2ccccc2n1 |
| Relative Density. | 1.1145 g/cm3 (Estimated) |
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 55 mg/mL (160.14 mM), Sonication is recommended.  | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.82 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 | ||||||||||||||||||||||||||||||||||||
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Calculator
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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