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Carazolol
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Catalog No. T3284Cas No. 57775-29-8
Alias Suacron, Conducton
Carazolol (Suacron) is a high-affinity antagonist/partial inverse agonist (also referred to as a beta blocker) of the β-adrenergic receptor.
Carazolol
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Purity: 99.53%
Catalog No. T3284Alias Suacron, ConductonCas No. 57775-29-8
Carazolol (Suacron) is a high-affinity antagonist/partial inverse agonist (also referred to as a beta blocker) of the β-adrenergic receptor.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | $30 | In Stock | In Stock | |
| 25 mg | $56 | In Stock | In Stock | |
| 50 mg | $81 | In Stock | In Stock | |
| 100 mg | $118 | In Stock | In Stock | |
| 1 mL x 10 mM (in DMSO) | $31 | 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:99.53%
Appearance:Solid
Color:White
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Product Introduction
Carazolol AI Summary
Carazolol exhibits multiple bioactivities and physicochemical properties of interest. It shows beta-blocking activity with a high affinity for beta1 and beta2 adrenergic receptors, having Ki values of 0.09 nM and 0.03 nM respectively. The compound’s dissociation constant (pKa) is 9.52, influencing its pH-dependent behavior. It demonstrates strong antiviral activity against SARS-CoV-2 strains, indicated by a 20.5% inhibition in the 3CL-Pro protease assay at 20 µM and notable activity in VERO-6 and HRCE cell assays. Carazolol also exhibits antiproliferative effects against SK-MEL-5, SK-MEL-28, and A375 cancer cell lines with IC50 values around 33,000 nM. Despite showing some antibacterial activity against various Staphylococcus aureus strains (with MIC values >50 µg/mL), its hemolytic activity (HC50 >200 µg/mL) suggests low toxicity to rabbit erythrocytes. Additionally, the compound demonstrates minor inhibitory activity against human HDAC6 enzyme, with inhibition rates of 6.05% and 3.77% using different substrates. These combined pharmacological profiles suggest compound 180370 holds potential for further development in various therapeutic areas..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Carazolol (Suacron) is a high-affinity antagonist/partial inverse agonist (also referred to as a beta blocker) of the β-adrenergic receptor. |
| Synonyms | Suacron, Conducton |
| Molecular Weight | 298.38 |
| Formula | C18H22N2O2 |
| Cas No. | 57775-29-8 |
| Smiles | CC(C)NCC(O)COc1cccc2[nH]c3ccccc3c12 |
| Relative Density. | 1.195 g/cm3 |
| Storage | 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 (184.33 mM), Sonication is recommended.  | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.7 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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