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N-Benzoyl-(2R,3S)-3-phenylisoserine
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Catalog No. T7054Cas No. 132201-33-3
Alias taxol side chain
N-Benzoyl-(2R,3S)-3-phenylisoserine (taxol side chain) is an intermediate in the synthesis of the potent anticancer drug Paclitaxel and is used to study the binding sites. It exhibits cytotoxic, antiviral, and immunomodulatory activities.
N-Benzoyl-(2R,3S)-3-phenylisoserine
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Purity: 99.10%
Catalog No. T7054Alias taxol side chainCas No. 132201-33-3
N-Benzoyl-(2R,3S)-3-phenylisoserine (taxol side chain) is an intermediate in the synthesis of the potent anticancer drug Paclitaxel and is used to study the binding sites. It exhibits cytotoxic, antiviral, and immunomodulatory activities.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $37 | In Stock | In Stock | |
| 50 mg | $55 | In Stock | In Stock | |
| 100 mg | $80 | In Stock | In Stock | |
| 200 mg | $117 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $29 | 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:99.10%
Appearance:Solid
Color:White
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Product Introduction
N-Benzoyl-(2R,3S)-3-phenylisoserine AI Summary
N-Benzoyl-(2R,3S)-3-phenylisoserine stimulates the assembly of tubulin into microtubules at a dose of 10 µM, with an ED50 greater than 10.0 µM. It exhibits cytotoxicity against the B16 melanoma cell line, achieving 62% inhibition at a dose of 42 µM and an ED50 greater than 10,000 nM. Additionally, it has a higher ratio of ED50 compared to taxol in both tubulin binding assays (Ratio > 14.0) and cytotoxicity against B16 melanoma cell lines (Ratio > 360.0). The compound shows antiplasmodial activity against the erythrocytic stage of multidrug-resistant Plasmodium falciparum Thailand K1 and chloroquine-resistant Plasmodium falciparum IndoChina W2, with IC50 values greater than 10,000 nM. Furthermore, N-Benzoyl-(2R,3S)-3-phenylisoserine exhibits cytotoxicity against rat L6 cells with an IC50 value greater than 100,000 nM..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | N-Benzoyl-(2R,3S)-3-phenylisoserine (taxol side chain) is an intermediate in the synthesis of the potent anticancer drug Paclitaxel and is used to study the binding sites. It exhibits cytotoxic, antiviral, and immunomodulatory activities. |
| Synonyms | taxol side chain |
| Molecular Weight | 285.29 |
| Formula | C16H15NO4 |
| Cas No. | 132201-33-3 |
| Smiles | O[C@H]([C@@H](NC(=O)c1ccccc1)c1ccccc1)C(O)=O |
| Relative Density. | 1.316g/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: 52 mg/mL (182.27 mM), Sonication is recommended. Ethanol: Soluble | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.01 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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