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10-Deacetylbaccatin III

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Catalog No. T2197Cas No. 32981-86-5

10-Deacetylbaccatin-III is an intermediate for the preparation of taxol analogs, possessing anti-cancer activity.

10-Deacetylbaccatin III

10-Deacetylbaccatin III

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🥰Excellent
Purity: 99.21%
Catalog No. T2197Cas No. 32981-86-5
10-Deacetylbaccatin-III is an intermediate for the preparation of taxol analogs, possessing anti-cancer activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$31In StockIn Stock
500 mg$64In StockIn Stock
1 g$98In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.21%
Appearance:solid
Color:White
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Product Introduction

10-Deacetylbaccatin III AI Summary
10-Deacetylbaccatin III demonstrates diverse biological activities across various assays and models. It shows high activity in affecting calcein accumulation in multidrug-resistant human 2780AD cells, with significant reductions at concentrations of 0.25 µg/ml (95.0%), 2.5 µg/ml (90.0%), and 25 µg/ml (93.0%) relative to the control. In human KB cells, it exhibits cytotoxic activity with an effective dose (ED50) of 1.0 µg/ml and an activity level of 16.0%. The compound also displays cytotoxicity against various human cell lines, including A498, NCI-H226, A549, PC-3, and H460 cells, with an IC50 of 3100 nM in H460 cells and moderate to low growth inhibition (1.6% to 27.0%) at 30 µg/ml after 48 hours. Additionally, it has antiproliferative activity against human cancer cell lines like MCF7, A549, A2780, and HCT8, with IC50 values ranging from 16000 nM to 25000 nM, and is less effective against mouse NIH/3T3 cells. 10-Deacetylbaccatin III also exhibits antiviral activity against SARS-CoV-2, inhibiting induced cytotoxicity in Caco-2 and VERO-6 cells, though the effectiveness was low. It shows antileishmanial activity in Leishmania donovani-infected BALB/c mice, reducing the parasitic load by 42.0% at a dose of 100 mg/kg. Additionally, it inhibits human HDAC6 enzyme activity in enzymatic assays, with inhibition percentages of -21.77% and -13.48% using commercial and custom peptide substrates, respectively..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
10-Deacetylbaccatin-III is an intermediate for the preparation of taxol analogs, possessing anti-cancer activity.
Chemical Properties
Molecular Weight544.59
FormulaC29H36O10
Cas No.32981-86-5
SmilesO(C(C)=O)[C@]12[C@]3([C@H](OC(=O)C4=CC=CC=C4)[C@@]5(O)C(C)(C)C([C@@H](O)C(=O)[C@]3(C)[C@@H](O)C[C@]1(OC2)[H])=C(C)[C@@H](O)C5)[H]
Relative Density.1.2007 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 91.7 mg/mL (168.38 mM), Sonication is recommended.
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
H2O: < 1 mg/mL (insoluble or slightly soluble)
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (7.34 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
DMSO
1mg5mg10mg50mg
1 mM1.8362 mL9.1812 mL18.3624 mL91.8122 mL
5 mM0.3672 mL1.8362 mL3.6725 mL18.3624 mL
10 mM0.1836 mL0.9181 mL1.8362 mL9.1812 mL
20 mM0.0918 mL0.4591 mL0.9181 mL4.5906 mL
50 mM0.0367 mL0.1836 mL0.3672 mL1.8362 mL
100 mM0.0184 mL0.0918 mL0.1836 mL0.9181 mL

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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:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 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 DMSOTargetMol | reagent 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent 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.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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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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