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(2S,3R)-Voruciclib hydrochloride

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Catalog No. T10096L2Cas No. 1253647-46-9
Alias (2S,3R)-Voruciclib hydrochloride (1253731-24-6 free base)

(2S,3R)-Voruciclib hydrochloride is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.

(2S,3R)-Voruciclib hydrochloride

(2S,3R)-Voruciclib hydrochloride

😃Good
Catalog No. T10096L2Alias (2S,3R)-Voruciclib hydrochloride (1253731-24-6 free base)Cas No. 1253647-46-9
(2S,3R)-Voruciclib hydrochloride is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$3,4203-6 months3-6 months
50 mg$4,2803-6 months3-6 months
100 mg$5,6003-6 months3-6 months
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
(2S,3R)-Voruciclib hydrochloride is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.
In vitro
(2S,3R)-Voruciclib (Compound B, formula I) is used in combination with a compound capable of inhibiting EGFR kinase activity and Gemcitabine to treat pancreatic cancer.
Synonyms(2S,3R)-Voruciclib hydrochloride (1253731-24-6 free base)
Chemical Properties
Molecular Weight506.3
FormulaC22H20Cl2F3NO5
Cas No.1253647-46-9
SmilesOC=1C(=C2C(C(=O)C=C(O2)C3=C(Cl)C=C(C(F)(F)F)C=C3)=C(O)C1)[C@@H]4[C@@H](CO)N(C)CC4.Cl
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: 250 mg/mL (493.78 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9751 mL9.8756 mL19.7511 mL98.7557 mL
5 mM0.3950 mL1.9751 mL3.9502 mL19.7511 mL
10 mM0.1975 mL0.9876 mL1.9751 mL9.8756 mL
20 mM0.0988 mL0.4938 mL0.9876 mL4.9378 mL
50 mM0.0395 mL0.1975 mL0.3950 mL1.9751 mL
100 mM0.0198 mL0.0988 mL0.1975 mL0.9876 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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