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DKFZ-633

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Catalog No. T219152 Copy Product Info
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DKFZ-633 is a potent inhibitor of KLK6 and a KLK6-specific probe, exhibiting an IC50 of 250 nM against human KLK6. It selectively covalently labels the active state of KLK6, allowing for the successful pull-down and capture of endogenous active KLK6 from conditioned cell media. DKFZ-633 serves as an important tool for studying the function and regulatory mechanisms of KLK6 in head and neck cancer.

DKFZ-633

Cas No. 2244425-14-5
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
DKFZ-633 is a potent inhibitor of KLK6 and a KLK6-specific probe, exhibiting an IC50 of 250 nM against human KLK6. It selectively covalently labels the active state of KLK6, allowing for the successful pull-down and capture of endogenous active KLK6 from conditioned cell media. DKFZ-633 serves as an important tool for studying the function and regulatory mechanisms of KLK6 in head and neck cancer.
In vitro
DKFZ-633 (compound 44) inhibits recombinant triple-mutant human KLK6 at a concentration of 0.25 μM following a 30-minute pre-incubation at room temperature, achieving an IC50 of 0.25 μM. At concentrations of 12-25 μM for 1 hour at room temperature, DKFZ-633 dose-dependently pulls down active endogenous human KLK6 from FaDu cell conditioned medium. When used at 50 μM for 1 hour at room temperature, DKFZ-633 can also pull down active endogenous human KLK6 from conditioned media of various human cancer cell lines, including two glycoform-dependent cell types.
Chemical Properties
Molecular Weight440.49
FormulaC26H24N4O3
Cas No.2244425-14-5
SmilesO=C(OCC(=O)NC=1C(=NN(C=2C=CC=CC2)C1C)C)CC=3C=4C=C(C#C)C=CC4NC3C
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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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.
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Related Tags: DKFZ-633 in vitro | DKFZ-633 formula | DKFZ-633 molecular weight