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QC6352

Catalog No. T16700Cas No. 1851373-36-8

QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).

QC6352

QC6352

Catalog No. T16700Cas No. 1851373-36-8
QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).
Pack SizePriceAvailabilityQuantity
25 mg$1,5208-10 weeks
50 mg$1,9808-10 weeks
100 mg$2,5008-10 weeks
1 mL x 10 mM (in DMSO)$4348-10 weeks
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Product Introduction

Bioactivity
Description
QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).
Targets&IC50
KDM4C:35 nM
In vitro
QC6352 is an effective KDM4C inhibitor (IC50: 35±8 nM). QC6352 blocks the proliferation and self-renewal of BCSCs. In a concentration-dependent manner QC6352 dramatically decreases the anchorage-independent sphere-forming capacity of BCSC1 and BCSC2. The protein levels of (Epidermal growth factor receptor) EGFR are reduced in both BCSC1 and BCSC2 upon treatment with QC6352 [1][2].
In vivo
QC6352 significantly inhibits tumor growth and final tumor weight in both BCSC1 and BCSC2 xenografts. The treatment is well tolerated, with no impact on mice body weight. Administration of the KDM4 inhibitor QC6352 effectively blocks BCSC xenograft tumor growth [2].
Chemical Properties
Molecular Weight387.47
FormulaC24H25N3O2
Cas No.1851373-36-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 25 mg/mL (64.52 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5808 mL12.9042 mL25.8084 mL129.0422 mL
5 mM0.5162 mL2.5808 mL5.1617 mL25.8084 mL
10 mM0.2581 mL1.2904 mL2.5808 mL12.9042 mL
20 mM0.1290 mL0.6452 mL1.2904 mL6.4521 mL
50 mM0.0516 mL0.2581 mL0.5162 mL2.5808 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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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

Keywords

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