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KAT6-IN-1

🥰Excellent
Catalog No. T75146Cas No. 2569008-99-5
Alias Prifetrastat, PF-07248144, PF07248144

KAT6-IN-1 (compound E) is a selective, orally available inhibitor of histone acetyltransferases KAT6A and KAT6B, exhibiting antitumour activity for cancer research.

KAT6-IN-1

KAT6-IN-1

🥰Excellent
Purity: 99.86%
Catalog No. T75146Alias Prifetrastat, PF-07248144, PF07248144Cas No. 2569008-99-5
KAT6-IN-1 (compound E) is a selective, orally available inhibitor of histone acetyltransferases KAT6A and KAT6B, exhibiting antitumour activity for cancer research.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$100-In Stock
5 mg$247-In Stock
10 mg$396-In Stock
25 mg$787-In Stock
50 mg$1,230-In Stock
100 mg$1,980-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.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:99.86%
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Product Introduction

Bioactivity
Description
KAT6-IN-1 (compound E) is a selective, orally available inhibitor of histone acetyltransferases KAT6A and KAT6B, exhibiting antitumour activity for cancer research.
In vitro
The combination of KAT6-IN-1 and Palbociclib exerts synergistic inhibitory effects on T47D, ZR-75-1, CAMA1, and MCF7 cancer cells [2].
In vivo
In the mouse ST340 Parazacco spilurus subsp. spilurus transplantation model, KAT6-IN-1 (3 mg/kg, orally administered once daily for 21 days) demonstrated antitumor activity [2].
SynonymsPrifetrastat, PF-07248144, PF07248144
Chemical Properties
Molecular Weight414.43
FormulaC19H18N4O5S
Cas No.2569008-99-5
SmilesO=S(=O)(NC1=NOC2=CC(=CC(OC)=C21)CN3N=CC=C3)C=4C=CC=CC4OC
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 3 mg/mL (7.24 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4130 mL12.0648 mL24.1295 mL120.6476 mL
5 mM0.4826 mL2.4130 mL4.8259 mL24.1295 mL

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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% Saline/PBS/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 μLSaline/PBS/ddH2OTargetMol | 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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