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FT709

🥰Excellent
Catalog No. T63375Cas No. 2413991-74-7
Alias FT 709

FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways.

FT709

FT709

🥰Excellent
Catalog No. T63375Alias FT 709Cas No. 2413991-74-7
FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways.
Pack SizePriceAvailabilityQuantity
1 mg$287In Stock
5 mg$928In Stock
10 mg$1,480In Stock
25 mg$2,970In Stock
1 mL x 10 mM (in DMSO)$987In Stock
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Product Introduction

Bioactivity
Description
FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways.
Targets&IC50
USP9X:82 nM
In vitro
In HCT116 cells, treatment with 10 µM FT709 for 24 hours downregulated the expression levels of ZNF598 (a ubiquitin E3 ligase) and centrosomal protein CEP55 [1].
SynonymsFT 709
Chemical Properties
Molecular Weight498.51
FormulaC23H22N4O7S
Cas No.2413991-74-7
SmilesS(=O)(=O)(N1CC2=C(C1)CN(C([C@@H](O)C3=C4C(OC(C)=N4)=CC=C3)=O)C2)C=5C=C6C(=NC5)OCCO6
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (160.48 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0060 mL10.0299 mL20.0598 mL100.2989 mL
5 mM0.4012 mL2.0060 mL4.0120 mL20.0598 mL
10 mM0.2006 mL1.0030 mL2.0060 mL10.0299 mL
20 mM0.1003 mL0.5015 mL1.0030 mL5.0149 mL
50 mM0.0401 mL0.2006 mL0.4012 mL2.0060 mL
100 mM0.0201 mL0.1003 mL0.2006 mL1.0030 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% 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.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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