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TH287 hydrochloride

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Catalog No. T2069LCas No. 1638211-05-8

TH287 is a selective MTH1 inhibitor(IC50 : 0.8 nM). It causees incorporation of oxidized dNTPs in cancer cells, leading to DNA damage, cytotoxicity and therapeutic responses in patient-derived mouse xenografts.

TH287 hydrochloride

TH287 hydrochloride

🥰Excellent
Purity: 99.5%
Catalog No. T2069LCas No. 1638211-05-8
TH287 is a selective MTH1 inhibitor(IC50 : 0.8 nM). It causees incorporation of oxidized dNTPs in cancer cells, leading to DNA damage, cytotoxicity and therapeutic responses in patient-derived mouse xenografts.
Pack SizePriceAvailabilityQuantity
1 mg43 €In Stock
2 mg60 €In Stock
5 mg87 €In Stock
10 mg132 €In Stock
25 mg238 €In Stock
50 mg356 €In Stock
1 mL x 10 mM (in DMSO)93 €In Stock
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Purity:99.5%
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Product Introduction

Bioactivity
Description
TH287 is a selective MTH1 inhibitor(IC50 : 0.8 nM). It causees incorporation of oxidized dNTPs in cancer cells, leading to DNA damage, cytotoxicity and therapeutic responses in patient-derived mouse xenografts.
Targets&IC50
MTH1:0.8 nM
In vitro
TH287 as first-in-class nudix hydrolase family inhibitor that potently and selectively engage and inhibit the MTH1 protein in cells.?Protein co-crystal structures demonstrate that the inhibitors bind in the active site of MTH1.?The inhibitors cause incorporation of oxidized dNTPs in cancer cells, leading to DNA damage, cytotoxicity and therapeutic responses in patient-derived mouse xenografts[1].
Chemical Properties
Molecular Weight305.59
FormulaC11H11Cl3N4
Cas No.1638211-05-8
SmilesNC1=NC(C2=CC=CC(Cl)=C2Cl)=CC(NC)=N1.[H]Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 27.5 mg/mL (89.99 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.2724 mL16.3618 mL32.7236 mL163.6179 mL
5 mM0.6545 mL3.2724 mL6.5447 mL32.7236 mL
10 mM0.3272 mL1.6362 mL3.2724 mL16.3618 mL
20 mM0.1636 mL0.8181 mL1.6362 mL8.1809 mL
50 mM0.0654 mL0.3272 mL0.6545 mL3.2724 mL

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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
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