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PolQi1

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Catalog No. T89335Cas No. 2607139-80-8

PolQi1 is a highly efficient and selective Polϴ (DNA polymerase theta) inhibitor with an IC50 of 2 nM, showing potential for cancer therapy.

PolQi1

PolQi1

😃Good
Purity: 98.97%
Catalog No. T89335Cas No. 2607139-80-8
PolQi1 is a highly efficient and selective Polϴ (DNA polymerase theta) inhibitor with an IC50 of 2 nM, showing potential for cancer therapy.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$195-In Stock
5 mg$483-In Stock
10 mg$692-In Stock
25 mg$1,080-In Stock
50 mg$1,490-In Stock
100 mg$1,970-In Stock
200 mg$2,690-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:98.97%
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Product Introduction

Bioactivity
Description
PolQi1 is a highly efficient and selective Polϴ (DNA polymerase theta) inhibitor with an IC50 of 2 nM, showing potential for cancer therapy.
In vitro
Methods:
SpCas9-inducible HEK293T cells and hiPSCs were treated with 0.3–10 μM PolQi1 in combination with AZD7648 (1 μM) for 3 hours to evaluate HDR knock-in efficiency and InDel levels.
Results:
In HEK293T cells, 3 μM PolQi1 increased HDR efficiency by 3.9-fold and reduced InDels by 17.4-fold, with no additional benefit observed at 10 μM. In hiPSCs, HDR efficiency was enhanced by 6.6-fold and InDels were reduced by 2.3-fold.[1]
Chemical Properties
Molecular Weight448.77
FormulaC18H14ClF5N4O2
Cas No.2607139-80-8
SmilesC(N(C)C1=C(F)C(Cl)=C(F)C=C1)(=O)[C@H]2N(C(=O)NC2)C3=CC(C(F)(F)F)=CC(C)=N3
ColorWhite
AppearanceSolid
Storage & Solubility Information
StoragePowder: -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 (6.68 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2283 mL11.1416 mL22.2831 mL111.4156 mL
5 mM0.4457 mL2.2283 mL4.4566 mL22.2831 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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