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USP1-IN-10

Catalog No. T88967Cas No. 2857051-98-8

USP1-IN-10 (compound 2) is an effective tricyclic USP1 inhibitor with an IC50 of 7.6 nM. It inhibits the viability of MDA-MB-436 cells with an IC50 of 21.58 nM, demonstrating potential for use in cancer research.

USP1-IN-10

USP1-IN-10

Catalog No. T88967Cas No. 2857051-98-8
USP1-IN-10 (compound 2) is an effective tricyclic USP1 inhibitor with an IC50 of 7.6 nM. It inhibits the viability of MDA-MB-436 cells with an IC50 of 21.58 nM, demonstrating potential for use in cancer research.
Pack SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
USP1-IN-10 (compound 2) is an effective tricyclic USP1 inhibitor with an IC50 of 7.6 nM. It inhibits the viability of MDA-MB-436 cells with an IC50 of 21.58 nM, demonstrating potential for use in cancer research.
Targets&IC50
USP1:7.6 nM
Chemical Properties
Molecular Weight545.52
FormulaC27H22F3N9O
Cas No.2857051-98-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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% 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
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