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UPF 1069

Catalog No. T6181Cas No. 1048371-03-4

UPF 1069 is a specific PARP2 inhibitor ( IC50: 0.3 μM). It is ~27-fold selective against PARP1.

UPF 1069

UPF 1069

Purity: 99.88%
Catalog No. T6181Cas No. 1048371-03-4
UPF 1069 is a specific PARP2 inhibitor ( IC50: 0.3 μM). It is ~27-fold selective against PARP1.
Pack SizePriceAvailabilityQuantity
5 mg$31In Stock
10 mg$50In Stock
25 mg$94In Stock
50 mg$153In Stock
100 mg$247In Stock
1 mL x 10 mM (in DMSO)$35In Stock
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Purity:99.88%
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Product Introduction

Bioactivity
Description
UPF 1069 is a specific PARP2 inhibitor ( IC50: 0.3 μM). It is ~27-fold selective against PARP1.
Targets&IC50
PARP2:0.3 μM
In vitro
UPF 1069 is a selective PARP2 inhibitor with IC50 of 0.3 μM while inhibiting PARP1 with IC50 of 8 μM. [1]
In vivo
In organotypic hippocampal slices, PARP-2 inhibition with UPF-1069 (0.01-1 mM) causes a concentration-dependent exacerbation (up to 155%) of oxygen-glucose deprivation (OGD)-induced CA1 pyramidal cell death. Higher concentrations, acting on both PARP-1 and PARP-2, have no effect on OGD injury. In mouse mixed cortical cells exposed to OGD, UPF-1069 (1-10 mM) significantly reduces post-ischaemic damage. [1]
Chemical Properties
Molecular Weight279.29
FormulaC17H13NO3
Cas No.1048371-03-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 27.9 mg/mL (100 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.5805 mL17.9025 mL35.8051 mL179.0254 mL
5 mM0.7161 mL3.5805 mL7.1610 mL35.8051 mL
10 mM0.3581 mL1.7903 mL3.5805 mL17.9025 mL
20 mM0.1790 mL0.8951 mL1.7903 mL8.9513 mL
50 mM0.0716 mL0.3581 mL0.7161 mL3.5805 mL
100 mM0.0358 mL0.1790 mL0.3581 mL1.7903 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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