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PARP-1-IN-2

PARP-1-IN-2
PARP-1-IN-2 is a potent PARP1 inhibitor that crosses the blood-brain barrier (IC50: 149 nM).PARP-1-IN-2 showed significant antiproliferative activity against the human lung adenocarcinoma epithelial cell line A549 in cellular assays.PARP-1-IN-2 induced apoptosis in A549 cells.
Catalog No. T62281Cas No. 684234-55-7
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Purity:98.82%
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PARP-1-IN-2

Catalog No. T62281Cas No. 684234-55-7

PARP-1-IN-2 is a potent PARP1 inhibitor that crosses the blood-brain barrier (IC50: 149 nM).PARP-1-IN-2 showed significant antiproliferative activity against the human lung adenocarcinoma epithelial cell line A549 in cellular assays.PARP-1-IN-2 induced apoptosis in A549 cells.
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Pack SizePriceAvailabilityQuantity
1 mg$98In Stock
5 mg$247In Stock
10 mg$397In Stock
25 mg$663In Stock
50 mg$945In Stock
100 mg$1,280In Stock
500 mg$2,570In Stock
1 mL x 10 mM (in DMSO)$262In Stock
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Product Introduction

Bioactivity
Description
PARP-1-IN-2 is a potent PARP1 inhibitor that crosses the blood-brain barrier (IC50: 149 nM).PARP-1-IN-2 showed significant antiproliferative activity against the human lung adenocarcinoma epithelial cell line A549 in cellular assays.PARP-1-IN-2 induced apoptosis in A549 cells.
Targets&IC50
PARP1:149 ± 11.0 nM
In vitro
PARP-1-IN-2 (compound 11g) (0-10 μM, 24-48 h) exhibits significant anti-proliferative activity against A549 cells without notable cytotoxicity on HFF cells.[1] PARP-1-IN-2 (0-10 μM, 24 h) reduces pro-caspase-3 and phosphorylated AKT expression, while increasing caspase-3, caspase-9 protein, and cleaved PARP-1 expression.[1]
Chemical Properties
Molecular Weight424.28
FormulaC22H15Cl2N3O2
Cas No.684234-55-7
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 9 mg/mL (21.21 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3569 mL11.7847 mL23.5693 mL117.8467 mL
5 mM0.4714 mL2.3569 mL4.7139 mL23.5693 mL
10 mM0.2357 mL1.1785 mL2.3569 mL11.7847 mL
20 mM0.1178 mL0.5892 mL1.1785 mL5.8923 mL

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