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MK-4827 Racemate

🥰Excellent
Catalog No. T22988Cas No. 1038915-75-1
Alias Niraparib Racemate, 2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide

MK-4827 Racemate (Niraparib Racemate) is a selective PARP1 and PARP2 inhibitor with IC50s of 3.8 nM and 2.1 nM, respectively, over 330-fold selectivity for PARP3, V-PARP and Tank1.

MK-4827 Racemate

MK-4827 Racemate

🥰Excellent
Purity: 99.86%
Catalog No. T22988Alias Niraparib Racemate, 2-(4-piperidin-3-ylphenyl)indazole-7-carboxamideCas No. 1038915-75-1
MK-4827 Racemate (Niraparib Racemate) is a selective PARP1 and PARP2 inhibitor with IC50s of 3.8 nM and 2.1 nM, respectively, over 330-fold selectivity for PARP3, V-PARP and Tank1.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$45In StockIn Stock
2 mg$63In StockIn Stock
5 mg$89In StockIn Stock
10 mg$156In StockIn Stock
25 mg$297In StockIn Stock
50 mg$518In StockIn Stock
100 mg$698In StockIn Stock
1 mL x 10 mM (in DMSO)$121In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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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Batch Information

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Purity:99.86%
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Product Introduction

Bioactivity
Description
MK-4827 Racemate (Niraparib Racemate) is a selective PARP1 and PARP2 inhibitor with IC50s of 3.8 nM and 2.1 nM, respectively, over 330-fold selectivity for PARP3, V-PARP and Tank1.
Targets&IC50
PARP1:3.8 nM, PARP2:2.1 nM
SynonymsNiraparib Racemate, 2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide
Chemical Properties
Molecular Weight320.39
FormulaC19H20N4O
Cas No.1038915-75-1
SmilesNC(=O)c1cccc2cn(nc12)-c1ccc(cc1)C1CCCNC1
Relative Density.1.34 g/cm3 (Predicted)
ColorYellow
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: 60 mg/mL (187.27 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1212 mL15.6060 mL31.2120 mL156.0598 mL
5 mM0.6242 mL3.1212 mL6.2424 mL31.2120 mL
10 mM0.3121 mL1.5606 mL3.1212 mL15.6060 mL
20 mM0.1561 mL0.7803 mL1.5606 mL7.8030 mL
50 mM0.0624 mL0.3121 mL0.6242 mL3.1212 mL
100 mM0.0312 mL0.1561 mL0.3121 mL1.5606 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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