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PF-06873600

PF-06873600
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Purity:99.36%
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PF-06873600

Catalog No. T8463Cas No. 2185857-97-8
PF-06873600 is a selective and orally bioavailable cyclin-dependent kinase (CDK) inhibitor(CDK2, CDK4 and CDK6 with Ki of 0.09 nM, 0.13 nM and 0.16 nM, respectively), has potential antineoplastic activity.
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.
Pack SizePriceAvailabilityQuantity
1 mg$113In Stock
5 mg$282In Stock
10 mg$448In Stock
25 mg$847In Stock
50 mg$1,130In Stock
100 mg$1,530In Stock
500 mg$2,970In Stock
1 mL x 10 mM (in DMSO)$349In Stock
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Product Introduction

Bioactivity
Description
PF-06873600 is a selective and orally bioavailable cyclin-dependent kinase (CDK) inhibitor(CDK2, CDK4 and CDK6 with Ki of 0.09 nM, 0.13 nM and 0.16 nM, respectively), has potential antineoplastic activity.
In vitro
PF-06873600 selectively targets, binds to and inhibits the activity of CDKs.?Inhibition of these kinases leads to cell cycle arrest, induction of apoptosis and inhibition of tumor cell proliferation.?CDKs, ATP-dependent serine/threonine kinases that are important regulators of cell cycle progression and cellular proliferation, are frequently overexpressed in tumor cells.
Chemical Properties
Molecular Weight471.52
FormulaC20H27F2N5O4S
Cas No.2185857-97-8
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 83.33 mg/mL (176.73 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1208 mL10.6040 mL21.2080 mL106.0400 mL
5 mM0.4242 mL2.1208 mL4.2416 mL21.2080 mL
10 mM0.2121 mL1.0604 mL2.1208 mL10.6040 mL
20 mM0.1060 mL0.5302 mL1.0604 mL5.3020 mL
50 mM0.0424 mL0.2121 mL0.4242 mL2.1208 mL
100 mM0.0212 mL0.1060 mL0.2121 mL1.0604 mL

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