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Ebvaciclib (PF-06873600) CDK inhibitor

Cat.No.S8816

PF-06873600 is an inhibitor of cyclin-dependent kinase 2 (CDK2), CDK4, and CDK6 with Ki values of 0.1, 1.2, and 0.1 nM, respectively, blocks the phosphorylation of retinoblastoma protein (RB1), and limits the proliferation of OVCAR-3 ovarian cancer cells with EC50s of 19 and 45 nM, respectively.
Ebvaciclib (PF-06873600) CDK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 471.52

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Quality Control

Batch: Purity: 98.95%
98.95

Products Often Used Together with Ebvaciclib (PF-06873600)

Fadraciclib (CYC065)

It and Fadraciclib efficiently inhibit growth of both sensitive and aromatase inhibitor (AI)-resistant cells.

Dinaciclib (SCH 727965)

Treatment with it and Dinaciclib dampens induction of gammaH2AX in FT282-hTERT cells.

Tagtociclib (PF-07104091)

It and PF-07104091 are used to understand the relationship between pNPAT and nascent histone mRNA in MCF10A cells.

Solubility

In vitro
Batch:

DMSO : 94 mg/mL (199.35 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 3 mg/mL

Water : Insoluble

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Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Chemical Information, Storage & Stability

Molecular Weight 471.52 Formula

C20H27F2N5O4S

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 2185857-97-8 -- Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
CDK2
(in a mobility shift assay (MSA))
0.1 nM(Ki)
CDK6
(in a mobility shift assay (MSA))
0.1 nM(Ki)
CDK4
(in a mobility shift assay (MSA))
1.2 nM(Ki)
In vitro

PF-06873600 is an inhibitor of cyclin-dependent kinase 2 (CDK2), CDK4, and CDK6 with Ki values of 0.1, 1.2, and 0.1 nM, respectively.

References

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