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AZD8421 CDK inhibitor

Cat.No.E1972

AZD8421 is a potent and highly selective inhibitor of Cyclin-dependent Kinase 2 (CDK2), with an IC50 against CDK2 of 9nM with selectivity over CDK1, CDK4 and CDK6. It also exhibits an anti-proliferative effect, effectively inhibits Rb phosphorylation, and shows strong activity both as a monotherapy and in combination with CDK4/6 inhibitors in breast and ovarian cancer models.
AZD8421 CDK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 440.57

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Quality Control

Batch: E197201 Ethanol]88 mg/mL]false]DMSO]44 mg/mL]false]Water]Insoluble]false Purity: 99.26%
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99.26

Solubility

In vitro
Batch:

Ethanol : 88 mg/mL

DMSO : 44 mg/mL (99.87 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.
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Chemical Information, Storage & Stability

Molecular Weight 440.57 Formula

C18H32N8O3S

Storage (From the date of receipt)
CAS No. 3047321-53-6 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
CDK2
References

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