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XMD16-5 ACK inhibitor

Cat.No.S8273

XMD16-5 is a novel tyrosine kinase nonreceptor 2(TNK2) inhibitor with IC50s of 16 nmol/L and 77 nmol/L for the D163E and R806Q mutations.
XMD16-5 ACK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 416.48

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Quality Control

Batch: S827301 DMSO]83 mg/mL]false]Ethanol]5 mg/mL]false]Water]Insoluble]false Purity: 99.05%
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99.05

Solubility

In vitro
Batch:

DMSO : 83 mg/mL (199.28 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 5 mg/mL

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.

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Chemical Information, Storage & Stability

Molecular Weight 416.48 Formula

C23H24N6O2

Storage (From the date of receipt)
CAS No. 1345098-78-3 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles CN1C2=CC=CC=C2C(=O)NC3=CN=C(N=C31)NC4=CC=C(C=C4)N5CCC(CC5)O

Mechanism of Action

Targets/IC50/Ki
TNK2
In vitro
XMD16-5 is found to be potent in the inhibition of TNK2 phosphorylation. This compound and XMD8-87 potently inhibit phosphorylation of TNK2 truncation mutations found in solid tumor types.
References

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