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Ulixertinib hydrochloride ERK inhibitor

Cat.No.E7772

Ulixertinib hydrochloride (BVD-523 hydrochloride, VRT752271 hydrochloride) is a highly selective, ATP-competitive, and reversible covalent inhibitor of ERK1/2 kinases, with an IC50 of <0.3 nM against ERK2. It also reduces A375 cell proliferation with an IC50 of 180 nM and inhibits phosphorylated ERK (pERK) and the downstream kinase RSK (pRSK) in the A375 melanoma cell line, with IC50 values of 4.1 μM and 0.14 μM, respectively.
Ulixertinib hydrochloride ERK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 469.79

Quality Control

Batch: E777201 DMSO]94 mg/mL]false]Ethanol]4 mg/mL]false]Water]Insoluble]false Purity: 98.56%
98.56

Chemical Information, Storage & Stability

Molecular Weight 469.79 Formula

C21H22Cl2N4O2.ClH

Storage (From the date of receipt)
CAS No. 1956366-10-1 Download SDF Storage of Stock Solutions

Solubility

In vitro
Batch:

DMSO : 94 mg/mL (200.08 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 4 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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References

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