| Name | Ulixertinib hydrochloride |
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| Description | Ulixertinib hydrochloride is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line[1][2]. |
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| References |
| Molecular Formula | C21H23Cl3N4O2 |
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| Molecular Weight | 469.79 |
| Storage condition | 2-8℃ |