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Product Name:ERK Inhibitor - CAS 1049738-54-6 - Calbiochem CAS:1049738-54-6 Purity:95% Package:25g、50g
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| ERK Inhibitor Basic information |
Product Name: | ERK Inhibitor | Synonyms: | (5Z)-3-(2-aminoethyl)-5-[(4-ethoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione:hydrochloride;ERK Inhibitor - CAS 1049738-54-6 - Calbiochem;3-(2-aminoethyl)-5-[(4-ethoxyphenyl)methylene]-2,4-thiazolidinedione,monohydrochloride | CAS: | 1049738-54-6 | MF: | C14H17ClN2O3S | MW: | 328.81 | EINECS: | | Product Categories: | | Mol File: | 1049738-54-6.mol | |
| ERK Inhibitor Chemical Properties |
storage temp. | +2C to +8C | solubility | DMSO: 2 mg/ml | form | Light yellow solid |
| ERK Inhibitor Usage And Synthesis |
Description | ERK inhibitor is a cell-permeable inhibitor that binds ERK2 near its docking domain (KD = 5 μM). This prevents its interaction with protein substrates without inhibiting catalytic activity. ERK inhibitor blocks ERK-specific phosphorylation of ribosomal S6 kinase-1 and ternary complex factor Elk-1 but does not affect ERK1/2 phosphorylation by MEK1/2. Presumably through its effects on ERK, ERK inhibitor completely prevents proliferation of HeLa cells (IC50 = 15-20 μM), A549 lung carcinoma cells (IC50 = 25 μM), Sum-159 estrogen receptor-negative breast cancer cells and HT1080 fibrosarcoma cells. | General Description | A cell-permeable and reversible thiazolidinedione compound that displays anti-proliferative properties (IC50 ≤ 25 μM in HeLa, A549, and SUM-159 tumor cells). Preferentially binds to ERK2 with a KD of ~5 μM and prevents its interaction with protein substrates. Shown to block ERK-mediated phosphorylation of ribosomal S6 kinase-1 (RSK-1) and ternary complex factor Elk-1 in HeLa cells, while exhibiting little effect on ERK1/2 phosphorylation by MEK1/2. | Biochem/physiol Actions | Primary TargetERK |
| ERK Inhibitor Preparation Products And Raw materials |
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