475858 Sigma-AldrichMet30 Antagonist, SMER3 - Calbiochem
The Met30 Antagonist, SMER3 controls the biological activity of Met30. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
More>> The Met30 Antagonist, SMER3 controls the biological activity of Met30. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Less<<Sinónimos: Small-Molecule Enhancer of Rapamycin-3, 9H-Indeno[1,2-b][1,2,5]oxadiazolo[3,4-e]pyrazin-9-one, Indeno[1,2-b]furazano[3,4-E]pyrazin-9-one, SCFMet30 Inhibitor
Descripción
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Tabla espec. clave
| Empirical Formula |
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| C₁₁H₄N₄O₂ |
| Description | |
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| Overview | This product has been discontinued. A cell-permeable indenofurazinopyrazinone compound that is shown to directly target the F-box protein Met30 subunit of the Skp1-cullin-F-box (SCF) E3 ubiquitin ligase complex, disrupting Met30-Skp1 interaction and selectively inhibiting SCFMet30, but not SCFCdc4, E3 ubiquitin ligase activity. SMER3 is reported to act in a synthetic lethal fashion with rapamycin (Cat. Nos. 553210, 553211, & 553212) in both human lung cancer A549 and in yeast cultures. SMER3 treatment (10 to 30 µM) results in cell cycle arrest and morphological phenotype resembling that seen with temperature-sensitive Met30, but not Skp1 or Cdc4, mutant under non-permissive temperature in yeast cultures. |
| Catalogue Number | 475858 |
| Brand Family | Calbiochem® |
| Synonyms | Small-Molecule Enhancer of Rapamycin-3, 9H-Indeno[1,2-b][1,2,5]oxadiazolo[3,4-e]pyrazin-9-one, Indeno[1,2-b]furazano[3,4-E]pyrazin-9-one, SCFMet30 Inhibitor |
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| References | Aghajan, M., et al. 2010. Nature Biotechnol. 28, 738. |
| Product Information | |
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| Form | Yellow solid |
| Hill Formula | C₁₁H₄N₄O₂ |
| Chemical formula | C₁₁H₄N₄O₂ |
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| Quality Level | MQ100 |
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| Purity | ≥97% by HPLC |
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| Packaged under inert gas | Packaged under inert gas |
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| Número de referencia | GTIN |
| 475858 | 0 |
Documentation
Met30 Antagonist, SMER3 - Calbiochem Ficha datos de seguridad (MSDS)
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Referencias bibliográficas
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| Aghajan, M., et al. 2010. Nature Biotechnol. 28, 738. |



