480060 Sigma-AldrichNecrosis Inhibitor, IM-54 - CAS 861891-50-1 - Calbiochem
The Necrosis Inhibitor, IM-54, also referenced under CAS 861891-50-1, selectively blocks oxidative stress-induced necrotic cell death. This small molecule/inhibitor is primarily used for Cancer applications.
More>> The Necrosis Inhibitor, IM-54, also referenced under CAS 861891-50-1, selectively blocks oxidative stress-induced necrotic cell death. This small molecule/inhibitor is primarily used for Cancer applications. Less<<Synonymes: 2-(1H-Indol-3-yl)-3-pentylamino-maleimide
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Aperçu
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Tableau de caractéristiques principal
CAS # | Empirical Formula |
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861891-50-1 | C₁₉H₂₃N₃O₂ |
Products
Référence | Conditionnement | Qté | |
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480060-5MG | Flacon en verre | 5 mg |
Description | |
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Overview | A cell-permeable mono-indolylmaleimide compound that selectively blocks oxidative stress-induced necrotic cell death (~3 µM IM-54 prevented ~50% cell death in HL60 cells exposed to 100 µM H2O2). Does not offer protection against Etoposide- (Cat. No. 341205) induced apoptosis or display antioxidant properties. Does not affect the kinase activities of S6K1 and PKC isozymes even at concentrations as high as 50 µM. |
Catalogue Number | 480060 |
Brand Family | Calbiochem® |
Synonyms | 2-(1H-Indol-3-yl)-3-pentylamino-maleimide |
References | |
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References | Dodo, K., et al. 2005. Bioorg. Med. Chem. Lett. 15, 3114. |
Product Information | |
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CAS number | 861891-50-1 |
ATP Competitive | N |
Form | Yellow orange solid |
Hill Formula | C₁₉H₂₃N₃O₂ |
Chemical formula | C₁₉H₂₃N₃O₂ |
Reversible | N |
Structure formula Image | |
Quality Level | MQ100 |
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Physicochemical Information | |
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Cell permeable | Y |
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Packaged under inert gas | Packaged under inert gas |
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Specifications |
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Global Trade Item Number | |
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Référence | GTIN |
480060-5MG | 04055977201864 |
Documentation
Necrosis Inhibitor, IM-54 - CAS 861891-50-1 - Calbiochem FDS
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Necrosis Inhibitor, IM-54 - CAS 861891-50-1 - Calbiochem Certificats d'analyse
Titre | Numéro de lot |
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480060 |
Références bibliographiques
Aperçu de la référence bibliographique |
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Dodo, K., et al. 2005. Bioorg. Med. Chem. Lett. 15, 3114. |