124005 Sigma-AldrichAkt Inhibitor - Calbiochem
This Akt inhibitor is a cell-permeable, reversible, and substrate competitive phosphatidylinositol ether analog that potently and selectively inhibits Akt (IC50 of 5.0 µM).
More>> This Akt inhibitor is a cell-permeable, reversible, and substrate competitive phosphatidylinositol ether analog that potently and selectively inhibits Akt (IC50 of 5.0 µM). Less<<Synonyme: 1L6-Hydroxymethyl-chiro-inositol-2-(R)-2-O-methyl-3-O-octadecyl-sn-glycerocarbonate
Empfohlene Produkte
Übersicht
Replacement Information |
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Key Spec Table
Empirical Formula |
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C₃₀H₅₈O₁₀ |
Preis & Verfügbarkeit
Bestellnummer | Verfügbarkeit | Verpackung | St./Pkg. | Preis | Menge | |
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124005-1MG |
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Kst.-Ampulle | 1 mg |
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References | |
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References | Hu, Y., et al. 2000 J. Med. Chem. 43, 3045. |
Product Information | |
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ATP Competitive | Y |
Form | White to off-white solid |
Hill Formula | C₃₀H₅₈O₁₀ |
Chemical formula | C₃₀H₅₈O₁₀ |
Hygroscopic | Hygroscopic |
Reversible | Y |
Structure formula Image | |
Quality Level | MQ100 |
Applications | |
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Application | This Akt inhibitor is a cell-permeable, reversible, and substrate competitive phosphatidylinositol ether analog that potently and selectively inhibits Akt (IC50 of 5.0 µM). |
Biological Information | |
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Primary Target | Akt |
Primary Target IC<sub>50</sub> | 5.0 µM for Akt (PKB) |
Purity | ≥98% by NMR |
Physicochemical Information | |
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Cell permeable | Y |
Dimensions |
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Materials Information |
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Toxicological Information |
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Safety Information according to GHS |
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Safety Information |
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Product Usage Statements |
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Packaging Information | |
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Packaged under inert gas | Packaged under inert gas |
Transport Information |
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Supplemental Information |
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Specifications |
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Global Trade Item Number | |
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Bestellnummer | GTIN |
124005-1MG | 07790788047979 |
Documentation
Akt Inhibitor - Calbiochem SDB
Titel |
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Akt Inhibitor - Calbiochem Analysenzertifikate
Titel | Chargennummer |
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124005 |
Literatur
Übersicht |
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Hu, Y., et al. 2000 J. Med. Chem. 43, 3045. |
Broschüre
Titel |
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Akt |
Biologics 31.1 |