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Buffer Detection Kit for Magnetic Beads
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528116
Sigma-AldrichPI 3-Kα Inhibitor VIII - CAS 372196-77-5 - Calbiochem
The PI 3-Kα Inhibitor VIII controls the biological activity of PI 3-Kα. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
More>>The PI 3-Kα Inhibitor VIII controls the biological activity of PI 3-Kα. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Less<<
MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
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Description
Overview
A cell-permeable imidazopyridine compound that acts as a highly potent and ATP-competitive DNA-PK and p110α-selective PI3-K inhibitor (IC50 = 0.3, 40, 100, and 850 nM for p110α, p110γ, PI 3-K C2β, and p110β, respectively). Shown to effectively block cellular PI3-K/Akt signaling and inhibit tumor growth both in vitro (IC50 ≤58 nM in MCF7, MCF7 ADR-res, HeLa, A375, and A549 cultures) and in mice in vivo (62% inhibition of HeLa xenograft in 2 weeks, 50 mg/kg/day, i.p.).
Catalogue Number
528116
Brand Family
Calbiochem®
Synonyms
N-((1E)-(6-Bromoimidazo[1,2-a]pyridin-3-yl)methylene)-Nʹ-methyl-Nʹʹ-(2-methyl-5-nitrobenzene)sulfonohydrazide, HCl, PI 3-K Inhibitor VIII, PIK-75
References
References
Kim, S., et al. 2007. Blood110, 4206. Hayakawa, M., et al. 2007. Bioorg. Med. Chem.15, 5837. Knight, Z.A., et al. 2007. Cell125, 733.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
13-December-2013 JSW
Synonyms
N-((1E)-(6-Bromoimidazo[1,2-a]pyridin-3-yl)methylene)-Nʹ-methyl-Nʹʹ-(2-methyl-5-nitrobenzene)sulfonohydrazide, HCl, PI 3-K Inhibitor VIII, PIK-75
Description
A cell-permeable imidazopyridine compound that acts as a highly potent and ATP-competitive DNA-PK and p110α-selective PI3-K inhibitor (IC50 = 0.3, 40, 100, and 850 nM for p110α, p110γ, PI 3-K C2β, and p110β, respectively). Shown to effectively block cellular PI3-K/Akt signaling and inhibit tumor growth both in vitro (IC50 ≤58 nM in MCF7, MCF7 ADR-res, HeLa, A375, and A549 cultures) and in mice in vivo (62% inhibition of HeLa xenograft in 2 weeks, 50 mg/kg/day, i.p.).
Form
Pale yellow solid
Intert gas (Yes/No)
Packaged under inert gas
CAS number
372196-77-5
Chemical formula
C₁₆H₁₄N₅O₄SBr • HCl • 2H₂O
Structure formula
Purity
≥95% by HPLC
Solubility
DMSO (10 mg/ml)
Storage
Protect from light +2°C to +8°C Hygroscopic
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Regulatory Review
References
Kim, S., et al. 2007. Blood110, 4206. Hayakawa, M., et al. 2007. Bioorg. Med. Chem.15, 5837. Knight, Z.A., et al. 2007. Cell125, 733.