124033

Akt Inhibitor XVI, AT7867

• Synonym(s): Akt Inhibitor XVI, AT7867, p70S6K Inhibitor III, 4-(4-Chlorophenyl)-4-(4-(1H-pyrazol-4-yl)-phenyl)-piperidine, PKA Inhibitor XIV, S6K1 Inhibitor III, Chlorophenyl-pyrazolyl-phenyl-piperidine
• Empirical Formula (Hill Notation): C₂₀H₂₀ClN₃
• Molecular Weight: 337.85
• UNSPSC Code: 12352200
• NACRES: NA.77

Properties

• assay: ≥99% (HPLC)
• Quality Level: 100
• form: powder
• manufacturer/tradename: Calbiochem^®
• storage condition: OK to freeze; protect from light
• color: white
• solubility: DMSO: 100 mg/mL
• shipped in: wet ice
• storage temp.: 2-8°C

Description

General description

A cell-permeable pyrazolo compound that acts as a potent inhibitor against Akt (IC₅₀ = 32, 17, and 47 nM against Akt1, Akt2, and Akt3, respectively), PKA (IC₅₀ = 20 nM), and p70S6K (IC₅₀ = 85 nM) in an ATP-competitive manner (K_i = 18 nM using AKT2), with much reduced activity toward RSK1 (IC₅₀ >100 nM) and a panel of 13 other cellular kinases (IC₅₀ >1 µM), including PDK1, PI 3-Kβ, SGK, GSK-3β, and MEK1. Shown to effectively reduce the phosphorylation levels of GSK-3β, S6R, and FKHRL1 (IC₅₀ range from 2.08 to 4.45 µM against GSK-3β pSer⁹ level), as well as inhibit the proliferation (IC₅₀ range from 0.94 to 11.86 µM) of cancer cells exhibiting constitutive Akt pathway activation, including the PTEN-deficient MES-SA uterine sarcoma and U87MG glioblastoma cell lines. AT7867 treatments via i.p. or p.o. (20 mg/kg and 90 mg/kg, respectively, once every 3 days) are also reported to result in Akt pathway and tumor growth inhibition in mice bearing MES-SA (~40% of untreated control on day 10 by i.p. or p.o.) or U87MG (~50% of untreated control on day 10 by i.p.) xenograft in vivo.

A cell-permeable pyrazolo compound that acts as a potent inhibitor against Akt (IC₅₀ = 32, 17, and 47 nM against Akt1, Akt2, and Akt3, respectively), PKA (IC₅₀ = 20 nM), and p70S6K (IC₅₀ = 85 nM) in an ATP-competitive manner (K_i = 18 nM using AKT2), with much reduced potency toward RSK1 (IC₅₀ >100 nM) and a panel of 13 other cellular kinases (IC₅₀ >1 µM). Shown to reduce cellular phosphorylation of GSK-3β (IC₅₀ range from 2.08 to 4.45 µM), S6R, FKHRL1, and inhibit the proliferation of cancer cells exhibiting constitutive Akt pathway activation both in vitro (IC₅₀ range from 0.94 to 11.86 µM) and in mice in vivo (20 mg/kg via i.p. or 90 mg/kg via p.o.).

Packaging

Packaged under inert gas

Warning

Toxicity: Standard Handling (A)

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Grimshaw, K.M., et al. 2010. Mol. Cancer Ther.9, 1100.
Saxty, G., et al. 2007. J. Med. Chem.50, 2293.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable