GNE-6776

GNE-6776 is a potent, non-covalent, selective and orally bioavailable inhibitor of USP7 with IC50 of 1.34 μM and 0.61 μM for full length USP7 and USP7 catalytic domain, respectively.

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库存: 现货

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5mg

￥2180.00

1962.00

- +
10mg

￥3467.00

3120.00

- +
50mg

￥10897.00

9807.00

- +
100mg

￥17832.00

16048.00

- +

已选 0 种 0 瓶

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Background

GNE-6776 is a potent, non-covalent, selective and orally bioavailable inhibitor of USP7 with IC50 of 1.34 μM and 0.61 μM for full length USP7 and USP7 catalytic domain, respectively.

[1] Lorna Kategaya, et al. Nature. 2017 Oct 26;550(7677):534-538.

Protocol

Cell experiment:

EOL-1 cells are seeded into 384-well plates 24?h before compound addition. Cells are then incubated with compound (e.g., GNE-6776; 0.003, 0.009, 0.027, 0.082, 0.25, 0.74, 2.22, 6.67, and 20 μM) for 72?h or 120?h before assaying viability. Assays are performed in biological triplicate. Cells are incubated (37°C, 5% CO2) in RPMI-1640, 2.5% FBS (72?h assay) or 5% FBS (120?h assay), and 2?mM glutamine throughout the assay. The reported IC50 and mean viability metrics are as follows: IC50 is the dose at which the estimated inhibition is 50% relative to untreated wells (that is, absolute IC50). The mean viability is calculated[1].

Animal experiment:

Mice[1]GNE-6776 is administered at 200?mg/kg (body weight) by oral gavage to female C.B-17 SCID mice, aged 12-16 weeks (n=3 per time point). No randomization is used for DMPK studies. At 0.5, 1, 2, 4, 8 and 24?h post-dose, blood samples are collected by terminal cardiac puncture into anticoagulant tubes (EDTA). Clarified plasma is then transferred to a fresh tube and snap frozen. GNE-6776 plasma concentrations are determined by LC-MS/MS[1].

参考文献:

[1]. Kategaya L, et al. USP7 small-molecule inhibitors interfere with ubiquitin binding. Nature. 2017 Oct 26;550(7677):534-538.