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XL177A

Catalog No.GC62517

XL177A est un inhibiteur USP7 irréversible très puissant et sélectif avec une IC50 de 0,34nM. XL177A provoque la destruction des cellules cancéreuses par un mécanisme dépendant de p53.

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XL177A Chemical Structure

Cas No.: 2417089-74-6

Taille Prix Stock Qté
5 mg
216,00 $US
En stock
10 mg
342,00 $US
En stock
25 mg
684,00 $US
En stock
50 mg
1 089,00 $US
En stock
100 mg
1 800,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

XL177A is a highly potent and selective irreversible USP7 inhibitor with an IC50 of 0.34 nM. XL177A elicits cancer cell killing through a p53-dependent mechanism[1].

XL177A is a potent USP7 inhibitor and p53 stabilizer in cyto. XL177A suppresses cancer cell growth predominantly through a p53-dependent mechanism. XL177A labels the catalytic cysteine, C223, of USP7 with exquisite selectivity for USP7 across the DUBome and human proteome[1]. XL177A (1 μM) induces complete G1 arrest in MCF7 cells after 24 hours[1].Treatment of MCF7 cells, which express WT TP53, with XL177A (0.001- 10 μM) induces rapid degradation of HDM2 within 2 hours, followed by increases in p53 and downstream p21 protein levels[1].

[1]. Nathan J Schauer, et al. Selective USP7 inhibition elicits cancer cell killing through a p53-dependent mechanism. Sci Rep.2020 Mar 24;10(1):5324.

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