Chemical Structure : USP15 inhibitor Z86
Catalog No.: PC-27904Not For Human Use, Lab Use Only.
USP15 inhibitor Z86 is a small molecule USP15 inhibitor, promotes the ubiquitination and degradation of Smad2/3 and disrupts TGF-β/Smad2/3 signaling pathway, does not inhibit USP8 and USP4.
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USP15 inhibitor Z86 is a small molecule USP15 inhibitor, promotes the ubiquitination and degradation of Smad2/3 and disrupts TGF-β/Smad2/3 signaling pathway, does not inhibit USP8 and USP4.
Z86 also is a Wnt signaling inhibitor, selectively inhibits the growth of CRC cells with constitutive Wnt signaling and caused obvious G1-phase arrest of the cell cycle.
Z86 inhibits GSK3β (Ser9) phosphorylation, leading to its overactivation and promoting the phosphorylation and degradation of β-catenin.
Z86 is also a novel PI3Kα inhibitor with potent inhibitory efficiency on PI3K-mediated CRCs growth and migration.
| M.Wt | 408.50 | |
| Formula | C27H24N2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Li X, et al. Novel beta-carbolines against colorectal cancer cell growth via inhibition of Wnt/beta-catenin signaling. Cell Death Discov. 2015;1:15033.
2. Nie S, et al. beta-carboline derivative Z86 attenuates colorectal cancer cell proliferation and migration by directly targeting PI3K. Nat Prod Bioprospect. 2024;14(1):3.
3. Wang Y, et al. Nat Prod Bioprospect. 2026 Aug 28;16(1):84.

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