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USP15 inhibitor Z86

Chemical Structure : USP15 inhibitor Z86

CAS No.: 1448711-61-2

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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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

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.

Physicochemical Properties

M.Wt 408.50
Formula C27H24N2O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

isopropyl 9-ethyl-1- (naphthalen-1-yl)-9H-pyrido[3,4-b]indole-3- carboxylate

References

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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