Chemical Structure : USP30i-3
Catalog No.: PC-23862Not For Human Use, Lab Use Only.
USP30i-3 is a potent, selective small molecule USP30 inhibitor with IC50 of 21 nM, selective over other DUBs (IC50=250->3000 nM) with exception of USP6 (IC50=60 nM).
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USP30i-3 is a potent, selective small molecule USP30 inhibitor with IC50 of 21 nM, selective over other DUBs (IC50=250->3000 nM) with exception of USP6 (IC50=60 nM).
USP30i-3 (3 µM) enhanced mitophagy in control and PARK2 KO neurons subjected to mitochondrial damage by CCCP. USP30i-3 reduced ROS levels in compromised (either by CCCP or parkin KO) neurons.
In TH-, but not TH+ neurons, 3 µM USP30i-3 reduced HSP60 areas in the absence of CCCP-induced mitochondrial damage, demonstrating a stronger effect of USP30 inhibition on basal mitophagy in the PARK2 KO TH- neurons.
M.Wt | 325.80 | |
Formula | C18H16ClN3O | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Okarmus J, et al. Cell Death Dis. 2024 Jan 15;15(1):52.
2. Patent WO2016156816 A1.
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