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USP30-IN-20

USP30-IN-20 is an orally active USP30 inhibitor (Kd = 1.61 μM, IC50 = 12.8 μM) . USP30-IN-20 induces ferroptosis by promoting ubiquitination-mediated degradation of GPX4. USP30-IN-20 inhibits the proliferation, migration, invasion, and stemness of prostate cancer cells. USP30-IN-20 induces G0/G1 cell cycle arrest and ROS levels in prostate cancer cells. USP30-IN-20 exhibits significant anti-tumor efficacy in PC3 cell subcutaneous xenografts in mice. USP30-IN-20 can be used for the study of advanced prostate cancer[1].

Product Specifications

UNSPSC

12352005

Target

Deubiquitinase; Ferroptosis; Glutathione Peroxidase; Reactive Oxygen Species (ROS)

Related Pathways

Apoptosis; Cell Cycle/DNA Damage; Immunology/Inflammation; Metabolic Enzyme/Protease; NF-κB

Applications

Cancer-programmed cell death

Field of Research

Cancer

Smiles

ClC(C=CC=C1)=C1[Se]C2=C(C)C3=C(O2)CC(C)CC3=O

Molecular Formula

C16H15ClO2Se

Molecular Weight

353.70

References & Citations

[1]Xu L, et al. Discovery of a selenium-containing compound as a promising ferroptosis inducer attenuates prostate cancer progression. Eur J Med Chem. 2025 Dec 5;299:118067.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

GPX4; USP30

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