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Highly Potent and Efficient PROTAC-induced Brd4 Degradation

for Leukemia Therapy

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Highly Potent and Efficient PROTAC-induced Brd4 Degradation

Drug Name ***0135
Description

A von Hippel–landau (VHL) E3 ligase-based proteolysis-targeting chimera consists of a potent Brd4 inhibitor conjugated to an antibody targeting c-type lectin domain family 12 member A (CLEC12) through a novel linker. The product showed significant antitumor activities without severe toxicity in preclinical studies.

Target Brd4; CLEC12
Drug Modality PROTAC
Indication Leukemia
Product Category Signal Transduction Modulators
Mechanism of Action Targeting CLEC12 expressed on tumor cells to induce Brd4 degradation
Status Preclinical
Patent Granted

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