a(PUBCHEM:33334) decreases act(p(HGNC:CSNK1A1))

PubMed:30444369

Screening previously synthesized frentizole derivatives for their efficiency to inhibit CK1 activity as well as ABAD, identified compound 13 which possessed an ABAD IC 50 = 1.67 µM, the most potent inhibitor of this chemotype identified to date.

MeSH

Neurons

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