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. 2020 Apr 13;11(6):1236–1243. doi: 10.1021/acsmedchemlett.0c00095

Table 2. Optimization of the Pyridine Hinge Binder.

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a

The activity against each class I PI3K was evaluated in in vitro kinase assays containing 2Km steady state concentrations of ATP (average of ≥2 determinations).

b

Numbers in parentheses represent fold selectivity (PI3Kα/δ/γ IC50 divided by PI3Kβ IC50).