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. 2020 Jan 8;7:873. doi: 10.3389/fchem.2019.00873

Figure 7.

Figure 7

(A) Presentation of the identified scaffolds by in vitro biochemical screening as PI3K inhibitors (hinge interacting moieties are labeled in red), Ar—presents carbocyclic or heterocyclic aromatic rings; (B) the scheme of lead optimization of the selected morpholine derivatives.