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. Author manuscript; available in PMC: 2021 Nov 19.
Published in final edited form as: Cell Chem Biol. 2020 Jul 28;27(11):1347–1358.e5. doi: 10.1016/j.chembiol.2020.07.007

Figure 5 |. 8-methoxy quinazoline and 3-nitrile quinoline tails achieve high potency.

Figure 5 |

(A) Chemical structures of the R group (head = phosphonate, core = piperidine). (B)–(C) Chemical structures of quinazoline (B) and quinoline (C) tails with corresponding Ki values (mean of at least 2 independent replicates) at pH 7.4. Ki values were determined using 3 nM ENPP1 and 5 μM cGAMP.