Design, Synthesis, and Biological Evaluation of Novel Cyclic Adenosine-Inosine Monophosphate (cAIMP) Analogs That Activate Stimulator of Interferon Genes (STING).

We describe novel STING-activating cyclic dinucleotides whose constituent nucleosides are adenosine and inosine and that vary by ribose substitution, internucleotide linkage position, and phosphate modification. In mammalian cells in vitro, some of these cAIMP analogs induce greater STING-dependent IRF and NF-κB pathway signaling than do the reference agonists for murine (DMXAA) or human (2',3'-cGAMP) STING. In human blood ex vivo, they induce type I interferons (IFNs) and proinflammatory cytokines: for the former, 3',3'-cAIMP (9; EC50 of 6.4 µM) and analogs 52-56 (EC50 of 0.4-4.7 µM), which contain one or two 2'-fluoro-2'-deoxyriboses and/or bis-phosphorothioate linkages, are more potent than 2',3'-cGAMP (EC50 of 19.6 µM). Interestingly, 9 induces type I IFNs more strongly than do its linkage isomers 2',3'-cAIMP (10), 3',2'-cAIMP (23), and 2',2'-cAIMP (27). Lastly, some of the cAIMP analogs are more resistant than 2',3'-cGAMP to enzymatic cleavage in vitro. We hope to exploit our findings to develop STING-targeted immunotherapies.

Qualitative colorimetric tests for solid phase synthesis.

Results obtained in the application of these tests are summarized in Table II. We have encountered some variations in the reproducibility and accuracy of some tests. Due to the numerous factors that can influence colorimetric test results (e.g., test reagent stability, resin type, functional group interference, and lability of protecting group) we highly recommend performing a positive and a negative control for any test applied to a new synthesis. We also emphasize the importance of reagent solution purity on the outcome of test results, hence we strongly encourage the use of correctly prepared and carefully stored reactants. To minimize false results due to lability of the resin-product bond or the product itself (such as Fmoc-protected amino acids), colorimetric tests should be performed with the utmost immediacy in regards to completion of the step to be monitored. Hence the storage of resin over long periods of time (more than 24 h) before testing is not advisable. When the result of a colorimetric test is in doubt we advise repeating the test a few times until a reproducible result is obtained. The use of multiple tests for the same functional group may elucidate ambiguous or otherwise challenging cases.