Abstract
Herein we report an efficient solid-phase synthesis of some N-1-alkyl-substituted analogs of cyclic inosine-diphosphate-ribose (cIDPR), a mimic of cyclic ADP-ribose (cADPR) which has been described as an agonist of the cADPR/Ca(2+) signalling system. The proposed synthetic strategy uses a polystyrene support bearing inosine by a 2',3'-acetal linkage which is converted into several N-1-alkylinosine-bis-phosphate derivatives which in turn were cyclized by a solid-phase pyrophosphate bond formation.
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CITATION STYLE
Oliviero, G., D’Errico, S., Borbone, N., Amato, J., Piccialli, V., Varra, M., … Mayol, L. (2008). Synthesis of N-1-alkyl analogues of cyclic inosine diphosphate ribose (cIDPR) by a new solid phase approach. Nucleic Acids Symposium Series (2004), (52), 573–574. https://doi.org/10.1093/nass/nrn290
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