Herein, we report on the synthesis of a small set of linear precursors of an inosine analogue of cyclic ADP-ribose (cADPR), a second messenger involved in Ca2+ mobilization from ryanodine receptor stores firstly isolated from sea urchin eggs extracts. The synthesized compounds were obtained starting from inosine and are characterized by an N1-alkyl chain replacing the “northern” ribose and a phosphate group attached at the end of the N1-alkyl chain and/or 5′-sugar positions. Preliminary Ca2+ mobilization assays, performed on differentiated C2C12 cells, are reported as well.
New linear precursors of cIDPR derivatives as stable analogs of cADPR: A potent second messenger with Ca2+-Modulating activity isolated from sea urchin eggs / D'Errico, S.; Basso, E.; Falanga, A. P.; Marzano, M.; Pozzan, T.; Piccialli, V.; Piccialli, G.; Oliviero, G.; Borbone, N.. - In: MARINE DRUGS. - ISSN 1660-3397. - 17:8(2019), p. 476. [10.3390/md17080476]
New linear precursors of cIDPR derivatives as stable analogs of cADPR: A potent second messenger with Ca2+-Modulating activity isolated from sea urchin eggs
D'Errico S.;Falanga A. P.;Marzano M.;Piccialli V.;Piccialli G.;Oliviero G.
;Borbone N.
2019
Abstract
Herein, we report on the synthesis of a small set of linear precursors of an inosine analogue of cyclic ADP-ribose (cADPR), a second messenger involved in Ca2+ mobilization from ryanodine receptor stores firstly isolated from sea urchin eggs extracts. The synthesized compounds were obtained starting from inosine and are characterized by an N1-alkyl chain replacing the “northern” ribose and a phosphate group attached at the end of the N1-alkyl chain and/or 5′-sugar positions. Preliminary Ca2+ mobilization assays, performed on differentiated C2C12 cells, are reported as well.File | Dimensione | Formato | |
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