This unit contains four basic protocols describing the synthesis of 5-aminoimidazole-4-carboxamide riboside (AICAR), 5-aminoimidazole-4-carboxamide riboside (ZPM), their 4-N functionalized derivatives, and two sugar-modified analogs of AICAR. The first and second basic protocols reveal the importance of solid-phase synthesis to obtain novel AICAR and ZMP imidazole-modified analogs in a short time, whereas the third and fourth basic protocols allow for the rapid preparation of 5'-F-AICAR and D-ribityl AICA.

Synthesis of 5-Aminoimidazole-4-Carboxamide Riboside (AICAR) and Its Derivatives Using Inosine as Starting Material / D'Errico, Stefano; Oliviero, Giorgia; Borbone, Nicola; Piccialli, Vincenzo; Piccialli, Gennaro. - 63:(2015), pp. 1.35.1-1.35.24. [10.1002/0471142700.nc0135s63]

Synthesis of 5-Aminoimidazole-4-Carboxamide Riboside (AICAR) and Its Derivatives Using Inosine as Starting Material

D'ERRICO, STEFANO;OLIVIERO, GIORGIA;BORBONE, NICOLA;PICCIALLI, VINCENZO;PICCIALLI, GENNARO
2015

Abstract

This unit contains four basic protocols describing the synthesis of 5-aminoimidazole-4-carboxamide riboside (AICAR), 5-aminoimidazole-4-carboxamide riboside (ZPM), their 4-N functionalized derivatives, and two sugar-modified analogs of AICAR. The first and second basic protocols reveal the importance of solid-phase synthesis to obtain novel AICAR and ZMP imidazole-modified analogs in a short time, whereas the third and fourth basic protocols allow for the rapid preparation of 5'-F-AICAR and D-ribityl AICA.
2015
Synthesis of 5-Aminoimidazole-4-Carboxamide Riboside (AICAR) and Its Derivatives Using Inosine as Starting Material / D'Errico, Stefano; Oliviero, Giorgia; Borbone, Nicola; Piccialli, Vincenzo; Piccialli, Gennaro. - 63:(2015), pp. 1.35.1-1.35.24. [10.1002/0471142700.nc0135s63]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/681257
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