Synthesis of alkylcarbonate analogs of O-acetyl-ADP-ribose
| Data(s) |
14/09/2013
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| Resumo |
The non-hydrolyzable alkylcarbonate analogs of O-acetyl-ADP-ribose have been synthesized from the phosphorylated ribose derivatives after coupling with AMP morpholidate promoted by mechanical grinding. The analogs were assessed for their ability to inhibit the human sirtuin homolog SIRT1. © 2013 The Royal Society of Chemistry. |
| Identificador |
http://dx.doi.org/10.1039/c3ob41016a http://www.scopus.com/inward/record.url?eid=2-s2.0-84882329933&partnerID=8YFLogxK |
| Idioma(s) |
eng |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
Dvorakova , M , Nencka , R , Dejmek , M , Zbornikova , E , Brezinova , A , Pribylova , M , Pohl , R , Migaud , M E & Vanek , T 2013 , ' Synthesis of alkylcarbonate analogs of O-acetyl-ADP-ribose ' Organic and Biomolecular Chemistry , vol 11 , no. 34 , pp. 5702-5713 . DOI: 10.1039/c3ob41016a |
| Tipo |
article |
