http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015218202-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c36b51422e483c9668800c2aff270102
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_62a25f73b51c70c44998457c37ec9170
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fdb273fab56777bf4930bcc01d0c15e2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-20
filingDate 2012-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2045c7fa77aa9992b5a887d41b322075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2523a1dda47aa97f33e02bd53fc63503
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_596b89275e2266ab82ad7285a28dbca1
publicationDate 2015-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2015218202-A1
titleOfInvention Non-enzymatic synthesis of o-acetyl-adp-ribose and analogues thereof
abstract Provided herein is a simple, one-step, non-enzymatic synthesis of O-Acetyl-ADP-ribose (OAADPR) from NAD and sodium acetate in acetic acid. The extension of this reaction to other carboxylic acids, demonstrates that the reaction between NAD, and NAD analogs produces mixtures of the corresponding 2′- and 3′-carboxylic esters. Included are O-carboxyl-ADP-ribose compounds and corresponding methods of synthesis (e.g., O-propionyl-ADP-ribose, O-succinyl-ADP-ribose, O-malonyl-ADP-ribose), as well as non-adenosine nucleoside compounds.
priorityDate 2011-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 506.