Synthesis of alkylcarbonate analogs of O-acetyl-ADP-ribose
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10209690" target="_blank" >RIV/00216208:11310/13:10209690 - isvavai.cz</a>
Alternative codes found
RIV/61389030:_____/13:00399579 RIV/61388963:_____/13:00399579
Result on the web
<a href="http://dx.doi.org/10.1039/c3ob41016a" target="_blank" >http://dx.doi.org/10.1039/c3ob41016a</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c3ob41016a" target="_blank" >10.1039/c3ob41016a</a>
Alternative languages
Result language
angličtina
Original language name
Synthesis of alkylcarbonate analogs of O-acetyl-ADP-ribose
Original language description
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.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Organic and Biomolecular Chemistry
ISSN
1477-0520
e-ISSN
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Volume of the periodical
11
Issue of the periodical within the volume
34
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
5702-5713
UT code for WoS article
000323800900017
EID of the result in the Scopus database
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