Synthesis and structure-activity relationships of C-glycosylated oxadiazoles as inhibitors of glycogen phosphorylase

Bioorganic and Medicinal Chemistry

Volumn 17, Issue 13, 2009, Pages 4773-4785

  Tóth, Marietta ^a   Kun, Sándor ^a   Bokor, Éva ^a   Benltifa, Mahmoud ^b,c,d,e   Tallec, Gaylord ^b,c,d,e   Vidal, Sébastien ^b,c,d,e   Docsa, Tibor ^f   Gergely, Pál ^g   Somsák, László ^a   Praly, Jean Pierre ^b,c,d,e  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b UNIVERSITÉ LYON 1   (France)

^c UNIVERSITÉ LYON 1   (France)

^d CNRS   (France)

^e CPE LYON   (France)

^f INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^g UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

1,2,4 Oxadiazoles; 1,3,4 Oxadiazoles; C Glycosyl compounds; Glycogen phosphorylase; Inhibitors

Indexed keywords

1,2,4 OXADIAZOLE DERIVATIVE; 1,3,4 OXADIAZOLE DERIVATIVE; 2,6 ANHYDRO ALDOSE BENZOYLHYDRAZONE DERIVATIVE; 5 BETA DEXTRO GLUCOPYRANOSYL 3 (2 NAPHTHYL) 1,2,4 OXADIAZOLE DERIVATIVE; 5 BETA DEXTRO GLUCOPYRANOSYL 3 (4 METHYLPHENYL) 1,2,4 OXADIAZOLE DERIVATIVE; BENZOYLHYDRAZONE DERIVATIVE; BETA DEXTRO GLUCOPYRANOSYL CYANIDE; CYANIDE; GLYCOGEN PHOSPHORYLASE; GLYCOGEN PHOSPHORYLASE B; GLYCOGEN PHOSPHORYLASE INHIBITOR; GLYCOSYLATED PROTEIN; IODOBENZENE; IODOBENZENE 1,1 DIACETATE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CATALYSIS; CYCLOADDITION; DRUG SYNTHESIS; ENZYME INHIBITION; ESTERIFICATION; NONHUMAN; OXIDATION; RABBIT; STRUCTURE ACTIVITY RELATION;

ORYCTOLAGUS CUNICULUS;

EID: 66749111878     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2009.04.036     Document Type: Article

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