117257-22-4Relevant articles and documents
FUCOSIDASE INHIBITORS
-
Page/Page column 24, (2017/02/24)
The present disclosure relates, in general, to compounds useful as inhibitors of fucosidase enzymes, and to methods and compositions for the treatment of tumors or cancers, such as liver disorders and liver tumors (e.g., hepatocellular carcinoma), with a compound as disclosed herein.
Synthesis of a novel uridine analogue and its use in attempts to form new cyclonucleosides using ring-closing metathesis
Zhong, Shi,Mondon, Martine,Len, Christophe
experimental part, p. 1932 - 1936 (2011/02/21)
One novel nucleoside analogue having a hex-5-enyl group and an allyl group in the 5′-C and 3-N position was synthesized regio- and diastereoselectively from d-glucose in twelve steps. In order to reach a particular conformation of nucleosides the nucleosi
Method of inhibiting virus
-
, (2008/06/13)
A group of five- and six-membered heterocyclic compounds having a nitrogen in the ring and 2 to 3 hydroxyl substituents on the ring are effective inhibitory agents of human immunodeficiency virus.