Fumio Sugawara and co-workers at the Tokyo University of Science have reported in JACS on the synthesis of MA026 and its anti-hepatitis C virus activity.
Archive for the ‘Hepatitis C’ Category
Myriberine A
Posted by naturalproductman on January 17, 2013
Xiao-Jiang Hao and co-workers from the Chinese Academy of Sciences have reported in Organic Letters on the isolation of myriberine A, a pentacyclic alkaloid.
Posted in Alkaloids, Diseases, Hepatitis C | Leave a Comment »
Manoalide vs. HCV
Posted by naturalproductman on March 30, 2012
Nobuyoshi Akimitsu and co-workers from the University of Tokyo have reported on the identification of manoalide A as an inhibitor for heptatitis C virus NS3 helicase.
Posted in Diseases, Enzymes, Hepatitis C, Protein Targets, Proteins, Terpenes | Leave a Comment »
HCV NS5B inhibitors
Posted by naturalproductman on January 11, 2012
Francisco Velasquez and co-workers at Merck have reported in Organic Letters on the synthesis of some HCV (hepatitis C virus) NS5B (non-structural 5B) polymerase inhibitors. Someone once told me that when industry publishes in academic journals, it usually means the project was a failure. I wonder if that is the case here.
Posted in Diseases, Hepatitis C, Methodology | Leave a Comment »
Olefin aminohydroxylation
Posted by naturalproductman on October 19, 2011
Istvan Marko and co-workers at Université catholique de Louvain in Belgium have reported in Tetrahedron on a nice synthesis of Telaprevir using an oxaziridine and a lithium amide to functionalize an alkene.
Posted in Cascade Reactions, Davies lithium amide, Diseases, Hepatitis C, Methodology, Multi-Component Coupling, Named Reagents, One pot | Leave a Comment »
Anti-Hepatitis C Virus Activity with Diosgenin
Posted by naturalproductman on March 11, 2011
Natural product chemists, whether they are isolation chemists or total synthesis type chemists, all must justify the existence of the field to the layman by claiming that the biological activities of the molecules they either uncover or synthesize are interesting. Sometimes these compounds are way too toxic and unrealistic to be used by patients with diseases, so they argue for those compounds by stating that the toxic compounds are “tools” used in biology. Some way or another there will always be biology intertwined with the chemical structure. Well here is an example of an old familiar compound having new biological activity:
Posted in Diseases, Hepatitis C, Steroids | Leave a Comment »