The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.
A new methodology has been developed for the synthesis of novel 2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylates from 2-aminonicotinaldehyde, Meldrum's acid, and the corresponding alcohols in the presence of anhydrous iron(III) chloride as a cheap and readily available catalyst. The structure of the synthesized compounds was established by IR, H-1 NMR, and mass spectral data and elemental analyses. All the synthesized compounds were evaluated for their in vitro antibacterial and antifungal activity, and the activity of some derivatives was comparable with the activity of Ciprofloxacin and Nystatin used as reference drugs.
GORECKI D. K. J.; HAWES E. M., J. MED. CHEM. <JMCM-AR>, 1977, 20, NO 1, 124-128
作者:GORECKI D. K. J.、 HAWES E. M.
DOI:——
日期:——
HCV NS3 PROTEASE INHIBITORS
申请人:Merck Sharp & Dohme Corp.
公开号:EP2086982B1
公开(公告)日:2018-08-29
POLYNUCLEOTIDE MOLECULES AND USES THEREOF
申请人:MODERNA THERAPEUTICS, INC.
公开号:US20160264614A1
公开(公告)日:2016-09-15
The present disclosure provides alternative nucleosides, nucleotides, and polynucleotides, and methods of use thereof.