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Divergent and stereocontrolled approach to the synthesis of uracil nucleosides branched at the anomeric position

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This article is published in Journal of Organic Chemistry.The article was published on 1995-02-01. It has received 56 citations till now.

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Patent

Methods and compositions for treating hepatitis C virus

TL;DR: A method and composition for treating a host infected with hepatitis C comprising administering an effective hepatitis C treatment amount of a described 1′, 2′ or 3′-modified nucleoside or a pharmaceutically acceptable salt or prodrug thereof, is provided in this paper.
Patent

3′-or 2′-hydroxymethyl substituted nucleoside derivatives for treatment of hepatitis virus infections

TL;DR: In this article, a composition for and a method of treating hepatitis B virus (HBV) infection, hepatitis C virus (HCV), hepatitis D virus (HDV), or a proliferative disorder in a patient using an effective amount of a compound selected from the group consisting of formulas (I)-(IV) below and mixtures of two or more thereof, wherein the substituents are as defined herein.
Patent

2-branched nucleosides and flaviviridae mutation

TL;DR: A method for the treatment of Flaviviridae infection that includes the administration of a 2-branched nucleoside, or a pharmaceutically acceptable prodrug and/or salt thereof, to a human in need of therapy in combination or alternation with a drug that directly or indirectly induces a mutation in the viral genome at a location other than a mutation of a nucleotide that results in a change from serine to a different amino acid in the highly conserved consensus sequence, XRXSGXXXT, or is associated with such a mutation as discussed by the authors
Patent

1'-substituted carba-nucleoside analogs for antiviral treatment

TL;DR: In this paper, pyrrolo, imidazo, triazolo and triazinyl nucleosides were used for the treatment of hepatitis C infection, where the 1′ position of the nucleoside sugar was substituted.
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