Inactivation of S‐Adenosyl‐L‐homocysteine Hydrolase with Novel 5′‐Thioadenosine Derivatives. Antiviral Effects.

Georges Guillerm; D. Guillerm; Corinne Vandenplas‐Vitkowski; Cederic Glapski; De Clercq Erik

doi:10.1002/chin.200338185

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Inactivation of S‐Adenosyl‐L‐homocysteine Hydrolase with Novel 5′‐Thioadenosine Derivatives. Antiviral Effects.

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Inactivation of S‐Adenosyl‐L‐homocysteine Hydrolase with Novel 5′‐Thioadenosine Derivatives. Antiviral Effects.

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Related publications

Inactivation of S-Adenosyl-l-Homocysteine hydrolase with novel 5′-thioadenosine derivatives. Antiviral effects

Sugar‐Modified Conjugated Diene Analogues of Adenosine and Uridine: Synthesis, Interaction with S‐Adenosyl‐L‐homocysteine Hydrolase, and Antiviral and Cytostatic Effects.

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S-Adenosyl-L-homocysteine Hydrolase Inhibitors as Anti-Viral Agents: 5′-Deoxyaristeromycin

9‐(2‐Aryloxyethyl) Derivatives of Adenine — A New Class of Non‐Nucleosidic Antiviral Agents.