The following articles (labelled with PubMed ID or TBD) are for your review
||Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-L-homocysteine hydrolase.
||4',5'-unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase.
||Merrell Dow Research Institute
||Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 11. Molecular dissections of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase.
||University of Kansas
||Synthesis of 2-fluoronoraristeromycin and its inhibitory activity against Plasmodium falciparum S-adenosyl-L-homocysteine hydrolase.
||(+)-7-Deaza-5'-noraristeromycin as an anti-trypanosomal agent.
||Antiviral enantiomeric preference for 5'-noraristeromycin.
||University of South Florida
||New neplanocin analogues. 1. Synthesis of 6'-modified neplanocin A derivatives as broad-spectrum antiviral agents.
||Toyo Jozo Company, Ltd.