Inactivation of S-adenosyl-L-homocysteine hydrolase and antiviral activity with 5′,5′,6′,6′-tetradehydro-6′-deoxy-6′-halohomoadenosine analogues (4′-haloacetylene analogues derived from adenosine) Article

Robins, MJ, Wnuk, SF, Yang, XD et al. (1998). Inactivation of S-adenosyl-L-homocysteine hydrolase and antiviral activity with 5′,5′,6′,6′-tetradehydro-6′-deoxy-6′-halohomoadenosine analogues (4′-haloacetylene analogues derived from adenosine) . JOURNAL OF MEDICINAL CHEMISTRY, 41(20), 3857-3864. 10.1021/jm980163m

International Collaboration

cited authors

  • Robins, MJ; Wnuk, SF; Yang, XD; Yuan, CS; Borchardt, RT; Balzarini, J; De Clercq, E

sustainable development goals

authors

publication date

  • September 24, 1998

published in

keywords

  • ACID RELATED-COMPOUNDS
  • ADENOSYLHOMOCYSTEINE HYDROLASE
  • ALCOHOLS
  • BROAD-SPECTRUM
  • Chemistry, Medicinal
  • DERIVATIVES
  • ENZYME
  • INHIBITORS
  • Life Sciences & Biomedicine
  • MECHANISM
  • NUCLEOSIDES
  • NUCLEOTIDES
  • Pharmacology & Pharmacy
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 3857

end page

  • 3864

volume

  • 41

issue

  • 20