Sugar-modified conjugated diene analogues of adenosine and uridine: Synthesis, interaction with S-adenosyl-L-homocysteine hydrolase, and antiviral and cytostatic effects Article

Wnuk, SF, Ro, BO, Valdez, CA et al. (2002). Sugar-modified conjugated diene analogues of adenosine and uridine: Synthesis, interaction with S-adenosyl-L-homocysteine hydrolase, and antiviral and cytostatic effects . JOURNAL OF MEDICINAL CHEMISTRY, 45(12), 2651-2658. 10.1021/jm020064f

International Collaboration

cited authors

  • Wnuk, SF; Ro, BO; Valdez, CA; Lewandowska, E; Valdez, NX; Sacasa, PR; Yin, D; Zhang, JS; Borchardt, RT; De Clercq, E

sustainable development goals

authors

publication date

  • June 6, 2002

published in

keywords

  • ACID RELATED-COMPOUNDS
  • ADENOSYLHOMOCYSTEINE HYDROLASE
  • ANTICANCER
  • Chemistry, Medicinal
  • DERIVATIVES
  • DISEASE
  • ESTERS
  • INACTIVATION
  • Life Sciences & Biomedicine
  • MECHANISM-BASED INHIBITORS
  • NUCLEOSIDES
  • Pharmacology & Pharmacy
  • STEREOSELECTIVE SYNTHESIS
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 2651

end page

  • 2658

volume

  • 45

issue

  • 12