Open-chain carbocyclic analogs of adenosine with dihalovinyl unit as potential inhibitors of S-adenosyl-L-homocysteine hydrolase Article

Lewandowska, E, Lalama, J, Yuan, CS et al. (2003). Open-chain carbocyclic analogs of adenosine with dihalovinyl unit as potential inhibitors of S-adenosyl-L-homocysteine hydrolase . NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 22(9), 1747-1755. 10.1081/NCN-120023270

International Collaboration

cited authors

  • Lewandowska, E; Lalama, J; Yuan, CS; Wnuk, SF

sustainable development goals

authors

publication date

  • January 1, 2003

published in

keywords

  • ADENOSYLHOMOCYSTEINE HYDROLASE
  • ANTIVIRAL ACTIVITY
  • Biochemistry & Molecular Biology
  • DERIVATIVES
  • HYDROLYTIC ACTIVITY
  • INACTIVATION
  • Life Sciences & Biomedicine
  • MECHANISM-BASED INHIBITORS
  • NUCLEOSIDES
  • S-adenosyl-L-homocysteine hydrolase
  • Science & Technology
  • acyclic nucleosides
  • carbocyclic nucleosides
  • enzyme inhibition

Digital Object Identifier (DOI)

publisher

  • TAYLOR & FRANCIS INC

start page

  • 1747

end page

  • 1755

volume

  • 22

issue

  • 9