A novel mechanism-based inhibitor (6′-bromo-5′,6′-didehydro-6′-deoxy-6′-fluorohomoadenosine) that covalently modifies human placental S-adenosylhomocysteine hydrolase Article

Yuan, CS, Wnuk, SF, Robins, MJ et al. (1998). A novel mechanism-based inhibitor (6′-bromo-5′,6′-didehydro-6′-deoxy-6′-fluorohomoadenosine) that covalently modifies human placental S-adenosylhomocysteine hydrolase . JOURNAL OF BIOLOGICAL CHEMISTRY, 273(29), 18191-18197. 10.1074/jbc.273.29.18191

Open Access

cited authors

  • Yuan, CS; Wnuk, SF; Robins, MJ; Borchardt, RT

sustainable development goals

authors

publication date

  • July 17, 1998

published in

keywords

  • ANALOGS
  • Biochemistry & Molecular Biology
  • CHEMOTHERAPY
  • DESIGN
  • INACTIVATION
  • L-HOMOCYSTEINE HYDROLASE
  • Life Sciences & Biomedicine
  • METHYLTRANSFERASES
  • NEPLANOCIN-A
  • NUCLEOSIDES
  • SPECTRUM ANTIVIRAL AGENTS
  • Science & Technology
  • TARGET

Digital Object Identifier (DOI)

publisher

  • AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

start page

  • 18191

end page

  • 18197

volume

  • 273

issue

  • 29