Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Michael B. Doughty"'
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 22:283-297
Nucleotides 2-(4-azidophenacyl)thio-1,N6-etheno-2'-deoxyadenosine 5'-triphosphate 1 and its tetrafluoro analog 2 inhibit HIV-1 reverse transcriptase (RT) competitively relative to template. These template-competitive RT inhibitors (TCRTIs) were analy
Publikováno v:
Bioorganic & Medicinal Chemistry. 10:4131-4141
Analogues of a novel class of template-competitive reverse transcriptase inhibitors (Li, K.; Lin, W.; Chong, K. H.; Moore, B. M.; Doughty, M. B. Bioorg. Med. Chem. 2002 , 10 , 507) were analyzed as photoprobes of HIV-1 reverse transcriptase (RT) hete
Publikováno v:
Bioorganic & Medicinal Chemistry. 10:507-515
We report the design, synthesis and activity studies on a novel class of template-competitive reverse transcriptase inhibitors (TCRTIs). The TCRTIs are 1,N(6)-etheno analogues of a series of dATP-based template-competitive DNA polymerase inhibitors s
Publikováno v:
Biochemistry. 35:11634-11641
DNA polymerase photoprobes 2-[(4-azidophenacyl)thio]-2'-deoxyadenosine 5'-triphosphate (1), 2-[(4-azidophenylsulfenyl)thio]-2'-deoxyadenosine 5'-triphosphate (2), and 2-[(4-azido-2-nitrophenyl)-thio]-2'-deoxyadenosine 5'-triphosphate (3) were designe
Publikováno v:
Journal of the American Chemical Society. 117:8502-8510
Publikováno v:
Nucleosides and Nucleotides. 14:65-76
We prepared 2-azido-1, N6-etheno-2′-deoxyadenosine 5′-monophosphate (7b) by activation of the 2-thio analog 4b by two methods. In the preferred method, 4b was treated with 2,4-dinitrofluorobenzene in 50% aqueous acetonitrile, and the resultant th
Autor:
Michael J. McLeish, Michael B. Doughty, Katherine J. Nielsen, Lidia V. Najbar, John D. Wade, David J. Craik, Feng Lin
Publikováno v:
Biochemistry. 33:11174-11183
The conformation, in solution, of a peptide corresponding to residues 59-81 from T4 lysozyme [LYS(59-81)] has been determined by H-1 NMR and CD spectroscopy. This peptide spans the region corresponding to helix C in the crystal structure of T4 lysozy
Publikováno v:
Journal of Medicinal Chemistry. 37:2242-2248
We synthesized a new series of benextramine analogs as neuropeptide Y (NPY) functional group mimetics and tested them for N-[propionyl-3H]NPY ([3]NPY) displacement activity in rat brain membrane homogenates and for NPY receptor antagonist activity in
Publikováno v:
Neuropeptides. 25:289-298
Effects of calcium-free buffer, nifedipine, or prior cumulative neuropeptide Y (NPY) receptor agonist concentration exposure on vasoconstrictive responsiveness to the agonists were assessed in norepinephrine (NE)-conditioned isolated rat femoral arte
Publikováno v:
ChemInform. 33
We report the design, synthesis and activity studies on a novel class of template-competitive reverse transcriptase inhibitors (TCRTIs). The TCRTIs are 1,N(6)-etheno analogues of a series of dATP-based template-competitive DNA polymerase inhibitors s