Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Howard J. Schaeffer"'
Autor:
Lilia M. Beauchamp, Howard J. Schaeffer, Gertrude B. Elion, Paulo de Miranda, James A. Fyfe, Phillip A. Furman
Publikováno v:
Reviews in Medical Virology. 9:147-153
Autor:
Thomas A. Krenitsky, W W Hall, Howard J. Schaeffer, Lilia M. Beauchamp, P de Miranda, P D Whiteman
Publikováno v:
Proceedings of the National Academy of Sciences. 81:3209-3213
Acyclovir [9-[(2-hydroxyethoxy)methyl]guanine] is an acyclic guanine nucleoside analogue that is widely used clinically as an antiherpetic agent. Its limited absorption in humans after oral administration prompted the search for prodrugs. A congener,
Autor:
John E. Kelsey, Jung-Chung Lin, John William Talbot Selway, Howard J. Schaeffer, Barbara L. Serling, Peter Collins, Lilia M. Beauchamp, Karen K. Biron
Publikováno v:
Journal of Medicinal Chemistry. 31:144-149
A series of pyrimidines related to the potent antiherpetic agent 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine (1, BW B759U), all containing the same acyclic chain, have been synthesized. Some of the compounds were derivatives of the naturally occurring
Autor:
Phillip A. Furman, James A. Fyfe, Carol M. Lubbers, Paul M. Keller, Howard J. Schaeffer, Lilia M. Beauchamp, Gertrude B. Elion
Publikováno v:
Biochemical Pharmacology. 30:3071-3077
The inhibitor and substrate specificities of deoxythymidine (dThd) kinase purified from herpes simplex virus (HSV Type 1) were studied. A number of nucleosides and nucleoside analogs were phosphorylated by the virus coded enzyme. These included sever
Autor:
Howard J. Schaeffer, Lilia M. Beauchamp, Gertrude B. Elion, Paulo de Miranda, Phillip A. Furman, James A. Fyfe
Publikováno v:
Proceedings of the National Academy of Sciences. 74:5716-5720
A guanine derivative with an acyclic side chain, 2-hydroxyethoxymethyl, at position 9 has potent antiviral activity [dose for 50% inhibition (ED 50 ) = 0.1 μM] against herpes simplex virus type 1. This acyclic nucleoside analog, termed acycloguanosi
Autor:
Howard J. Schaeffer, Bart L. Dolmatch, Peter Collins, James A. Fyfe, Paul M. Keller, D. J. Bauer, Lilia M. Beauchamp
Publikováno v:
Journal of Medicinal Chemistry. 28:982-987
A group of compounds was prepared in which variations of the ring portion of the acyclovir (ACV) structure were made. These modifications included monocyclic (isocytosine, triazole, imidazole), bicyclic (8-azapurine, pyrrolo[2,3-d]pyrimidine, pyrazol
Autor:
James A. Linn, Karen K. Biron, Peter Collins, James L. Kelley, Howard J. Schaeffer, John William Talbot Selway, Lilia M. Beauchamp
Publikováno v:
Nucleosides and Nucleotides. 8:475-489
The synthesis and antiherpetic activity of 9-[[[2-hydroxy-1-(hydroxymethyl)ethyl]thio]methy1]guanine (4) and 1-[[[2-hydroxy-1-(hydroxymethyl)ethyl]thio]methy]cytosine (6), the side-chain thio analogues of ganciclovir (3) and BW A1117U (5), are descri
Publikováno v:
Journal of Medicinal Chemistry. 24:1528-1531
A number of nitrogen analogues of 9-[(2-hydroxyethoxy)methyl]guanine [acylovir, Zovirax] containing amine functions in the side chain were synthesized and tested for antiviral activity. These purine acyclic nucleosides were prepared by reaction of tr
Autor:
Howard J. Schaeffer, Vijay K. Jain
Publikováno v:
The Journal of Organic Chemistry. 29:2595-2598
Publikováno v:
Journal of the American Chemical Society. 79:6160-6164