Zobrazeno 1 - 10
of 10
pro vyhledávání: '"R. J. Lindmark"'
Autor:
Wendy P. Gati, John S. Wilson, Stanislaw F. Wnukt, D. Lorne Tyrrell, R. J. Lindmark, Morris J. Robins, Danuta Madej
Publikováno v:
Journal of Heterocyclic Chemistry. 38:1297-1306
Selected 2,6-(disubstituted)purine 2′,3′-didehydro-2′,3′-dideoxynucleosides and 2′,3′-dideoxynucleosides were prepared and evaluated. Treatment of 5′-protected ribonucleosides with phenoxythiocarbonyl chloride and 4-(dimethylamino)pyrid
Autor:
Dudley E. McMackins, Mihaly V. Toth, Henry E. Dayringer, J. G. Rico, P. R. Bovy, Nancy S. Nicholson, Anita K. Salyers, Beatrice B. Taite, Jeffery Alan Zablocki, Larry P. Feigen, Thomas E. Rogers, Shashidhar N. Rao, Mark E. Zupec, Robert Bruce Garland, Steven Paul Adams, M. Herin, R. J. Lindmark, Foe S. Tjoeng, S.G. Panzer-Knodle, Masateru Miyano
Publikováno v:
Bioorganic & Medicinal Chemistry. 2:881-895
The evolutionary process from the Arg-Gly-Asp-Phe (RGDF) tetrapeptide to potent orally active anti-platelet agents is presented. The RGD sequence is an important component in the recognition of fibrinogen by its platelet receptor GP IIb-IIIa (integri
Publikováno v:
The Journal of Organic Chemistry. 58:7948-7951
Autor:
Nancy S. Nicholson, Jeffery Alan Zablocki, R. J. Lindmark, D Pireh, Robert Bruce Garland, Beatrice B. Taite, Masateru Miyano, Shashidhar N. Rao, L Schretzman, S.G. Panzer-Knodle
Publikováno v:
Journal of Medicinal Chemistry. 36:1811-1819
Peptide mimetics of the RGDF sequence in which Arg-Gly has been replaced with 5-(4-amidinophenyl)pentanoyl mimetic has led to a 1000-fold increase in inhibitory potency over the natural RGDF ligand. The guanidine residue of the arginine may be involv
Publikováno v:
ChemInform. 25
Autor:
Wendy P. Gati, D. Madej, John Wilson, D. Lorne J. Tyrrell, R. J. Lindmark, Stanislaw F. Wnuk, Morris J. Robins
Publikováno v:
ChemInform. 33
Autor:
J A, Zablocki, J G, Rico, R B, Garland, T E, Rogers, K, Williams, L A, Schretzman, S A, Rao, P R, Bovy, F S, Tjoeng, R J, Lindmark
Publikováno v:
Journal of medicinal chemistry. 38(13)
Our initial orally active fibrinogen receptor antagonist benzamidinopentanoyl (BAP) series which was discovered through truncation of our i.v. antiplatelet agent (SC-52012) demonstrated modest oral activity in canine studies (ethyl [5-(4-amindinophen
Autor:
Nancy S. Nicholson, J. G. Rico, Kenneth Williams, Foe S. Tjoeng, P. R. Bovy, Lucy W. King, Anita K. Salyers, Lori Ann Schretzman, Beatrice B. Taite, Robert B. Garland, Masateru Miyano, Susan G. Panzer-Knodle, Jeffery A. Zablocki, R. J. Lindmark, Mihaly V. Toth, Dudley E. McMackins, James G. Campion, Mark E. Zupec, Larry P. Feigen, Steven Paul Adams
Publikováno v:
Bioorganicmedicinal chemistry. 3(5)
A novel series of orally active fibrinogen receptor antagonists has been discovered through structural modification of our lead intravenous (iv) antiplatelet agent, 5-(4-amidinophenyl)pentanoyl-Asp-Phe 1 (SC-52012). The Asp-Phe amide bond was removed
Autor:
P. R. Bovy, F. S. Tjoeng, J. G. Rico, T. E. Rogers, R. J. Lindmark, J. A. Zablocki, R. B. Garland, D. E. McMackins, H. Dayringer, M. V. Tóth, M. E. Zupec, S. Rao, S. G. Panzer-Knodle, N. S. Nicholson, A. Salyers, B. B. Taite, M. F. Hérin, M. Miyano, L. P. Feigen, S. P. Adams
Publikováno v:
Peptides 1994 ISBN: 9789072199218
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::620b95f8fea5dddf6249efa11071a7a5
https://doi.org/10.1007/978-94-011-1468-4_25
https://doi.org/10.1007/978-94-011-1468-4_25
Autor:
D. E. Mcmackins, Nancy S. Nicholson, Jeffery Alan Zablocki, Thomas E. Rogers, Mihaly V. Toth, Steven Paul Adams, Beatrice B. Taite, Anita K. Salyers, M. Miyano, M. E. Zupec, R. B. Garland, R. J. Lindmark, F. S. Tjoeng, Larry P. Feigen, P. R. Bovy, J. G. Rico, S G Panzer-Knodle
Publikováno v:
Peptides ISBN: 9789401042956
Peptides
Peptides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dad2aa1184fb4053127c0246eabcc23b
https://doi.org/10.1007/978-94-011-0683-2_101
https://doi.org/10.1007/978-94-011-0683-2_101