Zobrazeno 1 - 10 of 97 pro vyhledávání: '"G. J. Koomen"'
2
Synthesis and properties of a fluorescent nucleotide derivative
Autor: D. G. I. Petra, R. F. de Boer, G. J. Koomen, N. J. Meeuwenoord, E. Kuyl-Yeheskiely, G. A. van der Marel, J. H. van Boom
Publikováno v: Recueil des Travaux Chimiques des Pays-Bas. 115:99-102
Strong fluorescent deoxyadenosine derivatives are of considerable research importance in cell biology. We prepared the deoxyriboside of methyl 3,7-dihydro-7-oxo-[2,1-i]pyrimidopurine-9-carboxylate (compound 1b, deoxyribofuranosyl A*)1 which was subse
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7414d875350218ed2ef3f34f0571bd34
https://doi.org/10.1002/recl.19961150117
Zobrazit plný text záznamu
5
Trans/cis (Z/E) photoisomerization of the chromophore of photoactive yellow protein is not a prerequisite for the initiation of the photocycle of this photoreceptor protein
Autor: R, Cordfunke, R, Kort, A, Pierik, B, Gobets, G J, Koomen, J W, Verhoeven, K J, Hellingwerf
Publikováno v: Proceedings of the National Academy of Sciences of the United States of America. 95(13)
The chromophore of photoactive yellow protein (PYP) (i.e., 4-hydroxycinnamic acid) has been replaced by an analogue with a triple bond, rather than a double bond (by using 4-hydroxyphenylpropiolic acid in the reconstitution, yielding hybrid I) and by
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9370ac622d1d343c240e490c9bafb2b7
https://pubmed.ncbi.nlm.nih.gov/9636160
Zobrazit plný text záznamu
6
Biomimetic Synthesis of Nitraria Alkaloids, based on Tetrahydropyridine Synthons
Autor: M. J. WANNER, G. J. KOOMEN
Publikováno v: Journal of the Indian Chemical Society, 899-903. Indian Chemical Society
ISSUE=74;STARTPAGE=899;ENDPAGE=903;ISSN=0019-4522;TITLE=Journal of the Indian Chemical Society
Amsterdam Institute of Molecular Studies, Laboratory of Organic Chemistry, University of Amsterdam, Nieuwe Achtergracht 129, 1 018 WS Amsterdam, The Netherlands Manuscript received 8 September 1997 Many of the alkaloids found in Nitraria and Lupine s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bac3f67720a12b18db6f29b55775520
https://dare.uva.nl/personal/pure/en/publications/biomimetic-synthesis-of-nitraria-alkaloids-based-on-tetrahydropyridine-synthons(86564861-4ae0-461f-924a-31fe176694ed).html
Zobrazit plný text záznamu
7
Inhibitors of Adenylosuccinate Lyase
Autor: G. J. Koomen, M. J. Wanner, W. A. Hartgers
Publikováno v: Bioorganic Chemistry in Healthcare and Technology ISBN: 9781468413564
Adenylosuccinate lyase is an essential enzyme in two steps of the biosynthesis of adenosine nucleotides. In the conversion IMP → AMP it catalyzes the elimination of fumaric acid from adenylosuccinate: We have been involved in the synthesis of adeny
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9c6f911a9d2d2d8226a436a92a230a7f
https://doi.org/10.1007/978-1-4684-1354-0_26
Zobrazit plný text záznamu
8
Abstracts of papers Symposium 'new therapeutic developments in human infectious diseases'
Autor: D. A. H. v. Maarschalkerwaart, N. Auzeil, L. Christiaens, H. Robaux, D. Schols, A. M. Ouero, Marcel J.E. Fischer, P. Wigerinck, P. Herdewiin, R. Bonaly, G. J. Koomen, M. Hooper, H. Galone, G. Schepers, E. De Clercg, F. A. W. Koeman, J. P. Kamerlina, J. P. Kamerling, S. Tounson, P. Claes, Hugo Vanden Bossche, G. Bram, J. Marchand-Brynaert, S. Labidalle, J. F. G. Vlieqenthart, R. Pauwels, E. De Vos, M. Baba, R. A. Dommisse, Carl H. Schwabe, Jaap Wilting, Georges J. Hoornaert, F. R. Opperdoes, F. Verberckmoes, H. Schellekens, J. A. Liepoivre, B. H. M. Mruthyunjayasuamy, W. G. J. Hol, Fred R. Opperdoes, J. Osuku Opio, A. F. M. Verheul, J. Cntto, N. De Meyer, L. Mishra, Octaaf J.M. Bos, D. Vanden Berghe, H. Snippe, Lambert H.M. Janssen, D. Van Der Taelen, Ashty Saleh, Ei. Esmans, E. L. Esmans, Frans Compernolle, Isabelle Coppens, J. L. Monal, M. Miocque, F. C. Alderweireldt, A. Jakobs, T. M. Slaghek, P. Joos, S. P. Hiremath, J. Balzarini, M. Renson, P. Herdewi in, Eugene L.M. Vansterkenburg, W. Van Dongen, A. Haemers, H. K. Pandey, L. Plaum, M. J. Wanner, A. Van Aerschot, J. A. Lepoivre, M. Q. Zhang, A. J. Vlietinck, H. Galons, N. Damianos, E. De Clercq, I. Nasri, V. Loppinet
Publikováno v: Pharmaceutisch Weekblad. 11:C3-C9
s of papers Symposium "New therapeutic developments in human infectious diseases" Organized by the Division Medicinal Chemistry of the Royal Dutch Chemistry Society (Sectie Farmacochemie van de Koninklijke Nederlandse Chemische Vereniging) and the Co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c667bc2fdd8d9b6b8704febb0262c8c9
https://doi.org/10.1007/bf02196043
Zobrazit plný text záznamu
9
Potential Antiviral Agents. Synthesis and Properties of Glutarimide-Nucleosides
Autor: M. J. Wanner, G. J. Koomen
Publikováno v: Nucleosides and Nucleotides. 7:511-517
The synthesis of 3- and 4-substituted glutarimide-ribosides via different approaches involving Wittig-reactions is described. Oxydation to 1-deazauridine failed, due to instability of the product. One of the compounds obtained exhibited slight activi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bb69974d424e6ce59826aa8dc8df81be
https://doi.org/10.1080/07328318808075393
Zobrazit plný text záznamu
10
Non-Sacccfaridal Nucleoside and Hucleotide Analocuses
Autor: A. P. Goores, G. J. Koomen, U. K. Pandit, A. P. Kroon
Publikováno v: Synthetic Communications. 1:41-45
The replacement of the sugar notsty of nucleosides and nueleotides by suitaole molecular systems, provides novel models of nucleic acid corpoonents for pnysico and biochemical studies. Several such “unconVentioral” analogues, based upon α-amino
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d767106178d15adbd8a0bab69cd9619a
https://doi.org/10.1080/00397917108081615
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje