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Book
Poly(ADP-ribose): an international symsposium
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Year: 1974 Publisher: Washington (D.C.): US. Government printing office

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Periodical
Nucleosides & nucleotides.
ISSN: 23323892 Year: 1982 Publisher: New York, N.Y. : M. Dekker,

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Periodical
Nucleosides, nucleotides & nucleic acids.
ISSN: 15322335 15257770 Year: 2000 Publisher: New York, NY : Marcel Dekker


Dissertation
Normal and abnormal expression of the human adenosine deaminase gene : a molecular analysis
Authors: ---
Year: 1988 Publisher: Amsterdam Rodopi

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Dissertation
Adenosine deaminase complexing protein as a marker in cancer studies
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Year: 1985 Publisher: Meppel Krips Repro

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Dissertation
Gene specific repair of UV-induced DNA damage in mammalian cells
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Year: 1991 Publisher: Enschede Febodruk

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Dissertation
Quels sont les nouveaux agents thérapeutiques prometteurs contre la péritonite infectieuse féline ?
Authors: --- --- --- ---
Year: 2020 Publisher: Liège Université de Liège (ULiège)

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La péritonite infectieuse féline (PIF) est une pathologie infectieuse ayant pour origine le coronavirus félin (FCoV), un mutant du coronavirus entérique félin (FECV). Cette pathologie est encore fréquemment rencontrée dans la pratique vétérinaire. Malheureusement, le pronostic est très mauvais avec un taux de mortalité qui approche les 100%. En plus d’un diagnostic difficile, il n’existe actuellement aucun traitement disponible contre la péritonite infectieuse féline. La recherche d’un traitement représente donc un enjeu important pour le monde vétérinaire. Deux principales stratégies curatives sont en cours de développement, l’une ciblant la protéase virale 3C avec un inhibiteur pharmacologique, l’autre ciblant la réplication virale avec un analogue de nucléoside. Le GC-376, l’inhibiteur de protéase 3C, présente peu d’effets indésirables et une efficacité correcte pour traiter les chats atteints de péritonite infectieuse féline. Cependant, l’analogue de nucléoside GS-441524 semble être une meilleure option. Effectivement, les effets indésirables sont également assez faibles et il montre un meilleur taux de survie chez les chats atteints de péritonite infectieuse féline. Ces résultats sont encourageants pour une pathologie mortelle dans la majorité des cas. Ces molécules, encore en développement, pourraient donc faire l’objet de demandes d’autorisation temporaire pour usage compassionnel ou d’inclusion dans un essai clinique par un vétérinaire en attendant leur mise sur le marché. Feline infectious peritonitis is an infectious disease caused by the feline coronavirus (FCoV), a mutant of feline enteric coronavirus (FECV). This pathology is still frequently encountered in veterinary practice. Unfortunatly, the prognosis is very poor with a mortality rate close to 100%. In addition to a complex diagnosis, no treatment is currently available for feline infectious peritonitis. Searching for a curative treatment is therefore an important challenge for veterinarians. Two main curative strategies are being developed, one targeting viral 3C protease with a pharmacological inhibitor, the other one targeting viral replication with a nucleoside analogue. GC-376, the 3C protease inhibitor, has few side effects and is correctly effictive in treating cats with feline infectious peritonitis. However, the nucleoside analogue GS-441524 seems to be a better option. Indeed, the side effects are also quite low and it shows a better survival rate in cats with feline infectious peritonitis. These results are encouraging for a pathology that turns out to be lethal in the majority of cases. These molecules, still in development, could therefore be subject to temporary authorization requests for compassionate use or inclusion in a clinical trial by a veterinarian pending their marketing.


Book
Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
Author:
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Marine natural products are characterized by high chemical diversity, biochemical specificity, and other molecular properties that make them favorable as lead structures for drug discovery. In this field, one of the main problems is often the reduced natural availability of isolated substances, which can complicate both the structural characterization and possible future developments. For these reasons, the study of bioactive marine metabolites should rely on the development of chemical synthesis and synthetic strategies aimed at the preparation of pure compounds and analogs both for structural confirmation and/or for the large-scale preparation necessary for future applications. Moreover, natural products can be a crucial starting point for the preparation of molecules structurally inspired by the latter, opening the path to new classes of biologically active compounds with pharmacological potential. This book collects original research articles regarding synthetic strategies for secondary marine metabolites and/or analogs that favor applications of these molecules and/or solve structural challenges common in the field of natural substances.


Book
Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
Author:
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Marine natural products are characterized by high chemical diversity, biochemical specificity, and other molecular properties that make them favorable as lead structures for drug discovery. In this field, one of the main problems is often the reduced natural availability of isolated substances, which can complicate both the structural characterization and possible future developments. For these reasons, the study of bioactive marine metabolites should rely on the development of chemical synthesis and synthetic strategies aimed at the preparation of pure compounds and analogs both for structural confirmation and/or for the large-scale preparation necessary for future applications. Moreover, natural products can be a crucial starting point for the preparation of molecules structurally inspired by the latter, opening the path to new classes of biologically active compounds with pharmacological potential. This book collects original research articles regarding synthetic strategies for secondary marine metabolites and/or analogs that favor applications of these molecules and/or solve structural challenges common in the field of natural substances.


Book
Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
Author:
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Marine natural products are characterized by high chemical diversity, biochemical specificity, and other molecular properties that make them favorable as lead structures for drug discovery. In this field, one of the main problems is often the reduced natural availability of isolated substances, which can complicate both the structural characterization and possible future developments. For these reasons, the study of bioactive marine metabolites should rely on the development of chemical synthesis and synthetic strategies aimed at the preparation of pure compounds and analogs both for structural confirmation and/or for the large-scale preparation necessary for future applications. Moreover, natural products can be a crucial starting point for the preparation of molecules structurally inspired by the latter, opening the path to new classes of biologically active compounds with pharmacological potential. This book collects original research articles regarding synthetic strategies for secondary marine metabolites and/or analogs that favor applications of these molecules and/or solve structural challenges common in the field of natural substances.

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