Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Catherine Verchère-Béaur"'
Autor:
Martine Perrée-Fauvet, Kosmas Kefokeris, Nikos Manoussakis, Leonidas Gryllos, Marie-Cecile G. Chalbot, Athanassios G. Coutsolelos, Catherine Verchère-Béaur
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 15:704-717
The DNA-binding modes and nuclease activity of methylpyridiniumyl/phenyl-hydroxamic acid porphyrin adducts (PHAs) have been studied. These compounds are derived from the tetracationic meso-tetrakis(N-methyl-4-pyridiniumyl)porphyrin (H2TMPyP-4) by rep
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 21:187-192
D-Sorbitol-6-phosphate 2-dehydrogenase catalyzes the NADH-dependent conversion of D-fructose 6-phosphate to D-sorbitol 6-phosphate and improved production and purification of the enzyme from Escherichia coli is reported. Preliminary inhibition studie
Autor:
Catherine Verchère-Béaur, Samia Far, Nohad Gresh, Alain Kossanyi, Martine Perrée-Fauvet, Eliane Taillandier
Publikováno v:
European Journal of Organic Chemistry. 2004:1781-1797
In order to increase the DNA binding affinity of a bis-arginyl-porphyrin which has been previously shown to bind preferentially in the major groove of the d(GGCGCC)2 sequence (Mohammadi et al., Biochemistry1998, 37, 9165), we have synthesized bis- an
Autor:
Fumiyuki Yamakura, Irène Morgenstern-Badarau, Malcolm Gerloch, Catherine Verchère-Béaur, Jean Philippe Renault
Publikováno v:
Inorganic Chemistry. 39:2666-2675
The problem of metal selectivity of iron/manganese superoxide dismutases (SODs) is addressed through the electronic structures of active sites using electron paramagnetic resonance and ligand field calculations. Studies of wild-type iron(III) SOD (Fe
Autor:
Gilles Anneheim-Herbelin, A. Gaudemer, Nathalie Bône, Catherine Verchère-Béaur, Martine Perrée-Fauvet, Eric Tarnaud
Publikováno v:
Tetrahedron. 52:13589-13604
Binding to a variety of natural and synthetic DNAs by cationic water-soluble porphyrins - having three N-methylpyridynium and one amino-acid derivatized phenyl ring as meso substituents - has been investigated. These studies indicate that amino acid
Autor:
Eric Tarnaud, Gilles Anneheim-Herbelin, Martine Perrée-Fauvet, Nathalie Bône, Catherine Verchère-Béaur, A. Gaudemer
Publikováno v:
Tetrahedron. 52:13569-13588
In order to obtain molecules that can bind to specific DNA-sequences, several new tri-(N-methyl-4-pyridiniumyl)porphyrins bearing an amino acid or peptide side-chain on the fourth meso aromatic substituent have been synthesized by efficient coupling
Autor:
Catherine Verchère-Béaur, C. Bied-Charreton, N. Robic, Laurent Salmon, Robert F. Pasternack, Alain Gaudemer, M. Perree-Fauvet
Publikováno v:
ChemInform. 22
A new water-soluble porphyrin containing benzyl-trimethylammonium groups was synthesized in a two-step sequence from tetraphenylporphyrin and preliminary studies show that it binds strongly to DNA in an outside manner and gives fairly stable complexe
Autor:
N. Bone, Alain Gaudemer, Catherine Verchère-Béaur, G. Anneheim‐Herbelin, Martine Perrée-Fauvet, E. Tarnaud
Publikováno v:
ChemInform. 28
Autor:
N. Bone, Catherine Verchère-Béaur, Martine Perrée-Fauvet, Alain Gaudemer, E. Tarnaud, G. Anneheim‐Herbelin
Publikováno v:
ChemInform. 28
Autor:
Alain Gaudemer, C. Bied-Charreton, Laurent Salmon, Catherine Verchère-Béaur, N. Robic, M. Perree-Fauvet, Robert F. Pasternack
Publikováno v:
Tetrahedron Letters. 31:4739-4742
A new water-soluble porphyrin containing benzyl-trimethylammonium groups was synthesized in a two-step sequence from tetraphenylporphyrin and preliminary studies show that it binds strongly to DNA in an outside manner and gives fairly stable complexe