Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Marcel Chassignol"'
Autor:
Julien Weiss, Ulysse Asseline, Victoria Roig, Gladys Mbemba, Marcel Chassignol, Jean-François Mouscadet, Hervé Meudal, Yves Aubert
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2009, 44 (12), pp.5029-5044. ⟨10.1016/j.ejmech.2009.09.007⟩
European Journal of Medicinal Chemistry, Elsevier, 2009, 44 (12), pp.5029-5044. ⟨10.1016/j.ejmech.2009.09.007⟩
International audience; The synthesis of a series of thirty-eight new modified dinucleotides and dinucleotide conjugate analogues of d-(5')ApC(3') is described. The inhibitory activity of these compounds toward HIV-1 integrase was examined in enzymat
Autor:
Marcel Chassignol, N.T. Thuong
Publikováno v:
Tetrahedron Letters. 39:8271-8274
Oligonucleotide thiophosphates react with 2-pyridyl-disulfide derivatives to give phosphodisulfide which can, upon reduction, be easily cleaved to give the starting oligonucleotide with a terminal thiophosphate group.
Autor:
Marcel Chassignol, O. Bornet, Nguyen Thanh Thuong, Chantal Prévost, Françoise Vovelle, Gérard Lancelot
Publikováno v:
Nucleic Acids Research. 23:788-795
Psoralen (pso) was attached via its C-5 position to the 5'-phosphate group of an oligodeoxynucleotide d(TAAGCCG) by a hexamethylene linker (m6). Complex formation between pso-m6-d(TAAGCCG) and the complementary strands d(CGGCTTA)[7-7mer] or d(CGGCTTA
Autor:
Claude Hélène, Alexandre Lebedev, Nguyen Thanh Thuong, Michel Rougee, Jean-Louis Mergny, Marcel Chassignol, Thérèse Garestier
Publikováno v:
Biochemistry. 33:15321-15328
An 11-mer oligopyrimidine was covalently linked via its 5'-phosphate to an acridine derivative (acridine-11-mer), and a 13-mer was covalently linked via its 3'-phosphate to an ethidium derivative (13-mer-ethidium). Each of them formed a triple helix
Autor:
Gérard Godard, Isabelle Duroux, Nguyen Thanh Thuong, Ulysse Asseline, Claude Hélène, Tula Saison-Behmoaras, Marcel Chassignol, Jean-Christophe François
Publikováno v:
Nucleic Acids Research. 22:4789-4795
Dodecadeoxyribonucleotides derivatized with 1,10-phenanthroline or psoralen were targeted to the point mutation (GU) in codon 12 of the Ha-ras mRNA. DNA and RNA fragments, 27 nucleotides in length, and containing the complementary sequence of the 12m
Autor:
Nguyen Thanh Thuong, Marcel Chassignol, R. Kurfuerst, Ulysse Asseline, Victoria Roig, Edwige Bonfils
Publikováno v:
ChemInform. 23
Autor:
Victoria Roig, Nguyen Thanh Thuong, Edwige Bonfils, Ulysse Asseline, Marcel Chassignol, Robin Kurfurst
Publikováno v:
Tetrahedron. 48:1233-1254
The solid-phase preparation of oligodeoxyribonucleotides attached to intercalator or reactive groups through their 5′- and (or) 3′-ends is reported. These syntheses implicate the introduction of suitable masked functional groups at the 5′-end o
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids
Nucleosides, Nucleotides and Nucleic Acids, Taylor & Francis, 2007, 26, pp.1669-1672
Nucleosides, Nucleotides and Nucleic Acids, Taylor & Francis, 2007, 26, pp.1669-1672
We recently reported the design of new fluorescent oligo-2'-deoxyribonucleotides (FODNs) for the detection of terminal mismatches on DNA duplexes in homogeneous assays. We now report the validation of this method in homogeneous assays with other sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3b4967e790f6bac2e6157b822d8c26a
https://hal.archives-ouvertes.fr/hal-00282396
https://hal.archives-ouvertes.fr/hal-00282396
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2006, 4 (10), pp.1949-1957. ⟨10.1039/b602262f⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2006, 4 (10), pp.1949-1957. ⟨10.1039/b602262f⟩
This paper describes the design of terminal-mismatch discriminating fluorescent oligonucleotides (TMDFOs). The method is based on the use of sets of oligo-2'-deoxyribonucleotide probes linked via their 5'-ends, and varying-sized flexible polymethylen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6023b0d46606fb3d11a9e9383603a0
https://hal.archives-ouvertes.fr/hal-00088833
https://hal.archives-ouvertes.fr/hal-00088833
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2003, 11, pp.3499-3511
Bioorganic and Medicinal Chemistry, Elsevier, 2003, 11, pp.3499-3511
Single and multiple incorporations of stereochemically pure modified dinucleoside-phosphoramidates involving substituent groups ending with bis-hydroxyethyl and bis-aminoethyl groups have been performed into pyrimidic triple helix-forming oligo-2'-de