Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Christelle Dupouy"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 436-469 (2018)
Oligonucleotides (ONs) have been envisaged for therapeutic applications for more than thirty years. However, their broad use requires overcoming several hurdles such as instability in biological fluids, low cell penetration, limited tissue distributi
Externí odkaz:
https://doaj.org/article/940694118b764537a14dbeff710a2beb
Autor:
Florian Gauthier, Jean-Rémi Bertrand, Jean-Jacques Vasseur, Christelle Dupouy, Françoise Debart
Publikováno v:
Molecules, Vol 25, Iss 11, p 2714 (2020)
Co-delivery systems of siRNA and chemotherapeutic drugs have been developed as an attractive strategy to optimize the efficacy of chemotherapy towards cancer cells with multidrug resistance. In these typical systems, siRNAs are usually associated to
Externí odkaz:
https://doaj.org/article/a3fee217948b4875be220b3f2d45c708
Autor:
Diallo Traoré, Elisa Biecher, Manon Mallet, Sonia Rouanet, Dr. Jean‐Jacques Vasseur, Prof. Michael Smietana, Dr. Christelle Dupouy
Publikováno v:
ChemistryOpen, Vol 13, Iss 8, Pp n/a-n/a (2024)
Abstract We recently reported the properties of RNA hairpins constrained by a dimethylene (DME) disulfide (S−S) linker incorporated between two adjacent nucleosides in the loop and showed that this linker locked the hairpin conformation thus distur
Externí odkaz:
https://doaj.org/article/bb0e8db1315b4704969c64fe26eb9c19
Publikováno v:
European Journal of Organic Chemistry. 2019:5636-5645
Autor:
Jean-Jacques Vasseur, Sonia Rouanet, Christelle Dupouy, Emmanuel Pfund, Rémi Legay, Thierry Lequeux, Cyril Lebargy
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2019, 21 (12), pp.4803-4807. ⟨10.1021/acs.orglett.9b01689⟩
Organic Letters, American Chemical Society, 2019, 21 (12), pp.4803-4807. ⟨10.1021/acs.orglett.9b01689⟩
The first synthesis of oligonucleotides incorporating URF, a uridine modified with a difluorophosphonylated allylic ether onto the 2'-position, is described. Fluorinated homouridylates and miR-342-3p analogues are efficiently prepared. UV-melting exp
Autor:
Françoise Debart, Florian Gauthier, Christelle Dupouy, Jean-Rémi Bertrand, Jean-Jacques Vasseur
Publikováno v:
Molecules
Molecules, MDPI, 2020, 25 (11), pp.2714. ⟨10.3390/molecules25112714⟩
Volume 25
Issue 11
Molecules, Vol 25, Iss 2714, p 2714 (2020)
Molecules, MDPI, 2020, 25 (11), pp.2714. ⟨10.3390/molecules25112714⟩
Volume 25
Issue 11
Molecules, Vol 25, Iss 2714, p 2714 (2020)
Co-delivery systems of siRNA and chemotherapeutic drugs have been developed as an attractive strategy to optimize the efficacy of chemotherapy towards cancer cells with multidrug resistance. In these typical systems, siRNAs are usually associated to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59410de283112e9bd79f5a3f28cc00f3
https://hal.archives-ouvertes.fr/hal-02991729/file/molecules-25-02714-1.pdf
https://hal.archives-ouvertes.fr/hal-02991729/file/molecules-25-02714-1.pdf
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 436-469 (2018)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2018, 14 (26), pp.436-469. ⟨10.3762/bjoc.14.32⟩
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2018, 14 (26), pp.436-469. ⟨10.3762/bjoc.14.32⟩
Oligonucleotides (ONs) have been envisaged for therapeutic applications for more than thirty years. However, their broad use requires overcoming several hurdles such as instability in biological fluids, low cell penetration, limited tissue distributi
Autor:
Sandra Claveau, Françoise Debart, Jean-Rémi Bertrand, Jean-Jacques Vasseur, Christelle Dupouy, Florian Gauthier
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2018, 26 (16), pp.4635-4643. ⟨10.1016/j.bmc.2018.07.033⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2018, 26 (16), pp.4635-4643. ⟨10.1016/j.bmc.2018.07.033⟩
International audience; Modified oligoribonucleotides used as siRNAs bearing biolabile disulfide-containing groups at some 2'-positions were synthesized following a post-synthesis transformation of solid-supported 2'-O-acetylthiomethyl RNA, previousl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89c36b725cbc99a6cd5f1fdf4ca0c662
https://hal.archives-ouvertes.fr/hal-02197153
https://hal.archives-ouvertes.fr/hal-02197153
Autor:
Frédéric Beltran, Christelle Dupouy, Annabelle Biscans, Jean-Jacques Vasseur, Florian Gauthier, Françoise Debart
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (17), pp.3181-3188. ⟨10.1039/c8ob00328a⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (17), pp.3181-3188. ⟨10.1039/c8ob00328a⟩
International audience; The synthesis and the impact of a disulfide bridge between 2'-O-positions of two adjacent nucleotides in an RNA duplex and in the loop of RNA hairpins are reported. The incorporation of this 2',2'-disulfide (S-S) bridge enable
Publikováno v:
RSC Advances
RSC Advances, Royal Society of Chemistry, 2014, 4 (90), pp.48821-48826. ⟨10.1039/c4ra09639h⟩
RSC Advances, 2014, 4 (90), pp.48821-48826. ⟨10.1039/c4ra09639h⟩
RSC Advances, Royal Society of Chemistry, 2014, 4 (90), pp.48821-48826. ⟨10.1039/c4ra09639h⟩
RSC Advances, 2014, 4 (90), pp.48821-48826. ⟨10.1039/c4ra09639h⟩
A constrained dinucleotide unit featuring a gauche(+) alpha torsional angle configuration was used to stabilize DNA hairpin or bulged structures. Large five nucleotides having looped hairpin structures can be stabilized up to +5 degrees C. Depending