Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Loïc René"'
Autor:
Loïc René Le Bourlegat
Publikováno v:
Biblioteca Digital de Teses e Dissertações do ITAInstituto Tecnológico de AeronáuticaITA.
O presente trabalho aborda o processamento e caracterização de um compósito híbrido obtido a partir da combinação de lâminas de titânio com pré-impregnados de fibra de carbono e epóxi. Atualmente, os compósitos híbridos vêm sendo amplame
Autor:
Loïc-René Labit
Publikováno v:
Journal of Physics: Conference Series. 2156:012156
During the last decades, several parameters describing the neutrino oscillation phenomenon have been characterized thanks to reactor neutrino experiments, in particular the precise measurement of the last-to-be-measured mixing angle θ 13. Following
Autor:
Loïc René, Ruth Pérez-Fernández, Pilar Prados, Michiel Luc Maria Van Gool, Michèle Reboud-Ravaux, Bernard Badet, Masayuki Takahashi, Javier de Mendoza, Perla Breccia, Nicole Boggetto
Publikováno v:
Journal of Medicinal Chemistry. 46:5196-5207
Original inhibitors of HIV-1 protease based on a chiral bicyclic guanidinium scaffold linked to short peptidic mimics of the terminal protease sequences and to a lipophilic group were designed. These inhibitors prevent dimerization of the native prot
Publikováno v:
The Journal of Organic Chemistry. 67:5408-5411
A general method giving access to protected alpha-alkyl amino glycines (A3G) 4 from the previously described precursor alpha-isopropylthioglycine 1 is described. In the presence of N-bromosuccinimide, displacement of the thiol by a large variety of a
Autor:
Michèle Reboud-Ravaux, Nicole Boggetto, Bernard Badet, Loïc René, I. Vergely, Eve de Rosny, Driss Qasmi
Publikováno v:
Bioorganic & Medicinal Chemistry. 5:707-714
A series of novel synthetic peptides containing an N-terminal glyoxylyl function (CHOCO-) have been tested as inhibitors of HIV-1 protease. The N-glyoxylyl peptide CHOCO-Pro-Ile-Val-NH2, which fulfills the specificity requirements of the MA/CA protea
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 36:1115-1121
1,2-anhydroglucitol-6P, a known inhibitor of glucose-6P isomerase, behaved as a fructose-6P site-directed irreversible inhibitor of bacterial glucosamine-6P synthase. The lack of reproducibility of the aldolase-mediated condensation of dihydroxyaceto
Publikováno v:
ChemInform. 24
The easily obtained and very stable title compound 1 can be used for direct diazoacetylation of aromatic or aliphatic amines, phenols, thiophenol, and peptides under mild conditions
Autor:
Loïc René, Bernard Badet
Publikováno v:
Synthetic Communications. 26:3237-3239
α-Boc-amino-Fmoc-glycine 6 was prepared in two steps from 9-fluorenyl-methylcarbamate 1, glyoxylic acid 3 and t-butyl carbamate 5. This compound is useful in Solid Phase Peptide Synthesis to prepare α-aminoglycine-containing peptides using Fmoc-str
Autor:
Elizabeth Anhalt, Patrice Courvalin, Loïc René, Bernard Badet, Romulo Aráoz, Marie-Ange Badet-Denisot
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 2000, 39 (51), pp.15971-15979. ⟨10.1021/bi001408b⟩
Biochemistry, 2000, 39 (51), pp.15971-15979. ⟨10.1021/bi001408b⟩
Biochemistry, American Chemical Society, 2000, 39 (51), pp.15971-15979. ⟨10.1021/bi001408b⟩
Biochemistry, 2000, 39 (51), pp.15971-15979. ⟨10.1021/bi001408b⟩
International audience; VanX is a zinc-dependent d-Ala-d-Ala amino dipeptidase required for high-level resistance to vancomycin. The enzyme is also able to process dipeptides with bulky C-terminal amino acids [Wu, Z., Wright, G. D., and Walsh, C. T.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f6b49009482b82c201a494776056d9
https://hal.sorbonne-universite.fr/hal-02144715
https://hal.sorbonne-universite.fr/hal-02144715
Publikováno v:
Tetrahedron Letters. 39:2569-2570
N-Boc-N′-Fmoc-imidazolidine-2-carboxylic acid, easily prepared from N-Boc-N′-Fmoc-ethylenediamine and glyoxylic acid, is a racemic proline surrogate which can be used in Solid Phase Peptide Synthesis.