Zobrazeno 1 - 10
of 69
pro vyhledávání: '"R Caujolle"'
Autor:
J. Vialard, M. J. Escorihuela, N. Jeannin, Yann Kerr, J. Costeraste, T. Amiot, R. Rodriguez-Suquet, Ahmad Al Bitar, Philippe Richaume, Baptiste Palacin, Francois Cabot, L. Costes, Arnaud Mialon, R. Caujolle, Ali Khazaal, Jacqueline Boutin, Eric Anterrieu, Thibaut Decoopman, Thierry Pellarin, Christophe Suere, L. Yu, Ghislain Picard, F. Vivier, Nemesio Rodriguez-Fernandez, Olivier Merlin
Publikováno v:
IGARSS
The Soil Moisture and Ocean Salinity (SMOS) satellite is performing systematic L-band observations since 2009, allowing a large number of science and operational applications. Several recent studies have shown the need of the continuity of L-band obs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b27d34c3546d4e16c883e34128e2c92e
https://doi.org/10.1109/igarss47720.2021.9554241
https://doi.org/10.1109/igarss47720.2021.9554241
Autor:
N. Jeannin, Baptiste Palacin, Jean-Michel Morel, T. Tournier, Y. H. Kerr, Eric Anterrieu, R. Caujolle, Miguel Colom, R. Rodriguez-Suquet, P. Richaume, B. Rouge, Thibaut Decoopman, J. Costerate, Francois Cabot, F. Payot, Ali Khazaal, Nemesio Rodriguez-Fernandez, L. Costes
Publikováno v:
IGARSS
The Soil Moisture and Ocean Salinity (SMOS) satellite has provided, for the very first time, systematic passive L-band (1420−1427 MHz) measurements from space with a spatial resolution of ~50 Km. This contribution presents preliminary results of st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b1d02c40aff91ad53c2c7655614030
https://doi.org/10.1109/igarss.2019.8898814
https://doi.org/10.1109/igarss.2019.8898814
Autor:
Cecile Tournaire‐Arellano, R Caujolle, A. Sanon, S. Younes El Hage, Christian Bories, Philippe M. Loiseau
Publikováno v:
Biomedicine & Pharmacotherapy. 59:245-248
Among chitinolytic activities previously described in Trichomonas vaginalis, N-acetyl-beta-D-hexosaminidase (NAHase) was the enzyme system expressing the highest level of specific activity. We report here some biochemical characteristics of NAHase pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3abf84c6274122d68ea48b90c9ed6dd
https://doi.org/10.1016/j.biopha.2004.09.013
https://doi.org/10.1016/j.biopha.2004.09.013
Autor:
R. Caujolle, J. P. Seguela, C. Tournaire‐Arellano, M. D. Linas, J. L. Stigliani, C. Recoche, Marc Payard
Publikováno v:
European Journal of Medicinal Chemistry. 32:1001-1007
Summary Ethers of 1-(2,4-dichlorophenyl)-2-(1- H -imidazolyl)ethanol bearing ramified and/or unsaturated chains have been synthesized in order to specify the role of lipophilicity or steric contributions on antifungal activity against yeast for micon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d04456e14014d93e3ab61e85c1ab884a
https://doi.org/10.1016/s0223-5234(97)89644-4
https://doi.org/10.1016/s0223-5234(97)89644-4
Autor:
C. Bories, Philippe Gayral, M. H. Bessieres, C Tournaire, Marc Payard, G. Commenges, R. Caujolle, Philippe M. Loiseau
Publikováno v:
European Journal of Medicinal Chemistry. 31:507-511
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6641184924dc23d6d593dd429f586d9
https://doi.org/10.1016/0223-5234(96)85172-5
https://doi.org/10.1016/0223-5234(96)85172-5
Publikováno v:
European Journal of Medicinal Chemistry. 30:955-962
Summary Aromatic ethers related to antifungal azole miconazole were synthesized and tested against various strains of Candida . We found that activity is related to the nature of the aromatic ring and the position of substituents on this ring. Activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09fa6dee717e1ef9c17adcf6a2bf4de0
https://doi.org/10.1016/0223-5234(96)88315-2
https://doi.org/10.1016/0223-5234(96)88315-2
Autor:
R Caujolle, Philippe M. Loiseau, Christian Bories, M. Payard, S. Labidalle, N. Kraouti, Philippe Gayral
Publikováno v:
European Journal of Medicinal Chemistry. 30:509-513
Summary A set of new analogs of pyrantel was synthesized in good yields by lithiation of 1,2-dimethyltetrahydropyrimidine with n -butyllithium in tetrahydrofuran and condensation with aromatic esters. Spectrometric studies showed the large influence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580ed5a8238dbe14e97188d12c7c76a4
https://doi.org/10.1016/0223-5234(96)88262-6
https://doi.org/10.1016/0223-5234(96)88262-6
Autor:
Philippe Gayral, J. P. Seguela, Christian Bories, H Amarouch, Linas, R Caujolle, Marc Payard, Philippe M. Loiseau
Publikováno v:
European Journal of Medicinal Chemistry. 30:801-807
Twenty-three arylthioureines bearing β-alanine or γ-aminobutyric alkyl ester chains were synthesized for in vitro screening toward 44 strains of fungi and 2 genera of nematodes. The nitro derivatives were the most potent compounds against Aspergill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::191e968f0e7f16faa73c7e0b24718c63
https://doi.org/10.1016/0223-5234(96)88299-7
https://doi.org/10.1016/0223-5234(96)88299-7
Publikováno v:
European Journal of Medicinal Chemistry. 29:701-706
Aliphatic ethers 2 and esters 3, which are closely related to antifungal azoles, were synthesized and tested against various strains of Candida. We found that their activity was strongly related to the length of the chains; the best activity was obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a621e16a470b8303ff259fbaaa2de9f
https://doi.org/10.1016/0223-5234(94)90032-9
https://doi.org/10.1016/0223-5234(94)90032-9
Autor:
G Baziard-Mouysset, Christian Bories, Philippe R Loiseau, Philippe Gayral, Linas, R Caujolle, H Amarouch, J. P. Seguela, J. D. Favrot, Philippe M. Loiseau, M. Payard
Publikováno v:
European Journal of Medicinal Chemistry. 28:29-35
Twenty-seven arylalkyl- or arylvinylthiazolines were synthesized and tested in vitro against three genera of nematodes, various yeasts and opportunistic fungi. Vinyl compounds seem to have an interesting filaricidal activity against Molinema dessetae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4c14c69ea0e6c170216c34173e6b176
https://doi.org/10.1016/0223-5234(93)90076-q
https://doi.org/10.1016/0223-5234(93)90076-q