Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jean-Philippe Ducoux"'
Autor:
G. Le Fur, S Daoul, J.C. Brelière, D. Van Broeck, M. Poncelet, Charles Advenier, Jean-Philippe Ducoux, Marco Landi, Emmanuel Naline, C Cognon, Philippe Soubrie, Vincenzo Proietto, X. Emonds-Alt, P. Vilain, Gervais Neliat, J P Maffrand, T. Croci
Publikováno v:
Neuropeptides. 31:449-458
(R)-3-(1-[2-(4-benzoyl-2-(3,4-difluorophenyl)-morpholin-2-yl)- ethyl]-4-phenylpiperidin-4-yl)-1-dimethylurea (SR 144190) is a new non-peptide antagonist of tachykinin NK2 receptors. SR 144190 potently and selectively inhibited neurokinin A binding to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635453df0e79e08dfa3ea9112dc64bd6
https://doi.org/10.1016/s0143-4179(97)90039-1
https://doi.org/10.1016/s0143-4179(97)90039-1
Autor:
Daniel Bichon, B. Miloux, M. Poncelet, J.C. Brele`ere, Gervais Neliat, X. Emonds-Alt, Jean-Philippe Ducoux, Vincenzo Proietto, P. Vilain, D. Van Broeck, Michel Heaulme, Philippe Soubrie, G. Le Fur
Publikováno v:
Life Sciences. 56:PL27-PL32
SR 142801 is the first potent and selective non-peptide antagonist of the tachykinin NK3 receptor. It inhibited [MePhe7]NKB binding to its receptor from various species, including humans. SR 142801 was a competitive antagonist of [MePhe7]NKB-mediated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cba3ece7eda5bf9198e2c8b7ed1fc4
https://doi.org/10.1016/0024-3205(94)00413-m
https://doi.org/10.1016/0024-3205(94)00413-m
Autor:
Vincenzo Proietto, Gervais Neliat, P. Vilain, Jean-Philippe Ducoux, Jean-Daniel Doutremepuich, Régis Steinberg, Philippe Soubrie, Xavier Emonds-Alt, Michel Heaulme, Gérard Le Fur, Didier Van Broeck, Jean-Claude Breliere, Vincent Santucci, Daniel Bichon
Publikováno v:
European Journal of Pharmacology. 250:403-413
(S)1-(2-[3-(3,4-dichlorophenyl)-1-(3-isopropoxyphenylacetyl)pip eridin-3- yl]ethyl)-4-phenyl-1-azoniabicyclo[2.2.2]octane chloride (SR140333) is a new non-peptide antagonist of tachykinin NK1 receptors. SR140333 potently, selectively and competitivel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2fb1e52b6a1f357aee3e05caa5d8387
https://doi.org/10.1016/0014-2999(93)90027-f
https://doi.org/10.1016/0014-2999(93)90027-f
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9372ca4477a70511c8d617da10e1f233
https://doi.org/10.1002/chin.199247264
https://doi.org/10.1002/chin.199247264
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f031f91918d96b0563f349f179e69e6f
https://doi.org/10.1002/chin.199323142
https://doi.org/10.1002/chin.199323142
Publikováno v:
Tetrahedron. 48:6403-6412
Three pheromones, (6Z,11Z)-hexadeca-6,11-dien-1-yl acetate (from Eudia pavonia), (5Z,9Z)-heptacosa-5,9-diene (from Drosophila melanogaster) and gossyplure, have been synthesized each by two consecutive consequences of nickel-assisted Grignard reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5f912733b9a48946d654d89d730279a
https://doi.org/10.1016/s0040-4020(01)88230-2
https://doi.org/10.1016/s0040-4020(01)88230-2
Publikováno v:
Tetrahedron Letters. 31:2595-2598
Two pheromones, (Z)-6,(Z)-11-hexadecadien-1-yl acetate (from Eudia pavonia ) and gossyplure, have been synthesized each by two consecutive sequences of nickel-assisted Grignard reactions with cyclic enol ethers and the preparation of Grignard reagent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c20ba79c437269cbd6c3532e176fb393
https://doi.org/10.1016/0040-4039(90)80134-8
https://doi.org/10.1016/0040-4039(90)80134-8
Publikováno v:
The Journal of Organic Chemistry. 58:1290-1292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffabadfcab540a2109e43162cd804bf4
https://doi.org/10.1021/jo00057a055
https://doi.org/10.1021/jo00057a055