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pro vyhledávání: '"I. Lesieur"'
Akademický článek
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Publikováno v:
Pharmacy and Pharmacology Communications. 5:177-181
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac96913ae418363b9672b1f62e7487a8
https://doi.org/10.1211/146080899128734767
https://doi.org/10.1211/146080899128734767
Autor:
P. Voisin, Philippe Delagrange, I. Lesieur, P. Depreux, I. Le Picard, Pierre Renard, Caroline Bennejean
Publikováno v:
Pharmacy and Pharmacology Communications. 5:183-188
Hydroxyindole-O-methyltransferase is an enzyme that catalyses the last step of melatonin biosynthesis. The objective of this work was to design and synthesize potential inhibitors of hydroxyindole-O-methyltransferase. Applying bioisosteric principles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::984bb5debc09fae56329c057622ccdd7
https://doi.org/10.1211/146080899128734578
https://doi.org/10.1211/146080899128734578
Autor:
M. Arborati, B. Guardiola-Lemaitre, Ewa Ninio, JG Bizot-Espiard, MJ Chapman, I. Lesieur, D. Benchorba
Publikováno v:
Fundamental & Clinical Pharmacology. 11:68-77
Cholesteryl esters in the hydrophobic core of low-density lipoprotein (LDL) particles constitute a major molecular target during copper-mediated oxidation. To facilitate the rapid analysis and quantitation of the oxidative degradation of LDL choleste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68be399bf1650c7eded54f3cc252440c
https://doi.org/10.1111/j.1472-8206.1997.tb00171.x
https://doi.org/10.1111/j.1472-8206.1997.tb00171.x
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:1912-1915
Although 6-benzoyl-2(3H)-benzothiazolone derivatives are known, their 4-benzoyl analogues have not been described previously. The title compound [2-(2-oxo-3H-1,3-benzothiazol-4-oyl)benzoic acid, C 15 H 9 NO 4 S] is the first of this series to be isol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d970a94836398fd73c70acddd340f26
https://doi.org/10.1107/s0108270195003179
https://doi.org/10.1107/s0108270195003179
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e446496ba20969b2a7c77e4732fb3ca
https://doi.org/10.1002/chin.199331175
https://doi.org/10.1002/chin.199331175
Publikováno v:
European Journal of Medicinal Chemistry. 25:361-368
The concept of bioisosterism between benzoxazolinone and pyrocatechol has led to the synthesis of benzoxazolinone analogues of the catecholamines which display β- and α-blocking properties. In this paper, we report the synthesis of analogues in whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14130164ad13e9bbb7fff75fe7d9027c
https://doi.org/10.1016/0223-5234(90)90120-r
https://doi.org/10.1016/0223-5234(90)90120-r
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 47:602-604
C 12 H 16 NO + •Cl − cristallise dans P2 1 /c avec a=9,903, b=11,331, c=11,272 A, β=98,18°, Z=4; affinement jusqu'a R=0,032. La molecule est dans une configuration etendue; le plan aromatique forme un angle de 57° avec le plan moyen du dimethy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94fabe600799ca09699a512d163ba972
https://doi.org/10.1107/s0108270190007545
https://doi.org/10.1107/s0108270190007545
Publikováno v:
Heterocyclic Communications. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca15aeb7edb246e72d8efed55f5d3d89
https://doi.org/10.1515/hc.1999.5.3.213
https://doi.org/10.1515/hc.1999.5.3.213
Akademický článek
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