Zobrazeno 1 - 10
of 230
pro vyhledávání: '"M Wakselman"'
Publikováno v:
Bioorganic & Medicinal Chemistry. 14:7023-7033
Beta-lactams with 6alpha (penicillins) or 7alpha (cephalosporins) substituents are often beta-lactamase inhibitors. This paper assesses the effect of such substituents on acyclic beta-lactamase substrates. Thus, a series of m-carboxyphenyl phenacetur
Publikováno v:
Bioorganic & Medicinal Chemistry. 9:1175-1183
6- and 7-Carboxy-3-phenylacetamido-3H-1-benzofuran-2-one have been synthesized as potential beta-lactamase substrates and/or inhibitors. These compounds were prepared by lactonization of the corresponding, appropriately substituted phenylglycines. Th
Publikováno v:
European Journal of Organic Chemistry. 2001:141-149
The title compounds can be considered as stabilized aza analogs of previously studied dihydrobenzopyranones and linear depsipeptides, which behave as substrates or inhibitors of β-lactamases. Treatment of substituted hydrazides 9b and 9b′ with a p
Publikováno v:
Bioorganic & Medicinal Chemistry. 2:757-771
A series of derivatives of phenyl phenylacetylglycinates (aryl phenaceturates) with a carboxylate substituent meta to the oxygen of the phenoxide leaving group and a functionalized methylene group in the ortho- or para-position have been synthesized.
Publikováno v:
ChemInform. 27
6-O-α- d - Galactopyranosyl - d - glucopyranose (melibiose) derivatives with alkyl groups at the terminal 1- O and 6′- O positions have been synthesized. They show thermotropic and lyotropic liquid-crystal properties. The d -spacings of the strong
Publikováno v:
ChemInform. 33
The title compounds can be considered as stabilized aza analogs of previously studied dihydrobenzopyranones and linear depsipeptides, which behave as substrates or inhibitors of β-lactamases. Treatment of substituted hydrazides 9b and 9b′ with a p
Autor:
C, Baldini, F, Formaggio, C, Toniolo, A, Toffoletti, C, Corvaja, J P, Mazaleyrat, K, Wright, J F, Lohier, M, Wakselman, B, Orioni, L, Stella, M, Venanzi
Publikováno v:
Advances in experimental medicine and biology. 611
Publikováno v:
30th European Peptide Symposium, Helsinki, 2008
info:cnr-pdr/source/autori:Wright K., Wakselman M., Mazaleyrat J.-P., Moretto A., Crisma M., Formaggio F., Toniolo C./congresso_nome:30th European Peptide Symposium/congresso_luogo:Helsinki/congresso_data:2008/anno:2008/pagina_da:/pagina_a:/intervallo_pagine
30th European Peptide Symposium, pp. 54–55, Helsinki, Finland, 31 agosto-5 settembre 2008
info:cnr-pdr/source/autori:K. Wright, M. Wakselman, J.-P. Mazaleyrat, A. Moretto, M. Crisma, F. Formaggio, C. Toniolo/congresso_nome:30th European Peptide Symposium/congresso_luogo:Helsinki, Finland/congresso_data:31 agosto-5 settembre 2008/anno:2009/pagina_da:54/pagina_a:55/intervallo_pagine:54–55
info:cnr-pdr/source/autori:Wright K., Wakselman M., Mazaleyrat J.-P., Moretto A., Crisma M., Formaggio F., Toniolo C./congresso_nome:30th European Peptide Symposium/congresso_luogo:Helsinki/congresso_data:2008/anno:2008/pagina_da:/pagina_a:/intervallo_pagine
30th European Peptide Symposium, pp. 54–55, Helsinki, Finland, 31 agosto-5 settembre 2008
info:cnr-pdr/source/autori:K. Wright, M. Wakselman, J.-P. Mazaleyrat, A. Moretto, M. Crisma, F. Formaggio, C. Toniolo/congresso_nome:30th European Peptide Symposium/congresso_luogo:Helsinki, Finland/congresso_data:31 agosto-5 settembre 2008/anno:2009/pagina_da:54/pagina_a:55/intervallo_pagine:54–55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::63a85020280377a839c7537034848d74
http://www.cnr.it/prodotto/i/104461
http://www.cnr.it/prodotto/i/104461
Autor:
K. Wright, M. Sarciaux, M. Wakselman, J.P. Mazaleyrat, M. Crisma, F. Formaggio, C. Peggion, A. Toffoletti, C. Corvaja, C. Toniolo
Publikováno v:
19th American Peptide Symposium, San Diego, CA, USA, 2005
info:cnr-pdr/source/autori:K. Wright, M. Sarciaux, M. Wakselman, J.P. Mazaleyrat, M. Crisma, F. Formaggio, C. Peggion, A. Toffoletti, C. Corvaja, C. Toniolo/congresso_nome:19th American Peptide Symposium/congresso_luogo:San Diego, CA, USA/congresso_data:2005/anno:2005/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:K. Wright, M. Sarciaux, M. Wakselman, J.P. Mazaleyrat, M. Crisma, F. Formaggio, C. Peggion, A. Toffoletti, C. Corvaja, C. Toniolo/congresso_nome:19th American Peptide Symposium/congresso_luogo:San Diego, CA, USA/congresso_data:2005/anno:2005/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::95123940495146243a8c018f4500067b
http://www.cnr.it/prodotto/i/104285
http://www.cnr.it/prodotto/i/104285
Autor:
K. Wright, A. de Castries, M. Sarciaux, F. Formaggio, C. Toniolo, A. Toffoletti, M. Wakselman, J.-P. Mazaleyrat
Publikováno v:
Tetrahedron letters 46 (2005): 5573–5576.
info:cnr-pdr/source/autori:K. Wright, A. de Castries, M. Sarciaux, F. Formaggio, C. Toniolo, A. Toffoletti, M. Wakselman, and J.-P. Mazaleyrat/titolo:Synthesis and Spectroscopic Characterization of Enantiopure Protected trans-4-Amino-1-Oxyl-2,2,6,6-Tetramethylpiperidine-3-Carboxylic Acid (trans b-TOAC)./doi:/rivista:Tetrahedron letters/anno:2005/pagina_da:5573/pagina_a:5576/intervallo_pagine:5573–5576/volume:46
info:cnr-pdr/source/autori:K. Wright, A. de Castries, M. Sarciaux, F. Formaggio, C. Toniolo, A. Toffoletti, M. Wakselman, and J.-P. Mazaleyrat/titolo:Synthesis and Spectroscopic Characterization of Enantiopure Protected trans-4-Amino-1-Oxyl-2,2,6,6-Tetramethylpiperidine-3-Carboxylic Acid (trans b-TOAC)./doi:/rivista:Tetrahedron letters/anno:2005/pagina_da:5573/pagina_a:5576/intervallo_pagine:5573–5576/volume:46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::85ce335b0f013b5abddbe8a5a7b03638
http://www.cnr.it/prodotto/i/15206
http://www.cnr.it/prodotto/i/15206