Zobrazeno 1 - 9
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pro vyhledávání: '"Kornienko A"'
Publikováno v:
In Tetrahedron 24 September 2022 123
Publikováno v:
In Tetrahedron 19 November 2021 101
Autor:
Masi, Marco, Andolfi, Anna, Mathieu, Veronique, Boari, Angela, Cimmino, Alessio, Moreno Y Banuls, Laetitia, Vurro, Maurizio, Kornienko, Alexander, Kiss, Robert, Evidente, Antonio
Publikováno v:
In Tetrahedron 2 September 2013 69(35):7466-7470
Publikováno v:
Tetrahedron. 123:132990
Publikováno v:
In Tetrahedron 2003 59(7):995-1007
Autor:
Véronique Mathieu, Anna Andolfi, Robert Kiss, Alessio Cimmino, Maurizio Vurro, Angela Boari, Antonio Evidente, Alexander Kornienko, Marco Masi, Laetitia Moreno Y Banuls
Publikováno v:
Tetrahedron (Oxf., Online) 69 (2013): 7466–7470. doi:10.1016/j.tet.2013.06.031
info:cnr-pdr/source/autori:Masi M, Andolfi A, Mathieu V, Boari A, Cimmino A, Banuls L, Vurro M, Kornienkoa, Kiss R, Evidente A/titolo:Fischerindoline, a pyrroloindole terpenoid isolated from Neosartorya pseudofischeri, with in vitro growth inhibitory activity in human cancer cell lines./doi:10.1016%2Fj.tet.2013.06.031/rivista:Tetrahedron (Oxf., Online)/anno:2013/pagina_da:7466/pagina_a:7470/intervallo_pagine:7466–7470/volume:69
info:cnr-pdr/source/autori:Masi M, Andolfi A, Mathieu V, Boari A, Cimmino A, Banuls L, Vurro M, Kornienkoa, Kiss R, Evidente A/titolo:Fischerindoline, a pyrroloindole terpenoid isolated from Neosartorya pseudofischeri, with in vitro growth inhibitory activity in human cancer cell lines./doi:10.1016%2Fj.tet.2013.06.031/rivista:Tetrahedron (Oxf., Online)/anno:2013/pagina_da:7466/pagina_a:7470/intervallo_pagine:7466–7470/volume:69
A novel pyrroloindole terpenoid, named fischerindoline (1), was isolated together with the known metabolites eurochevalierine, pyripyropenes A and E, sequiterpene, gliotoxin, and bis(dethio)bis(methylthio)gliotoxin from solid and liquid cultures of N
Publikováno v:
In Tetrahedron 16 April 2001 57(16):3255-3265
Publikováno v:
Tetrahedron. 59:995-1007
The l-amino group in amikacin was acylated with a variety of 2-hydroxy aminocarboxylic acids to probe the effect of acylation on ribosomal binding and antibacterial activity. The N-hydroxy urea analogue of amikacin ( 8a ) in which the 2-S-hydroxyl-be
Publikováno v:
Tetrahedron. 57:3255-3265
Based on the published NMR structure of the antibiotic paromomycin complexed with the A-site of Escherichia coli 16S ribosomal RNA, a set of C-5 functionalized analogs of paromamine was designed and synthesized, incorporating cyclic and acyclic appen