Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Giuditta Scialino"'
Autor:
Gabbriella Innocenti, Stefano Dall’Acqua, Giuditta Scialino, Elena Banfi, Silvio Sosa, Khilendra Gurung, Mariagnese Barbera, Maria Carrara
Publikováno v:
Molecules, Vol 15, Iss 4, Pp 2326-2338 (2010)
The essential oil of Rhododendron anthopogon was investigated by GC-MS, and seventeen compounds (representing approximately 98% of the oil) were identified. The major components of the aerial parts of the oil were the monoterpenes α-pinene, β-pinen
Externí odkaz:
https://doaj.org/article/c9a95a97e4a244318f128f4e5b2330b6
Autor:
Francesca Cateni, Paolo Bonivento, Elena Banfi, Marina Zacchigna, Giuditta Scialino, Giuseppe Procida
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:1971-1978
Monoglucosyl and monogalactosyl diglycerides (MGDGs) with medium-long length acyl chains, identified as active components in Euphorbiaceae, were synthesized. They were examined for antimicrobial activity against Gram-positive, Gram-negative bacteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6924f49387c7382143af3647a92c63d8
https://doi.org/10.1016/j.bmcl.2007.01.019
https://doi.org/10.1016/j.bmcl.2007.01.019
Autor:
Marina Zacchigna, Elena Banfi, Luciana Gabrielli Favretto, Giuditta Scialino, Giuseppe Procida, Francesca Cateni, Paolo Bonivento
Publikováno v:
Bioorganic & Medicinal Chemistry. 15:815-826
Monogalactosyl diglycerides with medium to long fatty acid acyl chains, were prepared and examined for antimicrobial activity against Gram positive, Gram negative bacteria and fungi. The study of their in vitro antimicrobial activity confirms the sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::350b5824f41e3da8e567a43c90dd9da0
https://doi.org/10.1016/j.bmc.2006.10.045
https://doi.org/10.1016/j.bmc.2006.10.045
Autor:
Giuditta Scialino, Maurizio Fermeglia, Elena Banfi, Daniele Zampieri, Maria Grazia Mamolo, Marco Ferrone, Sabrina Pricl, Luciano Vio
Publikováno v:
Bioorganic & Medicinal Chemistry. 13:3797-3809
3H-1,3,4-Oxadiazole-2-thione and 3H-1,3,4-oxadiazol-2-one derivatives were synthesized and tested for their in vitro antimycobacterial activity. Oxadiazolone derivatives showed an interesting antimycobacterial activity against the tested strain of My
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48cc6d1e14682702a62eae742a84379
https://doi.org/10.1016/j.bmc.2005.03.013
https://doi.org/10.1016/j.bmc.2005.03.013
Autor:
Giuditta Scialino, Elena Banfi, Daniele Zampieri, Luciano Vio, Maria Grazia Mamolo, Valeria Falagiani
Publikováno v:
Il Farmaco. 58:631-637
[5-(Pyridin-2-yl)-1,3,4-thiadiazol-2-ylthio]acetic acid (3,4-diaryl-3 H -thiazol-2-ylidene)-hydrazide derivatives were synthesized and tested for their in vitro antimycobacterial activity. Some compounds showed an interesting activity against a strai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57e185ce446214c5e0a7138b94e6e859
https://doi.org/10.1016/s0014-827x(03)00103-4
https://doi.org/10.1016/s0014-827x(03)00103-4
Autor:
Erik Laurini, Maria Grazia Mamolo, Giuditta Scialino, Elena Banfi, Daniele Zampieri, Luciano Vio
Publikováno v:
ChemInform. 41
2-Aryl-3-(1H-imidazol-1-yl and 1H-1,2,4-triazol-1-yl)-1H-indole derivatives were synthesized and tested for their in-vitro antifungal and antimycobacterial activities. These indole derivatives were devoid of antifungal activity against the tested str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e63cd0da1917a869f04300fb3f31ed6
https://doi.org/10.1002/chin.201016097
https://doi.org/10.1002/chin.201016097
Autor:
Maria Carrara, Mariagnese Barbera, Khilendra Gurung, Giuditta Scialino, Stefano Dall'Acqua, Gabbriella Innocenti, Silvio Sosa, Elena Banfi
Publikováno v:
Molecules
Molecules, Vol 15, Iss 4, Pp 2326-2338 (2010)
Molecules; Volume 15; Issue 4; Pages: 2326-2338
Molecules, Vol 15, Iss 4, Pp 2326-2338 (2010)
Molecules; Volume 15; Issue 4; Pages: 2326-2338
The essential oil of Rhododendron anthopogon was investigated by GC-MS, and seventeen compounds (representing approximately 98% of the oil) were identified. The major components of the aerial parts of the oil were the monoterpenes alpha-pinene, beta-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d06daec8828ac2f76957a63fe41cddc8
http://hdl.handle.net/11368/2297006
http://hdl.handle.net/11368/2297006
Autor:
Luciano Vio, Erik Laurini, Elena Banfi, Maria Grazia Mamolo, Daniele Zampieri, Giuditta Scialino
Publikováno v:
Archiv der Pharmazie. 342(12)
2-Aryl-3-(1H-imidazol-1-yl and 1H-1,2,4-triazol-1-yl)-1H-indole derivatives were synthesized and tested for their in-vitro antifungal and antimycobacterial activities. These indole derivatives were devoid of antifungal activity against the tested str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad5ac9560d2f20f935399cca757ecaa3
https://pubmed.ncbi.nlm.nih.gov/19921681
https://pubmed.ncbi.nlm.nih.gov/19921681
Autor:
Erik Laurini, Elena Banfi, Paola Posocco, Maurizio Fermeglia, Luciano Vio, Sabrina Pricl, Giuditta Scialino, Daniele Zampieri, Maria Grazia Mamolo
Publikováno v:
Bioorganicmedicinal chemistry. 17(13)
3H-1,3,4-Oxadiazol-2-one derivatives were synthesized and tested for their in vitro antimycobacterial activity. Oxadiazolone derivatives showed an interesting antimycobacterial activity against the reference strain of Mycobacterium tuberculosis H(37)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6179eb7252d93ff173ba78062c83c0
https://pubmed.ncbi.nlm.nih.gov/19467603
https://pubmed.ncbi.nlm.nih.gov/19467603
Autor:
Andrej Piltaver, Elena Banfi, Bojan Doljak, Marko Anderluh, Francesca Cateni, Marina Zacchigna, Giuditta Scialino
Publikováno v:
ChemInform. 39
From the fungus Stereum hirsutum have been isolated and identified two new epidioxysterols 1, 4, together with two known ones 2 and 3. Their structures were elucidated on the basis of spectroscopic analysis and chemical reactions. Epidioxysterols 1-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13bcc0b8c70333a5e2973752183becc5
https://doi.org/10.1002/chin.200809202
https://doi.org/10.1002/chin.200809202