Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Giovanni Biasoli"'
Publikováno v:
Tetrahedron Letters. 39:3551-3554
Aliphatic nitriles were obtained through functional group transformation of the corresponding unsubstituted aliphatic amidines with penta-atomic anhydrides. The best results were obtained with succinic anhydride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a721b66ea35efcea7b64ad585088444e
https://doi.org/10.1016/s0040-4039(98)00546-2
https://doi.org/10.1016/s0040-4039(98)00546-2
Autor:
Marina Caldarelli, Italo Beria, Laura Capolongo, Giovanni Biasoli, Paolo Cozzi, Cristina Geroni, Nicola Mongelli
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2979-2984
The design, synthesis, and in vitro and in vivo activities of novel benzoyl and cinnamoyl nitrogen mustard and half-mustard derivatives of distamycin A, in which the amidino moiety has been replaced by moieties of different physico-chemical features,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eefe6cf1a33e172bd34909e98c8d3e4a
https://doi.org/10.1016/s0960-894x(97)10120-2
https://doi.org/10.1016/s0960-894x(97)10120-2
Autor:
Italo Beria, Laura Capolongo, Marina Caldarelli, Giovanni Biasoli, Nicola Mongelli, Cristina Geroni, Paolo Cozzi
Publikováno v:
ChemInform. 29
The design, synthesis, and in vitro and in vivo activities of novel benzoyl and cinnamoyl nitrogen mustard and half-mustard derivatives of distamycin A, in which the amidino moiety has been replaced by moieties of different physico-chemical features,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c83cd41fa018e0f21ab39752ed3aa03
https://doi.org/10.1002/chin.199812235
https://doi.org/10.1002/chin.199812235
Autor:
Federico Corelli, Maurizio Botta, Giovanni Biasoli, Valentina Cappello, Nicola Mongelli, Fabrizio Manetti, Andrea Lombardi Borgia, M. Ciomei
Publikováno v:
Bioorganicmedicinal chemistry. 6(7)
The design, synthesis, and biological evaluation of a series of pyrrole and pyrazole congeners 2 of suramin, directed toward the development and identification of new ligands that complex the human fibroblast growth factor (bFGF), thereby inhibiting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c86e0155f3ccce2d3a1d2519f9f725c9
https://pubmed.ncbi.nlm.nih.gov/9730230
https://pubmed.ncbi.nlm.nih.gov/9730230
Autor:
Ettore Perrone, Giuliano Nannini, G. Meinardi, Dino Severino, Giovanni Biasoli, Angelo Bedeschi, Alberta Bianchi
Publikováno v:
The Journal of antibiotics. 34(4)
The synthesis and in vitro structure-activity relationships of 7-vinylenethioacetamido and thioacrylamido cephalosporins with various substituents at the 3-position are described. 7(Z)-beta-Vinylenethioacetamido cephalosporins proved the most active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a55408d640dac9eecc21bbd130e8fd7
https://pubmed.ncbi.nlm.nih.gov/7275820
https://pubmed.ncbi.nlm.nih.gov/7275820
Autor:
L. Sala, G. Vita, G. Galli, Alberta Bianchi, P. Cozzi, Dino Severino, C. Confalonieri, Ferruccio Casabuona, G. Meinardi, Gisella Monti, I. De Carneri, Pier Nicola Giraldi, G. Molgora, Giuliano Nannini, Giovanni Biasoli
Publikováno v:
Chemischer Informationsdienst. 8
A series of 7-substituted alkyl-thio-acylaminocephalosporins with the following general formula were prepared and tested for in vitro antibacterial activity: (formula: see text). We tried in our research to find any relationship between antibacterial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::699b3deaa24d1df0d88fd6d5eb96c6d7
https://doi.org/10.1002/chin.197722364
https://doi.org/10.1002/chin.197722364
Autor:
Roberto D'Alessio, Giovanni Biasoli, Enzio Ragg, Nicola Mongelli, Laura Capolongo, Carla Rossi, Stefania Mazzini, Marina Caldarelli, Cristina Geroni, Paolo Cozzi, Italo Beria
Publikováno v:
Scopus-Elsevier
The design, synthesis, in vitro and in vivo activities of novel benzoyl and cinnamoyl nitrogen mustard and half-mustard derivatives of distamycin A are described and structure-activity relationships are discussed. The equipotent activities of N-ethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63ae5713f09ea865e1ce964e012cd7a4
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030662587&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030662587&partnerID=MN8TOARS
