Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alessandro Altieri"'
Autor:
Alessandro Altieri, Antonello Alvino, Stephan Ohnmacht, Giancarlo Ortaggi, Stephen Neidle, Daniele Nocioni, Marco Franceschin, Armandodoriano Bianco
Publikováno v:
Molecules, Vol 18, Iss 11, Pp 13446-13470 (2013)
Following previous studies on anthraquinone and acridine-based G-quadruplex ligands, here we present a study of similar aromatic cores, with the specific aim of increasing G-quadruplex binding and selectivity with respect to duplex DNA. Synthesized c
Externí odkaz:
https://doaj.org/article/1695155e35b84d6f9727c48887f20964
Autor:
Armandodoriano Bianco, Lorenzo Cianni, Alessandro Altieri, Chiara Cingolani, Angela Maria Rizzo, Annamaria Biroccio, Marco Franceschin, Sara Iachettini, Carlo Leonetti, Emanuela Micheli, Stefano Cacchione
Publikováno v:
Biochimie. 125:223-231
A novel approach to cancer therapeutics is emerging in the field of G-quadruplex (G4) ligands, small molecules designed to stabilize four-stranded structures that can form at telomeres as well as in other genomic sequences, including oncogene promote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0581feb1de645bf358c2431896088b85
https://doi.org/10.1016/j.biochi.2016.04.008
https://doi.org/10.1016/j.biochi.2016.04.008
Autor:
Valentina Casagrande, Armandodoriano Bianco, Daniele Nocioni, Alessandro Altieri, Antonello Alvino, Maria Luisa Scarpati, Marco Franceschin
Publikováno v:
European Journal of Organic Chemistry. 2013:191-196
Taspine is an alkaloid found in the latex of certain trees belonging to the family of Euphorbiaceae, commonly called “Sangre de Drago” (Dragon's blood). Its structure and antineoplastic properties are well known. Here we report the total synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f79fe055f57f19aced1b2bb1f3d0d124
https://doi.org/10.1002/ejoc.201201034
https://doi.org/10.1002/ejoc.201201034
Publikováno v:
Natural Product Research. 28:586-588
In this study, the iridoidic content of two accessions of Crucianella maritima L., one from Sardinia and the second from Latium, was examined and compared. From a qualitative point of view, the iridoidic pattern of the two samples was similar, since
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36c39597bc52529d51ba8c4282da3b60
https://doi.org/10.1080/14786419.2014.882920
https://doi.org/10.1080/14786419.2014.882920
Publikováno v:
Natural Product Research. 27:2063-2065
The molecular pattern of two Gentiana species, G. dinarica and G. lutea, present in a protected area of Appennino Centrale in Italy, was examined. Results were compared with literature data, examining the differences between the two species.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0d885bfcee664d2846fcede84f6b91
https://doi.org/10.1080/14786419.2013.819863
https://doi.org/10.1080/14786419.2013.819863
Autor:
Armandodoriano Bianco, Alessandro Altieri, Chiara Cingolani, Annamaria Biroccio, Alessandro Venditti, Daniele Nocioni, Stefano Cacchione, Marco Franceschin, Pasquale Zizza, Emanuela Micheli
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (47), pp.9572-82. ⟨10.1039/c4ob01658k⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (47), pp.9572-82. ⟨10.1039/c4ob01658k⟩
International audience; Following the results we previously reported on a series of xanthene and xanthone derivatives as G-quad-ruplex stabilizing ligands, in order to obtain a more selective compound with respect to the previous generation of deriva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2832dbf7e20c92416ccd816a0cea6a
https://hal-riip.archives-ouvertes.fr/pasteur-01163662/file/c4ob01658k.pdf
https://hal-riip.archives-ouvertes.fr/pasteur-01163662/file/c4ob01658k.pdf
Autor:
Armandodoriano Bianco, Giancarlo Ortaggi, Stephan A. Ohnmacht, Antonello Alvino, Marco Franceschin, Alessandro Altieri, Daniele Nocioni, Stephen Neidle
Publikováno v:
Molecules
Molecules, Vol 18, Iss 11, Pp 13446-13470 (2013)
Molecules; Volume 18; Issue 11; Pages: 13446-13470
Molecules, Vol 18, Iss 11, Pp 13446-13470 (2013)
Molecules; Volume 18; Issue 11; Pages: 13446-13470
Following previous studies on anthraquinone and acridine-based G-quadruplex ligands, here we present a study of similar aromatic cores, with the specific aim of increasing G-quadruplex binding and selectivity with respect to duplex DNA. Synthesized c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b74f6667bddda7bcc3fea410040cb8
http://hdl.handle.net/11573/531038
http://hdl.handle.net/11573/531038
Autor:
Annamaria Biroccio, Alina Ciammaichella, Angela Maria Rizzo, Valentina Casagrande, Marco Franceschin, Carlo Leonetti, Alessandro Altieri, Manuela Porru, Armandodoriano Bianco, Giancarlo Ortaggi, Sara Iachettini, Erica Salvati, Antonello Alvino
Based on previous work on both perylene and coronene derivatives as G-quadruplex binders, a novel chimeric compound was designed: N,N′-bis[2-(1-piperidino)-ethyl]-1-(1-piperidinyl)-6-[2-(1-piperidino)-ethyl]-benzo[ghi]perylene-3,4:9,10-tetracarboxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67e2a8842a68f3b0118003732610578f
http://hdl.handle.net/11573/487207
http://hdl.handle.net/11573/487207