Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Claudia Percivalle"'
Autor:
John D. Sutherland, Cécile Caumes, Bhavesh H. Patel, Maria Tsanakopoulou, Colm D. Duffy, Claudia Bonfio, Claudia Percivalle
Publikováno v:
Journal of the American Chemical Society. 141:3934-3939
[Image: see text] The main aim of origins of life research is to find a plausible sequence of transitions from prebiotic chemistry to nascent biology. In this context, understanding how and when phospholipid membranes appeared on early Earth is criti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34e75171141d848c982dc6eb90f3bd4e
https://doi.org/10.1021/jacs.8b12331
https://doi.org/10.1021/jacs.8b12331
Publikováno v:
Current Organic Chemistry. 18:19-43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8766fec8902d60660031931e2fec98a4
https://doi.org/10.2174/13852728113176660135
https://doi.org/10.2174/13852728113176660135
Autor:
Caterina Musetti, Maria Laura Greco, Stefano Alcaro, Angelica Mariani, Maria Lucia Perrore, Giosuè Costa, Anna Artese, Mauro Freccero, Claudia Sissi, Claudia Percivalle
Publikováno v:
Org. Biomol. Chem.. 12:3744-3754
Aryl ethynyl anthraquinones have been synthesized by Sonogashira cross-coupling and evaluated as telomeric G-quadruplex ligands, by the FRET melting assay, circular dichroism, the DNA synthesis arrest assay and molecular docking. Both the binding pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::800455a702ae22ced45abf5f47695f2a
https://doi.org/10.1039/c4ob00220b
https://doi.org/10.1039/c4ob00220b
Publikováno v:
Org. Biomol. Chem.. 11:16-26
Widespread in nature, oligonucleotide-templated reactions of phosphodiester bond formation have inspired chemists who are now applying this elegant strategy to the catalysis of a broad range of otherwise inefficient reactions. This review highlights
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64a83b23e4032bd62e0497ea289f19e
https://doi.org/10.1039/c2ob26163d
https://doi.org/10.1039/c2ob26163d
Publikováno v:
MedChemComm. 4:211-215
We report the synthesis of an acridine-containing cyanine dye and demonstrate its potential as a pH-responsive colorimetric indicator and fluorescent probe. Similarly to its parent molecule BRACO-19, this tri-substituted acridine also binds strongly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eceb4d39b31efb66e4ce802abd258ff
https://doi.org/10.1039/c2md20173a
https://doi.org/10.1039/c2md20173a
A minimal cell can be thought of as comprising informational, compartment-forming and metabolic subsystems. To imagine the abiotic assembly of such an overall system, however, places great demands on hypothetical prebiotic chemistry. The perceived di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bef6e7dfcdceb43a762e0ced3918b07
https://europepmc.org/articles/PMC4568310/
https://europepmc.org/articles/PMC4568310/
Publikováno v:
ChemInform. 44
Widespread in nature, oligonucleotide-templated reactions of phosphodiester bond formation have inspired chemists who are now applying this elegant strategy to the catalysis of a broad range of otherwise inefficient reactions. This review highlights
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0314990f884af7e4f938c6b3bd37f8c
https://doi.org/10.1002/chin.201320232
https://doi.org/10.1002/chin.201320232
Publikováno v:
The Journal of organic chemistry. 77(7)
Irradiation of 2-alkynylphenols resulted in the generation of vinylidene-quinone methides (QMs), which were detected by laser flash photolysis in organic solvents and aqueous acetonitrile. QMs' spectroscopic properties and electrophilicity were both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a159f95fbb0384e25ea611e242add0df
https://pubmed.ncbi.nlm.nih.gov/22397717
https://pubmed.ncbi.nlm.nih.gov/22397717
Autor:
Marco Di Antonio, Marco Folini, Mauro Freccero, Claudia Percivalle, Luca Germani, Anna Artese, Stefano Alcaro, Nadia Zaffaroni, Filippo Doria, Claudia Sissi, Matteo Nadai, Sara N. Richter
The synthesis, physico-chemical properties and biological effects of a new class of naphthalene diimides (NDIs) capable of reversibly binding telomeric DNA and alkylate it through an electrophilic quinone methide moiety (QM), are reported. FRET and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e68721fdc221e99a762ecb3eb6dc61
http://hdl.handle.net/11577/2492014
http://hdl.handle.net/11577/2492014
Publikováno v:
ChemInform. 42
A straightforward route for the preparation of 6-substituted naphthols and 6,6′-disubstituted binols (binol = 2,2′-dihydroxy-1,1′-binaphthyl) is presented. The synthesis has been accomplished by a one-step procedure starting from 6-bromo deriva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ded9411226dead0b8d57908f9bbc08b
https://doi.org/10.1002/chin.201126091
https://doi.org/10.1002/chin.201126091