Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Irene Rovardi"'
Autor:
Johann Moschner, Anna Chentsova, Nicole Eilert, Irene Rovardi, Philipp Heretsch, Athanassios Giannis
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2328-2335 (2013)
The chemical synthesis and biological evaluation of new cyclopamine analogs bearing exocyclic methylenes in different positions is described. Bis-exo-cyclopamine 6 was identified as a potent inhibitor of the Gli1-dependent luciferase expression in Sh
Externí odkaz:
https://doaj.org/article/edbb78dd43eb4ac7a7c811fcbdb1621e
Autor:
Philipp Heretsch, Irene Rovardi, Anna Chentsova, Athanassios Giannis, Johann Moschner, Nicole Eilert
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2328-2335 (2013)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
The chemical synthesis and biological evaluation of new cyclopamine analogs bearing exocyclic methylenes in different positions is described. Bis-exo-cyclopamine 6 was identified as a potent inhibitor of the Gli1-dependent luciferase expression in Sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bec50068ce884f15ebf8da162096bfe
https://doaj.org/article/edbb78dd43eb4ac7a7c811fcbdb1621e
https://doaj.org/article/edbb78dd43eb4ac7a7c811fcbdb1621e
Autor:
Alessandra Bonamore, Eugenio Lendaro, Alessandra Comandini, Antonio Carraturo, R.M. Matarese, Alberto Macone, Irene Rovardi
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:6003-6007
Aromatic substrates tyrosol ( p -hydroxyphenylethanol) and 2,6-dihydroxynaphthalene (2,6-DHN) were converted into chromane derivatives by means of chemoenzymatic reactions catalyzed by the aromatic prenyltransferase of bacterial origin NovQ, using di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9dca2737769dd2eac4fca442b71e72
https://doi.org/10.1016/j.bmc.2009.06.061
https://doi.org/10.1016/j.bmc.2009.06.061
Autor:
Paola Baiocco, Alberto Macone, Alberto Boffi, Francesco Gasparrini, Marco Barba, Bruno Botta, Alessandra Bonamore, Carmela Molinaro, Irene Rovardi
An efficient, stereoselective, green synthesis of (S)-norcoclaurine (higenamine) has been developed using the recombinant (S)-norcoclaurine synthase (NCS) enzyme, starting from the cheap tyrosine and dopamine substrates in a one-pot, two step process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30fae0b0be74cc3ae968f3276a929b7f
http://hdl.handle.net/11573/376102
http://hdl.handle.net/11573/376102
Autor:
Alessandra Bonamore, Irene Rovardi, Francesco Gasparrini, Paola Baiocco, Marco Barba, Carmela Molinaro, Bruno Botta, Alberto Boffi, Alberto Macone
Publikováno v:
Green Chemistry; Sep2010, Vol. 12 Issue 9, p1623-1627, 5p