Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Paula López Rivas"'
Autor:
Lizeth Bodero, Paula López Rivas, Barbara Korsak, Torsten Hechler, Andreas Pahl, Christoph Müller, Daniela Arosio, Luca Pignataro, Cesare Gennari, Umberto Piarulli
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 407-415 (2018)
RGD-α-amanitin and isoDGR-α-amanitin conjugates were synthesized by joining integrin ligands to α-amanitin via various linkers and spacers. The conjugates were evaluated for their ability to inhibit biotinylated vitronectin binding to the purified
Externí odkaz:
https://doaj.org/article/b6aac4e1d16e4883ac5787d77551d159
Autor:
Gábor Mező, József Tóvári, Daniela Arosio, Paula López Rivas, Arianna Pina, Alberto Dal Corso, Cesare Gennari, Ivan Ranđelović, André Raposo Moreira Dias, Luca Pignataro
Publikováno v:
European Journal of Organic Chemistry. 2018:2902-2909
Autor:
Paula López Rivas, Eduard Figueras, Paola Gallinari, Umberto Piarulli, Cesare Gennari, Daniela Arosio, Marcel Frese, Arianna Pina, Ana Martins, Lizeth Bodero, Adina Borbély, Norbert Sewald, André Raposo Moreira Dias, Christian Steinkühler
Publikováno v:
ChemistryOpen 8 (2019): 737–742. doi:10.1002/open.201900110
info:cnr-pdr/source/autori:Borbély, Adina; Figueras, Eduard; Martins, Ana; Bodero, Lizeth; Raposo Moreira Dias, André; López Rivas, Paula; Pina, Arianna; Arosio, Daniela; Gallinari, Paola; Frese, Marcel; Steinkühler, Christian; Gennari, Cesare; Piarulli, Umberto; Sewald, Norbert/titolo:Conjugates of Cryptophycin and RGD or isoDGR Peptidomimetics for Targeted Drug Delivery/doi:10.1002%2Fopen.201900110/rivista:ChemistryOpen/anno:2019/pagina_da:737/pagina_a:742/intervallo_pagine:737–742/volume:8
ChemistryOpen, Vol 8, Iss 6, Pp 737-742 (2019)
ChemistryOpen
info:cnr-pdr/source/autori:Borbély, Adina; Figueras, Eduard; Martins, Ana; Bodero, Lizeth; Raposo Moreira Dias, André; López Rivas, Paula; Pina, Arianna; Arosio, Daniela; Gallinari, Paola; Frese, Marcel; Steinkühler, Christian; Gennari, Cesare; Piarulli, Umberto; Sewald, Norbert/titolo:Conjugates of Cryptophycin and RGD or isoDGR Peptidomimetics for Targeted Drug Delivery/doi:10.1002%2Fopen.201900110/rivista:ChemistryOpen/anno:2019/pagina_da:737/pagina_a:742/intervallo_pagine:737–742/volume:8
ChemistryOpen, Vol 8, Iss 6, Pp 737-742 (2019)
ChemistryOpen
RGD-cryptophycin and isoDGR-cryptophycin conjugates were synthetized by combining peptidomimetic integrin ligands and cryptophycin, a highly potent tubulin-binding antimitotic agent across lysosomally cleavable Val-Ala or uncleavable linkers. The con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5f6b95347262e1abd4af16e58236b7
https://publications.cnr.it/doc/405120
https://publications.cnr.it/doc/405120
Autor:
Christoph Müller, Luca Pignataro, Torsten Hechler, Daniela Arosio, Barbara Korsak, Cesare Gennari, Paula López Rivas, Umberto Piarulli, Andreas Pahl, Lizeth Bodero
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein journal of organic chemistry 14 (2018): 407–415. doi:10.3762/bjoc.14.29
info:cnr-pdr/source/autori:Bodero L.; Rivas P.L.; Korsak B.; Hechler T.; Pahl A.; Muller C.; Arosio D.; Pignataro L.; Gennari C.; Piarulli U./titolo:Synthesis and biological evaluation of RGD and isoDGR peptidomimetic-alpha-amanitin conjugates for tumor-targeting/doi:10.3762%2Fbjoc.14.29/rivista:Beilstein journal of organic chemistry/anno:2018/pagina_da:407/pagina_a:415/intervallo_pagine:407–415/volume:14
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 407-415 (2018)
Beilstein journal of organic chemistry 14 (2018): 407–415. doi:10.3762/bjoc.14.29
info:cnr-pdr/source/autori:Bodero L.; Rivas P.L.; Korsak B.; Hechler T.; Pahl A.; Muller C.; Arosio D.; Pignataro L.; Gennari C.; Piarulli U./titolo:Synthesis and biological evaluation of RGD and isoDGR peptidomimetic-alpha-amanitin conjugates for tumor-targeting/doi:10.3762%2Fbjoc.14.29/rivista:Beilstein journal of organic chemistry/anno:2018/pagina_da:407/pagina_a:415/intervallo_pagine:407–415/volume:14
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 407-415 (2018)
RGD-α-amanitin and isoDGR-α-amanitin conjugates were synthesized by joining integrin ligands to α-amanitin via various linkers and spacers. The conjugates were evaluated for their ability to inhibit biotinylated vitronectin binding to the purified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0953df6e3e8ef2e8f3a146ddc7a50dcd
http://hdl.handle.net/11383/2069651
http://hdl.handle.net/11383/2069651
Autor:
Simone Zanella, Simona Angerani, Arianna Pina, Paula López Rivas, Clelia Giannini, Silvia Panzeri, Daniela Arosio, Michele Caruso, Fabio Gasparri, Ivan Fraietta, Clara Albanese, Aurelio Marsiglio, Luca Pignataro, Laura Belvisi, Umberto Piarulli, Cesare Gennari
Publikováno v:
Chemistry-A European Journal
Autor:
Adina Borbély, Dr. Eduard Figueras, Ana Martins, Dr. Lizeth Bodero, Dr. André Raposo Moreira Dias, Dr. Paula López Rivas, Dr. Arianna Pina, Dr. Daniela Arosio, Dr. Paola Gallinari, Dr. Marcel Frese, Dr. Christian Steinkühler, Prof. Dr. Cesare Gennari, Prof. Dr. Umberto Piarulli, Prof. Dr. Norbert Sewald
Publikováno v:
ChemistryOpen, Vol 8, Iss 6, Pp 737-742 (2019)
Abstract RGD‐cryptophycin and isoDGR‐cryptophycin conjugates were synthetized by combining peptidomimetic integrin ligands and cryptophycin, a highly potent tubulin‐binding antimitotic agent across lysosomally cleavable Val‐Ala or uncleavable
Externí odkaz:
https://doaj.org/article/d3a79dc0bab74335b6cc1b9cbbeb2934