Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Carmela Salvatore"'
Autor:
Elisa Pierpaoli, Francesco Piacenza, Gaetano Fiorillo, Paolo Lombardi, Fiorenza Orlando, Carmela Salvatore, Cristina Geroni, Mauro Provinciali
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2653 (2021)
The natural isoquinoline alkaloid Berberine (BBR) has been shown to possess several therapeutic effects, including anticancer activity. Different BBR derivatives have been designed and synthesized in order to obtain new compounds with enhanced antica
Externí odkaz:
https://doaj.org/article/eb8561ad68db4a7294f63e2c2fbdeb26
Autor:
Elisa Pierpaoli, Francesco Piacenza, Gaetano Fiorillo, Paolo Lombardi, Fiorenza Orlando, Carmela Salvatore, Cristina Geroni, Mauro Provinciali
Publikováno v:
Perspective of Recent Advances in Medical Research Vol. 2 ISBN: 9788196055172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a929efb5a077901e9b3d4a001916ad25
https://doi.org/10.9734/bpi/pramr/v2/3905c
https://doi.org/10.9734/bpi/pramr/v2/3905c
Autor:
Carmela Salvatore, Mauro Provinciali, Gaetano Fiorillo, Paolo Lombardi, Fiorenza Orlando, Cristina Geroni, Elisa Pierpaoli, Francesco Piacenza
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2653, p 2653 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
The natural isoquinoline alkaloid Berberine (BBR) has been shown to possess several therapeutic effects, including anticancer activity. Different BBR derivatives have been designed and synthesized in order to obtain new compounds with enhanced antica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0fff5ff36c69b7c73d49fe5273a58d5
https://www.mdpi.com/1422-0067/22/5/2653
https://www.mdpi.com/1422-0067/22/5/2653
Autor:
Francesco Piacenza, Elisa Pierpaoli, Carmela Salvatore, Mauro Provinciali, Paolo Lombardi, Gaetano Fiorillo, Cristina Geroni
Publikováno v:
BioFactors. 44:443-452
Breast cancer (BC) is the most common malignancy and the most common cause of cancer death in elderly women. We recently demonstrated that innovative compounds structurally related to and semisynthetically derived from the plant alkaloid berberine re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b7d5f27387570fc04fd26010ec0471f
https://doi.org/10.1002/biof.1440
https://doi.org/10.1002/biof.1440
Autor:
Elisa, Pierpaoli, Gaetano, Fiorillo, Paolo, Lombardi, Carmela, Salvatore, Cristina, Geroni, Francesco, Piacenza, Mauro, Provinciali
Publikováno v:
BioFactors (Oxford, England). 44(5)
Breast cancer (BC) is the most common malignancy and the most common cause of cancer death in elderly women. We recently demonstrated that innovative compounds structurally related to and semisynthetically derived from the plant alkaloid berberine re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::989c251e05f0e489298f0771a52dfdca
https://pubmed.ncbi.nlm.nih.gov/30178609
https://pubmed.ncbi.nlm.nih.gov/30178609
Autor:
Franco Buzzetti, Carmela Salvatore, Mauro Provinciali, Elisa Pierpaoli, Paolo Lombardi, Andrea Guido Arcamone
Publikováno v:
BioFactors. 39:672-679
Breast cancer is the most common malignancy and the most common cause of cancer death in elderly women. Chemoprevention with dietary compounds and their synthetic analogs has emerged as an attractive strategy to prevent carcinogenic progression to in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e40cdd88952ff094f956e6afceb719d7
https://doi.org/10.1002/biof.1131
https://doi.org/10.1002/biof.1131
Autor:
Elisa Damiani, Fiorenza Orlando, Carmela Salvatore, Mauro Provinciali, Cristina Geroni, Paolo Lombardi, Abele Donati, Elisa Pierpaoli, Guendalina Lucarini, Beatrice Bartozzi
Publikováno v:
Carcinogenesis. 36(10)
Berberine (BBR) is a natural isoquinoline alkaloid with proven antiangiogenic and anticancer activities. We recently demonstrated that BBR and its synthetic derivative 13-(4-chlorophenylethyl)berberine iodide, NAX014, exert antiproliferative activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9423bf7ef96b546e52d8a75bd36c28ab
https://pubmed.ncbi.nlm.nih.gov/26168818
https://pubmed.ncbi.nlm.nih.gov/26168818
Autor:
Carmela Salvatore, Graziella Pratesi, Stefano Manzini, Cristina Goso, Angela Bullo, Fabio Animati, Mario Bigioni, Carlo Alberto Maggi, Giovanni Capranico, Daniela Bellarosa, Elisabetta Iafrate, Franco Zunino
Publikováno v:
Biochemical Pharmacology. 62:63-70
MEN 10755 is a disaccharide anthracycline endowed with a broader spectrum of antitumour activity than doxorubicin (DOX). To investigate the cellular and molecular basis of its action, cytotoxic activity, drug uptake, subcellular localisation, inducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19ab7bc28c991bb8f20d08dacfe83b26
https://doi.org/10.1016/s0006-2952(01)00645-1
https://doi.org/10.1016/s0006-2952(01)00645-1
Publikováno v:
Anti-Cancer Drugs. 10:663-670
We have developed a stable line of the human breast carcinoma cell line MCF-7 by in vitro continuous exposure to increasing concentrations of the antitumoral alkylating agent FCE 24517 (tallimustine). The selected line, MCF-7/24517(1), was resistant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422aef543fd91afdd4a2aa061369365c
https://doi.org/10.1097/00001813-199908000-00006
https://doi.org/10.1097/00001813-199908000-00006
Autor:
Rosanna Supino, Mario Bigioni, Amalia Cipollone, Michelandrea De Cesare, Claudia Caserini, Fabio Animati, Graziella Pratesi, Anna Maria Casazza, Edith Monteagudo, Marco Berettoni, Stefano Manzini, Franco Zunino, Andrea Madami, Paolo Lombardi, Federico Arcamone, Donatella Polizzi, Carmela Salvatore, Giovanni Capranico, Sabina C. Righetti, Maurizio Franciotti
Publikováno v:
Scopus-Elsevier
Background: Although doxorubicin re mains one of the most effective agent for the treatment of solid tumors, then is an intensive effort to synthesize doxo rubicin analogues (compounds with similar chemical structures) that may have improved antitumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb82281554b76494411de2e15b458246
https://doi.org/10.1093/jnci/89.16.1217
https://doi.org/10.1093/jnci/89.16.1217