Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Valeria Mascia"'
Autor:
Jean-Laurent Paparin, Thierry Convard, Catherine Caillet, Stéphanie Bot, Dominique Louis Nestor Ghislain Surleraux, Claire Pierra, Valeria Mascia, Maria Seifer, Jean-François Griffon, Efisio Sais, Agnès Amador, David Dukhan, Cyril B. Dousson, Elodie Rosinosky, Loredana Onidi, Anna Giulia Loi, Rachid Rahali, Eric Badaroux, Massimiliano LaColla, Frédéric Leroy, David Standring, Michel Liuzzi, Joe McCarville, Julien Milhau, Ludovic Griffe, Daniel Da Costa
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(11)
Hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase (RdRp) plays a central role in virus replication. NS5B has no functional equivalent in mammalian cells, and as a consequence is an attractive target for selective inhibition. This paper descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cabbb65889368ef3bd04a5068480e29
https://pubmed.ncbi.nlm.nih.gov/28416131
https://pubmed.ncbi.nlm.nih.gov/28416131
Autor:
Alessandra Cadeddu, Silvia Porcedda, Valeria Mascia, Laura Vargiu, Roberta Loddo, Alessandra Caredda, Bruno Marongiu, Alessandra Piras
Publikováno v:
Journal of Essential Oil Research. 16:256-261
By means of a supercritical fluid extractor, extract of Juniperus phoenicea L. was obtained in a single extraction stage. The yield was 0.2% by mass. The operative conditions were: extractor, pressure, P = 90 bar and temperature, T = 50°C; first sep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0518abacfd7709b4d7ddc3420beb85b
https://doi.org/10.1080/10412905.2004.9698715
https://doi.org/10.1080/10412905.2004.9698715
Autor:
Sergio Alleca, Paolo La Colla, Paola Corona, Mario Loriga, Valeria Mascia, Bernardetta Busonera, Giuseppe Paglietti, Roberta Loddo
Publikováno v:
Il Farmaco. 58:639-650
Twenty eight pyrrolo[1,2-a]quinoxalines bearing at position 4 various substituents related to the moieties present in classical and non classical antifolic agents were prepared and evaluated in vitro for antiproliferative activity. In an in vitro scr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd16b39981a08516b44dba6366eef73
https://doi.org/10.1016/s0014-827x(03)00101-0
https://doi.org/10.1016/s0014-827x(03)00101-0
Autor:
E. Arzedi, Sofia Cosentino, Valeria Mascia, F. Palmas, Carlo Ignazio Giovanni Tuberoso, M. Satta, B. Pisano
Publikováno v:
Letters in Applied Microbiology. 29:130-135
Essential oils and their components are becoming increasingly popular as naturally occurring antimicrobial agents. In this work the chemical composition and the antimicrobial properties of Thymus essential oils and of their main components were deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062c73fc01dd821a8472f4efbb1c7157
https://doi.org/10.1046/j.1472-765x.1999.00605.x
https://doi.org/10.1046/j.1472-765x.1999.00605.x
Publikováno v:
Le Lait. 79:607-613
This study was designed to compare the microbiological quality of Pecorino processed cheese spreads manufactured in a mechanized factory and in small artisanal dairies. The 118 factory- made spreads analyzed were characterized by generally low microb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39df517514c78505686efd02d9498e0d
https://doi.org/10.1051/lait:1999650
https://doi.org/10.1051/lait:1999650
Autor:
Elena Tamburini, Angelo Ranise, Giulia Menozzi, Paolo La Colla, Luisa Merello, Luisa Mosti, Chiara Murgioni, Roberta Loddo, Paola Fossa, Francesco Bondavalli, Silvia Schenone, Valeria Mascia
During the course of our studies in the azole antifungals area, we synthesized a number of 1,5-disubstituted 4-[1H-imidazol-1-yl(phenyl)methyl]-1H-pyrazoles, analogues of bifonazole. 1,5-Diphenyl-1H-pyrazole 3 showed weak antimycotic and antibacteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58b6c43337c086ffcc1f485d1fbc16fa
http://hdl.handle.net/11567/250408
http://hdl.handle.net/11567/250408
Autor:
Angelo Ranise, Maria Elena Marongiu, Silvia Schenone, Paolo La Colla, Roberta Loddo, Olga Bruno, Francesco Bondavalli, Valeria Mascia, Alessandra Pani, Andrea Spallarossa
Publikováno v:
Bioorganicmedicinal chemistry. 11(12)
Three series of 5-substituted 1,3-diphenyl-6-(omega-dialkyl- and omega-cyclo-aminoalkyl)thio-2-thiobarbiturates (11-13) were synthesized as polysubstituted thioanalogues of merbarone, a topoisomerase II inhibitor acting on the catalytic site. To bett
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ada646a7ddc3478ef194937f60c72fff
https://pubmed.ncbi.nlm.nih.gov/12757725
https://pubmed.ncbi.nlm.nih.gov/12757725