Zobrazeno 1 - 10
of 218
pro vyhledávání: '"Enzo Santaniello"'
Autor:
Jelena S Lazarevic, Ana Markovic, Andrija Smelcerovic, Gordana Stojanovic, Pierangela Ciuffreda, Enzo Santaniello
Publikováno v:
Acta Chimica Slovenica, Vol 69, Iss 3, Pp 571-583 (2022)
Chemical modifications of natural monoterpenoids to various derivatives have been reported to result in enhancement of biological activities when compared to parent compounds. In this context a well-known biocide and food additive, carvacrol, served
Externí odkaz:
https://doaj.org/article/7e1ca524e1ba4c2eb45c6bf42cb1a197
Autor:
Jelena S Lazarević, Ana Kolarević, Gordana Stojanović, Andrija Šmelcerović, Pierangela Ciuffreda, Enzo Santaniello
Publikováno v:
Acta Chimica Slovenica, Vol 65, Iss 4, Pp 801-810 (2018)
The results presented herein represent our continued study based on the modification of phenolic functionality in molecules originated from natural sources by acylation. A small focused library of nineteen eugenyl esters, with four of which are new c
Externí odkaz:
https://doaj.org/article/bacd4cf18c2b4c498220ae0e2d05ecbb
Autor:
Jelena S Lazarević, Ana Kolarević, Aleksandra Đorđević, Gordana Stojanović, Andrija Šmelcerović, Pierangela Ciuffreda, Enzo Santaniello
Publikováno v:
Acta Chimica Slovenica, Vol 64, Iss 3, Pp 603-612 (2017)
Derivatisation of parent structure in terpenoids often results in enhancement of biological activity of newly obtained compounds. Thymol, a naturally occurring phenol biosynthesized through the terpene pathway, is a well known biocide with strong ant
Externí odkaz:
https://doaj.org/article/c00f18a1dc164d969889286f924d2e10
Autor:
Pierangela Ciuffreda, Andrea Brizzolari, Silvana Casati, Ivano Eberini, Luca Palazzolo, Chiara Parravicini, Enzo Santaniello
Publikováno v:
ARKIVOC, Vol 2016, Iss 5, Pp 50-68 (2016)
Externí odkaz:
https://doaj.org/article/f7d64934422145ff8c34930e9e26b0bf
Autor:
Alice Dassano, Mariateresa Mancuso, Paola Giardullo, Loris De Cecco, Pierangela Ciuffreda, Enzo Santaniello, Anna Saran, Tommaso A. Dragani, Francesca Colombo
Publikováno v:
Redox Biology, Vol 2, Iss C, Pp 580-589 (2014)
N6-isopentenyladenosine (i6A), a naturally occurring modified nucleoside, inhibits the proliferation of human tumor cell lines in vitro, but its mechanism of action remains unclear. Treatment of MCF7 human breast adenocarcinoma cells with i6A or with
Externí odkaz:
https://doaj.org/article/42405e03332c4756aec73c1059b1dc65
Publikováno v:
ARKIVOC, Vol 2010, Iss 6, Pp 53-60 (2009)
Externí odkaz:
https://doaj.org/article/4e2b0489e0934b8a826862bf8a6597a4
Autor:
Andrea, Brizzolari, Mario C, Foti, Luciano, Saso, Pierangela, Ciuffreda, Jelena, Lazarević, Enzo, Santaniello
Publikováno v:
Natural product research. 36(24)
Cytokinins are naturally occurring adenine derivatives whose physiological role is that of growth regulators in plants and that show also many other activities either in plants and in mammalian cells. In plants, they can be found mainly as free bases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ed1a9ae7f3958f1b8be34c7fd4281d3
https://pubmed.ncbi.nlm.nih.gov/35130809
https://pubmed.ncbi.nlm.nih.gov/35130809
Autor:
Andrea Brizzolari, Mario C. Foti, Luciano Saso, Pierangela Ciuffreda, Jelena Lazarević, Enzo Santaniello
Cytokinins are naturally occurring adenine derivatives whose physiological role is that of growth regulators in plants and that show also many other activities either in plants and in mammalian cells. In plants, they can be found mainly as free bases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::562c600ee7034de7e60c99025263c4b7
Publikováno v:
Journal of Chromatography B. 1019:164-168
Four natural N(6)-substituted adenine derivatives (cytokinins) were evaluated for the first time in vitro for they antioxidant capacity by using fluorimetric and spectrophotometric assays, i.e., the oxygen radical absorbance capacity (ORAC), trolox e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a24e2d117077576756601a5b459129c
https://doi.org/10.1016/j.jchromb.2015.12.047
https://doi.org/10.1016/j.jchromb.2015.12.047
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 24:5652-5655
A few naturally occurring N(6)-substituted adenosine derivatives (cytokinin ribosides) were investigated as inhibitors of platelet aggregation induced in vitro by collagen and their activity range was demonstrated (IC50: 6.77-141 μM). A docking stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f56640df33ddaf2ab2f803848c078d4c
https://doi.org/10.1016/j.bmcl.2014.10.080
https://doi.org/10.1016/j.bmcl.2014.10.080