Alessandra Bertoli

ORCID: 0000-0002-0701-5163
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About
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Research Areas
  • Phytochemistry and Biological Activities
  • Essential Oils and Antimicrobial Activity
  • Natural product bioactivities and synthesis
  • Plant tissue culture and regeneration
  • Natural Compound Pharmacology Studies
  • Traditional Chinese Medicine Analysis
  • Transgenic Plants and Applications
  • Plant biochemistry and biosynthesis
  • Bioactive natural compounds
  • Phytochemicals and Antioxidant Activities
  • Sesquiterpenes and Asteraceae Studies
  • Herbal Medicine Research Studies
  • Mediterranean and Iberian flora and fauna
  • Chemical synthesis and alkaloids
  • Chromatography in Natural Products
  • Morinda citrifolia extract uses
  • Plant Parasitism and Resistance
  • Phytochemistry and Bioactive Compounds
  • Potato Plant Research
  • Plant and animal studies
  • Botanical Studies and Applications
  • Botanical Research and Chemistry
  • Plant Physiology and Cultivation Studies
  • Medicinal Plants and Neuroprotection
  • Phytochemistry Medicinal Plant Applications

Eni (Italy)
2024

University of Pisa
2011-2022

University of Trieste
2017

Policlinico Tor Vergata
2011

Agenzia Regionale per la Protezione Ambientale
2008

University of Calabria
2003-2006

University of Urbino
1997-1998

10.1007/978-1-4419-7347-4_15 article EN Advances in experimental medicine and biology 2010-01-01

A simple and rapid method is reported for the routine determination 1-phenylazo-2-naphthol (Sudan I) in chilli powder chilli-containing food products. The involved Soxtec extraction from products followed by high-pressure gel permeation chromatographic clean-up collecting appropriate fraction. Analysis of this fraction was HPLC with UV/VIS detection. limit detection 7 μg kg−1 quantification 13 kg−1. identity Sudan I established electrospray LC/MS MS/MS confirmation. From a small survey 30...

10.1080/02652030400007252 article EN Food Additives & Contaminants 2004-10-01

A wild strain of Agrobacterium rhizogenes was used to regenerate twelve in vitro plant lines from different hairy roots H. perforatum (St. John's Wort). The production the main bioactive constituents observed even though their yields varied lines. Two were selected for hyperoside (4.9-4.6 mg/gdw) while nine characterized by significant chlorogenic acid (ranged 0.47 1.09 mg/gdw). Furthermore, one out showed a 10-fold higher hypericin content (0.25 than that reported shoots literature....

10.1021/jf0729107 article EN Journal of Agricultural and Food Chemistry 2008-06-14

Context: Hypericum perforatum L. (Guttiferae) contains many bioactive secondary metabolites including hypericins, hyperforins, and essential oil.Objective: The present study was conducted to determine the variation in composition of oil H. accessions from Turkey.Material methods: At full flowering, aerial parts 30 plants were collected 10 sites northern Turkey assayed for components by GC-FID GC-MS.Results: chemical analysis revealed that main constituents all analyzed samples hydrocarbon...

10.3109/13880200903311136 article EN Pharmaceutical Biology 2010-08-01

Abstract The flower and leaf oil of Hypericum triquetrifolium Turra (Guttiferae, Hypericoideae) from Calabria (Italy) were studied by GC GC–MS. major components identified in each n ‐nonane (8%, 15%), β ‐pinene 4%), α (13%, 10%), myrcene (16%, 5%), ‐caryophyllene (5%, 11%), germacrene‐D (10%, 13%), sabinene 3%) caryophyllene oxide 12%) the oils, respectively. aerial parts same plant also analysed SPME. SPME analysis showed higher yields undecane (14%, 10%) comparison with corresponding...

10.1002/ffj.1161 article EN Flavour and Fragrance Journal 2003-03-01

A series of task-specific ionic liquids (TSILs) based on glycerylimidazolium cations have been prepared by reaction 1-chloropropanediol, a compound obtainable from glycerol (a widely available and in-expensive waste product), with the appropriate base (1-H-imidazole, 1,2-dimethylimidazole 1-methyl-1-H-imidazole). The 3-(1H-imidazol-1-yl)propane-1,2-diol chloroalkanes, bromoalkanes alkyl mesylates gave corresponding salts which were characterized. possibility to use these ILs in palladium...

10.1039/b821927c article EN Green Chemistry 2009-01-01

Essential oils (EOs) of Achillea millefolium, Myrtus communis, Rosmarinus officinalis, Helichrysum italicum, Foeniculum vulgare and Lavandula angustifolia were analysed with GC–FID GC–MS in order to define their aromatic profiles then toxicity repellent activity against Sitophilus zeamais Motsch. (Coleoptera Dryophthoridae) specific bioassays evaluated. Results from topical applications on insects showed that all EOs had variable significant insecticidal activity. Mortality rate never...

10.1080/14786419.2011.607453 article EN Natural Product Research 2011-08-23

Three new flavonoids (1-3) and 11 known compounds (genistein, isoprunetin, wighteone, laburnetin, alpinumisoflavone, genistin, genistein 8-C-glucoside, apigenin, isokaempferide, licoflavone C, D-pinitol) were isolated from the aerial parts of Genista ephedroides. The structures established as hydroxyalpinumisoflavone (1) [4', 5-dihydroxy-2"-methyl-2"-hydroxymethylpyrano(5",6":6,7)isoflavone], ephedroidin (2) [4',5, 7-trihydroxy-8-(2-hydroxy-3-methyl-3-butenyl)flavone], genisteone (3)...

10.1021/np980112s article EN Journal of Natural Products 1998-10-02

Abstract Smyrnium olusatrum L. is a biennal plant growing in western and southern Europe. Several phytochemical studies have identified flavonoids, phenolic acids sesquiterpene lactones as main constituents. In this work the root, stem leaf essential oils of (Umbelliferae) collected Urbino (Marche, Italy) were studied by GC GC‐MS. Myrcene (1, 13 14%), β ‐phellandrene (34, 17 9%), ‐caryophyllene 3 12%), furanodiene (19, 8 17%), curzerene (13, 6 germacrene B (7, 14 10%) germacrone (8, 7 8%)...

10.1002/ffj.1382 article EN Flavour and Fragrance Journal 2004-10-27
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