Search results for "taxonomy."

Chemical Constituents of Urospermum picroides

1992

Seven phenolic compounds were isolated from the aerial parts of U. picroides. They were identified by UV spectra, TLC and HPLC-DAD as luteolin, luteolin-7-glucoside, quercetin, quercetin-3-galactoside, kaempferol-3-galactoside, chlorogenic and isochlorogenic acids. Other phenolics were characterized by HPLC-DAD analysis: gallic, protocatechuic, caffeic, ferulic and isoferulic acids, quercetin-3-glucoside and luteolin-4′-glucoside.

Phenolic and acetylenic metabolites from Artemisia assoana

1987

Abstract Nine flavones, three coumarins, two flavone glycosides, p-hydroxyacetophenone and methyl caffeate have been isolated from the aerial parts of Artemisia assoana. Six diacetylenic spiroketal enol-ethers, a mixture of n-alkyl p-coumarates and a new phenylpropanoid metabolite, sinapyl alcohol diisovalerate, have been isolated from root extracts of the same plant. 1H and 13C NMR spectra of some of these compounds are given and taxonomic aspects are discussed.

A chemotaxonomic survey of Sonchus subgenus Sonchus

1993

Abstract Five species of Sonchus subgenus Sonchus were surveyed for their phenolic constituents. Seven flavonoids were identified: luteolin, luteolin-7-glucoside, apigenin, apigenin-3-glucoside, quercetin, quercetin-3-glucoside and quercetin-3-galactoside; three were phenolic acids; caffeic, chlorogenic and isochlorogenic; and two were coumarins: aesculetin and cichoriin. Their systematic significance for this genus is discussed.

Phytochemical constituents and chemosystematic significance of Pulicaria jaubertii E.Gamal-Eldin (Asteraceae)

2018

Abstract The chemical characterization of methylene chloride/methanol (1:1) extract of the air-dried whole medicinal plant, Pulicaria jaubertii E. Gamal-Eldin, led to isolation and identification of two new hydroquinone compounds; 2-(2-acetoxy propyl), 5-methyl hydroquinone (1) and 2-(2-hydroxy propyl), 5-methyl hydroquinone-4-O-β-D-glucopyranoside (2), four known flavonols (3-6) and 7 known dihydroflavonols (7-13). The structures were established depending upon comprehensive analysis of the NMR, IR and HR/EI-MS data. Herein, compounds 6, and 10-13 were isolated for the first time from this plant. The chemotaxonomic significance of the isolated flavonoids from P. jaubertii comparing with th…

Phenolic Compounds from Lactuca viminea L.

1992

Abstract The aerial part of Lactuca viminea L. was examined for the presence of phenolic compounds. Six different flavonoids were isolated and identified by UV spectra, TLC, HPLCDAD , 1H NMR and 13C NMR. They were identified as apigenin, luteolin, quercetin, luteolin-7-O-glucoside, quercetin-3-O-glucoside and luteolin-7-O-glucuronide-6″methyl ester. Three phenolic acids were also detected: caffeic, ferulic and chlorogenic acid.

Berberido aetnensis-Crataegion laciniatae, new orophilous pre-forestal alliance of the class Rhamno-Prunetea

2011

In this paper the results of a phytosociological study carried out on some aspects of shrub vegetation of forest margins are presented, investigated in the higher belt of the Madonie Mts. (Northern-Central Sicily), referred to the order Prunetalia spinosae (Rhamno-Prunetea). Through comparison with other known coenoses in the central- southern part of the Italian Peninsula and in Sicily – especially, the associations of Berberidion vulgaris and those of Pruno-Rubion ulmifolii – a coenological and phytogeographical autonomy has been made evident and has resulted in the recognition of a new alliance, described under the name Berberido aetnensis-Crataegion laciniatae Gianguzzi et al., all. nov…

Guaianolides from Centaurea babylonica

2005

The chemical composition of essential oil from Seseli bocconei (Apiaceae) aerial parts growing in Sicily (Italy)

2022

Seseli is a large genus of aromatic and economically important herbs of the Apiaceae family that includes eighty-seven taxa, mainly distributed in Europe and Asia. Several species of this genus are extensively used in various popular medicines and based on their traditional uses, much research concerning biological activities have been carried out. In the present study, the chemical composition of the essential oil from aerial parts of Seseli bocconei Guss., a rare plant endemic of Sicily, was analysed by GC-MS. No one report has been previously published on the essential oil of this species. The result showed the presence of large quantity of monoterpene and sesquiterpene hydrocarbons wher…

The chemical composition of essential oil from Seseli tortuosum subsp. tortuosum and S. tortuosum subsp. maritimum (Apiaceae) aerial parts growing in…

2022

Seseli L. genus, belonging to the Apiaceae family, includes more than eighty taxa, mainly growing in Europe and Asia. Due to the several biological properties, species of this genus have been largely investigated, showing to be a rich source of coumarins, as well as, of essential oils with anti-inflammatory, antiviral, antifungal, cytotoxic, etc. properties. In the present study, the chemical composition of the essential oils from aerial parts of Sicilian accessions of Seseli tortuosum subsp. tortuosum and S. tortuosum subsp. maritimum were analysed by GC-MS. No one report has been previously published on the subsp. maritimum. The results showed the presence, in both oils, of large quantity…

Taxonomy of generative adversarial networks for digital immunity of Industry 4.0 systems

2021

Abstract Industry 4.0 systems are extensively using artificial intelligence (AI) to enable smartness, automation and flexibility within variety of processes. Due to the importance of the systems, they are potential targets for attackers trying to take control over the critical processes. Attackers use various vulnerabilities of such systems including specific vulnerabilities of AI components. It is important to make sure that inappropriate adversarial content will not break the security walls and will not harm the decision logic of critical systems. We believe that the corresponding security toolset must be organized as a trainable self-protection mechanism similar to immunity. We found cer…