Common thyme (Thymus vulgaris L.) is a Mediterranean evergreen shrub of the Lamiaceae that shows chemical polymorphism in its natural populations. In Mediterranean habitats six basic chemotypes have been described according to the main component in its essential oil: thymol, carvacrol, linalool, geraniol, α-terpineol, thuyanol-4, of which the thymol chemotype is widely used in cultivation and as a

Phytochemical study of Pteris ensiformis Burm. resulted in the isolation of eleven compounds, including three sesquiterpenoids (1–3), one alkaloid (5), one amino acid (6), one flavonoid (7), four phenolic acids (4, 8, 9 and 10), and one coumarin (11). Structures of these compounds were deduced from the ESI-MS and NMR data. This is the first report on the isolation of compounds 1, 2, 7 and 11 from P

Emilia fosbergii is a member of the tribe Senecioneae (Asteraceae), most species of which contain pyrrolizidine alkaloids. Notwithstanding, the phytochemistry of E. fosbergii is poorly understood, and pyrrolizidine alkaloids produced by this species have yet to be characterized. In this work, the presence of 11 pyrrolizidine alkaloids, three caffeoylquinic acid derivatives, and six flavonoids were

Phytochemical investigation on the water-soluable portions of the EtOH extracts of the flowers of Coreopsis tinctoria Nutt. led to the isolation of six flavonoids, including a new okanin glycoside. The structures of these compounds were identified by spectroscopic analysis, chemical method, and comparison with the literature.

The European dewberry (Rubus caesius) is a perennial shrub that is widely distributed in Europe but can also be found in North America. In folk medicine, the European dewberry is used to treat hyperglycaemia, diarrhoea and inflammation. LC-MS analysis of the European dewberry confirmed the presence of 35 compounds, mostly flavonoids, phenolic acids and derivatives of ellagic acid. Phytochemical analysis

Phytochemical investigation of Silene schimperiana Boiss. ethanolic extract led to the isolation of fifteen compounds (1–15). The isolated compounds were identified by their NMR, MS spectral data analyses and comparing with published data as: vanillic acid (1), ferulic acid (2), caffeic acid (3), ethyl ferulate (4), apigenin (5), hesperetin (6), diosmetin (7), luteolin (8), kaempferol (9), quercetin

Phytochemical investigation of the leaves of Isatis tinctoria Linnaeus led to the isolation of thirty compounds, including thirteen indole alkaloids (1–13), seven quinazolinone alkaloids (14–20), two quinoline alkaloids (21–22), one quindoline alkaloid (23), one simple amide alkaloid (24) and six monoterpenes (25–30). According to spectroscopic data analysis and comparison with the previously reported

The present study evaluates the effects of severe drought stress on the content of phenolic compounds in olive leaves, namely hydroxytyrosol, tyrosol, p-hydroxybenzoic acid, catechin, luteolin 7-O-rutinoside, luteolin 7-O-glucoside, apigenin 7-O-glucoside, quercetin, apigenin, pinoresinol, oleuropein and verbascoside in greenhouse-grown plantlets. The results showed that oleuropein, verbascoside, luteolin

The Essential Oils (EOs) present numerous chemophenetic applications, mostly at infrageneric rank. EOs utilization for this purpose has been questioned because of the external stimulations that control their chemodiversity and quantitative composition. Therefore, they are considered as a class of natural products with questionable systematic significance. Present study exploiting the recent advances

The essential oil of the fresh leaves of Platycladus orientalis (L.), grown in four different biogeographic zones of Jordan,- (the Mediterranean, Irano-Turanian, Saharo-Arabian, and Sudanian penetration) -, were obtained by hydrodistillation and analysed by gas chromatography (GC) and gas chromatography-mass-spectrometry (GC/MS). The actual composition of the spontaneous emitted volatiles was obtained

Phytochemical characterization of the whole plants of Erigeron breviscapus (Vant.) Hand.-Mazz. Led to the isolation of two indole derivatives (1–2), seven monoterpenoids (3–9), two sesquiterpenoids (10–11), and four pyrone derivatives (12–15). The structures of these compounds were examined with spectroscopic methods, and also by comparing with previously reported spectroscopic data. Among them, ten

A new apotirucallane-type triterpenoid, 3α-benzoate triterpenoid A (1), along with six known triterpenoids (2–7), one aromatic ester (8) and eight lignans (9–16), were isolated from the fruits of Melia azedarach Linn. The structure of 1 was determined by spectral analyses, including HR-ESI-MS, 1D NMR (1H NMR and 13C NMR) and 2D NMR (HSQC and HMBC) analyses. 10, 11 and 16 were reported for the first

Sixteen compounds, including one polyacetylene (1), twelve coumarins (2–7, 9–14), one sterol (8), as well as two sugar derivatives (15, 16), were obtained from Libanotis laoshanensis by modern phytochemical isolation methods such as column chromatography and preparative TLC. Their structures were identified by spectroscopic methods and in comparison with the published data in the references. All the

Three perylenequinones, the methylated 12-epi-stemphytriol (1), dihydroalterperylenol (2), and alterperylenol (3), were isolated from cultures of Curvularia lunata (LBQM-04) on malt extract broth. All these compounds were obtained from this particular fungus for the first time. Structures of compounds were determined based on MS and NMR spectra, as well as by comparison with the literature reports

Mentha pulegium L. is an aromatic herb belonging to the Lamiaceae family, a wild plant which is distributed in different areas of Iran. In this research, we evaluated the variability of essential oil content and compositions of 12 M. pulegium populations. Essential oils were analyzed using gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS) methods. The essential oils content varied

A chemical investigation of the extract of the marine-sponge-associated fungus P. colombiensis resulted in the isolation of eight chlorinated benzophenone derivatives, named, pestalone (1), pestalachlorides A-C, E, and F (2-6), pestalalactone (7), and pestalalactone atropisomer (8). The structures of these compounds were identified by spectroscopic analysis (MS, 1D/2D NMR) and comparison with the previously

Miconia albicans (Sw.) Triana and Miconia chamissois Naudin, commonly known as “pixirica” and “pixirica-açu”, two Melastomataceae species, are commonly found in Cerrado areas. M. albicans species grows in dry and humid habitats, so it has adapted to both conditions and M. chamissois species grows in humid environment only. In this work, we have investigated the content of triterpenes, flavonols and

Processive phytochemistry and pharmacological investigation of Schefflera leucantha R.Vig. (Araliaceae) led to the isolation of fifteen known compounds: a nucleobase (1), six small aromatic molecules (2–7), three phenylpropanoids (8–10), four lignans (11–14) and a fatty acid derivative (15). Spectroscopic methods were used to establish the structure and configuration of isolates, followed by their

Phytochemical investigation on the flower buds of Daphne genkwa led to the isolation of 22 compounds, including 17 daphne diterpenes (1–17), three tigliane types (18–20), and two diphenylpentanes (21–22). Compounds 19–21 were isolated from D. genkwa for the first time. These compounds were elucidated using spectroscopic methods and by comparing their data to those reported in the literature. On the

From the Uncaria rhynchophlly (Miq.) Jacks, twelve monoterpene indole alkaloids, such as harman (1), strictosamide (2), vincosidelactam (3), cadambine (4), 3α-dihydrocadambine (5), 7-epi-javaniside (6), rhynchophylline (7), isorhynchophylline (8), hirsutine (9), vincosamide-6′-O-β-D-glucopyranoside (10), vincosamide-11-O-β-D-glucopyranoside (11) and 2′-O-[β-D-glucopyranosyl-(1 → 6)-β-D-glucopyrano

Fourteen compounds were isolated from fruits of Ziziphus jujuba Mill., including two flavonoids (1–2), one phenolic glycosides (3), one lignan (4), four phenols (5–8), three alkaloid (9–10, 14), three sesquiterpenoid (11–13). The structures of all the compounds were established by the NMR techniques, as well as by comparison with previously reported data in literature. Compounds 2″-glucosyl-8-C-gl

Diterpenoid alkaloids have been acknowledged as of chemotaxonomic significance in plants from the genus Aconitum (Ranunculaceae). Phytochemical investigation on the Aconitum spathulatum W. T. Wang, an endemic Aconitum species in China, has led to the isolation of twelve C19-diterpenoid alkaloids. The chemotaxonomic significance of these compounds are summarized.

The phytochemical investigations on the rhizome of Menispermum dauricum DC. led to the isolation of 18 compounds, including eleven alkaloids (1–11), four amides (12–15) and three fatty acids (16–18). All chemical structures were established on the basis of NMR (1H NMR and 13C NMR) spectroscopic data. Meanwhile, compounds 5–6, 9–10 and 13–18 are reported for the first time from Menispermum genus, as

Phytochemical study on the stems and leaves of Clausena dunniana H. Lév. led to the isolation and identification of 14 coumarins (1–14). Their chemical structures were determined on the basis of MS, NMR, and further supported by comparison with those reported in the literature. This is the first report that compounds 1–2, 4, 8, and 12–14 are present in the genus Clausena, and all of these compounds

Phytochemical analysis of isolates from the aerial parts of Clausena lansium Lour. Skeels (Rutaceae) led to the identification of 14 alkaloids, including two indole alkaloids (1 and 2), one quinoline alkaloid (3), two pyridine alkaloids (4 and 5), four carbazole alkaloids (6–9) and five amides alkaloids (10–14). The phytochemical structures of the alkaloids were established by means of NMR and MS spectral

Black locust (Robinia pseudoacacia L.) is one of the important biomass sources used to produce bioenergy and bioethanol. In this study, we examined variations in chemical composition as well as genetic diversity and differentiation among 165 black locust plants from seven populations in five provinces (Beijing, Hebei, Gansu, Shanxi, Shandong) of Northern China using microsatellite markers(SSR). The

Phytochemical study of the aerial parts of Senefelderopsis croizatii Steyerm., led to the isolation and characterization of 14 known compounds, 10 triterpenoids with different skeletons type, friedelane, oleanane, ursanes, lupanes, and cycloartanes, two glycosylates flavonoid, and one iridoid. The chemical structure of those isolated metabolites was obtained by extensive spectrometric, and spectroscopy

Essential oil (EO) properties of six L. angustifolia (LA) and two L. x intermedia (LI) cultivars were evaluated during summer harvest periods of 2017 and 2018, The cultivars were grown in Dörgicse, Hungary. According to our results, the essential oil (EO) content was highly dependent on the varieties in both experimental years (2017: p < 0.0001 and 2018: p < 0.0001). In 2017, the EO content values

Chemical biodiversity of essential oils of natural populations of Deverra scoparia growing in different regions in Algeria, and spreading from of semiarid to Saharan territories, was assessed. More than 60 compounds were identified by GC and GC-MS. Both phenylpropanoids and phathalids classes of bioactive components in leaves part were exhibiting drastic variations: (0.77–59.46%) and (0.04–28.55%)

Since Myrtaceae is considered a complex family concerning the taxonomic classification due to the elevated number of components, difficult morphologic differentiation, and relatively low amount of studies in area, this article describes the potentiality of classification using chemometrics applied to UPLC-qToF/MS-MS dataset for chemotaxonomy investigation of leaves of fifteen species from the genus