Phytochemical and chemotaxonomic study on the leaves of Rhododendron amesiae

The phytochemical study of the leaves of Rhododendron amesiae (Ericaceae) led to the isolation and identification of 19 compounds, including six diterpenoids (1–6), six triterpenoids (7–12) and seven flavonoids (13–19). The chemical structures of these compounds were identified by spectroscopic data, as well as by comparison with previously reported data in literature. This is the first systematic study on the chemical constituents of Rhododendron amesiae. All the compounds were isolated from this plant for the first time. Compounds 12, 14 and 15 were first isolated and reported from the genus Rhododendron and the family Ericaceae. Furthermore, the chemotaxonomic significance of these compounds was discussed.     

Sesquiterpene lactones and other constituents from Stevia jorullensis

A chemical study of the aerial parts of Stevia jorullensis was carried out as a contribution to the knowledge of the chemistry of the genus Stevia. In this investigation the sesquiterpene lactones 11β,13-dihydrocostunolide (1), 11,13-dihydroreynosin (4), and 1β-hydroxycolartin (5) were isolated for the first time in the genus. Additionally, chlorogenic acid (8), the steroidal compounds β-sitosterol (2), stigmasterol (3), β-sitosteryl glucopyranoside (6), and stigmasteryl glucopyranoside (7) were also isolated. This is the third report of the presence of a 11,13-dihydrogermacranolide and the second of 11,13-dihydroeudesmanolides in the genus Stevia.     

A new acorane sesquiterpenes of Lysionotus pauciflorus maxim. Form Guizhou province,China

A new acorane sesquiterpene (1), together with fourteen known compounds were isolated from the whole plant of Lysionotus pauciflorus Maxim. The chemical structures of the compounds were identified by physio-chemical properties and 1D-NMR, 2D-NMR, ESI-MS, IR and ECD spectra. Among them, six compounds (1, 4, 6, 7, 13, 15) were first found in the genus Lysionotus. The chemotaxonomic significance of the isolated compounds in the genus Lysionotus and family Gesneriaceae were discussed.     

Monoterpene and sesquilignan compounds from the leaves of Crataegus pinnatifida

Detailed chemical investigation of the secondary metabolites from the extract of the leaves of Crataegus pinnatifida led to the isolation of 12 monoterpene and sesquilignan compounds, including a new monoterpene, pinnatifidanoid A (1), a new sesquilignan, pinnatifidanin A (12). To our knowledge, this is the first report of the presence of compounds 1–12 in this genus.     

α-pyrone derivatives from endophytic fungus Diaporthe sp. RJ-41

A new α-pyrone derivative 1 and six known α-pyrone derivatives 2–7, along with known compounds 8–10 were isolated from the fermentation products of the endophytic fungus Diaporthe sp. RJ-41. Among them, nine compounds (1–9) were reported for the first time from the genus Diaporthe. This work expanded the knowledge of the chemical diversity of the genus Diaporthe, and the chemotaxonomic significance of the isolates was also discussed.     

Phenylethaniod glycosides from Orobanche pycnostachya Hance and their chemotaxonomic significance

In this current study, we investigated the chemical ingredients of the whole plants of Orobanche pycnostachya Hance. Eighteen compounds, including fifteen phenylethaniod glycosides (2–16), two lignans (17, 18), and one flavonoid (1) were obtained from this plant and they were elucidated utilizing spectroscopic methods. This is the first study to describe the isolation of compounds 1-5, 7–11, 13, and 15–18 from O. pycnostachya and compound 2, 4, 7, and 9 from the genus Orobanche L.     

Chemical constituents from the stem bark of Clausena excavata Burm. f

Phytochemical study on the stem bark of Clausena excavata Burm. f. led to the isolation and identification of 11 compounds, including four prenylated coumarins (1–4), three carbazole alkaloids (5–7), a limonoid (8), a sterol (9), a depside (10) and a xanthone (11). The chemical structures of the compounds were elucidated based on NMR and mass spectroscopic data, and further supported by comparison with previously literature values. This is the first report on the isolation of compounds 10 and 11 from the genus Clausena. The chemotaxonomic significance of the isolated compounds is discussed.     

Chemical constituents from Euphorbia hirta

Thirty-one compounds, including fourteen triterpenoids (1–14), seven coumarins (15–21), four lignans (22–25), and six diterpenes (26–31) were isolated from the aerial part of Euphorbia hirta. The structures were elucidated by spectroscopic methods and by comparison of their reported spectroscopic data. These compounds have shown the chemical relationships between this plant and other species from the genus Euphorbia.     

Investigation of chemical compounds from Chlamydomonas sp. KSF108 (Chlamydomonadaceae)

Nine compounds (1–9) including one norisoprenoid (1), one polyol-glycoside (2), three sterols (3–5), three phenols (6, 8, and 9), and one fatty acid (7) were isolated from Chlamydomonas sp. KSF108. Their chemical structures were established using NMR spectroscopic techniques and compared with published data. None of the compounds have been previously reported from the genus Chlamydomonas and they may therefore serve as chemotaxonomic markers for Chlamydomonas sp. KSF108 within the genus.     

Chemical constituents from the roots and rhizomes of Silene tatarinowii Regel

Chemical investigation of the root and rhizome of Silene tatarinowii Regel led to the isolation of nine ecdysteroids (1–9) and one sterol (10). All the compounds were determined on the basis of MS and NMR and by comparison with those in the literature. All these compounds were isolated from S. tatarinowii for the first time. Furthermore, compounds 7–10 were isolated from Silene genus for the first time, of which compounds 7 and 8 were isolated from Caryophyllaceae family members for the first time. This is the first study to report the chemical constituents of S. tatarinowii and the chemotaxonomic relationships between Silene and other genera of Caryophyllaceae.     

Chemical constituents from the rhizome of Menispermum dauricum DC. and their chemotaxonomic significance

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 well as the rhizome of Menispermum dauricum DC. Notably, this is the first study to report compounds 10, 15–18 from the family Menispermaceae. These compounds laid the foundation for the chemical classification of this species.     

Chemical constituents from the calyces of Physalis alkekengi var. franchetii

One new monoterpenoid glycoside (1), together with seven known compounds, including two alkaloids (2–3), three phenylpropanoids (4–6), and two nucleosides (7–8) were isolated from the calyces of Physalis alkekengi var. franchetii. Their structures were elucidated by a combination of detailed spectroscopic analyses, chemical methods, and comparison with reported data. These eight compounds were isolated for the first time from the genus Physalis. The chemotaxonomic significance of these compounds was summarized.     

Secondary metabolites from Spiranthes sinensis (Orchidaceae)

One new flavonol glycoside (1) and nine known compounds (2–10) were obtained from the n-BuOH soluble fraction of the whole plants of Spiranthes sinensis. The structure of compound 1 was elucidated based on the combination of spectroscopic (¹H-NMR, ¹³C-NMR, HSQC, and HMBC as well as HR-ESI-MS) and chemical methods. The occurrences of eight compounds (2-9) in this genus were firstly reported while five of them (2–6) were obtained from Orchidaceae for the first time. Furthermore, the chemotaxonomic significance of these compounds was discussed.     

Mammea-type coumarins from Mammea usambarensis Verdc.

Phytochemical investigations of Mammea usambarensis resulted into the isolation a δ-tocotrienol (1) and five known mammea-type coumarins (2–6). Their structures were determined by NMR, IR, and LC-MS spectroscopic methods and by comparison of their spectral and physical data with those reported previously in the literature. The presence of these compounds is consistent with the compound classes reported from other members of the genus Mammea. Compound 6 is isolated from the Mammea genus for the first time. This is the new source of mammea-type coumarin compounds while the chemotaxonomic significance of this investigation is summarized.     

Coumarins from the stems and leaves of Clausena dunniana H. Lév

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 were isolated from C. dunniana for the first time. The chemotaxonomic significance of these isolated compounds was discussed.     

Sterols,aromatic compounds,and cerebrosides from the Hericium erinaceus fruiting body

Chemical investigation of the methanolic extract from the fruiting bodies of Hericium erinaceus, led to the isolation of fifty-one compounds including thirty-five ergostane-type sterols (1–35), fourteen aromatic compounds (36–49), and two cerebrosides (50 and 51). Their structures were identified based on spectroscopic analyses and by comparison of their spectral data with those reported in literature. This is the first comprehensive low-polarity chemical investigation of H. erinaceus. Thirty-one of the compounds (6–8, 11–35, 39, 41, and 49) were isolated for the first time from the genus Hericium and the family Hericiaceae. The chemotaxonomic relationship between H. erinaceus and other Hericium species was also discussed.     

Chemical constituents from the roots of Asarum sieboldii Miq. var. Seoulense Nakai

Fourteen compounds were isolated from the 95% ethanol reflux extract of Asarum sieboldii Miq. var. Seoulense Nakai, including five phenanthrene derivatives (1–5), three isobutyl amides (6–8), three phenylpropanoids (9–11) and three lignins (12–14). The structures of these compounds were identified by spectroscopic methods and by comparison with the reported spectroscopic data. Among them, compounds 6 and 11 were firstly reported from the family Aristolochiaceae, and compounds 3 and 4 were reported for the first time from the genus Asarum. Additionally, compounds 1, 2 and 8 were isolated from A. sieboldii Miq. var. Seoulense Nakai for the first time. These compounds have shown chemical relationships between A. sieboldii Miq. var. Seoulense Nakai and other species of Asarum as well as those found in the genus Aristolochia in the family Aristolochiaceae.     

Phytochemical and chemotaxonomic studies on Dioscorea collettii

A chemical investigation of Dioscorea collettii led to the isolation of twenty-nine compounds, including six steroid saponins (1–6), thirteen monocyclic phenols (7–19), two flavonoids (20–21), three sterols (22–24), and five cyclodipeptides (25–29). The chemical structures of these compounds were elucidated using spectroscopic methods and by comparing their data to that reported in the literature. This study is the first report of compounds 2–4, 7, 14–17, 21, and 23–24 in D. collettii, while compounds 8–13, 18–20, and 25–29 were first isolated from the genus Dioscorea and the family Dioscoreaceae. The chemotaxonomic significance of the isolated compounds is discussed.     

Chemical constituents of Stenotaenia macrocarpa Freyn & Sint. (Apiaceae)

Phytochemical investigation of Stenotaenia macrocarpa Freyn & Sint. (Apiaceae) led to the isolation of ten known compounds: eight flavonoids (1–8) and two furanocoumarins (9–10). The chemical structures of the compounds were elucidated based on 1D and 2D NMR and MS spectra, as well as comparison with the relevant literature data. To the best of our knowledge, this is the first detailed phytochemical study about Stenotaenia macrocarpa and the first report on the isolation of all the compounds from the genus Stenotaenia, and manghaslin (2) and its methoxylated derivative typhaneoside (3) from Apiaceae. The chemotaxonomic significance of isolates was also discussed.     

Chemical constituents from the leaves of Ilex urceolatus

Eighteen compounds, including four hemiterpene glycosides (1–4), three triterpenoid saponins (5–7), four triterpenes (8–11), five sterols (12-16) and two monoterpene glucosides (17 and 18), were isolated from the leaves of Ilex urceolatus C. B. Shang, K. S. Tang et D. Q. Du, which was identified as a new species belonging to the genus Ilex. Among them, compounds 14–18 were firstly isolated from the genus Ilex, others were obtained from I. urceolatus for the first time. This work represented the initially phytochemical study on this plant. The isolated compounds have significant chemotaxonomic characteristics with the other species from this genus.