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Four new monoterpenoids, including two new acyclic monoterpenoids (2R, 6R)-2, 6-dimethyl-8-isovaleroxyoctan-1-ol (1) and (2S, 6S)-2, 6-dimethyl-8-isovaleroxyoctan-1-ol (2), as well as two new iridoids stenopterins F-G (3 and 4), together with fifteen known compounds (5–19), were isolated from whole dried material of Valeriana stenoptera. Stenopterin F was the first reported iridoids with n-butoxyl in the Valerianaceae family. The structures of new compounds were established on the basis of extensive spectroscopic analysis. [ABSTRACT FROM AUTHOR]

A new bibenzyl derivative, dendrocandin V ( 1 ) and a new sesquiterpene amino ether, wardianumine A ( 2 ), together with eleven known compounds, including phenanthrenes (denbinobin ( 3 ), 9,10-dihydro-denbinobin ( 4 ), mostatin ( 5 ), loddigesiinols A ( 6 )), bibenzyls (moscatilin ( 7 ), 5-hydroxy-3,4′-dimethoxybibenzyl ( 8 ), 3,4-dihydroxy-5,4′-dimethoxy bibenzyl ( 9 ), dendrocandin A ( 10 ), gigantol ( 11 ), dendrocandin U ( 12 )) and an alkaloids (dihydroshihunine, 13 ) were isolated from the EtOH extraction of stems of Dendrobium wardianum Warner. Isolation of the new compound 2 indicated that N , N -dimethylethanolamine as the key adduction in the synthesis of dendroxine and its analogs in Dendrobium species. The hypothetical biosynthetic pathway of 2 was then postulated. Inspired by literature and traditional usage of the herbal medicine, some compounds were sent for cytotoxic activity and the results indicated that compounds 1 , 3 , 4 , 5 showed cytotoxic activities against five human cancer cell lines (HL-60, A-549, SMMC-7721, MCF-7, and SW-480) with IC50 from 2.33–38.48 μM. Among those compounds, 3 and 4 showed cell line selectivity with strong activity comparable to DDP. [ABSTRACT FROM AUTHOR]

The traditional Chinese medicine (TCM) "Shihu" has a long history of medicinal use in China from some species of Dendrobium. D. officinale is a major source of "Shihu" and is widely cultivated in south of China and listed separately as "Tiepi Shihu" by the Chinese Pharmacopoeia in now time. Traditionally, D. officinale has been widely used in daily health care and the treatment of diabetes and gastrointestinal diseases. In order to better develop and utilize D. officinale , we conducted this systematic review of previous studies, showed clear structure of all isolates from D. officinale together with pharmacological progress, hoping to provide references for further research and utilization. In addition, specific display of the chemical components and the research progress of related activities can help to better understand the traditional records and modern pharmaceutical applications of the plant medicine. Information on phytochemistry and pharmacological studies of D. officinale was collected from various scientific databases including Web of Science, SciFinder, ACS, Springer, Scopus, PubMed, ScienceDirect, Google Scholar and CNKI. More than 180 compounds isolated from D. officinale , including bibenzyls, phenols, phenylpropanoids, lignans, flavonoids and polysaccharides are listed in this review. Furthermore, modern pharmacological researches such as hypoglycemia, immune regulation, antioxidant, cardiovascular regulation and gastrointestinal protection are summarized. Based on the summary of the research work of D. officinale , we systematically show the chemical composition of the plant, and concluded the relationship of those composition with plant habitat together with the relationship between the structure of chemical components and pharmacological activity. Moreover, we suggest that some of small molecule compounds could also be quality control of D. officinale besides polysaccharides. [Display omitted] • D. officinale is widely used in Asia as a precious folk herbal medicine or health food. • Traditional application of D. officinale and modern diseases, especially diabetes, were discussed. • Active ingredients and their action mechanism of D. officinale were systematically summarized. • The relationship between habitat and chemical composition of D. officinale was discussed. • This review intends to provide a comprehensive understanding and appraisal of D. officinale. [ABSTRACT FROM AUTHOR]

Three new iridoids, jatamanvaltrates R–S ( 1 – 2 ) and jatamanin Q ( 3 ), as well as three new sesquiterpenoids, valeriananoids D–E ( 4 , 5 ) and clovane-2 β -isovaleroxy-9 α -ol ( 6 ), together with nine known compounds were isolated from the roots of Valeriana jatamansi Jones. Compound 2 was the first reported iridoid with fatty acid esters in the Valerianaceae family. The structures of new compounds were established on the basis of extensive spectroscopic analysis. Moreover, all the isolates were evaluated for inhibitory activity on acetylcholinesterase (AChE). [ABSTRACT FROM AUTHOR]

One new phenanthrene, aphyllone A ( 1 ) and four new bibenzyl derivatives, aphyllone B ( 2 ) and aphyllals C–D ( 3 – 5 ), together with nine known compounds ( 6–14 ), were isolated from the stems of Dendrobium aphyllum (Roxb.) C. E. Fischer. The structures of these new compounds were elucidated by means of extensive spectroscopic analyses, and the absolute configuration of compound 1 was determined by single crystal X-ray diffraction and quantum calculations. Compounds 6 , 8 and 14 inhibited NO production at the concentration of 25 μM in LPS-stimulated RAW264.7 cells with the inhibition (%) of 32.48, 35.68, and 38.50. Compound 2 possessed significant DPPH radical scavenging activity with scavenging percentage of 87.97% at the concentration of 100 μg/mL. [ABSTRACT FROM AUTHOR]

Abstract: Three tigliane-type diterpenoids named excoecafolins A–C and two daphnane-type diterpenoids named excoecafolins D and E, together with 13 known compounds, were isolated from the EtOAc extract of Excoecaria acerifolia Didr. Their structures were elucidated through the analysis of the spectroscopic data. The anti-HIV-1 activity evaluation of five of these compounds showed that four possessed moderate anti-HIV-1 activities with EC50 0.258, 0.036, 0.046, and 0.978 ?M, SI >1,836.9, 431.1, 298.7, and >503.7, respectively. Additionally, the chemotaxonomic issue of the affinity correlation between Thymelaeceae and Euphorbiaceae is discussed based on the isolates. [Copyright &y& Elsevier]

Abstract: Ethnopharmacological relevance: Various species of genus Passiflora have been used as traditional folk medicines owing to their sedative and anti-hypertensive properties. Passiflora edulis Sims most widely grown in the warm temperate for their fragrant fruits and their twigs and leaves are used as a folk medicine for treating both anxiety and nervousness in American countries. The present study was to evaluate the antidepressant-like effect and the active components of this plant. Materials and methods: The alcohol extracts of the stems (PES, 10 and 2g/kg of the plant materials) and leaves (PEL, 10 and 2g/kg of the plant materials) of Passiflora edulis Sims were orally administered to mice for 7 day. The animals were tested in the forced swim test (FST) and tail suspension test (TST). After behavioral assay of ethanol extract, phytochemical research of the stems and leaves (5.7kg) of Passiflora edulis Sims were developed and further bioactive verification of monomeric compounds were conducted. Results: There are mainly cycloartane triterpenoids and their saponins isolated from this plant, including two new cycloartane triterpenoid saponins named cyclopassifloside ХII (1) and ХIII (2), together with six known cycloartane triterpenoids, cyclopassifloic acids B and E, cyclopassiflosides II, VI, IX and XI. The ethanol extract of Passiflora edulis Sims together with isolated compounds cyclopassiflosides IX and XI may possess antidepressant-like effect. Conclusions: Cycloartane triterpenoid was one of the main compositions of Passiflora edulis Sims and possess antidepressant-like activity. [Copyright &y& Elsevier]

Two unusual dendrobine-type alkaloids, findlayines E and F (1 , 2), along with five known dendrobine-type alkaloids (3 – 7), were isolated from the stems of Dendrobium findlayanum Par. et Rchb. f. Compound 1 is the first example of dendrobine-type alkaloids with a 2-ethoxy-2-oxoethyl group attaching to the C-2, and compound 2 is a nor-dendrobine-type alkaloid, featuring a 5-decarboxylated structure. The structures of compounds 1 and 2 were elucidated by means of extensive spectroscopic analyses, and their absolute configuration were confirmed by electronic circular dichroism (ECD) calculations. All isolates were evaluated for their cytotoxicity against HL-60, SMMC-7721, A-549 and MCF-7 human cancer cells. Unlabelled Image [ABSTRACT FROM AUTHOR]

One hitherto unknown 24-nor-13,27-cycloursane-type triterpenoid, lucumic acid A (1), one new 24-nor-ursane triterpenoid, lucumic acid B (2), along with six known triterpenoids were isolated from the ethanol extract of the leaves of Lucuma nervosa. Their structures were established on the basis of spectroscopic data interpretation. Lucumic acid A (1) is the first example of a 24-nor-triterpenoid with a 13,27-cyclopropane ring. Unlabelled Image [ABSTRACT FROM AUTHOR]