Polybenzyls from Gastrodia elata,their agonistic effects on melatonin receptors and structure-activity relationships

Gastrodia elata is a famous traditional Chinese herb with medicinal and edible application. In this study, nine polybenzyls (1?9), including six new ones (2?5, 7 and 9), were isolated from the EtOAc extract of G. elata. Five compounds 1, 3, 4, 6 and 8 were found to activate melatonin receptors. Especially, compound 1 showed agonistic effects on MT₁ and MT₂ receptors with EC₅₀ values of 237 and 244 μM. For better understanding their structure-activity relationships (SARs), ten polybenzyl analogs were further synthesized and assayed for their activities on melatonin receptors. Preliminary SARs study suggested that two para-hydroxy groups were the key pharmacophore for maintaining activity. Molecular docking simulations verified that compound 1 could strongly interact with MT₂ receptor by bonding to Phe 118, Gly 121, His 208, Try 294 and Ala 297 residues.     

Medicinal Uses,Phytochemistry, and Pharmacology of Origanum onites (L.): A Review

Origanum onites L., known as Turkish oregano, has great traditional, medicinal, preservative, and commercial importance. It is used for the treatment of several kinds of ailments, such as gastrointestinal disorders, diabetes, high cholesterol, leukemia, bronchitis, etc. In this review, traditional use, phytochemistry, and pharmacology of O. onites reported between 1988 and 2014 were discussed. This review was prepared based on literature survey on scientific journals and books from libraries and electronic sources, such as Web of Science, PubMed, Scopus, Google Scholar, etc. All databases were searched up to June 2014. Several different classes of terpenoids, triterpene acids, phenolic acids, hydroquinones, flavonoids, hydrocarbons, sterols, pigments, fatty acids, tocopherols, and inorganic compounds were detected mainly in the aerial parts of this plant. Pharmacological studies revealed that extracts obtained from several solvents and individual compounds exhibited antimicrobial, antiviral, antioxidant, insecticidal, anticancer, hepatoprotective, genotoxic, antidiabetic, cholinesterase inhibitory, anti‐inflammatory, analgesic activities, etc. O. onites, in general, exhibited remarkable activity potential in almost all test systems. The results of toxicity studies indicated that O. onites did not show any significant toxicity and mutagenicity on Drosophila and Salmonella. Toxicity of the extracts/essential oils and also individual compounds should be evaluated on mammalian cells to ensure their safety. The bioactivity of individual compounds aside from terpenoids should also be assessed in detail. Additionally, mode of action for the bioactive compounds should be evaluated to understand the complex pharmacological effects of these phytochemicals.     

Rapid shifts in the chemical composition of aspen forests: an introduced herbivore as an agent of natural selection

The global ecological impacts of introduced and exotic species can be dramatic, leading to losses in biodiversity and ecosystem “meltdown”, however, the evolutionary impacts of introduced species are much less understood. Further, very few studies have examined whether mammalian herbivores can act as agents of natural selection for plant traits. We examined the hypothesis that variation in aspen phytochemistry resulted in selective herbivory by Cervus elaphus (elk), an introduced mammalian herbivore. With the experimental removal of a large elk exclosure, elk selectively eliminated 60% of an aspen population previously protected from herbivory resulting in a dramatic shift in the phytochemical composition of the aspen forest. Selection gradients (β) varied from 0.52 to 0.66, well above average relative to other studies of selection. These results indicate that introduced herbivores can have rapid evolutionary consequences even on long lived native species. Because there are fundamental links between phytochemistry, biodiversity and ecosystem processes, the effects of an introduced herbivore are likely to have cascading impacts on the services ecosystems provide.     

Phytochemical and chemotaxonomic studies on Pteris wallichiana J. Agardh

A systematic phytochemical investigation of Pteris wallichiana J. Agardh resulted in the isolation of twenty compounds, including five sesquiterpenes (1–5), six flavonoids (6–11), seven phenolic acids (12–18) and two fatty acids (19 and 20). Their structures were deduced from MS, NMR and ORD data. This is the first report of compounds dehydropterosin B (2), (2R,3S)-pterosin C (4), (2R,3R)-pterosin L (5), apigenin (6), luteolin (7), luteolin-7-O-glucoside (10), caffeic acid (13), vanillin (14), 3,4-dihydroxybenzaldehyde (15), chlorogenic acid (17), 3,5-dicaffeoylquinic acid (18), suberic acid (19) and azelaic acid (20) from P. wallichiana and of compounds 15, 19 and 20 from the family Pteridaceae. Furthermore, a chemotaxonomic study of the isolates was performed.     

Tetrahydroquinolinyl phosphinamidates and phosphonamidates enhancing tolerance towards drought stress in crops via interaction with ABA receptor proteins

New phosphorous-containing lead structures against drought stress in crops interacting with RCAR/(PYR/PYL) receptor proteins were identified starting from in-depth SAR studies of related sulfonamide lead structures and protein docking studies. A converging 6-step synthesis via phosphinic chlorides and phosphono chloridates as key intermediates afforded envisaged tetrahydroquinolinyl phosphinamidates and phosphonamidates. Whilst tetrahydroquinolinyl phosphonamidates 13a,b exhibited low to moderate target affinities, the corresponding tetrahydroquinolinyl phosphinamidates 12a,b revealed confirmed strong affinities for RCAR/ (PYR/PYL) receptor proteins in Arabidopsis thaliana on the same level as essential plant hormone abscisic acid (ABA) combined with promising efficacy against drought stress in vivo (broad-acre crops wheat and canola).     

热喷雾液质联用技术在药用植物化学研究中的应用

本文对近年来国内外学者利用热喷雾液质联用技术进行药用植物化学研究的情况进行了综述 ,并介绍了几个较为重要的应用实例。     

AP-I型低压液相层析仪的研制及其在植物化学研究中的应用

本文介绍AP-I型低压液相层析仪,以及利用该仪器进行制备性分离的快速层析技术。应用AP-I型低压液相层析仪,采用高细度层析材料、短粗柱和上行洗脱法,在1—5kg.cm~(-2)压力下进行柱层析,具有设备简单、操作方便、分离快速、纯化效率高,重现性好等优点。     

Interaction between growth environment and host progeny shape fungal endophytic assemblages in transplanted Fagus sylvatica

Fungal endophytes are an integral part of the leaf microbiome of forest trees. Most of these endophytes are horizontally transmitted, however little is known about their assembly drivers. Endophytic assemblages differ in composition according to geography and host individuals. In addition, climate and genetic diversity are also reported to lead to host plant adaptation. To determine the impact of the host progeny and respective adaptation to environmental conditions on endophytic assemblages, we designed a transplantation experiment in beech trees (Fagus sylvatica). Beech nuts were collected from distant geographical regions and germinated in a common greenhouse. One-year-old beech seedlings were transplanted to the different locations and the leaf-endophytic assemblages were characterized in the second growth season after planting by cultivation-independent metabarcoding. The chlorophyll and flavonoid content of the respective leaves were also measured. The results revealed host progeny effects in shaping leaf-endophytic fungal assemblages, that might be concealed by major geographical effects. We hypothesise and discuss possible interactions of different assembly drivers.     

Identifying new lead structures to enhance tolerance towards drought stress via high-throughput screening giving crops a quantum of solace

Novel synthetic lead structures interacting with RCAR/(PYR/PYL) receptor proteins were identified based on the results of a high-throughput screening campaign of a large compound library followed by focused SAR studies of the three most promising hit clusters. Whilst indolinylmethyl sulfonamides 8y,z and phenylsulfonyl ethylenediamines 9y,z showed strong affinities for RCAR/ (PYR/PYL) receptor proteins in wheat, thiotriazolyl acetamides 7f,s exhibited promising efficacy against drought stress in vivo (wheat, corn and canola) combined with confirmed target interaction in wheat and arabidopsis thaliana. Remarkably, binding affinities of several representatives of 8 and 9 were on the same level or even better than the essential plant hormone abscisic acid (ABA).     

Cissampeloflavone,a chalcone-flavone dimer from Cissampelos pareira

From the aerial parts of Cissampelos pareira L. (Menispermaceae), a chalcone-flavone dimer has been isolated which, mainly from NMR spectroscopic and MS data, was proved to be 2-(4-hydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)-6-(2-hydroxy-4,6-dimethoxybenzoyl)-furano[3,2-g]benzopyran-4-one. This has been assigned the trivial name cissampeloflavone. The compound has good activity against Trypanosoma cruzi and T. brucei rhodesiense and has a low toxicity to the human KB cell line.