桥环萜类化合物的合成及其对蚂蚁驱避活性的研究

由β-蒎烯合成了诺卜醇、诺卜甲基醚、诺卜乙基醚、诺卜丙基醚、甲酸诺卜酯、乙酸诺卜酯、丙酸诺卜酯,测试以上7个桥环类萜类化合物对小黄家蚁(Monomorium pharaonis)的驱避活性,结果显示它们对小黄家蚁具有很强的驱避活性,在质量浓度为20 mg/mL时,驱避率分别为80%、100%、80%、100%、100%、100%和86%,并对驱避率较高的诺卜甲基醚、诺卜丙基醚、甲酸诺卜酯、乙酸诺卜酯进行了剂量—活性关系进行研究。

类胡萝卜素在水产动物养殖上的应用

类胡萝卜素是广泛存在于自然界中的各种动植物及微生物体中的一类由异戊二烯残基组成的共轭双键长链类萜化合物。大多数难溶于水,易溶于油脂等有机溶剂中。大量试验表明,类胡萝卜素对改善动物体色和肉质;提高水产动物的饵料转化率;促进生长;提高水产动物的繁殖力和卵的受精率等多方面有重大的作用。

Triterpenes and Other Constituents from Rhaponticum uniflorum

From the roots of Rhaponticum uniflorum a new triterpene was isolated together with ursolic acid(2), 3-oxo-19a-hydroxyurs-12-en-28-oic acid (3), pomolic acid (4), 2a,3a,19a-trihydroxyurs-12-en-28-oic acid (5), arctic acid (6), catechin (7) and b-sitosterol (8). The structure of the new compound was elucidated as 2a,3a,19a,25-tetrahydroxyurs-12-en-23,28-dioic acid (1) on the basis of spectral and chemical methods.

Bioinformatics Analysis of IPIs in Five Northern Medicinal Plants

This study analyzed and predicted following aspects of isopentenyl py- rophosphate isomerases （IPIs） of five north medicinal plants using bioinformatics methods and tools： physical and chemical properties, hydrophobicity/hydrophilicity, trans-membrane domain, secondary structure, subcellular localization and so on. The results showed that： there was no notable difference among the physical and chem- ical properties of IPIs of the five north medicinal plants; the IPIs were mainly hy- drophilic; the IPIs were mainly located in chloroplasts by subcellular localization; serine phosphorylation sites were the most; the secondary structures mainly consist- ed of c^-helixes and random coils; no signal peptide existed, indicating that the pro- tein IPI was non-secreted protein; no trans-membrane domain existed; and one functional domain was shown, Le., Nudix Hydrolase Superfamily. This study is of great significance to research on IPI gene functions, deep research on north medic- inal plants, improvement of efficacy of north medicinal plants and rational develop- ment and utilization of medicinal plant resources.

ent-Kaurene Diterpenoids from Isodon adenanthus

Three new ent-kaurene diterpenoids, adenanthins N, 0 and P (1-3), and four known diterpenoids, leucophyllin E (4), glabcensin C (5), adenanthin A (6), leucophyllin B (7), together with a highly unsaturated fatty acid, 9,16-dioxo-10,1 2,14-octadeca-trienoic acid (8), were isolated from Isodon adenanthus (Diels) Kudo. The structure of compound 4 was revised accordingly. Compound I showed significant cytotoxic activity against K562 cells with IC50 = 0.45 mug/mL.

A New Sesquiterpenoid from Russula lepida

new aristolane sesquiterpenoid named rulepidol was isolated from the fruiting body of Russula lepida Fr. Its structure was elucidated as (1a alpha ,5 alpha ,7 alpha ,7a alpha, 7b alpha)-1, 1a,4,5,6,7,7a, 7b-octahydro-5-hydroxy-1,1,7,7a-tetramethyl-5H-cyclopropa [alpha] naphthalen-2-one mainly by 1D and 2D-NMR techniques.

植物的相克相生

有些植物之间，由于种类不同，习性各异，在其生长过程中，为了争夺营养空间，从叶面或根系分泌出对其他植物有杀伤作用的有毒物质，致使其与邻近的它种植物“结怨成伤、你死我活”。如胡桃的根系能分泌出一种叫胡桃醌的物质，在土壤中水解氧化后、有极大的毒性，能造成松树、军果、马铃薯、西红柿、桦木及多种草木植物受害或致死。

Chemical constituents of marine medicinal mangrove plant Sonneratia caseolaris

Twenty-four compounds including eight steroids （1-8）, nine triterpenoids （9-16, 24）, three flavonoids （20-22）, and four benzenecarboxylic derivatives （17-19, 23） were isolated and identified from stems and twigs of medicinal mangrove plant Sonneratia caseolaris. The structures of the isolated compounds were determined by extensive analysis of their spectroscopic data. Among these rnetabolites, compounds 1, 4-20 and 22-24 were isolated and identified for the first time from S. caseolaris. In the in vitro cytotoxic assay against SMMC-7721 human hepatoma cells, compound 21 （3＇,4＇,5,7-tetrahydroxyflavone） exhibited significant activity with IC50 2.8 μg/mL, while oleanolic acid （14）, 3,3＇-di-O-methyl ether ellagic acid （18）, and 3,3＇,4-O-tri-O-methyl ether ellagic acid （19） showed weak activity. None of these compounds displayed significant antibacterial activites.

Systematic analysis of components and contents in Houttuynia cordata Thunb

Objective:This study aims to provide the material basis for the molecular mechanism of Yuxingcao(Houttuynia cordata Thunb,HCT)through the method of evidence-based study to summarize the natural constituents isolated from HCT.Methods:We searched CNKI,Wanfang,VIP,Pubmed and relevant conference compilations.The keywords were'Yuxingcao or Houttuynia cordata Thunb'and'components'or'ingredients'or'constituent'or'volatile oil'or'flavonoids'or'terpene'or'content',both in Chinese and English.According to the inclusion and exclusion criteria,the reported compositions and contents have been summarized,and SPSS software was used to draw the boxplot of contents.Results:A total of 603 natural compounds in 11 categories were obtained from pooled articles.In the diverse components,the number of aliphatic compounds(n=259)and terpenoids(n=158)are more than those of flavonoids(n=26),alkaloids(n=42)and aromatics(n=42).While,in the part of volatile oils of HCT,the largest components are aliphatic compounds(mainly distributed on the ground)and terpenoids(mainly distributed in the underground).Although,methyl n-nonylketone is distributed in the whole herb plant,a large proportion is present in the underground parts.As for non-volatiles,the flavonoid content(mainly distributed on the ground)was the highest,among which quercetin and its glycosyl derivatives were the prominent.Conclusion:The results of this study provide a more comprehensive material basis for the further study of HCT.It is also helpful to explain the mechanisms of anti-oxidant,anti-inflammatory,anti-bacterial,anti-viral and anti-cancer effects from the molecular target and molecular network levels.

The Roles of Plant Secondary Metabolites from Cowpea Floral Structures in Resistance to the Flower Bud Thrips

Floral structures of six cowpea （Vigna unguiculata） cultivars were analysed for secondary plant metabolites （polyphenols, terpenoids and flavonoids） to study their relationships with resistance to Megalurothrips sjostedti （Trybom）. Polyphenols varied significantly （P 〈 0.001） among the floral structures of the cultivars at the same growth stage. Significant negative correlations were obtained between polyphenols and damage indices （r = -0.57）, mean adult counts （r = -0.56） and mean larval counts （r = -0.64） of resistant cowpea cultivars especially in the late season, indicating that polyphenols play a significant role in cowpea resistance to M. sjostedti. High levels of polyphenols obtained from Sanzibanili and Sewe cultivars, coupled with highly significant correlations between the polyphenols and thrips population on resistant cultivars, and their damage indices, suggests that these polyphenols could be inhibitors or deterrents in this case. Terpenoid extracts （10 mg/mL） of IT90K-277-2, Sewe, Sanzibanili, TVu 1509 and KV - 404-8-1 racemes; KV ~ 404-8-I and TVu 1509 floral buds; IT90K-277-2, Sewe and Sanzibanili flowers caused significant （P 〈 0.001） larval mortalities, since mortality ranged between 56.7%-96.7%. Hence terpenoid extracts from floral structures of the cultivars are biologically active and confers antibiotic resistance to M. sjostedti larvae; this compound could be promising candidates for genetic transformation of cowpea cultivars.

A Review of Triterpenoids and Their Pharmacological Activities from Genus Kadsura

Plants in genus Kadsura,belong to the Schisandraceae family including genus Schisandra and genus Kadsura,revealed folk efficacy and medicinal application in the treatment of rheumatoid arthritis and gastroenteric disorders for a long history.Previous study indicated that plants from genus Kadsura mainly contain lignans,triterpenoids and essential oils,and showed the active compounds were lignans and triterpenoids.Among all compounds from Schisandraceae family,the triterpenoids between the genus Schisandra and genus Kadsura had obvious differences.In this paper,we reviewed214triterpenoids and their pharmacological activities reported from genus Kadsura in the past30years(from1987to2017),aiming to provide reference for further study.

Maqui Aristotelia chilensis （Mol.） Stuntz]-the Amazing Chilean Tree： A Review

A. chilensis （Elaeocarpaceae） is commonly known as maqui, a species widely distributed in Chile. The plant participates in the structure of the Chilean temperate rainforest, currently being found mainly as fragmented forest. Maqui has been listed as the plant with the highest content of phenols when compared with other berries. Multiplication by both, seeds and vegetative has been obtained, opening the possibility to cultivate the plant. Leaves ofmaqui have been traditionally used in the native herbal medicine to treat diverse ailments. Studies indicate the presence of indolic alkaloids, flavonoids, cyaniding glucosides, delfidine, malvidine, petunidine, cumarines and triterpenes. Recent studies support therapeutic properties of maqui leaves, concluding that extracts obtained with polar solvents showed stabilizing capacity of free radicals and antioxidant capacity of plasma in humans. Other works show that fruits could be useful as antioxidant and cardioprotective source. The high contents of anthocyanins and polyglycosylated derivatives make berries of maqui an interesting p｜ant for food and pharmaceutical uses. A. chilensis polyphenols molecular mechanism of action and toxicity can be attributed to functional perturbation of cell membrane lipid bilayers. This review summarizes the research up to date, from propagation methods to chemical properties, indicating weak and lacking aspects.

Phytochemical Constituents and Allelopathic Effects of Some Medicinal Plants Extract on the Soil Algal Diversity

Phytochemical constituents of the shoots and roots extract of chosen eight medicinal plants （Plantago major, Verbesina encelioides, Glinus lotoides, Helotropium supinum, Mentha microphylla, Euphorbia hirta, Juncus subulatus and Convolvulus arvensis） were estimated using standard qualitative analysis. The extract contained alkaloids, glycosides, saponins, phenols, tannins, f[avonoids and terpenoids in some medicinal plants while others contain some only of these phytochemical components. Allelopathic effect of the various concentrations of the extracts on the soil algal diversity was also investigated. Wollea saccata was the only algal species disappeared from all applied investigated plant extracts. Phormidium richardsii, Monoraphidium braunii, Eunotia verneris and Nitzschia bilobata were the highly sensitive algal species to all applied shoot and root extract from all tested plants, they disappeared from most of the studied plants. On the other hand, Phormidium animale and Chlorella neustonice were highly tolerant algal species to all applied extracts. Counts of Cyanophyceae, Chlorophyceae and Bacillariophyceae were decreased by addition of some investigated medicinal plants extracts such as Juncus subulatus, Convolvulus arvensis and Euphorbia hirta. So the authors can use these plants extracts in biocontrol of the nuisance of algal bloom or any other microorganisms. Also, these plants may be useful to recover eutrophic water which needs further investigation.

Anti-promastigote Activity of the Amazon Plants

This study evaluated in vitro activity of ethanol extract, fractions, and isolated substance from Amazon species against promastigotes of L. amazonensis. The ethanol extracts were concentrated and fractionation. The anti-promastigote activity was evaluated through the cell viability assessment method （MTT）. The ethanol extract, fractions, and isolated substance from Himatanthus articulatus and Parahancorniafasciculata were inactive in promastigote ofL. amazonensis, as the ethanol extract ofPhysalis angulata. The hexane fractions from different parts ofMontrichardia linifera showed anti-promastigote activity probably due to the presence of steroids and terpenes. All species in studies were inactive, except ofM. linifera. The few polar constituents can be responsible for the activity. Therefore, the isolation and purification of the active on L. amazonensis promastigotes are urgently required.

Enzyme engineering in microbial biosynthesis of terpenoids:progress and perspectives

Terpenoids,known for their structural and functional diversity,are highly valued,especially in food,cosmetics,and cleaning products.Microbial biosynthesis has emerged as a sustainable and environmentally friendly approach for the production of terpenoids.However,the natural enzymes involved in the synthesis of terpenoids have problems such as low activity,poor specificity,and insufficient stability,which limit the biosynthesis efficiency.Enzyme engineering plays a pivotal role in the microbial synthesis of terpenoids.By modifying the structures and functions of key enzymes,researchers have significantly improved the catalytic activity,specificity,and stability of enzymes related to terpenoid synthesis,providing strong support for the sustainable production of terpenoids.This article reviews the strategies for the modification of key enzymes in microbial synthesis of terpenoids,including improving enzyme activity and stability,changing specificity,and promoting mass transfer through multi-enzyme collaboration.Additionally,this article looks forward to the challenges and development directions of enzyme engineering in the microbial synthesis of terpenoids.

Two terpenoids and a polyketide from the endophytic fungus Trichoderma sp. Xy24 isolated from mangrove plant Xylocarpus granatum

Three known compounds were isolated from the endophytic fungus Trichoderma sp Xy24 from a mangrove plant Xylocarpus granatum by using various column chromatography techniques. Their structures were identified as harzianone （1）, trichoacorenol （2）, and trichodimerol （3） by extensive spectroscopic analysis. Among them, 1 was a harziane diterpene, 2 was a sesquiterpene alcohol, and 3 was a polyketide with a completely symmetric configuration. Compound 3 exhibited medium inhibitory activity with an IC50 value of 74.6 μM using a NA （H7N9）/MUNANA model.

Inhibition of protein tyrosine phosphatase 1B activity by triterpenes isolated from Aceriphyllum rossii

An organic layer prepared from the seed of Aceriphyllum rossii was studied to identify the active compounds for protein tyrosine phosphatase 1B（PTP1B） inhibition.Bioassay guided fractionation resulted in the isolation of PTP1B inhibitory activity of triterpenes（1-4）.These four compounds were identified as aceriphyllic acid C（1）,aceriphyllic acid D（2）,aceriphyllic acid E（3） and aceriphyllic acid F（4）.The isolated 1-4 compounds inhibited PTP1B with IC50 values ranged from（2.1±1.5） μmol/L to（11.2±2.5） μmol/L.Kinetic analysis of PTP1B inhibition by aceriphyllic acid C（1） and aceriphyllic acid D（2） suggested that oleanane-type triterpenes inhibited PTP1B activity in a mixed-type manner.

Inhibition of protein tyrosine phosphatase 1B by triterpenes isolated from Potentilla discolor Bge

Seven oleanene triterpenes were isolated from the roots of Potentilla discolor Bge and their structures were identified as 3-oxoolean-12-en-27-oic acid（1）, gypsogenic acid（2）, 3α-hydroxyolean-12-en-27-oic acid（3）, 3β-hydroxyolean-12-en-27-oic acid（4）, aceriphyllic acid A（5）, aceriphyllic acid A methyl ester（6）, and oleanolic acid（7）. Compounds 1–7 inhibited protein tyrosine phosphatase 1B（PTP1B） activity, with IC50 values ranging from（7.5±0.5） to（22.7±0.5） μmol/L. Among the isolates, compounds 1, 2, 3 and 7 from the Potentilla discolor Bge were found to exhibit selective PTP1 B inhibitory activity.

Progress on the total synthesis of natural products in China:From 2006 to 2010

This paper summarizes the progress on the total syntheses riod from 2006 to 2010. The overview focuses on the first of natural products accomplished in rnainland China during the petotal synthesis of natural products of contemporary interest includ- ing alkaloids, cyclopeptides and cyclic depsipeptides, macrolides, terpenoids and steroids, saponins and glycosides. The development of novel synthetic strategies and methodologies, and application of new selective synthetic methods in the total syntheses of natural products are included as well.

A comparative study of conventional and supercritical fluid extraction methods for the recovery of secondary metabolites from Syzygium campanulatum Korth

Syzygium campanulatum Korth is a plant, which is a rich source of secondary metabolites （especially flavanones, chalcone, and triterpenoids）. In our present study, three conventional solvent extraction （CSE） techniques and supercritical fluid extraction （SFE） techniques were performed to achieve a maximum recovery of two flavanones, chalcone, and two triterpenoids from S. campanulatum leaves. Furthermore, a Box-Behnken design was constructed for the SFE technique using pressure, temperature, and particle size as independent variables, and yields of crude extract, individual and total secondary metabolites as the dependent variables. In the CSE procedure, twenty extracts were produced using ten different solvents and three techniques （maceration, soxhletion, and reflux）. An enriched extract of five secondary metabolites was collected using n-hexane：methanol （1：1） soxhletion. Using food-grade ethanol as a modifier, the SFE methods produced a higher recovery （25.5%-84.9%） of selected secondary metabo- lites as compared to the CSE techniques （0.92%-66.00%）.