Cycloartanone derivatives from Viguiera dentata

In addition to previously known compounds, three new cycloartanone derivatives were obtained from the aerial parts of Viguiera dentata collected in Mexico.     

Sesquiterpene lactones from glandular trichomes of Viguiera radula (Heliantheae; Asteraceae)

In addition to known compounds, the floral parts of Viguiera radula afforded two new sesquiterpene lactones. All compounds were detected in glandular trichomes, which were micromechanically collected from the anther appendages and analyzed by HPLC. Structure identification was performed by NMR and MS techniques.     

Sesquiterpene lactones from Viguiera species

Viguiera eriophora yielded the sesquiterpene lactones erioflorin, acetylerioflorin and 17,18-dehydroviguiepinin, which was correlated with tetrahyd     

Kaurane and pimarane-type diterpenes from the Viguiera species inhibit vascular smooth muscle contractility

The research, development and use of natural products as therapeutic agents, especially those derived from plants, have been increasing in recent years. Despite the fact that plants provide a rich source of novel biologically active compounds, only a small percentage have been phytochemically investigated and studied for their medical potential. Viguiera is a genus that belongs to the family Asteraceae and to the sunflower tribe Heliantheae, which is widespread mostly in Mexico and in other areas of the Andes and upland areas of Brazil. A review on the secondary metabolites pointed out that sesquiterpene lactones and diterpenes, of the kaurane and pimarane-type, are the main compounds produced by these plants. Some reports have shown that kaurane- and pimarane-type diterpenes exert several biological activities such as anti-inflammatory action, antimicrobial and antispasmodic activities. Kaurenoic and pimaradienoic acids, which are the main secondary metabolites isolated by our research group from the roots of Viguiera robusta and V. arenaria, respectively, have been evaluated on vascular smooth muscle contractility. We showed that these diterpenoids are able to inhibit the vascular contractility mainly by blocking extracellular Ca(2+) influx. Additionally, in this review we discuss the structure-activity relationship of the diterpenes regarding their inhibitory activity on vascular contractility.     

Sesquiterpene lactones and a myoinositol from glandular trichomes of Viguiera quinqueremis (Heliantheae; Asteraceae)

The extract of the floral parts of Viguiera quinqueremis afforded, in addition to known compounds, six new sesquiterpene lactones as well as a new myoinositol derivative. All compounds were detected in glandular trichomes which were collected micromechanically from the anther appendages and were analyzed by HPLC. Structure identification was performed by 1H NMR measurements including LC NMR and LC MS experiments.     

Sesquiterpene lactones from Viguiera hypargyrea

The new sesquiterpene lactones 8β-[epoxyangeloyloxy]-14-hydroxytithifolin and 8-[epoxyangeloyl]-14-acetoxy-eupatolide, were isolated from Viguiera hypargyrea. The structures were established by chemical and spectroscopic means. The chemotaxonomic implications of the chemical constituents of Viguiera are briefly discussed.     

15-Hydroxy-acetylerioflorin and other constituents from Viguiera linearis

Aerial parts of Viguiera linearis afforded 16α-hydroxy-ent-kauranoic acid, viguiestenin, leptocarpin, acetylleptocarpin, budlein B, clovandiol and the new heliangolide 15-hydroxy-acetylerioflorin.     

Cadina-4,11-diene from Viguiera oblongifolia

Viguiera oblongifolia afforded two known furanoheliangolides and a new cadinane derivative whose structure was established by spectroscopic methods. From V. lanceolata 17,18-dihydrobudlein A was isolated.     

Bioactive oleanolic acid saponins and other constituents from the roots of Viguiera decurrens

The bisdesmoside oleanolic acid saponin, 3-0-(methyl-beta-D-glucuronopyranosiduronoate)-28-0-beta-D-glucopyranosyl-oleanolate along with nine known compounds (two diterpenic acids, one chromene, three triterpenes, one steroidal glycoside, and two monodesmoside oleanolic acid saponins), were obtained from Viguiera decurrens roots. The chemical structure of the bisdesmoside oleanolic saponin was determined by chemical and NMR spectral evidence. A mixture of monodesmoside saponins displayed cytotoxic activity against P388 and COLON cell lines (ED50= 2.3 and 3.6 microg/ml, respectively). Two of the known compounds showed insecticidal activity against the Mexican bean beetle larvae (Epilachna varivestis).     

15-oxo-zoapatlin,a diterpene lactone from Viguiera maculata

The isolation of a new diterpene lactone and two known diterpenoid acids from the aerial parts of Viguiera maculata is reported.     

Further sesquiterpene lactones from Viguiera robusta and the potential anti-inflammatory activity of a heliangolide: inhibition of human neutrophil elastase release

In addition to known heliangolides, a new eudesmanolide was isolated from the leaf rinse extract of Viguiera robusta (Asteraceae). Structural elucidation was based on spectral analysis. It is the first report on eudesmanolides in members of the subgenus Calanticaria of Viguiera. In this work, the main isolated compound, the furanoheliangolide budlein A, besides its previously reported in vitro and in vivo anti-inflammatory activities, inhibited human neutrophil elastase release. The inhibition was at the concentration of (16.83 +/- 1.96) microM for formylated bacterial tripeptide (fMLP) stimulation and (11.84 +/- 1.62) microM for platelet aggregation factor (PAF) stimulation, being slightly less active than the reference drug parthenolide. The results are important to demonstrate the potential anti-inflammatory activities of sesquiterpene lactones and corroborate the previous studies using other targets.     

A new species of Viguiera (Asteraceae: Heliantheae) from Mexico

AlthoughViguiera hidalgoana, a new species from Hidalgo, Mexico, bears a superficial resemblance toV. dentata, it is clearly related to certain woody species of seriesGrammatoglossae.     

The germacranolides of Viguiera buddleiaeformis structures of budlein-A and -B

The structure of budlein-A, the main sesquiterpene lactone of Viguiera buddleiaeformis was established as the 8 angeloyl ester of 1 keto, 8-β, 14-dihydroxy germacra-2,4,11 (13)-trien-3, (10 β) oxido-6 α, 12-olide. Its structure and stereochemistry was determined by chemical and spectroscopic means. Budlein-B, found in the same plant as a minor constituent, is 8 α, 15-dihydroxygermacra-1 (10), 4, 11 (13)-trien-6 α, 12-olide.     

Fructan Variations in Tuberous Roots of Viguiera discolor Baker (Asteraceae): the Influence of Phenology

The content and composition of fructans in tuberous roots ofViguiera discolor Baker (Asteraceae), a perennial herbaceousspecies native to the Brazilian cerrado, are analysed accordingto season and in sequence from late dormancy (winter) to thebeginning of the next dormant period (autumn). The general patternof fructose found in decreasing concentrations of ethanol extractsis similar at each phenological phase. Hot water soluble fructans(high molecular mass inulin) are predominant throughout, particularlyin the dormant period, and account for more than half the totalfructan. Lower molecular mass components, especially free fructose,are present in higher amounts during the sprouting phase; thiswould indicate that hydrolysis occurs in association with thebreaking of dormancy. The absence of oligosaccharides of intermediatesize during the flowering/fruiting phase suggests they mightbe metabolized in the course of this process. The total concentrationof fructans and the mean molecular mass of inulin remain highin spite of these variations. (Received July 15, 1992; Accepted May 10, 1993)     

Effects of elevated CO2 concentration and water deficit on fructan metabolism in Viguiera discolor Baker

Elevated [CO₂] is suggested to mitigate the negative effects of water stress in plants; however responses vary among species. Fructans are recognised as protective compounds against drought and other stresses, as well as having a role as reserve carbohydrates. We analysed the combined effects of elevated [CO₂] and water deficit on fructan metabolism in the Cerrado species Viguiera discolor Baker. Plants were cultivated for 18 days in open‐top chambers (OTC) under ambient (～380 ppm), and high (～760 ppm) [CO₂]. In each OTC, plants were submitted to three treatments: (i) daily watering (control), (ii) withholding water (WS) for 18 days and (iii) re‐watering (RW) on day 11. Analyses were performed at time 0 and days 5, 8, 11, 15 and 18. High [CO₂] increased photosynthesis in control plants and increased water use efficiency in WS plants. The decline in soil water content was more distinct in WS 760 (WS under 760 ppm), although the leaf and tuberous root water status was similar to WS 380 plants (WS under 380 ppm). Regarding fructan active enzymes, 1‐SST activity decreased in WS plants in both CO₂ concentrations, a result consistent with the decline in photosynthesis and, consequently, in substrate availability. Under WS and both [CO₂] treatments, 1‐FFT and 1‐FEH seemed to act in combination to generate osmotically active compounds and thus overcome water deficit. The proportion of hexoses to sucrose, 1‐kestose and nystose (SKN) was higher in WS plants. In WS 760, this increase was higher than in WS 380, and was not accompanied by decreases in SKN at the beginning of the treatment, as observed in WS 380 plants. These results suggest that the higher [CO₂] in the atmosphere contributed to maintain, for a longer period, the pool of hexoses and of low DP fructans, favouring the maintenance of the water status and plant survival under drought.     

Biological activities from extracts of endophytic fungi isolated from Viguiera arenaria and Tithonia diversifolia

A total of 39 endophytic fungi have been isolated from Viguiera arenaria and Tithonia diversifolia, both collected in S?o Paulo State, Brazil. The isolates were identified based on their ribosomal DNA sequences. The ethyl acetate (EtOAc) extracts of all endophytic fungi were evaluated for their antimicrobial, antiparasitic and antitumoral activity. Antimicrobial screening was conducted using an agar diffusion assay against three pathogenic microorganisms: Staphylococcus aureus, Escherichia coli and Candida albicans. Antiparasitic activity was determined by enzymatic inhibition of gGAPDH of Trypanosoma cruzi and adenine phosphorybosiltransferase (APRT) of Leishmania tarentolae. Antitumoral activity was tested against human T leukemia cells by the Mosmann colorimetric method. All extracts showed activity in at least one assay: 79.5% of the extracts were cytotoxic against leukemia cells, 5.1% of the extracts were active against S. aureus, 25.6% against E. coli and 64.1% against Candida albicans. Only one extract showed promising results in the inhibition of parasitic enzymes gGAPDH (95.0%) and three were found to inhibit APRT activity. The cytotoxic extract produced by the strain VA1 (Glomerella cingulata) was fractionated and yielded nectriapyrone and tyrosol. Nectriapyrone showed relevant cytotoxic activity against both human T leukemia and melanoma tumor cell lines.     

Germacranolides and diterpenes from Viguiera species

The investigation of six Viguiera species afforded in addition to known compounds two new diterpenes, the 9,11-dehydro derivatives of trachylobanic and stachenic acid, two new heliangolides closely related to viguiestenin, and the acetate of falcarinol. The chemotaxonomic situation is discussed briefly.     

Diketopiperazines produced by endophytic fungi found in association with two Asteraceae species

Diketopiperazine (DKP) derivatives, named colletopiperazine, fusaperazine C and E as well as four known DKPs were isolated from cultures of Colletotrichum gloeosporioides, Penicillium crustosum, both endophytic fungi isolated from Viguiera robusta, and a Fusarium spp., an endophyte of Viguiera arenaria, respectively. Their structures were established on the basis of their spectroscopic data. Conformational analysis of two known DKPs showed that folded conformations were as energetically stable as the extended one.     

A revised classification of subtribe Helianthinae (Asteraceae: Heliantheae). I. Basal lineages

Results for nuclear ITS sequences were combined with previously obtained data from cpDNA restriction site studies to provide a comprehensive molecular phylogeny for subtribe Helianthinae. Results from the two molecular data sets were mostly congruent for basally diverging branches of the subtribe. Based on the results, combined with morphological observations, the basally diverging branches are placed in six genera, including one newly described. Bahiopsis is resurrected to accommodate species previously placed in Viguiera subgenus Bahiopsis . Calanticaria is newly proposed for the five species of Viguiera ser. Brevifolieae . Heliomeris is retained for the group sometimes included within Viguiera as sect. Heliomeris . Hymenostephium is revived and enlarged to include a number of species of similar habit and involucre, including members of Viguiera sect. Diplostichis , Haploca-lymma and Garcilassa . Although cpDNA results place the morphologically distinctive Sclerocarpus within the clade including species of Hymenostephium , the ITS data were consistent with morphology in suggesting it to be a distinctive lineage.  © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 140 , 65–76.