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1.
Life Sci ; 333: 122166, 2023 Nov 15.
Article in English | MEDLINE | ID: mdl-37827232

ABSTRACT

Ovarian cancer presents a significant challenge due to its high rate of chemoresistance, which complicates the effectiveness of drug-response therapy. This study provides a comprehensive metabolomic analysis of ovarian cancer cell lines OVCAR-3 and SK-OV-3, characterizing their distinct metabolic landscapes. Metabolomics coupled with chemometric analysis enabled us to discriminate between the metabolic profiles of these two cell lines. The OVCAR-3 cells, which are sensitive to doxorubicin (DOX), exhibited a preference for biosynthetic pathways associated with cell proliferation. Conversely, DOX-resistant SK-OV-3 cells favored fatty acid oxidation for energy maintenance. Notably, a marked difference in glutathione (GSH) metabolism was observed between these cell lines. Our investigations further revealed that GSH depletion led to a profound change in drug sensitivity, inducing a shift from a cytostatic to a cytotoxic response. The results derived from this comprehensive metabolomic analysis offer potential targets for novel therapeutic strategies to overcome drug resistance. Our study suggests that targeting the GSH pathway could potentially enhance chemotherapy's efficacy in treating ovarian cancer.


Subject(s)
Ovarian Neoplasms , Humans , Female , Ovarian Neoplasms/drug therapy , Ovarian Neoplasms/metabolism , Drug Resistance, Neoplasm , Apoptosis , Cell Line, Tumor , Doxorubicin/pharmacology , Doxorubicin/therapeutic use , Glutathione/metabolism
2.
Plant Sci ; 336: 111858, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37673219

ABSTRACT

The Sirex noctilio's climatic adaption and rapid proliferation have caused Pinus mortality worldwide. The infestation combines the early effect of female S. noctilio gland secretion and the spreading symbiotic fungus Amylostereum areolatum. 'Lipidomics' is the study of all non-water-soluble components of the metabolome. Most of these non-water-soluble compounds correspond to lipids which can provide information about a biological activity, an organelle, an organism, or a disease. Using HPLC-MS/MS based lipidomics, 122 lipids were identified in P. radiata needles during S. noctilio infestation. Phosphatidic acids, N-acylethanolamines, and phosphatidylinositol-ceramides accumulated in infested trees could suggest a high level of phospholipases activities. The phosphatidylcholines were the most down-regulated species during infection, which could also suggest that they may be used as a substrate for up-regulated lipids. The accumulation of very long-chain fatty acids and long-chain fatty acids during the infestation could imply the tree defense response to create a barrier in the drilled zone to avoid larvae development and fungus proliferation. Also, the growth arrest phase of the trees during the prolonged infestation suggests a resistance response, regulated by the accumulation of NAE, which potentially shifts the tree energy to respond to the infestation.


Subject(s)
Hymenoptera , Pinus , Animals , Lipid Metabolism , Lipidomics , Tandem Mass Spectrometry , Hymenoptera/physiology , Fungi , Trees , Fatty Acids , Lipids
4.
J Plant Res ; 136(6): 827-839, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37486392

ABSTRACT

The ecological niche centrality hypothesis states that population abundance is determined by the position in the ecological niche, expecting higher abundances towards the center of the niche and lower at the periphery. However, the variations in the conditions that favor the persistence of populations between the center and the periphery of the niche can be a surrogate of stress factors that are reflected in the production of metabolites in plants. In this study we tested if metabolomic similarity and diversity in populations of the tree species Eucryphia cordifolia Cav. vary according to their position with respect to the structure of the ecological niche. We hypothesize that populations growing near the centroid should exhibit lower metabolites diversity than plants growing at the periphery of the niche. The ecological niche of the species was modeled using correlative approaches and bioclimatic variables to define central and peripheral localities from which we chose four populations to obtain their metabolomic information using UHPLC-DAD-QTOF-MS. We observed that populations farther away from the centroid tend to have higher metabolome diversity, thus supporting our expectation of the niche centrality hypothesis. Nonetheless, the Shannon index showed a marked variation in metabolome diversity at the seasonal level, with summer and autumn being the periods with higher metabolite diversity compared to winter and spring. We conclude that both the environmental variation throughout the year in combination with the structure of the ecological niche are relevant to understand the variation in expression of metabolites in plants.


Subject(s)
Ecosystem , Metabolome , Seasons , Trees , Plants
5.
Antioxidants (Basel) ; 12(2)2023 Jan 28.
Article in English | MEDLINE | ID: mdl-36829862

ABSTRACT

Polyphenols are bioactive substances that participate in the prevention of chronic illnesses. High content has been described in Berberis microphylla G. Forst (calafate), a wild berry extensively distributed in Chilean-Argentine Patagonia. We evaluated its beneficial effect through the study of mouse plasma metabolome changes after chronic consumption of this fruit. Characterized calafate extract was administered in water, for four months, to a group of mice fed with a high-fat diet and compared with a control diet. Metabolome changes were studied using UHPLC-DAD-QTOF-based untargeted metabolomics. The study was complemented by the analysis of protein biomarkers determined using Luminex technology, and quantification of OH radicals by electron paramagnetic resonance spectroscopy. Thirteen features were identified with a maximum annotation level-A, revealing an increase in succinic acid, activation of tricarboxylic acid and reduction of carnitine accumulation. Changes in plasma biomarkers were related to inflammation and cardiovascular disease, with changes in thrombomodulin (-24%), adiponectin (+68%), sE-selectin (-34%), sICAM-1 (-24%) and proMMP-9 (-31%) levels. The production of OH radicals in plasma was reduced after calafate intake (-17%), especially for the group fed with a high-fat diet. These changes could be associated with protection against atherosclerosis due to calafate consumption, which is discussed from a holistic and integrative point of view.

6.
Plants (Basel) ; 11(23)2022 Dec 05.
Article in English | MEDLINE | ID: mdl-36501417

ABSTRACT

Plant growth-stimulation bioactivity of triterpenoid saponins is well known, especially for oleanane-type compounds. Nevertheless, a few phytotoxicity bioassays performed on some steroidal saponins have shown hormesis profiles and growth stimulation on Lactuca sativa roots. The focus of the work described here was on the use of the wheat coleoptile bioassay to evaluate plant growth stimulation, and on the search for a commercially available source of active saponins by bio-guided fractionation strategy. Selected saponins were tested and a cluster analysis showed that those saponins with a sugar chain of more than five units had a hormesis profile, while saponins with growth enhancement had fewer sugar residues. Two saponins showed similar activity to the positive control, namely the phytohormone indole-3-butyric acid (IBA). As a potential source of these metabolites, a commercial extract of Yucca schidigera used as a fertilizer was selected. Bio-guided fractionation led to the identification of two fractions of defined composition and these showed stimulation values similar to the positive control. It was observed that the presence of a carbonyl group at C-12 on the aglycone skeleton led to improved activity. A saponin-rich fraction from Y. schidigera could be proposed to enhance crop quality and production.

7.
Food Res Int ; 160: 111642, 2022 10.
Article in English | MEDLINE | ID: mdl-36076377

ABSTRACT

A comprehensive study of bioactive compounds was carried out in the leaves of the main Berberis species growing in Chile (Berberis microphylla, Berberis darwinii, Berberis empetrifolia, Berberis trigona, and the introduced Berberis vulgaris). We identified 117 compounds, by a detailed analysis of each molecule, including phenolic acids, alkaloids, flavonols, and other compounds, using high-performance liquid chromatography and high-resolution mass spectrometry. Quantitative analysis of main compound was also included for all species. Hydroxycinnamic acid derivatives were the main compounds in all the studied leaves, with the highest concentration in Berberis microphylla. Quercetin derivatives were the most relevant flavonols in all species, except in Berberis vulgaris, in which isorhamnetin-3-rutinoside was the most concentrated. The fatty acid profile, determined by gas chromatography mass spectrometry revealed the presence of linoleic and linolenic acids in all species studied. Berberis vulgaris showed higher levels of these fatty acids. The antioxidant capacity, explored by three in vitro methods, showed high values for all studied Berberis species. The obtained levels are higher than those of other prominent foods. The findings will inform novel approaches for the valorization of these leaves as natural food or ingredient.


Subject(s)
Berberis , Antioxidants/analysis , Berberis/chemistry , Flavonols/analysis , Metabolome , Plant Extracts/chemistry
8.
Phytochemistry ; 203: 113350, 2022 Nov.
Article in English | MEDLINE | ID: mdl-35973612

ABSTRACT

Defense-related metabolome traits in pine species after infestation by Sirex noctilio are largely unknown, despite, in most cases, trees being overwhelmed. Using LC-MS-based untargeted metabolomics, we revealed the systemic metabolic changes induced by this insect in 14-year-old Pinus radiata trees, the most affected species worldwide. An immediate metabolome alteration was expressed in needles after infestation, including the up-regulation of flavonols, flavan-3-ols, oxyneolignans, auxins, proline, and tryptophan, among others. The flavan-3-ols (catechin and procyanidin B1) suggested a rapidly induced photoprotection mechanism aided by diverting proline as an alternative substrate for respiration to compensate for the progressive chlorosis that degrades photosystems. Meanwhile, glutathione, glutamate, and ascorbate levels significantly dropped in needles, which may indicate the critical oxidative stress that trees had to face since the onset of the infestation. They were not fully replenished after long-term infestation, and redox homeostasis was probably not achieved, compromising tree survival. Nevertheless, a huge auxins overexpression detected in needles throughout the infestation may reflect tolerance against the premature senescence caused by the woodwasp venom. In contrast, the metabolome of wood tissues remained initially unchanged, although it seems to collapse after three months. Overall, the metabolomics strategy adopted in this work evidenced its usefulness in uncovering the fundamental roles of plants' chemical defense that govern interactions with specific stressors.


Subject(s)
Catechin , Hymenoptera , Pinus , Animals , Flavonols , Glutamates , Glutathione , Hymenoptera/physiology , Indoleacetic Acids , Proline , Trees , Tryptophan
10.
MethodsX ; 8: 101406, 2021.
Article in English | MEDLINE | ID: mdl-34430302

ABSTRACT

The validation of protocols for carrying out the experimental analysis of amination reactions is of paramount importance to enhance the scientific knowledge and reproducibility of results. Accordingly, in the present paper, a protocol has been proposed for the study of the amination of cyclohexanone-to-secondary amines (Diphenylamine and N-Cyclohexylaniline) over heterogeneous catalysts. The results of activity and selectivity, and the elucidation of a plausible reaction pathway were described in a parent paper. Therefore, the purpose of this document is to inform about the details of the experimental setups, the methods, and the analytical techniques to identify and quantify the reaction products. Finally, some practical and safety considerations are also included.•One-pot catalytic amination of cyclohexanone with aniline was performed efficiently in liquid phase on Pd/C.•Stirring, He atmosphere and temperature control were critical to achieve reproducible activity results.•Ultra-High Performance Liquid Chromatography allows identifying products and reaction intermediates, while nonane performed well as internal standard for GC-FID quantification.

11.
Phytochem Anal ; 32(1): 38-61, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32515107

ABSTRACT

INTRODUCTION: The analysis and detection of steroidal saponins is mainly performed using chromatographic techniques coupled with mass spectrometry. However, nuclear magnetic resonance (NMR) spectroscopy is a potential tool that can be combined with these techniques to obtain unambiguous structural characterisation. OBJECTIVE: This work provides a review of the carbon-13 (13 C)- and proton (1 H)-NMR spectroscopic data of aglycones from Agave saponins reported in the literature and also the development of an easy identification method for these natural products. METHODS: The database Scifinder was used for spectroscopic data collection in addition to data obtained from the Cadiz Allelopathy research group. The keywords used were Agave, spirostanic, furostanic, and saponin. RESULTS: The shielding variations produced by functional groups on the aglycone core and the structural features of the most representative aglycones from Agave species are described. The effects are additive for up to four long-range connectivities. A method for the identification of aglycones (HMAI) is proposed to classify aglycones from Agave spp. through the use of 1 H-NMR and heteronuclear multiple bond correlation (HMBC) experiments. CONCLUSIONS: The HMBC spectrum is representative of the structural features of aglycones from Agave spp. The HMBC method for aglycone identification (HMAI) method allowed the identification of pure saponins or mixtures thereof and this method can be used in combination with chromatographic techniques coupled with mass spectrometry to provide a more thorough analysis of Agave samples that contain aglycones.


Subject(s)
Agave , Saponins , Magnetic Resonance Spectroscopy , Plant Extracts
12.
Antioxidants (Basel) ; 9(12)2020 Nov 24.
Article in English | MEDLINE | ID: mdl-33255435

ABSTRACT

Calafate (Berberis microphylla G. Forst) is a Patagonian barberry very rich in phenolic compounds. Our aim was to demonstrate, through in vitro models, that a comprehensive characterized calafate extract has a protective role against oxidative processes associated to cardiovascular disease development. Fifty-three phenolic compounds (17 of them not previously reported in calafate), were tentatively identified by Ultra-Liquid Chromatography with Diode Array Detector, coupled to Quadrupole-Time of Fly Mass Spectrometry (UHPLC-DAD-QTOF). Fatty acids profile and metals content were studied for the first time, by Gas Chromatography Mass Spectrometry (GC-MS) and Total X-ray Fluorescence (TXRF), respectively. Linolenic and linoleic acid, and Cu, Zn, and Mn were the main relevant compounds from these groups. The bioactivity of calafate extract associated to the cardiovascular protection was evaluated using Human Umbilical Vein Endothelial Cells (HUVECs) and human low density lipoproteins (LDL) to measure oxidative stress and lipid peroxidation. The results showed that calafate extract reduced intracellular Reactive Oxygen Species (ROS) production (51%) and completely inhibited LDL oxidation and malondialdehyde (MDA) formation. These findings demonstrated the potential of the relevant mix of compounds found in calafate extract on lipoperoxidation and suggest a promising protective effect for reducing the incidence of cardiovascular disease.

13.
Nutrients ; 12(1)2019 Dec 24.
Article in English | MEDLINE | ID: mdl-31878160

ABSTRACT

Raisins are dried grapes consumed worldwide that contain beneficial components for human health. They are rich in fiber and phytochemicals such as phenolic compounds. Despite a 60% sugar content, several studies have reported health-promoting properties for raisins and this review compiles the intervention studies, as well as the cell line and animal model studies carried out to date. It has been demonstrated that raisins possess a low-to-moderate glycemic index, which makes them a healthy snack. They seem to contribute to a better diet quality and may reduce appetite. Their antioxidant capacity has been correlated to the phenolic content and this may be involved in the improvement of cardiovascular health. In addition, raisins maintain a good oral health due to their antibacterial activity, low adherence to teeth and an optimum oral pH. Raisin consumption also seems to be favorable for colon function, although more studies should be done to conclude this benefit. Moreover, gut microbiota could be affected by the prebiotic content of raisins. Cell line and animal model studies show other potential benefits in specific diseases, such as cancer and Alzheimer's disease. However, deeper research is required and future intervention studies with humans are needed. Overall, incorporating an 80-90 g portion of raisins (half a cup) into the daily diet may be favorable for human health.


Subject(s)
Fruit , Vitis , Animals , Diet , Food Handling , Humans , Snacks
14.
J Agric Food Chem ; 65(23): 4611-4623, 2017 Jun 14.
Article in English | MEDLINE | ID: mdl-28535679

ABSTRACT

For centuries oak wood (Quercus robur) has been used in aging of wines and spirits, which is based on pleasant flavors given to beverages by phenolics transferred to the liquid during the maturation process. Other metabolites, such as triterpenoids, can also be released. Searching for extractable triterpenoids in oak heartwood, 12 new, 1-12, and five known, 13-17, oleanane types were isolated and characterized. Their cytotoxicities were tested against cancer cells (PC3 and MCF-7) and lymphocytes. Breast cancer cells (MCF-7) were the most affected by triterpenoids, with roburgenic acid, 4, being the most active compound (IC50 = 19.7 µM). Selectivity was observed for compounds 1-3, 8, 9, and 16, exhibiting an IC50 > 200 µM against lymphocytes, while active against cancer cells. A galloyl unit attached to the triterpenoid moiety was established as the key feature for such effect. These results highlight the occurrence of triterpenoids in oak heartwood and their relevance for chemoprevention of breast cancer.


Subject(s)
Plant Extracts/chemistry , Quercus/chemistry , Triterpenes/chemistry , Wood/chemistry , Alcoholic Beverages/analysis , Cell Line, Tumor , Cell Proliferation/drug effects , Chromatography, High Pressure Liquid , Flavoring Agents/chemistry , Flavoring Agents/pharmacology , Gas Chromatography-Mass Spectrometry , Humans , Plant Extracts/pharmacology , Triterpenes/pharmacology
15.
Food Chem Toxicol ; 109(Pt 2): 863-870, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28363853

ABSTRACT

For centuries wood containers have been used in aging of wines and spirits, due to the pleasant flavors they give to the beverages. Together with oak, sweet chestnut wood (Castanea sativa) have been often used for such purpose. The maturation process involves the transfer of secondary metabolites, mainly phenolics, from the wood to the liquid. At the same time, other metabolites, such as triterpenoids and their glycosides, can also be released. Searching for the extractable triterpenoids from sweet chestnut heartwood (C. sativa), two new ursane-type triterpenoid saponins named chestnoside A (1) and chestnoside B (2), together with two known oleanen-type analogs (3 and 4) were isolated and characterized. The cytotoxicity of isolated compounds was tested against two cancer cell lines (PC3 and MCF-7), and normal lymphocytes. Breast cancer cells (MCF-7) were more affected by tested compounds than prostate cancer cells (PC3). Chestnoside B (2) exhibited the strongest cytotoxicity with an IC50 of 12.3 µM against MCF-7 cells, lower than those of positive controls, while it was moderately active against normal lymphocytes (IC50 = 67.2 µM). These results highlight the occurrence of triterpenoid saponins in sweet chestnut heartwood and their potential for the chemoprevention of breast cancer.


Subject(s)
Fagaceae/chemistry , Plant Extracts/toxicity , Triterpenes/toxicity , Humans , MCF-7 Cells , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Triterpenes/chemistry , Triterpenes/isolation & purification , Wood/chemistry
16.
Nat Prod Res ; 31(17): 2024-2031, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28049352

ABSTRACT

A fingerprint of steroid saponins, the major constituent in 80% methanolic fraction from the male flowers of Phoenix dactylifera has been established. Under ESI-MS/MS conditions, the fragmentation patterns of [M - H]- ions exclusively displayed signals corresponding to the cleavage of the glycosidic bonds, thus allowing a rapid identification of 21 steroidal saponins. Moreover, two unique among them conjugated with histidine were detected by LC-ESI (-)-MS and DFT and were given tentative names of 3-o-histidine-26-o-hexosyl-dioscin and 3-o-histidine-26-o-dihexosyl-hydroxydioscin. Their steroidal saponins exhibited a significant improvement of the sperm cells count, motility and viability in male rats. These effects could be attributed to enhancing the levels of sex hormones.


Subject(s)
Phoeniceae/chemistry , Saponins/chemistry , Saponins/pharmacology , Spermatogenesis/drug effects , Animals , Chromatography, Liquid , Drug Evaluation, Preclinical/methods , Flowers/chemistry , Male , Rats, Wistar , Saponins/analysis , Spectrometry, Mass, Electrospray Ionization , Sperm Count , Spermatozoa/drug effects , Steroids/chemistry , Steroids/pharmacology , Tandem Mass Spectrometry
17.
J Nat Prod ; 79(11): 2903-2911, 2016 11 23.
Article in English | MEDLINE | ID: mdl-27797203

ABSTRACT

Four new steroidal saponins (1-4) along with 13 known saponins were isolated from the leaves of Furcraea hexapetala. The new compounds were identified as (20R,22R,25R)-3ß-hydroxy-5α-spirostan-12-one 3-O-{α-l-rhamnopyranosyl-(1→4)-O-ß-d-glucopyranosyl-(1→3)-O-[ß-d-glucopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (1), (25R)-3ß-hydroxy-5α-spirost-20(21)-en-12-one 3-O-{α-l-rhamnopyranosyl-(1→4)-O-ß-d-glucopyranosyl-(1→3)-O-[ß-d-glucopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (2), (25R)-5α-spirostan-3ß-ol 3-O-{ß-d-glucopyranosyl-(1→2)-O-ß-d-glucopyranosyl-(1→2)-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (3), and (25R)-5ß-spirostan-3ß-ol 3-O-{ß-d-glucopyranosyl-(1→6)-O-ß-d-galactopyranoside} (4) by spectroscopic analysis, including one- and two-dimensional NMR techniques, mass spectrometry, and chemical methods. The phytotoxicity of the isolated compounds against the standard target species Lactuca sativa was evaluated. Structure-activity relationships for these compounds with respect to phytotoxic effects are discussed.


Subject(s)
Alkaloids/isolation & purification , Alkaloids/pharmacology , Asparagaceae/chemistry , Phytosterols/isolation & purification , Phytosterols/pharmacology , Plant Leaves/chemistry , Saponins/isolation & purification , Saponins/pharmacology , Alkaloids/chemistry , Cuba , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Phytosterols/chemistry , Saponins/chemistry , Stereoisomerism , Structure-Activity Relationship
18.
J Agric Food Chem ; 64(22): 4686-94, 2016 Jun 08.
Article in English | MEDLINE | ID: mdl-27192362

ABSTRACT

Several species of Brachiaria (Poaceae) currently cover extensive grazing areas in Brazil, providing valuable source of feed for a large cattle population. However, numerous cases of toxicity outbreaks in livestock have raised concerns on safety of using these plants, especially B. decumbens. In this study, chemometric analysis of ultrahigh-performance liquid chromatography-high-resolution quadrupole time-of-flight mass spectrometry (UHPLC-HR-QTOF-MS) data has for the first time uncovered qualitative and quantitative differences between metabolomes of toxic B. decumbens and nontoxic B. brizantha. The steroidal saponin protoneodioscin was established as the main biomarker for B. decumbens when compared to B. brizantha, and therefore the key explanation for their phytochemical differentiation. Quantification of protodioscin in both plants showed no significant differences; consequently, the idea that this compound is solely responsible for toxicity outbreaks must be discarded. Instead, we propose that the added occurrence of its stereoisomer, protoneodioscin, in B. decumbens, can be considered as the probable cause of these events. Interestingly, the greatest concentrations of saponins for both species were reached during winter (B. decumbens = 53.6 ± 5.1 mg·g(-1) dry weight (D.W.); B. brizantha = 25.0 ± 1.9 mg·g(-1) D.W.) and spring (B. decumbens = 49.4 ± 5.0 mg·g(-1) D.W.; B. brizantha = 27.9 ± 1.4 mg·g(-1) D.W.), although in the case of B. decumbens these values do not vary significantly among seasons.


Subject(s)
Brachiaria/chemistry , Chromatography, High Pressure Liquid/methods , Diosgenin/analogs & derivatives , Mass Spectrometry/methods , Metabolomics/methods , Saponins/analysis , Sterols/analysis , Animal Feed/analysis , Animals , Brachiaria/classification , Brachiaria/metabolism , Brachiaria/toxicity , Brazil , Cattle , Diosgenin/analysis , Diosgenin/metabolism , Diosgenin/toxicity , Saponins/metabolism , Saponins/toxicity , Seasons , Sterols/metabolism , Sterols/toxicity
19.
Phytochemistry ; 105: 92-100, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24939800

ABSTRACT

A bioassay-guided fractionation of Agave offoyana leaves led to the isolation of five steroidal saponins (1-5) along with six known saponins (6-11). The compounds were identified as (25R)-spirost-5-en-2α,3ß-diol-12-one 3-O-{α-l-rhamnopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (1), (25R)-spirost-5-en-3ß-ol-12-one 3-O-{α-l-rhamnopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (2), (25R)-spirost-5-en-3ß-ol-12-one 3-O-{ß-d-xylopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (3), (25R)-26-O-ß-d-glucopyranosylfurost-5-en-3ß,22α,26-triol-12-one 3-O-{α-l-rhamnopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (4) and (25R)-26-O-ß-d-glucopyranosylfurost-5-en-3ß,22α,26-triol-12-one 3-O-{ß-d-xylopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (5) by comprehensive spectroscopic analysis, including one- and two-dimensional NMR techniques, mass spectrometry and chemical methods. The phytotoxicity of the isolated compounds on the standard target species Lactuca sativa was evaluated.


Subject(s)
Agave/chemistry , Phytosterols/isolation & purification , Phytosterols/pharmacology , Saponins/isolation & purification , Saponins/pharmacology , Nuclear Magnetic Resonance, Biomolecular , Phytosterols/chemistry , Plant Leaves/chemistry , Saponins/chemistry , Stereoisomerism , Structure-Activity Relationship
20.
Phytochemistry ; 95: 298-307, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23859261

ABSTRACT

Bioguided studies of flowers of Agave offoyana allowed the isolation of five steroidal saponins never described previously, Magueyosides A-E (1-5), along with six known steroidal saponins (6-11). The structures of compounds were determined as (25R)-spirost-5-en-2α,3ß-diol-12-one 3-O-{ß-d-xylopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (1), (25R)-spirost-5-en-2α,3ß-diol-12-one 3-O-{ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (2), (25R)-spirost-5-en-2α,3ß,12ß-triol 3-O-{ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (3), (25R)-5α-spirostan-2α,3ß-diol-12-one 3-O-{ß-d-xylopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (4), and (25R)-5α-spirostan-2α,3ß-diol-9(11)-en-12-one 3-O-{ß-d-xylopyranosyl-(1→3)-O-ß-d-glucopyranosyl-(1→2)-O-[ß-d-xylopyranosyl-(1→3)]-O-ß-d-glucopyranosyl-(1→4)-O-ß-d-galactopyranoside} (5), by comprehensive spectroscopic analysis, including one- and two-dimensional NMR techniques, mass spectrometry and chemical methods. The bioactivities of the isolated compounds on the standard target species Lactuca sativa were evaluated. A dose-dependent phytotoxicity and low dose stimulation were observed.


Subject(s)
Agave/chemistry , Plant Extracts/pharmacology , Saponins/pharmacology , Flowers/chemistry , Lactuca/drug effects , Molecular Structure , Plant Extracts/chemistry , Saponins/chemistry , Saponins/isolation & purification
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