The genus Aristolochia stands out as the most representative of the Aristolochiaceae plant family, with approximately 550 species distributed around the world, many of which have little or no studies reported in the literature. Investigation of the acetone extract from leaves of Aristolochia warmingii Mast. resulted in the isolation and identification of twenty-three compounds, mostly lignans and neolignans, including the new furofuran lignans warminin A (1), warminin B (2) and warminin C (3). The structures of the compounds were established by comprehensive spectroscopic and spectrometric analyses. A large amount of (–)-epieudesmin (4) was isolated from the extract, which suggests that A. warmingii could be a potential source of this compound. The hexane, acetone, ethanol, and ethanol Soxhlet extracts, in addition to fourteen of the isolated compounds, were evaluated for their ability to inhibit the formation of advanced glycation end products (AGEs), but they did not show significant activities. family 55 world literature Mast twentythree twenty three neolignans 1, 1 , (1) 2 (2 3. 3 . (3) analyses –epieudesmin epieudesmin – 4 (4 compound hexane extracts AGEs, AGEs (AGEs) activities 5 (1 ( (3 (AGEs

A new compound, (6R,7S,2E,4E)-6,7-dihydroxy-4,6-dimethylocta-2,4-dienoic acid (1), together with eight known compounds were isolated from the co-culture of Saccharicola sp. and Botryosphaeria parva, an endophytic fungi associated with Eugenia jambolana Lam. (Myrtaceae) plant species. The structures were elucidated by spectroscopic analysis of the one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) and mass spectrometry (MS) data as well as by comparison with literature data. The bioactivity (antioxidant and antifungal) of the crude EtOAc was evaluated. All crude extracts presented antioxidant activity and only the crude extract from the co-culture was active on the fungus Cladosporium sphaerospermum. This investigation contributed to the knowledge about the metabolic production of two endophytic fungi Saccharicola sp. and Botryosphaeria parva in co-culture, once, until the present date, there are no studies in the literature that report the understanding of the chemical interaction of both grown in the same environment. compound 6R,7S,2E,4E6,7dihydroxy4,6dimethylocta2,4dienoic 6R7S2E4E67dihydroxy46dimethylocta24dienoic RSEEdihydroxydimethyloctadienoic 6R,7S,2E,4E 6,7 dihydroxy 4,6 dimethylocta 2,4 dienoic 6R 7S 2E 4E 6 7 4 2 R S E 1, 1 , (1) coculture co culture sp Lam Myrtaceae (Myrtaceae species onedimensional one dimensional 1D D (1D twodimensional 2D (2D NMR (NMR MS (MS antifungal evaluated sphaerospermum coculture, culture, once date environment 4E6 7dihydroxy4 6dimethylocta2 4dienoic 6R7S2E4E RSEE 67 6, 46 4, 24 2, (1 7dihydroxy 6dimethylocta (

A new isoflavone named pratensein-7-O-β-D-rutinoside [(-)-7-O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranosyl-5,3’-dihydroxy-4’-methoxyisoflavone] and the known compounds biochanin A-7-O-β-D-rutinoside, 6-deoxyclitoriacetal 11-O-β-D-glucopyranoside, 6-deoxyclitoriacetal, (2S)-naringenin-6-C-β-D-glucopyranoside, (2R)-naringenin-6-C-β-D-glucopyranoside, tachioside, and koaburaside were isolated from the roots of Clitoria guianensis (Aubl.) Benth var. guianensis (Fabaceae), a subshrub found in the Brazilian Cerrado biome. The structures of the compounds were identified by physical and spectroscopic data measurements (specific rotation ([α]D), circular dichroism (CD), ultraviolet (UV), infrared (IR), 1D and 2D nuclear magnetic resonance (NMR), and mass spectrometry (MS)). The EtOAc fraction of the roots exhibited high toxicity against Artemia salina with median lethal dose (LD50) value of 8.53 mg L-1.

A new flavonol triglycoside, named kaempferol-3-O-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside, was isolated from flowers of Aristolochia trulliformis (Aristolochiaceae) together with 15 known compounds, including six flavonoids and four lignans. The structures of the compounds were determined by spectroscopic analyses, including 1D and 2D nuclear magnetic resonance (NMR) techniques and high-resolution mass spectrometry (HRMS).

A new pyranone, (S)-2-(4-hydroxyphenylethyl)-6-methyl-2,3-dihydro-4H-pyran-4-one, with unusual carbon skeleton, and three new aristolochic acid derivatives (7-O-methylaristolochic acid F, sodium 7-O-methylaristolochate F and sodium aristolochate F) were isolated from Aristolochia urupaensis (Aristolochiaceae) stems together with 31 known compounds. The structures of the compounds were determined by spectroscopic analyses, including Fourier transform infrared (FTIR) and 1D and 2D nuclear magnetic resonance (NMR) techniques, and high-resolution mass spectrometry (HRMS).

The water hyacinth (Eichhornia crassipes (Mart.) Solms, Pontederiaceae) is considered as one of the most productive plants on earth, and an aquatic weed, which causes serious environmental problems. In this study, this species is presented as an alternative of a renewable source of shikimic acid. Although this acid is an important intermediate in the biosynthesis of aromatic compounds in plants and microorganisms, its occurrence is described for the first time in a species of the Pontederiaceae family. Shikimic acid is the lead compound for the production of the antiviral agent oseltamivir phosphate (Tamiflu®). Semi-quantitative analyses of the plant extracts by HPLC-PDA showed that the aerial parts of E. crassipes contain higher shikimic acid concentration (0.03%-2.70% w/w) than the roots (0.05%-0.90% w/w), and that methanol is a better solvent than water for shikimic acid extraction.