A Rare Dirhamnosyl Flavonoid and Other Radical-Scavenging Metabolites from Cynophalla mollis (Kunth) J. Presl and Colicodendron scabridum (Kunt) Seem. (Capparaceae) of Ecuador.
Vladimir MorochoLeslye Paola ValarezoDavid Andrés TapiaLuis CartucheNixon CumbicusGianluca GilardoniPublished in: Chemistry & biodiversity (2021)
The phytochemistry of Cynophalla mollis (Kunth) J. Presl and Colicodendron scabridum (Kunth), both belonging to the family Capparaceae, were investigated in this study for the first time. Lupeol, betulin, lutein, stachydrine and quercetin-3,4'-di-O-rhamnoside were isolated from C. mollis, whereas C. scabridum afforded lupeol, lutein, stachydrine, β-sitosterol, stigmasterol, betonicine and narcissoside. All these compounds were purified by preparative liquid chromatography, in both open column and instrumental (MPLC) separation systems. Preparative TLC was also applied. They were all identified by 1 H- and 13 C-NMR experiments. The complete structure of the very rare flavonoid quercetin-3,4'-di-O-rhamnoside was fully elucidated through DEPT-135, COSY, HMQC and HMBC experiments, together with UV/VIS and FT-IR spectrophotometry. Complete NMR data for quercetin-3,4'-di-O-rhamnoside in deuterated methanol were presented here for the first time. All the extracts did not exert antioxidant activity at the maximum tested dose of 1 mg/mL. Three out of the nine isolated compounds exerted a good spectrum of antioxidant capacity, being narcissoside the most active against ABTS radicals, with SC50 =12.43 μM. It was followed by lutein and quercetin-3,4'-di-O-rhamnoside, with 40.92 μM and 46.10 μM, respectively.
Keyphrases
- liquid chromatography
- biofilm formation
- mass spectrometry
- magnetic resonance
- high resolution
- high resolution mass spectrometry
- tandem mass spectrometry
- solid state
- ms ms
- escherichia coli
- pseudomonas aeruginosa
- minimally invasive
- staphylococcus aureus
- big data
- artificial intelligence
- single molecule
- atomic force microscopy