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1.
Nat Prod Res ; 35(4): 641-645, 2021 Feb.
Article in English | MEDLINE | ID: mdl-30887819

ABSTRACT

For the first time, the cytotoxic and phytochemical investigation of the leaves of Stereospermum binhchauensis V.S. Dang, a new species discovered in Viet Nam were finalized and led to purify nine compounds, including one furancoumarin (1), one chromone (3), two triterpenoids (2, 4), two flavonoids (5, 8), two flavanoids (6, 7) and one iridoid (9) using various chromatography methods. Their structures were verified by HR-ESI-MS, NMR experiments and compared with previous literatures. For the first time, compounds (5-8) were realized from the genus Stereospermum, while compounds (1, 2, 3, 4 & 9) were designated from the species S. binhchauensis. Furthermore, the furancoumarin, chromone and flavanoid classes were notified for the first time from the genus Stereospermum.


Subject(s)
Antineoplastic Agents/pharmacology , Bignoniaceae/chemistry , Phytochemicals/analysis , Phytochemicals/pharmacology , Plant Leaves/chemistry , Antineoplastic Agents/analysis , Cell Death/drug effects , Cell Line, Tumor , Humans , Phytochemicals/chemistry , Plant Extracts/chemistry
2.
Nat Prod Res ; 30(21): 2389-95, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27228410

ABSTRACT

From the fruit of Pandanus tectorius Parkinson ex Du Roi, one new dihydrofurocoumarin, named pandanusin A (1) and 15 known compounds, including one furanocoumarin (2), two coumarins (3, 4), four lignans (5-8), one neolignan (9), two flavonoids (10, 11), three phenolics (12-14), one monoglyceride (15) and one monosaccharide (16) were isolated by various chromatography methods. Among them, compounds (3-5) were obtained from the Pandanus genus for the first time and compounds (9-14, 16) were reported from this species for the first time. Their structures were elucidated by HR-ESI-MS, NMR 1D and 2D experiments and comparison with previous reported data. The α-glucosidase inhibitory activity of all compounds was measured. The isolated compounds (1-12, 14) showed better α-glucosidase inhibitory activity (IC50 = 42.2, 36.5, 84.7, 73.2, 40.8, 26.7, 76.5, 33.8, 68.1, 14.4, 22.1, 81.5, 43.8 µM, respectively) than the standard drug acarbose (IC50 = 214.5 µM).


Subject(s)
Coumarins/isolation & purification , Glycoside Hydrolase Inhibitors/isolation & purification , Pandanaceae/chemistry , Coumarins/chemistry , Coumarins/pharmacology , Fruit/chemistry , Glycoside Hydrolase Inhibitors/chemistry , Glycoside Hydrolase Inhibitors/pharmacology
3.
J Asian Nat Prod Res ; 17(4): 338-42, 2015.
Article in English | MEDLINE | ID: mdl-25367696

ABSTRACT

From the leaves of Cleome chelidonii L.f., two new flavonol glycosides, named cleomesides A (1) and B (2), and four known compounds, quercetin 3-O-ß-glucopyranosyl(1 â†’ 2)-α-rhamnoside-7-O-α-rhamnoside (3), ethyl α-galactopyranoside (4), adenine (5) and glycerol monostearate (6), were isolated. The structures of all isolated compounds (1-6) were determined by NMR spectroscopy and mass spectrometry. The data of known compounds (3-6) were further compared with the reported data for these compounds.


Subject(s)
Cleome/chemistry , Flavonols/isolation & purification , Glycosides/isolation & purification , Flavonols/chemistry , Glycosides/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Plant Leaves/chemistry , Quercetin/analogs & derivatives , Quercetin/chemistry , Quercetin/isolation & purification
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