1999
DOI: 10.1248/cpb.47.1029
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Studies on Constituents with Cytotoxic Activity from the Stem Bark of Syringa velutina.

Abstract: Cytotoxic compounds, oleuropein (1) and a phenylethanoid glycoside (2) were isolated from the stem bark of Syringa velutina KOM. along with coniferylaldehyde 4-O-glucoside, syringin, ligstroside, (+)-syringaresinol 4-O-glucoside, (+)-medioresinol 4"-O-glucoside and (-)-olivil 4"-O-glucoside. Phenylethanoid glycoside (2) was identified to be 3,4-dihydroxyphenylethyl alcohol 8-O-beta-D-glucopyranoside. This compound showed the most potent cytotoxic effect on several tumor cell lines (P-388, L-1210, SNU-5 and HL-… Show more

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Cited by 44 publications
(24 citation statements)
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“…Among them, secoiridoid glucosides showed free radical scavenging activity [5] and antihypertensive activity [6]. Furthermore, some lignan glycosides displayed hypotensive activity [7] and cytotoxicity [8].…”
Section: Introductionmentioning
confidence: 99%
“…Among them, secoiridoid glucosides showed free radical scavenging activity [5] and antihypertensive activity [6]. Furthermore, some lignan glycosides displayed hypotensive activity [7] and cytotoxicity [8].…”
Section: Introductionmentioning
confidence: 99%
“…The known compounds were identified as oleoside-11-methylester (3), 16) oleoside-7,11-dimethylester (4), 17) 10-hydroxyoleuropein (5), 14) oleuropein (6), 16) ligstroside (7), 18) (2″R)-2″-methoxyoleuropein (8), 19) neonuezhenide (9) 14) by comparison of their spectroscopic and physical data with previously reported values.…”
Section: Resultsmentioning
confidence: 93%
“…The main FCC from Sw-leaves, named Sw-FCC-62, was remarkably abundant (>13% of the Chl in a green leaf). The structure of Sw-FCC-62 was deduced and it was revealed to carry ) is a natural product, that occurs e.g., in (extracts of) several species of the genus Chelone (Scrophulariaceae) [24], the stem bark of Syringa velutina [25], and the thalloid liverwort Marchantia polymorpha [26].…”
Section: Discussionmentioning
confidence: 99%