2013
DOI: 10.1080/01496395.2012.710887
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Effective and Preparative Separation of Bioactive Flavonoids FromGynostemma PentaphyllumTea Using Elution-Extrusion Counter-Current Chromatography

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Cited by 6 publications
(7 citation statements)
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“…The E1 products of gypenosides LVI and XLVI, the damulins A (15) and B (16) (C-2-OH) and the C-3-OH isomers, damulins E (17) and F (18), exhibited low to moderate monolayer permeability with P app values ranging from 1.33 (±0.073) to 6.2 (±0.248) × 10 −6 cm/s. Damulins A and B (15 and 16) differ only in the position of the double bond at C-20 of the side chain, with 15 being the Δ 20,22 isomer and 16 the less stable terminal double-bond isomer (Δ 20,21 ). Damulins E and F (17 and 18) share the same structural relationship (Figure 1).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…The E1 products of gypenosides LVI and XLVI, the damulins A (15) and B (16) (C-2-OH) and the C-3-OH isomers, damulins E (17) and F (18), exhibited low to moderate monolayer permeability with P app values ranging from 1.33 (±0.073) to 6.2 (±0.248) × 10 −6 cm/s. Damulins A and B (15 and 16) differ only in the position of the double bond at C-20 of the side chain, with 15 being the Δ 20,22 isomer and 16 the less stable terminal double-bond isomer (Δ 20,21 ). Damulins E and F (17 and 18) share the same structural relationship (Figure 1).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Reports suggest that approximately 165 saponins are present in G. pentaphyllum . 18 , 21 The major saponins present in G. pentaphyllum belong to the dammarane class of saponins (known as gypenosides, if isolated from G. pentaphyllum ). Dammarane saponins are characterized by a dammarane aglycone with an acyclic side chain ( Figure 1 ).…”
Section: Introductionmentioning
confidence: 99%
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