Medicinal flowers. XI. Structures of new dammarane-type triterpene diglycosides with hydroperoxide group from flower buds of Panax ginseng (Q80100054)

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28 December 2019

title

Medicinal flowers. XI. Structures of new dammarane-type triterpene diglycosides with hydroperoxide group from flower buds of Panax ginseng (English)

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28 December 2019

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UOOOLBYCGFVHQY-WZFQGTCTSA-N

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UOOOLBYCGFVHQY-RHKQBYAPSA-N

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20-(6-O-alpha-L-Arabinofuranosyl-beta-D-glucopyranosyloxy)-25-hydroperoxydammara-23-ene-3beta,6alpha,12beta-triol

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2-[2-[[3,12-dihydroxy-17-(2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

panaxoside A progenin

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DBARXZWYGPCWKH-XCDFCMFKSA-N

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(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[(2R)-6-methyl-2-[(6R,10R,12S,13R,14R,17S)-3,6,12-trihydroxy-4,4,10,14,17-pentamethyl-2,3,5,6,7,8,9,11,12,13,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-5-en-2-yl]oxyoxane-3,4,5-triol

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IUHBPCFXZYBDIY-HWJWAWHJSA-N

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LBEQBAUYSPUYAY-ZQQZZLNPSA-N

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AYMHVZBATCNDEX-HAMMYILSSA-N

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Guanine, 9-beta-D-xylofuranosyl-

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2-(Hydroxymethyl)-6-[[12-hydroxy-4,4,8,10,14-pentamethyl-17-[6-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol

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2-(hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol

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17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

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beta-Sitosterol 3-O-beta-D-galactopyranoside

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Masayuki Yoshikawa

1

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28 December 2019

Sachiko Sugimoto

series ordinal

2

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28 December 2019

Seikou Nakamura

series ordinal

3

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28 December 2019

Hisashi Matsuda

series ordinal

4

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28 December 2019

language of work or name

English

1 reference

Chemical & Pharmaceutical Bulletin

publication date

2007

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16 September 2022

16 September 2022

full work available at URL

https://www.jstage.jst.go.jp/article/cpb/55/4/55_4_571/_pdf

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19 March 2024

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published in

Chemical & Pharmaceutical Bulletin

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28 December 2019

volume

55

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28 December 2019

issue

4

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28 December 2019

page(s)

571-576

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28 December 2019

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access restriction status

open access

1 reference

based on heuristic

inferred from online access status

cites work

Studies on the Constituents of Gynostemma pentaphyllum MAKINO. II. Structures of Gypenoside XV-XXI

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Structures of new dammarane-type Triterpene Saponins from the flower buds of Panax notoginseng and hepatoprotective effects of principal Ginseng Saponins

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Saponins of buds and flowers of Panax ginseng C.A. Meyer. 1. Isolation of ginsenosides-Rd, -Re, and -Rg.

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Chemical Studies on Crude Drug Precession. I. On the Constituents of Ginseng Radix Rubra (1)

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Bioactive saponins and glycosides. VIII. Notoginseng (1): new dammarane-type triterpene oligoglycosides, notoginsenosides-A, -B, -C, and -D, from the dried root of Panax notoginseng (Burk.) F.H. Chen

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Triterpene saponins from Vietnamese ginseng (Panax vietnamensis) and their hepatocytoprotective activity

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Further studies on dammarane-saponins of sanchi-ginseng.

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12 April 2024

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Medicinal flowers. VIII. Radical scavenging constituents from the flowers of Prunus mume: structure of prunose III.

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Bioactive saponins and glycosides. XIX. Notoginseng (3): immunological adjuvant activity of notoginsenosides and related saponins: structures of notoginsenosides-L, -M, and -N from the roots of Panax notoginseng (Burk.) F. H. Chen

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12 April 2024

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Bioactive saponins and glycosides. XI. Structures of new dammarane-type triterpene oligoglycosides, quinquenosides I, II, III, IV, and V, from American ginseng, the roots of Panax quinquefolium L

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Floratheasaponins A-C, acylated oleanane-type triterpene oligoglycosides with anti-hyperlipidemic activities from flowers of the tea plant (Camellia sinensis).

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Enzymatic synthesis of two ginsenoside Re-beta-xylosides

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Identifiers

DOI

10.1248/CPB.55.571

1 reference

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28 December 2019

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