(Q83229496)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Monoterpene constituents from Cistanche tubulosa--chemical structures of kankanosides A-E and kankanol- (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

1 reference

2-(hydroxymethyl)-6-[(7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl)oxy]oxane-3,4,5-triol

1 reference

(2S,3R,4S,5S,6R)-2-[[(1S,4aR,7S,7aS)-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(2R,3S,4S,5S,6R)-2-[[(1S,4aS,7S,7aS)-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1 reference

7-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid

1 reference

(2S,3R,4S,5S,6R)-2-{[(1S,4aR,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

5-Chloro-2,10-dioxatricyclo[5.3.1.04,11]undecan-4-ol

1 reference

2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undecane-4,5-diol

1 reference

(2S,3S,4R,5R,6R)-2-[[(1S,4aS,7aS)-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(2e,6z)-8-beta-d-Glucopyranosyloxy-2,6-dimethyl-2,6-octadienoic acid

1 reference

(1S,4aS,7aS)-7-(hydroxymethyl)-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid

1 reference

1 reference

(3R)-3-hydroxy-1-methylpyrrolidin-2-one

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(2R,3S,4S,5S,6R)-2-[[(1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1 reference

(2S,3S,4R,5R,6S)-2-[[(1S,4aS,6S,7aS)-6-hydroxy-7-methylidene-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

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Bartsioside, >=95% (LC/MS-ELSD)

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(2Z,6Z)-2,6-dimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyocta-2,6-dienoic acid

1 reference

1 reference

1A-(Hydroxymethyl)-1A,1B,2,5A,6,6A-hexahydrooxireno[4,5]cyclopenta[1,2-C]pyran-2-YL hexopyranoside

1 reference

1 reference

1 reference

1 reference

1 reference

(1R,4S,5R,7S,11S)-5-chloro-2,10-dioxatricyclo[5.3.1.04,11]undecan-4-ol

1 reference

6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid

1 reference

1 reference

(1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid

1 reference

(R)-3-Hydroxy-2-pyrrolidone

1 reference

(1S,4aS,6S,7S,7aR)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid

1 reference

1 reference

(2S,3R,4S,5R,6R)-2-[[(1S,4aS,6R,7S,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1 reference

1 reference

(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-[[(1S,2S,4S,6S,10S)-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]oxane-3,4,5-triol

1 reference

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Cistanche deserticola

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1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Haihui Xie

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Hisashi Matsuda

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Seikou Nakamura

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Osamu Muraoka

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Masayuki Yoshikawa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

language of work or name

English

1 reference

Chemical & Pharmaceutical Bulletin

publication date

2006

1 reference

Crossref

full work available at URL

16 September 2022

https://www.jstage.jst.go.jp/article/cpb/54/5/54_5_669/_pdf

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1248/cpb.54.669?email=unpaywall_01@example.com

published in

Chemical & Pharmaceutical Bulletin

1 reference

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20 January 2020

volume

1 reference

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20 January 2020

issue

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20 January 2020

page(s)

669-675

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20 January 2020

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19 March 2024

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access restriction status

open access

1 reference

based on heuristic

inferred from online access status

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(2E,6R)-8-hydroxy-2,6-dimethyl-2-octenoic acid, a novel anti-osteoporotic monoterpene, isolated from Cistanche salsa

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Rotundial, a new natural mosquito repellent from the leaves of Vitex rotundifolia

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Bioactive constituents from Chinese natural medicines. XVII. constituents with radical scavenging effect and new glucosyloxybenzyl 2-isobutylmalates from Gymnadenia conopsea

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12 April 2024

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Absolute Stereostructures of Hydramacrosides A and B, New Bioactive Secoiridoid Glucoside Complexes from the Leaves of Hydrangea macrophylla SERINGE var. thunbergii MAKINO

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Chemical Studies on Crude Drug Processing. VII. On the Constituents of Rehmanniae Radix. (1): Absolute Stereostructures of Rehmaglutins A, B, and D Isolated from Chinese Rehmanniae Radix,the Dried Root of Rehmannia glutinosa Libosch.

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Glucosyloxybenzyl 2-Isobutylmalates from the tubers of Gymnadenia conopsea

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Structures of new beta-carboline-type alkaloids with antiallergic effects from Stellaria dichotoma(1,2)

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Iridoid glucosides from Linaria japonica

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Absolute stereostructures of new arborinane-type triterpenoids and inhibitors of nitric oxide production from Rubia yunnanensis

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Bioactive constituents from Chinese natural medicines. XIV. New glycosides of beta-carboline-type alkaloid, neolignan, and phenylpropanoid from Stellaria dichotoma L. var. lanceolata and their antiallergic activities.

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12 April 2024

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12 April 2024

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Chemical constituents from the leaves of Hydrangea macrophylla var. thunbergii (III): Absolute stereostructures of hydramacrosides A and B, secoiridoid glucoside complexes with inhibitory activity on histamine release

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Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene

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Studies on the constituents of Cistanchis Herba. II. Isolation and structures of new iridoids, cistanin and cistachlorin.

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Synthesis and glycosylation shift of 1,1'-disaccharides

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Three monoterpenes from Mussaenda pubescens

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The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

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Studies on the constituents of Cistanchis Herba. VI. Isolation and structure of a new iridoid glycoside, 6-deoxycatalpol.

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Identifiers

DOI

10.1248/CPB.54.669

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16651763%20AND%20SRC:MED&resulttype=core&format=json