(Q31988449)

5 July 2017

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris (English)

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(1Z)-1-phenylhex-1-en-4-yn-3-one

5 July 2017

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2',6-Bis(beta-D-glucopyranosyloxy)-4',5,5',7-tetrahydroxyflavone

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

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5,7,8-trimethoxychromen-2-one

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(1R,2S,14R,15R)-5,24-dimethoxy-7,9,12,17,20,22-hexaoxaheptacyclo[13.11.0.02,14.03,11.06,10.018,26.019,23]hexacosa-3,5,10,18,23,25-hexaene-13,16-dione

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8H-1,3-Dioxolo[4,5-h][1]benzopyran-8-one, 4-hydroxy-

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(7-phenyldodeca-2,4,8,10-tetrayn-6-yl)benzene

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isorhamnetin 3-robinobioside

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2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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(1E)-1-phenylhex-1-en-4-yn-3-one

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Homoeriodictyol 7-O-rutinoside

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3,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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4,9-dimethoxy-2H-[1,3]dioxolo[4,5-g]chromen-6-one

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SVNJLRKERVRIRJ-BTMCAZCFSA-N

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4',5,7-Trihydroxy-8-(beta-D-glucopyranosyloxy)flavone

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5-hydroxy-6,7-dimethoxychromen-2-one

6-Demethoxycapillarisin

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6,7-Bis(2-methoxyphenyl)-2,4,8,10-dodecatetryne

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(+)-(7S,8R,8'R)-acuminatolide

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4,5-dimethoxy-2H-[1,3]dioxolo[4,5-h]chromen-8-one

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AMVFDCTXPYHACR-FWCAKJNKSA-N

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4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-methoxyphenoxy)-

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(1S,3R,4S,5R)-1,3,5-trihydroxy-4-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}cyclohexane-1-carboxylic acid

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4-Hydroxy-9-methoxy-[1,3]dioxolo[4,5-g]chromen-6-one

5,6,7-trimethoxycoumarin

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methyl hydroxycinnamate

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1-(hexa-2,4-diyn-1-yl)-2-methoxybenzene

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methyl (E)-4-hydroxycinnamate

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1-(2-methoxyphenyl)hexa-2,4-diyn-1-one

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5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one

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7,3',4'-Tri-O-methylluteolin

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(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one

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5-Hydroxy-2-(4-hydroxyphenoxy)-6,7-dimethoxychromen-4-one

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6,7,8-trimethoxy-1-benzopyran-2-one

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4-Methoxy-2H,8H-[1,3]dioxolo[4,5-h][1]benzopyran-8-one

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1-Phenylhexa-2,4-diyn-1-ol

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Wu TS

1

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5 July 2017

Tsang ZJ

2

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5 July 2017

Wu PL

3

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5 July 2017

Lin FW

4

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5 July 2017

Li CY

5

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5 July 2017

Teng CM

6

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5 July 2017

Lee KH

7

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Bioorganic & Medicinal Chemistry

5 July 2017

language of work or name

English

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publication date

January 2001

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16 September 2022

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5 July 2017

9

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5 July 2017

77-83

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5 July 2017

1

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Studies on "Inchinko". I. Capillarisin, a new choleretic substance (author's transl)

5 July 2017

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

A flavone from Artemisia capillaris

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Studies on the constituents of Formosan Leguminosae. II. The constituents in the leaves of Uraria crinita Desv (author's transl)

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Three germacranolides and other constituents from Eremanthus species

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Isorhamnetin 3-O-Robinobioside From Gomphrena martiana

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Flavone and flavonol 5-glucosides

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Flavonol glycosides from leaves of Strychnos variabilis

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Flavonoids of Striga asiatica

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

C-glycosylflavones in Lespedeza cuneata.

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Phenylalkynes from Artemisia capillaris

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Volatile components of Artemisia capillaris

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

A new polyacetylene from Artemisia capillaris

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Coumarins of Artemisia tridentat ssp. vaseyana

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

6-Methoxy-7,8-Methylenedioxycoumarin from Artemisia dracunculoides and Artemisia vulgaris

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Flavonoids of Various Prunus Species X

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

The heartwood constituents of Tetradium glabrifolium

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Study on the Constituents of Marsdenia tinctoria var. tomentosa MASAMUNE

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Lignans and Other Constituents from South and Central AmericanZanthoxylumSpecies

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Studies on constituents of medicinal plants. XXII. Constituents of Schizandra nigra Max. 4

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Chemistry and biochemistry of Chinese drugs. VII. Cytostatic pheophytins from silkworm excreta, and derived photocytotoxic pheophorbides

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https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Identification of ent-16 beta, 17-dihydroxykauran-19-oic acid as an anti-HIV principle and isolation of the new diterpenoids annosquamosins A and B from Annona squamosa.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

Vasorelaxing effect in rat thoracic aorta caused by fraxinellone and dictamine isolated from the Chinese herb Dictamnus dasycarpus Turcz: comparison with cromakalim and Ca2+ channel blockers

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2900225-X

7 January 2021

10.1016/S0968-0896(00)00225-X

Identifiers

DOI

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5 July 2017

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