(Q104945318)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900730-0

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(1S,2R,3R,9S,10S,17S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol

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(1S,2S,3S,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol

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(1E,2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol

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(2R,3R,10S,11S,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-20-oxahexacyclo[16.6.1.02,10.04,9.012,17.021,25]pentacosa-1(25),4(9),5,7,12(17),13,15,21,23-nonaene-7,13,15,23-tetrol

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(1R,4R,5R,11S,12S,15R,16R,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol

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(1R,2S,3R,4R,10S,11S)-4-(3,5-dihydroxyphenyl)-3,11-bis(4-hydroxyphenyl)hexacyclo[8.7.6.12,5.012,17.018,23.09,24]tetracosa-5(24),6,8,12(17),13,15,18(23),19,21-nonaene-6,8,14,19,21-pentol

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(1R,2R,3S,4S,10R,11R)-4-(3,5-dihydroxyphenyl)-3,11-bis(4-hydroxyphenyl)hexacyclo[8.7.6.12,5.012,17.018,23.09,24]tetracosa-5(24),6,8,12(17),13,15,18(23),19,21-nonaene-6,8,14,19,21-pentol

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(1R,4R,5R,11R,12S,15R,16R,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol

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(1R,8R,9S,16S)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol

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(1S,8R,9S,16S)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,9,12-tetrol

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(2R,3R,10S,11S,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-20-oxahexacyclo[16.6.1.02,10.04,9.012,17.021,25]pentacosa-1(25),4(9),5,7,12(17),13,15,21,23-nonaene-5,13,15,23-tetrol

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(1R,2R,3R,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol

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(2R,3R,10S,11S,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-20-oxahexacyclo[16.6.1.02,10.04,9.012,17.021,25]pentacosa-1(25),4(9),5,7,12(17),13,15,21,23-nonaene-5,7,13,15,23-pentol

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2-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol

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(5beta,10beta,12S)-10,11-Dihydro-11beta,12-bis(4-hydroxyphenyl)-5,10-methano-5H-dibenzo[a,d]cycloheptene-1,3,6,8-tetrol

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(1S,2R,3S)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-1-[(S)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol

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(1S,2R,3R,9R,10R,17S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.0⁴,¹⁸.0⁷,¹⁹.0¹¹,¹⁶]nonadeca-4(18),5,7(19),11,13,15-hexaene-5,13,15-triol

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(1S,2R,3R,9S,10S,17S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.0⁴,¹⁸.0⁷,¹⁹.0¹¹,¹⁶]nonadeca-4,6,11,13,15,18-hexaene-5,13,15-triol

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YQQUILZPDYJDQJ-PZPRHIMESA-N

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3

Munekazu Iinuma

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900730-0

Toshiyuki Tanaka

2

object named as

Toshiyuki Tanaka

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900730-0

Jin Murata

10

object named as

Jin Murata

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Ryuichi Sawa

8

object named as

Ryuichi Sawa

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author name string

Tetsuro Ito

1

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Ibrahim Iliya

4

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Ken-ichi Nakaya

5

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Zulfiqar Ali

6

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Yoshikazu Takahashi

7

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Yoshiaki Shirataki

9

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900730-0

Dedy Darnaedi

11

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publication date

July 2003

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16 September 2022

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volume

59

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issue

28

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page(s)

5347-5363

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Heimiol A, a new dimeric stilbenoid from Neobalanocarpus heimii

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Resveratrol Tetramers fromVaticadiospyroides

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HIV-inhibitory and cytotoxic oligostilbenes from the leaves of Hopea malibato

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7 January 2021

Shoreaphenol, a polyphenol from Shorea robusta

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7 January 2021

Canaliculatol, an antifungal resveratrol trimer from Stemonoporous canaliculatus

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7 January 2021

Distichol an antibacterial polyphenol from Shorea disticha

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7 January 2021

Further evidence for the structure of vaticaffinol and a revision of its stereochemistry

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7 January 2021

Another antibacterial polyphenol, copalliferol B, from Vateria copallifera (dipterocarpaceae)

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7 January 2021

Polyphenols from dipterocarp species. Vaticaffinol and Îµ-viniferin

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7 January 2021

Balanocarpol, a new polyphenol from Balanocarpus zeylanicus(trimen) and Hopea jucunda(Thw.)(Dipterocarpaceae)

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Polyphenols from dipterocarp species. Copalliferol A and stemonoporol

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Polyphenols from Stemonoporus species

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Novel resveratrol tetramer, vaticaffinol, from Vatica affinis Thw. (dipterocarpaceae)

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7 January 2021

New antibacterial polyphenol, copalliferol A, from Vateria copallifera(retz.) alston (dipterocarpaceae)

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7 January 2021

Identity of the polyphenol of shorea species with hopeaphenol

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7 January 2021

Two new stilbenetetramers from the stem of Vitis vinifera ‘Kyohou’

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7 January 2021

A novel oligostilbene named (+)-viniferol A from the stem of Vitis vinifera ‘Kyohou’

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7 January 2021

Anti-inflammatory tetramers of resveratrol from the roots of Vitis amurensis and the conformations of the seven-membered ring in some oligostilbenes

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Four Novel Oligostilbenes from the Roots of Vitis amurensis

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Ampelopsins E, E, H and cis-ampelopsin E, oligostilbenes from Ampelopsis brevipedunculata var. Hancei roots

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Ampelopsins A, B and C, new oligostilbenes of VAR. Hancei

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Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus

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7 January 2021

Stilbene oligomers in roots of Sophora davidii

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7 January 2021

Phenolic Compounds Isolated from the Roots of Sophora stenophylla.

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7 January 2021

Five novel oligostilbenes from the roots of Caragana sinica

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7 January 2021

An isorhapontigenin tetramer and a novel stilbene dimer from Gnetum hainanense

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7 January 2021

Four New Stilbene Oligomers in the Root of Gnetum gnemon

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7 January 2021

Five Stilbene Glucosides from Gnetum gnemonoides and Gnetum africanum

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7 January 2021

Cancer chemopreventive activity of resveratrol, a natural product derived from grapes

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7 January 2021

Antitumor agents 200. Cytotoxicity of naturally occurring resveratrol oligomers and their acetate derivatives

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7 January 2021

Vaticanol C, a novel resveratrol tetramer, inhibits cell growth through induction of apoptosis in colon cancer cell lines

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7 January 2021

(+)-Alpha-viniferin, an anti-inflammatory compound from Caragana chamlagu root

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7 January 2021

A new resveratrol octamer, vateriaphenol A, in Vateria indica

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7 January 2021

Two new oligostilbenes with dihydrobenzofuran from the stem bark of Vateria indica

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7 January 2021

Hopeafuran and a C-glucosyl resveratrol isolated from stem wood of Hopea utilis

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7 January 2021

Stilbenoids in the stem bark of Hopea parviflora

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7 January 2021

A novel bridged stilbenoid trimer and four highly condensed stilbenoid oligomers in Vatica rassak

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7 January 2021

Five New Oligostilbenes with One or Two Dihydrofurans from the Stem Bark of Vatica rassak

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7 January 2021

Vaticanol D, a novel resveratrol hexamer isolated from Vatica rassak

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7 January 2021

Oligostilbenoids in stem bark of Vatica rassak

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7 January 2021

Six New Heterocyclic Stilbene Oligomers from Stem Bark of Shorea hemsleyana

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7 January 2021

Four new stilbenoid C-glucosides isolated from the stem bark of Shorea hemsleyana

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7 January 2021

Stilbenoids isolated from stem bark of Shorea hemsleyana

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7 January 2021

Identification and ecdysteroid antagonist activity of three resveratrol trimers (suffruticosols A, B and C) from Paeonia suffruticosa

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7 January 2021

Lophirone A, A biflavonoid with unusual skeleton from Lophira lanceolata.

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7 January 2021

Possible inhibitor of tumor promotion and related polyphenol from Lophira alata, a medicinal plant in tropical west Africa.

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7 January 2021

Chemical determination of the absolute structures of resveratrol dimers, ampelopsins A, B, D and F

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7 January 2021

A resveratrol dimer from Parthenocissus tricuspidata

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7 January 2021