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Vitis coignetiae

Vitis coignetiae - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffae350804835184461
Scientific name Vitis coignetiae
Authority Pulliat ex Planch.
First published in Vigne Amer. Vitic. Eur. 7(1): 186. 1883 [Jan 1883]

Description Top

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Synonyms Top

Scientific name Authority First published in
Vitis austrokoreana Hatus. J. Jap. Bot. 16: 530 (1940)
Vitis amurensis var. coignetiae (Pulliat ex Planch.) Nakai

Common names Top

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Language Common/alternative name
English crimson glory vine
Danish pragt-vin
German rostrote weinrebe
German rostrote rebe
Persian ویتیس کیگنتیا
Finnish ruosteviini
French vigne de coignet
Japanese ヤマブドウ
Japanese やまぶどう
Japanese 山ブドウ
Japanese 山葡萄
Korean 머루
Lithuanian japoninis vynmedis
lzh 紫葛
Polish winorośl japońska
Russian Виноград японский
Russian Виноград Куанье
Chinese 紫葛
Chinese 紫葛葡萄

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000421604
Tropicos 34000016
KEW urn:lsid:ipni.org:names:68634-1
The Plant List kew-2456654
Missouri Botanical Garden 287540
Open Tree Of Life 925462
Observations.org 123574
NCBI Taxonomy 694578
NBN Atlas NHMSYS0000464932
IPNI 327401-2
iNaturalist 559123
GBIF 5658476
Freebase /m/080bg7s
EPPO VITCO
EOL 5537979
Elurikkus 564198
USDA GRIN 41864
Wikipedia Vitis_coignetiae

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Studies on pollen micro-morphology, pollen storage methods, and cross-compatibility among grape (Vitis spp.) genotypes Rane P, Thakre M, Verma MK, Kumar C, Prakash J, Srivastava V, P. R. S, Murukan N, Chawla G, Mandal PK, Kumar H, Jadhav AK, Varghese E, Patel VB, Singh SK Front Plant Sci 21-Feb-2024
PMCID:PMC10922203
doi:10.3389/fpls.2024.1353808
PMID:38463567
Grapevine Virome of the Don Ampelographic Collection in Russia Has Concealed Five Novel Viruses Belkina D, Karpova D, Porotikova E, Lifanov I, Vinogradova S Viruses 14-Dec-2023
PMCID:PMC10747563
doi:10.3390/v15122429
PMID:38140672
Anthocyanins Inhibits Oxidative Injury in Human Retinal Pigment Epithelial ARPE-19 Cells via Activating Heme Oxygenase-1 Park C, Hwangbo H, Kim SO, Noh JS, Park SH, Hong SH, Hong SH, Kim GY, Choi YH J Microbiol Biotechnol 13-Nov-2023
PMCID:PMC11016763
doi:10.4014/jmb.2310.10011
PMID:38044685
Effects of Functional and Nutraceutical Foods in the Context of the Mediterranean Diet in Patients Diagnosed with Breast Cancer Flore G, Deledda A, Lombardo M, Armani A, Velluzzi F Antioxidants (Basel) 11-Oct-2023
PMCID:PMC10603973
doi:10.3390/antiox12101845
PMID:37891924
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Annual (2023) taxonomic update of RNA-directed RNA polymerase-encoding negative-sense RNA viruses (realm Riboviria: kingdom Orthornavirae: phylum Negarnaviricota) Kuhn JH, Abe J, Adkins S, Alkhovsky SV, Avšič-Županc T, Ayllón MA, Bahl J, Balkema-Buschmann A, Ballinger MJ, Kumar Baranwal V, Beer M, Bejerman N, Bergeron É, Biedenkopf N, Blair CD, Blasdell KR, Blouin AG, Bradfute SB, Briese T, Brown PA, Buchholz UJ, Buchmeier MJ, Bukreyev A, Burt F, Büttner C, Calisher CH, Cao M, Casas I, Chandran K, Charrel RN, Kumar Chaturvedi K, Chooi KM, Crane A, Dal Bó E, Carlos de la Torre J, de Souza WM, de Swart RL, Debat H, Dheilly NM, Di Paola N, Di Serio F, Dietzgen RG, Digiaro M, Drexler JF, Duprex WP, Dürrwald R, Easton AJ, Elbeaino T, Ergünay K, Feng G, Firth AE, Fooks AR, Formenty PB, Freitas-Astúa J, Gago-Zachert S, Laura García M, García-Sastre A, Garrison AR, Gaskin TR, Gong W, Gonzalez JP, de Bellocq J, Griffiths A, Groschup MH, Günther I, Günther S, Hammond J, Hasegawa Y, Hayashi K, Hepojoki J, Higgins CM, Hongō S, Horie M, Hughes HR, Hume AJ, Hyndman TH, Ikeda K, Jiāng D, Jonson GB, Junglen S, Klempa B, Klingström J, Kondō H, Koonin EV, Krupovic M, Kubota K, Kurath G, Laenen L, Lambert AJ, Lǐ J, Li JM, Liu R, Lukashevich IS, MacDiarmid RM, Maes P, Marklewitz M, Marshall SH, Marzano SY, McCauley JW, Mirazimi A, Mühlberger E, Nabeshima T, Naidu R, Natsuaki T, Navarro B, Navarro JA, Neriya Y, Netesov SV, Neumann G, Nowotny N, Nunes MR, Ochoa-Corona FM, Okada T, Palacios G, Pallás V, Papa A, Paraskevopoulou S, Parrish CR, Pauvolid-Corrêa A, Pawęska JT, Pérez DR, Pfaff F, Plemper RK, Postler TS, Rabbidge LO, Radoshitzky SR, Ramos-González PL, Rehanek M, Resende RO, Reyes CA, Rodrigues TC, Romanowski V, Rubbenstroth D, Rubino L, Runstadler JA, Sabanadzovic S, Sadiq S, Salvato MS, Sasaya T, Schwemmle M, Sharpe SR, Shi M, Shimomoto Y, Kavi Sidharthan V, Sironi M, Smither S, Song JW, Spann KM, Spengler JR, Stenglein MD, Takada A, Takeyama S, Tatara A, Tesh RB, Thornburg NJ, Tian X, Tischler ND, Tomitaka Y, Tomonaga K, Tordo N, Tu C, Turina M, Tzanetakis IE, Maria Vaira A, van den Hoogen B, Vanmechelen B, Vasilakis N, Verbeek M, von Bargen S, Wada J, Wahl V, Walker PJ, Waltzek TB, Whitfield AE, Wolf YI, Xia H, Xylogianni E, Yanagisawa H, Yano K, Ye G, Yuan Z, Zerbini FM, Zhang G, Zhang S, Zhang YZ, Zhao L, Økland AL J Gen Virol 25-Aug-2023
PMCID:PMC10721048
doi:10.1099/jgv.0.001864
PMID:37622664
The Endophytic Microbiome of Wild Grapevines Vitis amurensis Rupr. and Vitis coignetiae Pulliat Growing in the Russian Far East Aleynova OA, Nityagovsky NN, Ananev AA, Suprun AR, Ogneva ZV, Dneprovskaya AA, Beresh AA, Tyunin AP, Dubrovina AS, Kiselev KV Plants (Basel) 15-Aug-2023
PMCID:PMC10460016
doi:10.3390/plants12162952
PMID:37631163
Anthocyanins Reduce Cell Invasion and Migration through Akt/mTOR Downregulation and Apoptosis Activation in Triple-Negative Breast Cancer Cells: A Systematic Review and Meta-Analysis Rabelo AC, Guerreiro CD, Shinzato VI, Ong TP, Noratto G Cancers (Basel) 14-Apr-2023
PMCID:PMC10137251
doi:10.3390/cancers15082300
PMID:37190229
Inhibitory effect of natural extract mixtures on microbial growth and lipid oxidation of sausages during storage Woo SH, Sung JM, Park H, Kim J, Kim YJ, Kim TK, Lee H, Choi YS J Anim Sci Technol 31-Jan-2023
PMCID:PMC10119476
doi:10.5187/jast.2022.e92
PMID:37093932
Dietary Phytochemicals as Potential Chemopreventive Agents against Tobacco-Induced Lung Carcinogenesis Ding Y, Hou R, Yu J, Xing C, Zhuang C, Qu Z Nutrients 17-Jan-2023
PMCID:PMC9920588
doi:10.3390/nu15030491
PMID:36771198
Anticancer applications of phytochemicals in gastric cancer: Effects and molecular mechanism Liang Z, Xu Y, Zhang Y, Zhang X, Song J, Jin J, Qian H Front Pharmacol 12-Jan-2023
PMCID:PMC9877357
doi:10.3389/fphar.2022.1078090
PMID:36712679
A strategy for healthy eating habits of daily fruits revisited: A metabolomics study Song J, Jeong J, Kim EH, Hong YS Curr Res Food Sci 12-Jan-2023
PMCID:PMC9868340
doi:10.1016/j.crfs.2023.100440
PMID:36699116
Anthocyanins: Metabolic Digestion, Bioavailability, Therapeutic Effects, Current Pharmaceutical/Industrial Use, and Innovation Potential Ayvaz H, Cabaroglu T, Akyildiz A, Pala CU, Temizkan R, Ağçam E, Ayvaz Z, Durazzo A, Lucarini M, Direito R, Diaconeasa Z Antioxidants (Basel) 26-Dec-2022
PMCID:PMC9855055
doi:10.3390/antiox12010048
PMID:36670910
Research Progress on Absorption, Metabolism, and Biological Activities of Anthocyanins in Berries: A Review Xue H, Sang Y, Gao Y, Zeng Y, Liao J, Tan J Antioxidants (Basel) 20-Dec-2022
PMCID:PMC9855064
doi:10.3390/antiox12010003
PMID:36670865
Chemopreventive effects and anti-tumorigenic mechanisms of Actinidia arguta, known as sarunashi in Japan toward 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)- induced lung tumorigenesis in a/J mouse Takata J, Miyake N, Saiki Y, Tada M, Sasaki K, Kubo T, Kiura K, Arimoto-Kobayashi S Genes Environ 09-Dec-2022
PMCID:PMC9733242
doi:10.1186/s41021-022-00255-0
PMID:36494703

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1R,8S,9S,16R)-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 131874109 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O 454.50 unknown https://doi.org/10.1007/BF01964921
Ampelopsin F 102004746 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O 454.50 unknown https://doi.org/10.1007/BF01964921
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Methyl 3-(8-acetyloxy-1'-ethyl-4',5,10-trimethyl-3-oxo-6-prop-1-en-2-ylspiro[15-oxatetracyclo[7.4.2.01,10.04,9]pentadecane-13,3'-2,7-dioxabicyclo[2.2.1]heptane]-5-yl)propanoate 101914581 Click to see CCC12CCC(O1)(C3(O2)CCC4(C35CC(=O)C6C4(C(CC(C6(C)CCC(=O)OC)C(=C)C)OC(=O)C)OC5)C)C 558.70 unknown https://doi.org/10.1007/BF01964921
https://doi.org/10.1021/JO00056A016
> Organoheterocyclic compounds / Benzodioxoles
7-(1,3-Benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 75069493 Click to see CC1C(C2(C(C1(C=C(C2=O)OC)CC=C)O)OC)C3=CC4=C(C=C3)OCO4 372.40 unknown https://doi.org/10.1007/BF01964921
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(+/-)-Tricholomalide B 44240398 Click to see CC(C)C1CC(=O)C2=CC(C3(CC(=O)OC3CC12C)C)(C(=C)CO)O 348.40 unknown https://doi.org/10.1007/BF01964921
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-epsilon-Viniferin 5315233 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1007/BF01964921
(1R,2S,3S,9R,10R,17R)-2-(3,5-dihydroxyphenyl)-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 59409135 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1007/BF01964921
(1S,2R,3R,9S,10S,17S)-2-(3,5-dihydroxyphenyl)-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 9917932 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1007/BF01964921
(1S,8S,9R,16S)-8,16-bis(4-hydroxyphenyl)-9-[2-hydroxy-5-[(1S,8S,16S)-4,6,12-trihydroxy-16-(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-8-yl]phenyl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 102120914 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=CC(=CC1=C34)O)C5=CC=C(C=C5)O)C6=CC(=C(C=C6)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O 906.90 unknown https://doi.org/10.3987/COM-97-S62
(1S,8S,9R,16S)-9-[5-[(Z)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-hydroxyphenyl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 102120913 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)C=CC8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1016/S0040-4020(98)00332-9
(3R,4R,10S,11S,18S)-3-(3,5-dihydroxyphenyl)-4,10,18-tris(4-hydroxyphenyl)-5,9-dioxapentacyclo[9.8.1.02,6.08,20.012,17]icosa-1,6,8(20),12(17),13,15-hexaene-14,16-diol 46892318 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=C3C1=C5C(C(OC5=C4)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O 680.70 unknown https://doi.org/10.3987/COM-97-S62
3-(3,5-Dihydroxyphenyl)-4,10,18-tris(4-hydroxyphenyl)-5,9-dioxapentacyclo[9.8.1.02,6.08,20.012,17]icosa-1,6,8(20),12(17),13,15-hexaene-14,16-diol 75228949 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=C3C1=C5C(C(OC5=C4)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O 680.70 unknown https://doi.org/10.3987/COM-97-S62
5-[(2R,3R)-6-[(2R,3R)-5-[(E)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzouran-4-yl]ethenyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzouran-3-yl]-4-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzouran-3-yl]benzene-1,3-diol 16133855 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8=CC(=C9C(C(OC9=C8)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
5-[(2S,3S)-4-[(1S,2S)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 162844411 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C(C(C4=CC=C(C=C4)O)O)O)C5=CC(=CC(=C5)O)O)O 488.50 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
5-[4-[(E)-2-[3-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-4-yl]-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-5-yl]vinyl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrobenzofuran-3-yl]benzene-1,3-diol 122370780 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC5=C(C=C4)OC(C5C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
5-[4-[1,2-Dihydroxy-2-(4-hydroxyphenyl)ethyl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 162844410 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C(C(C4=CC=C(C=C4)O)O)O)C5=CC(=CC(=C5)O)O)O 488.50 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
5-[4-[2-[3-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]ethenyl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 91995939 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC5=C(C=C4)OC(C5C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
5-[6-Hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 366354 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1007/BF01964921
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 2289 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O)O 470.50 unknown https://doi.org/10.1007/BF01964921
8,16-Bis(4-hydroxyphenyl)-9-[2-hydroxy-5-[4,6,12-trihydroxy-16-(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-8-yl]phenyl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 75228950 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=CC(=CC1=C34)O)C5=CC=C(C=C5)O)C6=CC(=C(C=C6)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O 906.90 unknown https://doi.org/10.3987/COM-97-S62
9-[5-[2-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-hydroxyphenyl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 75214669 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)C=CC8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1021/JO00056A016
https://doi.org/10.1007/BF01964921
cis-Vitisin B 163193967 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC5=C(C=C4)OC(C5C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1016/0040-4020(95)00757-Y
Epsilon-viniferin 5281728 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/JO00056A016
https://doi.org/10.1007/BF01964921
Viniferol D 182979 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 680.70 unknown https://doi.org/10.1007/BF01964921
Vitisin A 16131430 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)C=CC8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown https://doi.org/10.1007/BF01964921
https://doi.org/10.1021/JO00056A016

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