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Vitis chunganensis

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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 UUID64404fcea2caf924678883
Scientific name Vitis chunganensis
Authority Hu
First published in J. Arnold Arbor. 6: 143 (1925)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 小果野葡萄藤
Chinese 东南葡萄
Chinese 東南葡萄

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001145973
Tropicos 34002339
KEW urn:lsid:ipni.org:names:870682-1
The Plant List tro-34002339
Open Tree Of Life 816134
NCBI Taxonomy 1046259
IPNI 870682-1
GBIF 5658551
Freebase /m/0c011r3
USDA GRIN 456057
Wikipedia Vitis_chunganensis

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
Acuminatol and Other Antioxidative Resveratrol Oligomers from the Stem Bark of Shorea acuminata Muhammad N, Din LB, Sahidin I, Hashim SF, Ibrahim N, Zakaria Z, Yaacob WA Molecules 30-Jul-2012
PMCID:PMC6268933
doi:10.3390/molecules17089043
PMID:22847143
Chunganenol: an unusual antioxidative resveratrol hexamer from Vitis chunganensis. He S, Jiang L, Wu B, Li C, Pan Y J Org Chem 16-Oct-2009
doi:10.1021/JO901354P
PMID:19757796

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
> Organoheterocyclic compounds / Tetrahydrofurans
11-Hydroxy-5,5,8-trimethyl-10-oxatricyclo[7.2.1.03,7]dodec-2-ene-2-carbaldehyde 78148074 Click to see CC1C2CC(C(O2)O)C(=C3C1CC(C3)(C)C)C=O 250.33 unknown https://doi.org/10.1021/JO901354P
> 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/10.1021/JO901354P
(1S,8S,9R,16S)-8,16-bis(4-hydroxyphenyl)-9-[(1S,8S,9R,16S)-4,6,12-trihydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 21669381 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)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)O 906.90 unknown https://doi.org/10.1021/JO901354P
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 73800061 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1021/JO901354P
3-[2-[[4-[5-(3,5-Dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-3-yl]-2,6-dihydroxyphenyl]methyl]-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 162869508 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=C(C(=C6)O)CC7=C(C=C(C=C7O)O)C8C(C9C(C1=C(C=C(C=C1O)O)C1C(OC2=C1C9=C8C(=C2)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 1373.40 unknown https://doi.org/10.1021/JO901354P
5-[(2S,3S,5S,6R)-3-(3,5-dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-5-yl]benzene-1,3-diol 163186864 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO901354P
5-[3-(3,5-Dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-5-yl]benzene-1,3-diol 73091958 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO901354P
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/10.1021/JO901354P
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/JO901354P
Hopeaphenol 495605 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)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)O 906.90 unknown https://doi.org/10.1021/JO901354P
Pauciflorol B 21674271 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1021/JO901354P
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/10.1021/JO901354P
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1021/JO901354P
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1021/JO901354P

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