Parthenocissus laetevirens - Unknown
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Internal ID UUID64404fc896c4d510719387
Scientific name Parthenocissus laetevirens
Authority Rehder
First published in Mitt. Deutsch. Dendrol. Ges. 21: 190 (1912 publ. 1913)

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Language Common/alternative name
Chinese 五叶壁藤
Chinese 大绿藤
Chinese 绿叶地锦
Chinese 绿叶爬山虎
Chinese 青叶爬山虎

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Distribution (via POWO/KEW) Top

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

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Database ID/link to page
World Flora Online wfo-0001145732
Tropicos 34001978
KEW urn:lsid:ipni.org:names:870494-1
The Plant List tro-34001978
Open Tree Of Life 941913
NCBI Taxonomy 926023
IPNI 870494-1
GBIF 4054791
Freebase /m/0gtty_q
EPPO PRTLA
EOL 2907637
Wikipedia Parthenocissus_laetevirens

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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
Response of plant diversity and soil physicochemical properties to different gap sizes in a Pinus massoniana plantation Lyu Q, Liu J, Liu J, Luo Y, Chen L, Chen G, Zhao K, Chen Y, Fan C, Li X PeerJ 21-Sep-2021
PMCID:PMC8462388
doi:10.7717/peerj.12222
PMID:34616636
Seed Geometry in the Vitaceae Cervantes E, Martín-Gómez JJ, Gutiérrez del Pozo D, Tocino Á Plants (Basel) 18-Aug-2021
PMCID:PMC8399696
doi:10.3390/plants10081695
PMID:34451740
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
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
Covalent interaction of ascorbic acid with natural products Kesinger NG, Stevens JF Phytochemistry 28-Oct-2009
PMCID:PMC2787919
doi:10.1016/j.phytochem.2009.09.028
PMID:19875138
Two Novel Antioxidative Stilbene Tetramers from <i>Parthenocissus laetevirens</i> Shan He, Liyan Jiang, Bin Wu, Jing Zhou, Yuan‐Jiang Pan Wiley 10-Sep-2009
doi:10.1002/HLCA.200800371
Preliminary studies on the chemical characterization and antioxidant properties of acidic polysaccharides from Sargassum fusiforme Zhou J, Hu N, Wu YL, Pan YJ, Sun CR J Zhejiang Univ Sci B 01-Sep-2008
PMCID:PMC2528887
doi:10.1631/jzus.B0820025
PMID:18763305
Stilbene oligomers from Parthenocissus laetevirens: isolation, biomimetic synthesis, absolute configuration, and implication of antioxidative defense system in the plant. He S, Wu B, Pan Y, Jiang L J Org Chem 18-Jul-2008
doi:10.1021/JO8001112
PMID:18549269

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
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
5-(3,5-Dihydroxyphenyl)-4-(4-hydroxyphenyl)-4,5-dihydroacephenanthrylene-1,3,9-triol 162881111 Click to see C1=CC(=CC=C1C2C(C3=C4C2=C(C=C(C4=C5C=C(C=CC5=C3)O)O)O)C6=CC(=CC(=C6)O)O)O 452.50 unknown https://doi.org/10.1021/JO8001112
Laetevirenol A 25016671 Click to see C1=CC(=CC=C1C2C(C3=C4C2=C(C=C(C4=C5C=C(C=CC5=C3)O)O)O)C6=CC(=CC(=C6)O)O)O 452.50 unknown https://doi.org/10.1021/JO8001112
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1E,2S,3S)-2-(3,5-dihydroxyphenyl)-1-[[(2R,3R)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 25016921 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C7=C2C(=CC(=C7)O)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO8001112
(1Z,2R,3R)-2-(3,5-dihydroxyphenyl)-1-[[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 163195595 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC7=C(C=C6)OC(C7C8=CC(=CC(=C8)O)O)C9=CC=C(C=C9)O)C1=C2C(=CC(=C1)O)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1002/HLCA.200800371
(1Z,2R,3R)-2-(3,5-dihydroxyphenyl)-1-[[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 163188617 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC7=C(C=C6)OC(C7C8=CC(=CC(=C8)O)O)C9=CC=C(C=C9)O)C1=C2C(=CC(=C1)O)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1002/HLCA.200800371
(1Z,2S,3S)-2-(3,5-dihydroxyphenyl)-1-[[(2R,3R)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 163193965 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C7=C2C(=CC(=C7)O)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO8001112
(1Z,2S,3S)-2-(3,5-dihydroxyphenyl)-1-[[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 25016922 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C7=C2C(=CC(=C7)O)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO8001112
(6R,7R,13S,14S)-7,13-bis(3,5-dihydroxyphenyl)-6,14-bis(4-hydroxyphenyl)-5-oxapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(19),2,4(8),9,11,15,17-heptaene-16,18-diol 25016919 Click to see C1=CC(=CC=C1C2C(C3=CC4=CC5=C(C=C4C6=C3C2=C(C=C6O)O)OC(C5C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 678.70 unknown https://doi.org/10.1021/JO8001112
2-(3,5-Dihydroxyphenyl)-1-[[3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 162915582 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C7=C2C(=CC(=C7)O)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO8001112
2-(3,5-Dihydroxyphenyl)-1-[[3-(3,5-dihydroxyphenyl)-2-[3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydro-1-benzofuran-5-yl]methylidene]-3-(4-hydroxyphenyl)-2,3-dihydroindene-4,6-diol 74955776 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC7=C(C=C6)OC(C7C8=CC(=CC(=C8)O)O)C9=CC=C(C=C9)O)C1=C2C(=CC(=C1)O)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1002/HLCA.200800371
7,13-Bis(3,5-dihydroxyphenyl)-6,14-bis(4-hydroxyphenyl)-5-oxapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(19),2,4(8),9,11,15,17-heptaene-16,18-diol 162990490 Click to see C1=CC(=CC=C1C2C(C3=CC4=CC5=C(C=C4C6=C3C2=C(C=C6O)O)OC(C5C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O 678.70 unknown https://doi.org/10.1021/JO8001112
Laetevirenol C 25016920 Click to see C1=CC(=CC=C1C2C(C(=CC3=CC4=C(C=C3)OC(C4C5=CC(=CC(=C5)O)O)C6=CC=C(C=C6)O)C7=C2C(=CC(=C7)O)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown https://doi.org/10.1021/JO8001112
> Phenylpropanoids and polyketides / Stilbenes
(1E,2S,3S)-2-(3,5-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 71028026 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/JO8001112
(1Z,2S,3S)-2-(3,5-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 95790137 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/JO8001112
2-(3,5-Dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol 73194217 Click to see C1=CC(=CC=C1C=C2C(C(C3=C2C=C(C=C3O)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1021/JO8001112

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