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Internal ID UUID644028e03a535225822491
Scientific name Gnetum leyboldii
Authority Tul.
First published in Ann. Sci. Nat., Bot. , sér. 4, 10: 115 (1858)

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Synonyms Top

Scientific name Authority First published in
Gnemon leyboldii Kuntze Revis. Gen. Pl. 2: 796. 1891 [5 Nov 1891]
Gnetum dioicum Leyb. ex Tul. Ann. Sci. Nat., Bot. , sér. 4, 10: 115 (1858)
Gnetum paraense Huber Bol. Mus. Paraense Hist. Nat. Ethnogr. 3: 403 (1902)
Thoa leyboldii (Tul.) Doweld Turczaninowia 3(4): 33 (2000).

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Subspecies (abbr. subsp./ssp.) 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
  • Southern America
    • Brazil
      • Brazil North
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000795625
Tropicos 14300033
KEW urn:lsid:ipni.org:names:111368-2
The Plant List kew-334154
Open Tree Of Life 425764
NCBI Taxonomy 29812
IUCN Red List 194946
IPNI 111368-2
iNaturalist 135985
GBIF 2653166
EOL 1156254

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
Leaf-cutter ants – mycorrhizal fungi: observations and research questions from an unexpected mutualism Allen MF, Shulman H, Rundel PW, Harmon TC, Aronson EL Front Fungal Biol 16-Nov-2023
PMCID:PMC10687443
doi:10.3389/ffunb.2023.1241916
PMID:38033376
CAM photosynthesis: the acid test Winter K, Smith JA New Phytol 05-Nov-2021
PMCID:PMC9298356
doi:10.1111/nph.17790
PMID:34637529
Resveratrol oligomer structure in Dipterocarpaceaeous plants Ito T J Nat Med 30-Apr-2020
PMCID:PMC7456419
doi:10.1007/s11418-020-01412-x
PMID:32356240
Significance of Photosynthetic Characters in the Evolution of Asian Gnetum (Gnetales) Deng N, Hou C, Liu C, Li M, Bartish I, Tian Y, Chen W, Du C, Jiang Z, Shi S Front Plant Sci 05-Feb-2019
PMCID:PMC6370715
doi:10.3389/fpls.2019.00039
PMID:30804953
Chemistry and Biology of Resveratrol-Derived Natural Products Keylor MH, Matsuura BS, Stephenson CR Chem Rev 02-Apr-2015
PMCID:PMC4566929
doi:10.1021/cr500689b
PMID:25835567
The influence of Brazilian plant extracts on Streptococcus mutans biofilm BARNABÉ M, SARACENI CH, DUTRA-CORREA M, SUFFREDINI IB J Appl Oral Sci 01-Sep-2014
PMCID:PMC4245747
doi:10.1590/1678-775720140085
PMID:25466471
Gnetins: Resveratrol Oligomers From Gnetum Species Arlete P. Lins, M. Nilce De S. Ribeiro, Otto R. Gottlieb, Hugo E. Gottlieb American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50024A022

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 / Anthracenes / Anthraquinones
1,2,3,5,8-Pentamethoxy-6-methylanthracene-9,10-dione 15118838 Click to see CC1=CC(=C2C(=C1OC)C(=O)C3=CC(=C(C(=C3C2=O)OC)OC)OC)OC 372.40 unknown https://doi.org/10.1021/NP50024A022
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-[(2R,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,3-diol 21575178 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=C(C=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 470.50 unknown https://doi.org/10.1021/NP50024A022
4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-4-hydroxy-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,3-diol 102377293 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=C(C=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 470.50 unknown https://doi.org/10.1021/NP50024A022
5-[(2R,3R)-4-hydroxy-6-[(2R,3S)-4-hydroxy-2-(4-hydroxyphenyl)-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 154496689 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=C6C(C(OC6=C5)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O)O)O 680.70 unknown https://doi.org/10.1021/NP50024A022
5-[(2S,3S)-4-hydroxy-6-[(2S,3S)-4-hydroxy-2-(4-hydroxyphenyl)-6-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 102377294 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=C6C(C(OC6=C5)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O)O)O 680.70 unknown https://doi.org/10.1021/NP50024A022
5-[4-Hydroxy-6-[4-hydroxy-2-(4-hydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 76028173 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=C6C(C(OC6=C5)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O)O)O 680.70 unknown https://doi.org/10.1021/NP50024A022
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1R,5S,6S,7S)-6-(3,5-dihydroxyphenyl)-7-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]bicyclo[3.2.1]oct-3-ene-2,8-dione 102522790 Click to see C1=CC(=CC=C1C=CC2=CC(=O)C3C(C(C2C3=O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O 454.50 unknown https://doi.org/10.1021/NP50024A022
(1S,4R,7S,8R)-7-(3,5-dihydroxyphenyl)-1-hydroxy-8-(4-hydroxyphenyl)-5-[(E)-2-(4-hydroxyphenyl)ethenyl]bicyclo[2.2.2]oct-5-en-2-one 163105075 Click to see C1C2C(C(C(C1=O)(C=C2C=CC3=CC=C(C=C3)O)O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O 456.50 unknown https://doi.org/10.1021/NP50024A022
6-(3,5-Dihydroxyphenyl)-7-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]bicyclo[3.2.1]oct-3-ene-2,8-dione 5090127 Click to see C1=CC(=CC=C1C=CC2=CC(=O)C3C(C(C2C3=O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O 454.50 unknown https://doi.org/10.1021/NP50024A022
8-(3,5-Dihydroxyphenyl)-4-hydroxy-7-(4-hydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]bicyclo[2.2.2]oct-5-en-2-one 162820481 Click to see C1C(=O)C2C(C(C1(C=C2C=CC3=CC=C(C=C3)O)O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O 456.50 unknown https://doi.org/10.1021/NP50024A022
Gnetin A 5281714 Click to see C1=CC(=CC=C1C=CC2=CC(=O)C3C(C(C2C3=O)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O)O 454.50 unknown https://doi.org/10.1021/NP50024A022

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