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Cyphostemma crotalarioides

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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 UUID64401520cb6ff840436398
Scientific name Cyphostemma crotalarioides
Authority (Planch.) Desc. ex Wild & R.B.Drumm.
First published in Fl. Zambes. 2: 466 (1966)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cissus crotalarioides Planch. Monogr. Phan. 5: 577 (1887)
Cissus variifolia Gilg & M.Brandt Bot. Jahrb. Syst. 46: 452, 500 (1912)
Cyphostemma variifolium (Baker) Desc. Naturalia Monspel., Sér. Bot. 18: 230 (1967)
Vitis variifolia Baker Bull. Misc. Inform. Kew 1897: 248 (1897)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Burkina
      • Ivory Coast
      • Mali
      • Nigeria
      • Senegal
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000634504
Tropicos 34000727
KEW urn:lsid:ipni.org:names:870208-1
The Plant List kew-2752696
Open Tree Of Life 6045084
IPNI 870208-1
iNaturalist 701190
GBIF 4052519
Freebase /m/0111354l
EPPO CWMCR
EOL 5540667
Wikipedia Cyphostemma_crotalarioides

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)!
Title Authors Publication Released IDs
Cis ε-viniferin: A New Antifungal Resveratrol Dehydrodimer from Cyphostemma crotalarioides Roots A. E. A. Bala, A. Kollmann, P.-H. Ducrot, A. Majira, L. Kerhoas, P. Leroux, R. Delorme, J. Einhorn Wiley 01-May-2008
doi:10.1111/J.1439-0434.2000.TB04620.X
Antifungal activity of resveratrol oligomers from<i>Cyphostemma crotalarioides</i> Adil E Bala, Albert Kollmann, Paul-Henri Ducrot, Amel Majira, Lucien Kerhoas, Robert Delorme, Jacques Einhorn Wiley 28-Jan-2005
doi:10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae) Paul-Henri Ducrot, Albert Kollmann, Adil E. Bala, Amel Majira, Lucien Kerhoas, Robert Delorme, Jacques Einhorn Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(98)02207-2

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Indanes
5,10-Bis-(4-hydroxy-phenyl)-4b,5,9b,10-tetrahydro-indeno[2,1-a]indene-1,3,6,8-tetraol 57518717 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O 454.50 unknown https://doi.org/10.1016/S0040-4039(98)02207-2
Pallidol 484757 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O 454.50 unknown https://doi.org/10.1111/J.1439-0434.2000.TB04620.X
https://doi.org/10.1016/S0040-4039(98)02207-2
https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
> 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/10.1111/J.1439-0434.2000.TB04620.X
(Z)-epsilon-Viniferin 11236373 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/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
https://doi.org/10.1111/J.1439-0434.2000.TB04620.X
5-[(2R,3R)-4-hydroxy-6-[(2S,3R)-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 163187947 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/10.1016/S0040-4039(98)02207-2
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/10.1016/S0040-4039(98)02207-2
https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
https://doi.org/10.1111/J.1439-0434.2000.TB04620.X
5-[4-Hydroxy-2-(4-hydroxyphenyl)-6-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 73816509 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O 454.50 unknown https://doi.org/10.1016/S0040-4039(98)02207-2
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/10.1016/S0040-4039(98)02207-2
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/10.1016/S0040-4039(98)02207-2
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/10.1016/S0040-4039(98)02207-2
https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
Gnetin C 21633857 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O 454.50 unknown https://doi.org/10.1016/S0040-4039(98)02207-2
Gnetinc 100920621 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O 454.50 unknown https://doi.org/10.1016/S0040-4039(98)02207-2
https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
https://doi.org/10.1111/J.1439-0434.2000.TB04620.X
> 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/10.1016/S0040-4039(98)02207-2
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/10.1016/S0040-4039(98)02207-2
parthenocissin A 15411553 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/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z
https://doi.org/10.1016/S0040-4039(98)02207-2
quadrangularin A 5318096 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/10.1016/S0040-4039(98)02207-2
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1111/J.1439-0434.2000.TB04620.X
https://doi.org/10.1016/S0040-4039(98)02207-2
https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<206::AID-PS871>3.0.CO;2-Z

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