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Robynsiophyton vanderystii

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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 UUID643fde6e91622399292329
Scientific name Robynsiophyton vanderystii
Authority R.Wilczek
First published in Bull. Jard. Bot. État Bruxelles23: 128 (1953)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
      • Zambia
    • West-central Tropical Africa
      • Congo
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000211135
Tropicos 13062473
KEW urn:lsid:ipni.org:names:517803-1
The Plant List ild-6221
Open Tree Of Life 431316
NCBI Taxonomy 508336
IPNI 517803-1
GBIF 2945817
EOL 695607
USDA GRIN 437019

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)!
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Title Authors Publication Released IDs
Chemotaxonomic significance of alkaloids in the genus Robynsiophyton Ben-Erik Van Wyk, Gerhard H. Verdoorn Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(91)90086-F

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
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
[(1S,2R,4R,5S,9S,10S)-5-hydroxy-6-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-2-methylbut-2-enoate 14589033 Click to see CC=C(C)C(=O)OC1CC2C3CC(CN2C(=O)C1O)C4CCCCN4C3 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R,13S,17R)-13,17-dihydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-2-methylbut-2-enoate 14589036 Click to see CC=C(C)C(=O)OC1CCN2CC3C4CCC(C(=O)N4CC(C2C1)C3O)O 378.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R,13S,17S)-13,17-dihydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (Z)-2-methylbut-2-enoate 102437380 Click to see CC=C(C)C(=O)OC1CCN2CC3C4CCC(C(=O)N4CC(C2C1)C3O)O 378.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R,13S)-13-hydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (Z)-2-methylbut-2-enoate 102437378 Click to see CC=C(C)C(=O)OC1CCN2CC3CC(C2C1)CN4C3CCC(C4=O)O 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R,17R)-17-hydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-2-methylbut-2-enoate 14589039 Click to see CC=C(C)C(=O)OC1CCN2CC3C4CCCC(=O)N4CC(C2C1)C3O 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R,17S)-17-hydroxy-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (Z)-2-methylbut-2-enoate 102437381 Click to see CC=C(C)C(=O)OC1CCN2CC3C4CCCC(=O)N4CC(C2C1)C3O 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
3beta-Hydroxy-13alpha-tigloyloxylupanine 14589027 Click to see CC=C(C)C(=O)OC1CCN2CC3CC(C2C1)CN4C3CCC(C4=O)O 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(91)90086-F
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(91)90086-F

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