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Rauvolfia biauriculata

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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 UUID643feabc3296f563855525
Scientific name Rauvolfia biauriculata
Authority Müll.Arg.
First published in Linnaea 30: 396 (1860)

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
  • Southern America
    • Caribbean
      • Cuba
      • Haiti
      • Leeward Islands
      • Trinidad-Tobago
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000295004
Tropicos 1802537
INPN 630532
KEW urn:lsid:ipni.org:names:81513-1
The Plant List kew-176813
Open Tree Of Life 837362
NCBI Taxonomy 947876
IPNI 81513-1
GBIF 3169788
EOL 481709
USDA GRIN 414461

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
Alcaloïdes Indoliques de Rauvolfia biauriculata J. Abaul, E. Philogène, P. Bourgeois, G. Mérault, C. Poupat, A. Ahond, P. Potier American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50047A011
Indole alkaloids from Rauvolfia media Christiane Kan, Pierre Potier, Siew-Kwon Kan, Reija Jokela, Mauri Lounasma Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81266-2
Antimycobacterial activity of chemically defined natural substances from the Caribbean flora in Guadeloupe. Rastogi N, Abaul J, Goh KS, Devallois A, Philogène E, Bourgeois P FEMS Immunol Med Microbiol 01-Apr-1998
doi:10.1111/J.1574-695X.1998.TB01136.X
PMID:9626931

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 / Ajmaline-sarpagine alkaloids
(1R,9R,10S,12S,13S,14R,16S,17S,18R)-13-ethyl-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-14,18-diol 98054312 Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C 326.40 unknown https://doi.org/10.1021/NP50047A011
[(1R,10S,12R,13E,14S,16S,17S,18R)-13-ethylidene-14-hydroxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 163067976 Click to see CC=C1C2CC3C4=NC5=CC=CC=C5C46CC(C2C6OC(=O)C)N3C1O 350.40 unknown https://doi.org/10.1021/NP50047A011
[(1R,10S,12R,13R,14S,16S,17S,18R)-13-formyl-14-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 13579079 Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)C=O 350.40 unknown https://doi.org/10.1021/NP50047A011
Ajmaline 6100671 Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C 326.40 unknown https://doi.org/10.1016/S0031-9422(00)81266-2
Vomilenine 11953806 Click to see CC=C1C2CC3C4=NC5=CC=CC=C5C46CC(C2C6OC(=O)C)N3C1O 350.40 unknown https://doi.org/10.1016/S0031-9422(00)81266-2
> Alkaloids and derivatives / Macroline alkaloids
[(1S,12S)-15-ethylidene-7-methoxy-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-13-yl]methanol 138113843 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=C(C=C5)OC)CO 324.40 unknown https://doi.org/10.1016/S0031-9422(00)81266-2
https://doi.org/10.1111/J.1574-695X.1998.TB01136.X
2-[13-(Hydroxymethyl)-7-methoxy-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-15-ylidene]ethanol 163105641 Click to see COC1=CC2=C(C=C1)NC3=C2CC4C(C5CC3N4CC5=CCO)CO 340.40 unknown https://doi.org/10.1016/S0031-9422(00)81266-2
Lochnerine 6436184 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=C(C=C5)OC)CO 324.40 unknown https://doi.org/10.1111/J.1574-695X.1998.TB01136.X
> Alkaloids and derivatives / Yohimbine alkaloids
Corynanthine 92766 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/S0031-9422(00)81266-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl 4a-hydroxy-5-(8-hydroxy-2,6-dimethylocta-2,6-dienoyl)oxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162988114 Click to see CC1CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C(=CCCC(=CCO)C)C 572.60 unknown https://doi.org/10.1021/NP50047A011

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