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Rauvolfia bahiensis

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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 UUID643feabb8cac3982618632
Scientific name Rauvolfia bahiensis
Authority A.DC.
First published in Prodr. 8: 339 (1844)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000294997
Tropicos 1800501
KEW urn:lsid:ipni.org:names:81511-1
The Plant List kew-176807
Open Tree Of Life 837358
NCBI Taxonomy 947874
IUCN Red List 148752461
IPNI 81511-1
GBIF 3618452

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
Alkaloids as Inhibitors of Malate Synthase from Paracoccidioides spp.: Receptor-Ligand Interaction-Based Virtual Screening and Molecular Docking Studies, Antifungal Activity, and the Adhesion Process Costa FG, Neto BR, Gonçalves RL, da Silva RA, de Oliveira CM, Kato L, Freitas CD, Giannini MJ, da Silva JD, Soares CM, Pereira M Antimicrob Agents Chemother 14-Aug-2015
PMCID:PMC4538557
doi:10.1128/AAC.04711-14
PMID:26124176
Indole alkaloids from Rauvolfia bahiensis A.DC. (Apocynaceae). Kato L, Marques Braga R, Koch I, Sumiko Kinoshita L Phytochemistry 01-Jun-2002
doi:10.1016/S0031-9422(02)00122-X
PMID:12031452

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
(13Z)-13-ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-one 6325046 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4=O 306.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(17R,19E)-19,20-Didehydro-12-methoxyajmalan-17-ol 162965316 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=C5C=CC=C6OC)C)C4O 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(1R,9R,10S,12R,13E,16S,17S,18R)-13-ethylidene-6-methoxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-18-ol 162939665 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=C5C=CC=C6OC)C4O 324.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(1R,9R,10S,12R,13E,16S,17S)-13-ethylidene-6-methoxy-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-18-one 162843588 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=C5C=CC=C6OC)C)C4=O 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(1R,9R,10S,12R,13E,16S,17S)-13-ethylidene-6-methoxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-18-one 163092668 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=C5C=CC=C6OC)C4=O 322.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(1R,9R,12S,13E,17S)-13-ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-one 163186402 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4=O 306.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(9R,12R,13Z,16S,17S)-13-ethylidene-6-methoxy-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-18-one 101967087 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=C5C=CC=C6OC)C)C4=O 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
[(10S,12S,13E,16S,18R)-13-ethylidene-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 91820597 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56 334.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
[(1R,10R,16S)-13-ethylidene-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate 138113894 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56 334.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
13-Ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-one 78384781 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4=O 306.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
21-Deoxyvomilenine 124389565 Click to see CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56 334.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
3Dff5qdk46 15599715 Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)CO 352.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
Demethoxypurpeline 163184341 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4=O 306.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
Raucaffrinoline 56927714 Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)CO 352.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
Seredamine, 1-demethyl- 5379001 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=C5C=CC=C6OC)C4O 324.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
> Alkaloids and derivatives / Macroline alkaloids
(12S,13R,14S,15E)-15-ethylidene-5-methoxy-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraene-13-carbaldehyde 163193299 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=C4C=CC=C5OC)C)C=O 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(12S,13R,14S,15E)-15-ethylidene-5-methoxy-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraene-13-carbaldehyde 163195014 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=CC=C5OC)C=O 322.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(1S,12S,13R,14S,15E)-15-ethylidene-5-methoxy-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraene-13-carbaldehyde 162995542 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=C4C=CC=C5OC)C)C=O 336.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
(E)-16-Epi-normacusine B 5460548 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
[(1S,12S,13R,14R,15E)-15-ethylidene-5-methoxy-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-13-yl]methanol 11244657 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=C4C=CC=C5OC)C)CO 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
[(1S,14R,15Z)-15-ethylidene-5-methoxy-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-13-yl]methanol 102357238 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=C4C=CC=C5OC)C)CO 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
12-Methoxy-vellosimine 163184343 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=CC=C5OC)C=O 322.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
12-Methoxyvellosimine 101190312 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=CC=C5OC)C=O 322.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
Lochnerine 6436184 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=C(C=C5)OC)CO 324.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
Tombozine 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(4S,6S)-6-[(2R,3R)-4-(3,4-dimethoxyphenyl)-3-hydroxybutan-2-yl]-4-methoxy-6-prop-2-enylcyclohex-2-en-1-one 163190867 Click to see CC(C(CC1=CC(=C(C=C1)OC)OC)O)C2(CC(C=CC2=O)OC)CC=C 374.50 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
CID 5478940 5478940 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
methyl (1R,9R,11S,14E,15R,17S,19S)-14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate 85473463 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X
methyl (1R,9R,11S,14E,17S)-14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate 102004475 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(02)00122-X

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