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Rauvolfia volkensii

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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
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Details Top

Internal ID UUID643feac28462a425001493
Scientific name Rauvolfia volkensii
Authority Stapf
First published in Fl. Trop. Afr. 6(1): 116 (1902)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rauvolfia oreogiton Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 8: 287 (1923)
Tabernaemontana volkensii K.Schum. Pflanzenw. Ost-Afrikas , C: 316 (1895)

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-0000295212
Tropicos 50177388
KEW urn:lsid:ipni.org:names:81672-1
The Plant List kew-177000
Open Tree Of Life 382822
NCBI Taxonomy 947905
IUCN Red List 158214
IPNI 81672-1
iNaturalist 133419
GBIF 3616192

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
A Picrinine N-Methyltransferase Belongs to a New Family of γ-Tocopherol-Like Methyltransferases Found in Medicinal Plants That Make Biologically Active Monoterpenoid Indole Alkaloids Levac D, Cázares P, Yu F, De Luca V Plant Physiol 04-Feb-2016
PMCID:PMC4825134
doi:10.1104/pp.15.01813
PMID:26848097
Alkaloid distribution in some african rauvolfia species. Court WE Planta Med 01-Aug-1983
doi:10.1055/S-2007-969925
PMID:17404988
The alkaloids of Rauwolfia volkensii. Akinloye BA, Court WE J Ethnopharmacol 01-Jul-1981
doi:10.1016/0378-8741(81)90022-2
PMID:7253681

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
(13-Ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-yl) acetate 631680 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4OC(=O)C 350.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
(1R,10S,13E,16S)-13-ethylidene-8-methyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-trien-18-ol 118701737 Click to see CC=C1CN2C3CC1C4C2CC5(C3N(C6=CC=CC=C65)C)C4O 308.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
[(1R,10R,16S)-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 138113842 Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)C=O 350.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
17-O-acetylajmaline 15942893 Click to see CCC1C2CC3C4C5(CC(C2C5OC(=O)C)N3C1O)C6=CC=CC=C6N4C 368.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Ajmaline 6100671 Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C 326.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
Aritmina 2073 Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C 326.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
Nortetraphyllicine 133561861 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=CC=CC=C65)C4O 294.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
Raucaffrinoline 56927714 Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)CO 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> Alkaloids and derivatives / Aporphines
1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol 23930365 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)O)OC)OC 327.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (19E)-16-formylcoryn-19-en-17-oate 5280491 Click to see CC=C1CN2CCC3=C(C2CC1C(C=O)C(=O)OC)NC4=CC=CC=C34 352.40 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
methyl (Z)-2-[(3E)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxyprop-2-enoate 10043592 Click to see CC=C1CN2CCC3=C(C2CC1C(=CO)C(=O)OC)NC4=CC=CC=C34 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
> Alkaloids and derivatives / Hasubanan alkaloids
(1S,11R,13S,14S,15R,19R)-14,15-dimethoxy-20-methyl-19-(2-oxopropyl)-5,7,21-trioxa-20-azahexacyclo[11.4.3.111,14.01,13.02,10.04,8]henicosa-2,4(8),9-trien-16-one 44577171 Click to see CC(=O)CC1CC23CC(=O)C(C4(C2(N1C)CC(O4)C5=CC6=C(C=C35)OCO6)OC)OC 429.50 unknown https://doi.org/10.1055/S-2007-969925
> Alkaloids and derivatives / Macroline alkaloids
(16S)-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-17-ol 6325796 Click to see CC1C2COC(C3C2CC4N1C3CC5=C4NC6=CC=CC=C56)O 310.40 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
(1R,12S)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4(9),5,7-tetraen-7-ol 137795317 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=C4C=C(C=C5)O)CO 310.40 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
(2S,13S,15R,20S,21S)-21-methyl-18-oxa-1,11-diazahexacyclo[11.8.0.02,16.04,12.05,10.015,20]henicosa-4(12),5,7,9-tetraen-17-ol 102004388 Click to see CC1C2COC(C3C2CC4N1C3CC5=C4NC6=CC=CC=C56)O 310.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
[(1S,14R)-15-formyl-16-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methyl acetate 102063626 Click to see CC1C(C2CC3N1C(C2COC(=O)C)CC4=C3NC5=CC=CC=C45)C=O 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716693 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Tombozine 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> Alkaloids and derivatives / Pleiocarpaman alkaloids
Pleiocarpamine 5385014 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
https://doi.org/10.1055/S-2007-969925
> Alkaloids and derivatives / Strychnos alkaloids
Akuammicine 10314057 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Aricine 251575 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=C(C=C5)OC 382.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Isoreserpiline 161345 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Melinonine A 20054968 Click to see CC1C2C[N+]3(CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45)C 367.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
methyl (1S,15S,19S,20S)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 120635 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Methyl 18-hydroxy-7-methoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4(9),5,7-tetraene-19-carboxylate 163049844 Click to see CC1C2CN3CCC4=C(C3CC2C(C(O1)O)C(=O)OC)NC5=C4C=C(C=C5)OC 400.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Rauwolscine 643606 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Rescinnamine 5280954 Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C=CC6=CC(=C(C(=C6)OC)OC)OC 634.70 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
Reserpiline 67228 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
Reserpine 5770 Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC 608.70 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> 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/10.1016/0378-8741(81)90022-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 44584413 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)O)O)C)C)C)CO)O)O 675.90 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
17-Ethyl-3-methyl-3,15,20-triazapentacyclo[10.7.1.02,10.04,9.013,18]icosa-2(10),4,6,8,13(18),14,16-heptaene 12443111 Click to see CCC1=CN=CC2=C1CC3C4=C(CC2N3)C5=CC=CC=C5N4C 303.40 unknown https://doi.org/10.1016/0378-8741(81)90022-2
2H,12H-6,12a-Epoxy-2,7a-methanoindolo(2,3-a)quinolizine-14-carboxylic acid, 3-ethylidene-1,3,4,6,7,12b-hexahydro-9,10-dimethoxy-, methyl ester, (2R,3E,6S,7aR,12aR,12bS,14R)- 6437858 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC(=C(C=C64)OC)OC)OC2C5)C(=O)OC 398.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
Alstonine 441979 Click to see CC1C2CN3C=CC4=C5C=CC=CC5=NC4=C3CC2C(=CO1)C(=O)OC 348.40 unknown https://doi.org/10.1055/S-2007-969925
https://doi.org/10.1016/0378-8741(81)90022-2
CID 5478940 5478940 Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC 338.40 unknown https://doi.org/10.1055/S-2007-969925
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/10.1055/S-2007-969925
Methyl 14-ethylidene-5,6-dimethoxy-2-methyl-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate 78410245 Click to see CC=C1CN2C3CC1C(C45C3(N(C6=CC(=C(C=C64)OC)OC)C)OC2C5)C(=O)OC 412.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2
> Organoheterocyclic compounds / Indolizidines
Carapanaubine 442037 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC(=C(C=C5NC4=O)OC)OC 428.50 unknown https://doi.org/10.1016/0378-8741(81)90022-2

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