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Rauvolfia mannii

Rauvolfia mannii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643feabe39813989916248
Scientific name Rauvolfia mannii
Authority Stapf
First published in Bull. Misc. Inform. Kew 1894: 21 (1894)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rauvolfia cardiocarpa K.Schum. Nat. Pflanzenfam. 4(2): 154 (1895)
Rauvolfia cumminsii Stapf Fl. Trop. Afr. 4(1): 114 (1902)
Rauvolfia ivorensis A.Chev. Explor. Bot. Afrique Occ. Franç. 1: 412 (1920)
Rauvolfia liberiensis Stapf Fl. Trop. Afr. 4(1): 601 (1904)
Rauvolfia longeacuminata De Wild. & T.Durand Bull. Soc. Roy. Bot. Belgique , Compt.-Rend. 38: 205 (1899)
Rauvolfia obscura K.Schum. Nat. Pflanzenfam. 4(2): 154 (1893)
Rauvolfia preussii K.Schum. Pflanzenw. Ost-Afrikas , C: 318 (1895)
Rauvolfia rosea K.Schum. Pflanzenw. Ost-Afrikas , C: 317 (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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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
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Angola
      • Malawi
    • West Tropical Africa
      • Ghana
      • Ivory Coast
      • Liberia
      • Nigeria
    • West-central Tropical Africa
      • Burundi
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000295086
Tropicos 1800039
KEW urn:lsid:ipni.org:names:81579-1
The Plant List kew-176888
Open Tree Of Life 1050235
NCBI Taxonomy 4062
IUCN Red List 144310524
IPNI 81579-1
GBIF 3617543
Freebase /m/0whzk_c
USDA GRIN 451509
Wikipedia Rauvolfia_mannii

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
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Traditional knowledge, use and conservation of plants by the communities of Tharaka-Nithi County, Kenya Kathambi V, Mutie FM, Rono PC, Wei N, Munyao JN, Kamau P, Gituru RW, Hu GW, Wang QF Plant Divers 30-Dec-2020
PMCID:PMC7936104
doi:10.1016/j.pld.2020.12.004
PMID:33733015
In silico analysis and homology modeling of strictosidine synthase involved in alkaloid biosynthesis in catharanthus roseus Sahay A, Piprodhe A, Pise M J Genet Eng Biotechnol 28-Aug-2020
PMCID:PMC7455670
doi:10.1186/s43141-020-00049-3
PMID:32857261
First large-scale ethnobotanical survey in the province of Uíge, northern Angola Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C J Ethnobiol Ethnomed 25-Jul-2018
PMCID:PMC6060550
doi:10.1186/s13002-018-0238-3
PMID:30045744
Class II Cytochrome P450 Reductase Governs the Biosynthesis of Alkaloids Parage C, Foureau E, Kellner F, Burlat V, Mahroug S, Lanoue A, Dugé de Bernonville T, Londono MA, Carqueijeiro I, Oudin A, Besseau S, Papon N, Glévarec G, Atehortùa L, Giglioli-Guivarc’h N, St-Pierre B, Clastre M, O’Connor SE, Courdavault V Plant Physiol 29-Sep-2016
PMCID:PMC5100751
doi:10.1104/pp.16.00801
PMID:27688619
The Evolution of Function in Strictosidine Synthase-like Proteins Hicks MA, Barber AE II, Giddings LA, Caldwell J, O’Connor SE, Babbitt PC Proteins 21-Sep-2011
PMCID:PMC3561908
doi:10.1002/prot.23135
PMID:21948213
The Alkaloids of Rauwolfia cumminsii. M. Iwu, W. Court Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1097468
The Structure of Rauvolfia serpentina Strictosidine Synthase Is a Novel Six-Bladed β-Propeller Fold in Plant Proteins Ma X, Panjikar S, Koepke J, Loris E, Stöckigt J Plant Cell 01-Apr-2006
PMCID:PMC1425862
doi:10.1105/tpc.105.038018
PMID:16531499
Improved production of raucaffricine by cultivated Rauwolfia cells Helmut Schübel, Carl Michael Ruyter, Joachim Stöckigt Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80038-X
Alkaloid distribution in some african rauvolfia species. Court WE Planta Med 01-Aug-1983
doi:10.1055/S-2007-969925
PMID:17404988

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
(9R,12R,13S,14R,16S,17S,18R)-13-ethyl-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-14,18-diol 102271367 Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4 312.40 unknown https://doi.org/10.1055/S-2007-969925
(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/10.1055/S-0028-1097468
13-Ethylidene-4-methoxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-18-one 163045391 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=C5C=C(C=C6)OC)C4=O 322.40 unknown https://doi.org/10.1055/S-0028-1097468
Nortetraphyllicine 133561861 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=CC=CC=C65)C4O 294.40 unknown https://doi.org/10.1055/S-0028-1097468
Seredamine, 1-demethyl- 5379001 Click to see CC=C1CN2C3CC1C4C2CC5(C3NC6=C5C=CC=C6OC)C4O 324.40 unknown https://doi.org/10.1055/S-0028-1097468
> 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-0028-1097468
(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/10.1055/S-0028-1097468
Tombozine 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1055/S-0028-1097468
> 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/10.1055/S-0028-1097468
Aricine 251575 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=C(C=C5)OC 382.50 unknown https://doi.org/10.1055/S-0028-1097468
methyl (1S,15R,16S,18R,19R,20S)-18-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraene-19-carboxylate 14413744 Click to see CC1C2CN3CCC4=C(C3CC2C(C(O1)O)C(=O)OC)NC5=CC=CC=C45 370.40 unknown https://doi.org/10.1055/S-0028-1097468
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-0028-1097468
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-0028-1097468
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1055/S-0028-1097468
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 2-[[3-[(3,3-dimethyloxiran-2-yl)methyl]-4-hydroxyphenyl]methyl]-4-hydroxy-3-(4-hydroxyphenyl)-5-oxofuran-2-carboxylate 16681743 Click to see CC1(C(O1)CC2=C(C=CC(=C2)CC3(C(=C(C(=O)O3)O)C4=CC=C(C=C4)O)C(=O)OC)O)C 440.40 unknown https://doi.org/10.1016/0031-9422(89)80038-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[(1S,3R,5R,6aS,7S,8S,9R,10R,10aS)-1,3,10-triacetyloxy-5-methoxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-9-yl] acetate 163014705 Click to see CC1C(C(C23C(C1(C)CC=C(C)C=C)CC(C=C2C(OC3OC(=O)C)OC(=O)C)OC)OC(=O)C)OC(=O)C 548.60 unknown https://doi.org/10.1055/S-0028-1097468
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-[(2R,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]ethanol 101287731 Click to see C=CC1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1055/S-0028-1097468
2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 21595545 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1055/S-2007-969925

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