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Rauvolfia sumatrana

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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 UUID643feac222747992391208
Scientific name Rauvolfia sumatrana
Authority Jack
First published in Malayan Misc. 1(5): 22 (1820)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rauvolfia blumeana Valeton ex Koord.-Schum. Syst. Verz. 1(247): 176 (1912)
Rauvolfia madurensis Burck ex Koord.-Schum. Syst. Verz. 1(247): 174 (1912)
Rauvolfia palawanensis Elmer Leafl. Philipp. Bot. 4: 1162 (1912)
Rauvolfia reflexa Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 3: 329 (1852)
Rauvolfia samarensis Merr. Philipp. J. Sci., C 4: 316 (1909)
Rauvolfia spectabilis Boerl. Handl. Fl. Ned. Ind. 2: 393 (1899)
Rauvolfia sumatrana var. longifolia Blume Bijdr. Fl. Ned. Ind. 1034. 1826
Cyrtosiphonia madurensis Teijsm. & Binn. Cat. Hort. Bot. Bogor. : 125 (1866)
Cyrtosiphonia reflexa Miq. Fl. Ned. Ind. 2: 402 (1857)
Cyrtosiphonia spectabilis Miq. Fl. Ned. Ind. 2: 402 (1857)
Cyrtosiphonia sumatrana Miq. Fl. Ned. Ind. 2: 401 (1857)
Rauvolfia madurensis (Teijsm. & Binn.) Boerl. Handl. Fl. Ned. Ind. 2: 393 1899

Common names Top

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Language Common/alternative name
mad polay lalakè'
Chinese 苏门答腊萝芙木
Chinese 巴拉望萝芙木
Chinese 苏门答腊鬼椒
Chinese 蘇門答臘蘿芙木

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
  • Asia-tropical
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000295190
Tropicos 1802566
KEW urn:lsid:ipni.org:names:81660-1
The Plant List kew-176982
Open Tree Of Life 638940
NCBI Taxonomy 478094
IUCN Red List 156220634
IPNI 81660-1
GBIF 3616339
Freebase /m/0wx_3t0
USDA GRIN 432079
Wikipedia Rauvolfia_sumatrana

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
Anti-aging and antioxidant of four traditional malaysian plants using simplex centroid mixture design approach Ranneh Y, Abu Bakar MF, Ismail NA, Kormin F, Mohamed M, Md Akim A, Isha A Saudi J Biol Sci 22-Jul-2021
PMCID:PMC8626306
doi:10.1016/j.sjbs.2021.07.048
PMID:34866970
Novel Indole Alkaloids from the Leaves of Rauwolfia sumatrana JACK. in Thailand. Sanan SUBHADHIRASAKUL, Hiromitsu TAKAYAMA, Norio AIMI, Dhavadee PONGLUX, Shin-ichiro SAKAI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.42.1427
Screening of α-Glucosidase Inhibitory Activity from Some Plants of Apocynaceae, Clusiaceae, Euphorbiaceae, and Rubiaceae Elya B, Basah K, Mun'im A, Yuliastuti W, Bangun A, Septiana EK J Biomed Biotechnol 07-Dec-2011
PMCID:PMC3236488
doi:10.1155/2012/281078
PMID:22187534

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,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/10.1248/CPB.42.1427
[(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/10.1248/CPB.42.1427
methyl (1R,9R,12R,13E,18S)-13-ethylidene-5-[(1R,9R,10S,12R,13E,16S,17R)-13-ethylidene-5-methoxy-8-methyl-18-oxo-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2(7),3,5-trien-4-yl]-4-oxo-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,5,7-triene-18-carboxylate 102274937 Click to see CC=C1CN2CCC34C2(CCC1C3C(=O)OC)N=C5C4=CC(=O)C(=C5)C6=CC7=C(C=C6OC)N(C8C79CC1C(C9=O)C2CC8N1CC2=CC)C 672.80 unknown https://doi.org/10.1248/CPB.42.1427
> Alkaloids and derivatives / Akuammilan and related alkaloids
Methyl 13-ethylidene-5-methoxy-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2(7),3,5,8-tetraene-18-carboxylate 74030970 Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=C4C=CC(=C5)OC)C(=O)OC 352.40 unknown https://doi.org/10.1248/CPB.42.1427
> Alkaloids and derivatives / Harmala alkaloids
Harmalan 160510 Click to see CC1=NCCC2=C1NC3=CC=CC=C23 184.24 unknown https://doi.org/10.1248/CPB.42.1427
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1248/CPB.42.1427
> 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/10.1248/CPB.42.1427
(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/10.1248/CPB.42.1427
> Alkaloids and derivatives / Strychnos alkaloids
Curan-17-oic acid, 2,16-didehydro-19,20-dihydroxy-, methyl ester, (19S)- 614664 Click to see CC(C1(CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O)O 356.40 unknown https://doi.org/10.1248/CPB.42.1427
> 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/10.1248/CPB.42.1427
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl (methylthio)acetate 78199 Click to see CCOC(=O)CSC 134.20 unknown https://doi.org/10.1248/CPB.42.1427
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
3-Cylcohexylpropanoic acid [(S)-2-(3,5-difluorophenyl)-1-((3S,9S,13S,15R,19S,22S)-15,19-Dimethyl-2,8,12,18,21-pentaoxo-11-oxa-1,7,17,20-tetraaza-tetracyclo[20.4.0.03,7.013,17] hexacos-9-ylcarbamoyl)-ethyl]-amide 11578672 Click to see CC1CC2C(=O)OCC(C(=O)N3CCCC3C(=O)N4CCCCC4C(=O)NC(C(=O)N2C1)C)NC(=O)C(CC5=CC(=CC(=C5)F)F)NC(=O)CCC6CCCCC6 798.90 unknown https://doi.org/10.1248/CPB.42.1427
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(6S)-6-hydroxy-2,3,4,4-tetramethylcyclohex-2-en-1-one 89098932 Click to see CC1=C(C(CC(C1=O)O)(C)C)C 168.23 unknown https://doi.org/10.1248/CPB.42.1427
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
9H-Pyrido[3,4-B]indole 64961 Click to see C1=CC=C2C(=C1)C3=C(N2)C=NC=C3 168.19 unknown https://doi.org/10.1248/CPB.42.1427
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
methyl (1S,6Z,7S,9S,10S,12S,20R)-6-ethylidene-10-hydroxy-13-methyl-11-oxa-4,13-diazahexacyclo[10.7.1.01,10.04,9.07,20.014,19]icosa-14,16,18-triene-20-carboxylate 101712482 Click to see CC=C1CN2CCC34C5=CC=CC=C5N(C6C3(C1CC2C4(O6)O)C(=O)OC)C 382.50 unknown https://doi.org/10.1248/CPB.42.1427

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