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Tabernaemontana robinsonii

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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 UUID644034388e508561361496
Scientific name Tabernaemontana robinsonii
Authority (Woodson) A.O.Simões & M.E.Endress
First published in Taxon 59: 787 (2010)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stemmadenia lagunae Woodson Ann. Missouri Bot. Gard. 29: 364 (1942)
Stemmadenia macrantha Standl. Publ. Field Columb. Mus., Bot. Ser. 4: 253 (1929)
Stemmadenia minima A.H.Gentry Ann. Missouri Bot. Gard. 64: 322 (1977 publ. 1978)
Stemmadenia robinsonii Woodson Ann. Missouri Bot. Gard. 15: 369 (1928)

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
    • Central America
      • Costa Rica
      • Nicaragua
      • Panamá
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000916153
Tropicos 100361755
KEW urn:lsid:ipni.org:names:77105798-1
The Plant List kew-461108
Open Tree Of Life 6068037
IUCN Red List 149997550
IPNI 77105798-1
iNaturalist 631615
GBIF 7938215

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)!
Title Authors Publication Released IDs
New Lignan Glucosides from Stemmadenia minima*. Achenbach H, Löwel M, Waibel R, Gupta M, Solis P Planta Med 01-Jun-1992
doi:10.1055/S-2006-961451
PMID:17226467
Phytochemical and Biological Study of Slemmadenia minima. Gupta MP, Alvarez D, Solis PN, Löwel M, Achenbach H Planta Med 01-Oct-1991
doi:10.1055/S-2006-960186
PMID:17226192

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 / Ibogan-type alkaloids
(1R,15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene 51055165 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1055/S-2006-960186
(1S)-1-[(1R,15R,17R,18R)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraen-17-yl]ethanol 44566758 Click to see CC(C1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45)O 296.40 unknown https://doi.org/10.1055/S-2006-960186
6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole, 7-ethyl-6,6a,7,8,9,10,12,13-octahydro-, [6R-(6alpha,6abeta,7beta,9alpha)]- 500053 Click to see CCC1CC2CC3C1N(C2)CCC4=C3NC5=CC=CC=C45 280.40 unknown https://doi.org/10.1055/S-2006-960186
Coronaridine 73489 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1055/S-2006-960186
Ibogamine-18-carboxylic acid, 12-methoxy-, methyl ester 363270 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1055/S-2006-960186
methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate 137628478 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC 338.40 unknown https://doi.org/10.1055/S-2006-960186
methyl (1R,15S,17R,18S)-17-ethyl-7-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-1-carboxylate 134688048 Click to see CCC1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC 368.50 unknown https://doi.org/10.1055/S-2006-960186
Voacristine 196982 Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=C4C=C(C=C5)OC)C(=O)OC)O 384.50 unknown https://doi.org/10.1055/S-2006-960186
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Lyoniresinol 9'-O-glucoside 10483388 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O 582.60 unknown https://doi.org/10.1055/S-2006-961451

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