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Stillingia sanguinolenta

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fedd77be44714785271
Scientific name Stillingia sanguinolenta
Authority Müll.Arg.
First published in Linnaea 32: 88 (1863)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Sapium angulatum Klotzsch ex Pax Pflanzenr. , IV, 147, V: 191 (1912)
Stillingia sanguinolenta var. angustifolia Müll.Arg. Linnaea 32: 88 (1863)
Stillingia sanguinolenta var. lanceolata Müll.Arg. Linnaea 32: 88 (1863)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000317023
Tropicos 12805049
KEW urn:lsid:ipni.org:names:356592-1
The Plant List kew-197963
Open Tree Of Life 3911750
IPNI 356592-1
iNaturalist 275451
GBIF 3055150
EOL 1150042
Wikipedia Stillingia_sanguinolenta

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
Tonantzitlolone and other Diterpenes from <i>Stillingia sanguinolenta</i> Gerald Dräger, Frank Jeske, Eike Kunst, Elda G. Lopez, Humberto V. Sanchez, Fotini Tsichritzis, Andreas Kirschning, Jasmin Jakupovic Wiley 17-Aug-2007
doi:10.1002/EJOC.200700184

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2R,4aR,6R,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-2,6-diol 23731227 Click to see 304.50 unknown https://doi.org/10.1002/EJOC.200700184
(4aR,7S,8aS,10aS)-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-3,4,8,9,10,10a-hexahydrophenanthrene-2,6-dione 23731228 Click to see 316.40 unknown https://doi.org/10.1002/EJOC.200700184
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
1,5,9-Cyclotetradecatriene, 1,5,9-trimethyl-12-(1-methylethenyl)- 328947 Click to see 272.50 unknown https://doi.org/10.1002/EJOC.200700184
1,5,9-Cyclotetradecatriene, 13-isopropenyl-2,6,10-trimethyl-, (-)- 11208039 Click to see CC1=CCCC(=CCC(CCC(=CCC1)C)C(=C)C)C 272.50 unknown https://doi.org/10.1002/EJOC.200700184
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,9R,10S,13S,14R)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 11001752 Click to see 320.50 unknown https://doi.org/10.1002/EJOC.200700184
(1R,4R,9R,10S,13S,14R)-5,5,9-trimethyl-6-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylic acid 162908862 Click to see 318.40 unknown https://doi.org/10.1002/EJOC.200700184
(1R,4R,9R,10S,13S,14S)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 21143852 Click to see 320.50 unknown https://doi.org/10.1002/EJOC.200700184
(1S,4R,9S,10R,12R,13S,14S)-5,5,9-trimethyl-6-oxopentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-13-carboxylic acid 162896888 Click to see 316.40 unknown https://doi.org/10.1002/EJOC.200700184
(1S,4S,6S,9S,10R,13R,14S)-6-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-7-one 23731230 Click to see 320.50 unknown https://doi.org/10.1002/EJOC.200700184
(1S,4S,9S,10R,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 162870465 Click to see 286.50 unknown https://doi.org/10.1002/EJOC.200700184
(3R)-ent-Kaur-16-en-3-ol 101630627 Click to see 288.50 unknown https://doi.org/10.1002/EJOC.200700184
ent-17-Hydroxykauran-3-one 23731229 Click to see 304.50 unknown https://doi.org/10.1002/EJOC.200700184
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,4S,9R,10S,12S,13R,15S)-13-hydroxy-5,5,9-trimethylpentacyclo[11.3.1.01,10.04,9.012,15]heptadecan-6-one 162995193 Click to see CC1(C2CCC34CC5CC(C3)(C5CC4C2(CCC1=O)C)O)C 302.50 unknown https://doi.org/10.1002/EJOC.200700184
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
(3S)-N-[(3R,6R,9R,12R,15R,18S,19R)-6-(2-amino-2-oxoethyl)-9-[(1S)-1-hydroxyethyl]-12-[(4-hydroxyphenyl)methyl]-3,19-dimethyl-2,5,8,11,14,17-hexaoxo-15-propan-2-yl-1-oxa-4,7,10,13,16-pentazacyclononadec-18-yl]-15-(diaminomethylideneamino)-3-hydroxypentadecanamide 162893516 Click to see 947.10 unknown https://doi.org/10.1002/EJOC.200700184

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