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Solanum fraxinifolium

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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 UUID644041a880cef124297646
Scientific name Solanum fraxinifolium
Authority Dunal
First published in Prodr. [A. P. de Candolle] 13(1): 39. 1852.

Description Top

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Synonyms Top

Scientific name Authority First published in
Solanum fraxinifolium var. protoxanthum (Bitter) Bitter Repert. Spec. Nov. Regni Veg. 12: 147. 1913.
Solanum grossularia subsp. protaxanthum Bitter Repert. Spec. Nov. Regni Veg. 10: 538. 1912.

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
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001028028
Tropicos 29601443
KEW urn:lsid:ipni.org:names:819253-1
The Plant List tro-29601443
Open Tree Of Life 81458
NCBI Taxonomy 265242
IPNI 819253-1
GBIF 2932789
USDA GRIN 408311

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)!
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Title Authors Publication Released IDs
(23S)-23-Hydroxysolasodine from two Solanum species Helmut Ripperger, Andrea Porzel Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95220-8
25-Isoetioline from twoSolanum species Helmut Ripperger Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80224-5

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 / Triterpenoids
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/0031-9422(90)80224-5
Spirost-5-en-3-ol 234096 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/0031-9422(90)80224-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
10,13-dimethyl-17-[1-(3-methyl-2,3,4,5-tetrahydropyridin-6-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 12309790 Click to see CC1CCC(=NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 413.60 unknown https://doi.org/10.1016/0031-9422(90)80224-5
25-Iso-etioline 12309793 Click to see CC1CCC(=NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 413.60 unknown https://doi.org/10.1016/S0031-9422(00)95220-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-3',16-diol 10938908 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1)O 429.60 unknown https://doi.org/10.1016/S0031-9422(00)95220-8
(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol 137704740 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1016/0031-9422(90)80224-5
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-3',16-diol 85323274 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1)O 429.60 unknown https://doi.org/10.1016/S0031-9422(00)95220-8
Soladulcamaridine 91871142 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1016/0031-9422(90)80224-5
> Organoheterocyclic compounds / Naphthopyrans
(1R,2S,4R,5R,10R,11S,17S)-11-hydroxy-5-[(2R)-2-hydroxy-1-methylsulfinylpropan-2-yl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadec-8-ene-7,15-dione 102354698 Click to see CC12CCC(C3(C1C(C4C5(C3=CC(=O)OC5C(C)(CS(=O)C)O)O4)OC2=O)C)O 426.50 unknown https://doi.org/10.1016/0031-9422(90)80224-5

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