Solanum asperum - Unknown
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Internal ID UUID6440418869648612430789
Scientific name Solanum asperum
Authority Rich.
First published in Actes Soc. Hist. Nat. Par. 1: 107. 1792.

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Synonyms Top

Scientific name Authority First published in
Solanum asperum Vahl Eclog. Amer. 2: 17. 1798.
Solanum asperum var. angustifolium Sendtn. Fl. Bras. (Martius) 10: 40. 1846.
Solanum radula (Vahl) M.Gómez (V. ) M.Gómez, (V. ) M.Gómez, (R. ) M.Gómez, and (V. ) M.Gómez, Anales Sci. Nat. 23: 268. 1894., 1894.
Solanum canescens Rich. ex Dunal Prodr. [A. P. de Candolle] 13(1): 107. 1852.
Solanum lima Banks ex Dunal Prodr. [A. P. de Candolle] 13(1): 107. 1852.
Solanum radula Vahl Eclog. Amer. 2: 16. 1798.
Solanum salviifolium Lam. Tabl. Encycl. 2: 14. 1794.

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
    • Central America
      • Belize
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001026357
Tropicos 29604138
INPN 735155
KEW urn:lsid:ipni.org:names:818335-1
The Plant List tro-29604138
Open Tree Of Life 651350
NCBI Taxonomy 681489
IPNI 818335-1
iNaturalist 83968
GBIF 2930051

Genomes (via NCBI) Top

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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
Solanaceae Family Phytochemicals as Inhibitors of 3C-Like Protease of SARS-CoV-2: An In Silico Analysis Mahmood RA, Hasan A, Rahmatullah M, Paul AK, Jahan R, Jannat K, Bondhon TA, Mahboob T, Nissapatorn V, de Lourdes Pereira M, Paul TK, Rumi OH, Wiart C, Wilairatana P Molecules 25-Jul-2022
PMCID:PMC9331421
doi:10.3390/molecules27154739
PMID:35897915
Comparative Molluscicidal and Schistosomicidal Potentiality of Two Solanum Species and Its Isolated Glycoalkaloids Alsherbiny MA, El Badawy SA, Elbedewy H, Ezzat SM, Elsakhawy FS, Abdel-Kawy MA Pharmacognosy Res 01-Jan-2018
PMCID:PMC5855367
doi:10.4103/pr.pr_71_17
PMID:29568198
Thirty Years of Forest Census at Barro Colorado and the Importance of Immigration in Maintaining Diversity Condit R, Chisholm RA, Hubbell SP PLoS One 30-Nov-2012
PMCID:PMC3511510
doi:10.1371/journal.pone.0049826
PMID:23226222
Structure of Solaparnaine, a New Spirosolane Alkaloid from the Green Berries of Solanum asperum Vahl Jnanabrata Bhattacharyya The Japan Institute of Heterocyclic Chemistry 24-Feb-2009
doi:10.3987/R-1985-12-3111
Plant Sexual Systems and a Review of the Breeding System Studies in the Caatinga, a Brazilian Tropical Dry Forest MACHADO IC, LOPES AV, SAZIMA M Ann Bot 01-Feb-2006
PMCID:PMC2803361
doi:10.1093/aob/mcj029
PMID:16377654
Floral Traits and Pollination Systems in the Caatinga, a Brazilian Tropical Dry Forest Machado IC, Lopes AV Ann Bot 30-Jul-2004
PMCID:PMC4242177
doi:10.1093/aob/mch152
PMID:15286010

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 / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol 21573754 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(CN6)CO 429.60 unknown https://doi.org/10.3987/R-1985-12-3111
5'-(Hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol 73796886 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(CN6)CO 429.60 unknown https://doi.org/10.3987/R-1985-12-3111

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