Eremosis triflosculosa

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Internal ID UUID643fc7d3f38d7695216073
Scientific name Eremosis triflosculosa
Authority Gleason
First published in Bull. New York Bot. Gard. 4: 233 (1906)

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Synonyms Top

Scientific name Authority First published in
Vernonia triflosculosa subsp. palmeri (Rose) S.B.Jones Brittonia 25: 100 (1973)
Critoniopsis triflosculosa (Kunth) H.Rob. Proc. Biol. Soc. Washington 106: 624 (1993)
Vernonia triflosculosa Kunth Nov. Gen. Sp. 4: 40 (1818)
Vernonia luxensis Coult. Bot. Gaz. (Crawfordsville) 20: 41. 1895.
Vernonia chacalana S.F.Blake Contr. Gray Herb. 52: 19 (1917)
Eremosis palmeri Gleason Bull. New York Bot. Gard. 4: 233 (1906)
Vernonia luxensis J.M.Coult. Bot. Gaz. 20: 41 (1895)
Vernonia triflosculosa var. palmeri (Rose) B.L.Turner Phytologia 66: 464 (1989)
Cacalia triantha (S.Schauer) Kuntze Revis. Gen. Pl. 2: 971 (1891)
Vernonia palmeri Rose Contr. U.S. Natl. Herb. 1: 101. 1891
Cacalia triflosculosa (Kunth) Kuntze Revis. Gen. Pl. 2: 971 (1891)
Gymnanthemum congestum Cass. Dict. Sci. Nat., ed. 2. 20: 110 (1821)
Vernonia dumeta Klatt. Bull. Soc. Roy. Bot. Belgique 35: 277. 1896.

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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 Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000017743
Tropicos 2711673
KEW urn:lsid:ipni.org:names:93420-2
The Plant List gcc-117169
Open Tree Of Life 7052625
NCBI Taxonomy 2067267
IUCN Red List 150432477
IPNI 93420-2
iNaturalist 867096
GBIF 5695203

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
Ent-kaurane glycosides and sesquiterpene lactones of the hirsutinolide type from Vernonia triflosculosa. Kos O, Castro V, Murillo R, Poveda L, Merfort I Phytochemistry 01-Jan-2006
doi:10.1016/J.PHYTOCHEM.2005.07.006
PMID:16129464

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 / Kaurane diterpenoids
16-Hydroxy-(-)-kauranoic acid 494329 Click to see 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
Kauran-18-oic acid, 16-hydroxy-, (4alpha)- 15214986 Click to see 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 101391409 Click to see 630.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 101391410 Click to see 614.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl] 14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 163022542 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(CO6)O)O)O 630.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl] 14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 163093651 Click to see 614.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
[(1R,2E,8S,10R,11S)-10-hydroxy-11-methoxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 101391408 Click to see 424.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[(1R,2E,8S,10R,11S)-10,11-dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 15689665 Click to see 410.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[10-Hydroxy-11-methoxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 162989038 Click to see CC12CCC(O1)(C(CC(C3=C(C(=O)OC3=C2)COC)OC(=O)C(=C)CO)(C)O)OC 424.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[10,11-Dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 163059474 Click to see CC12CCC(O1)(C(CC(C3=C(C(=O)OC3=C2)COC)OC(=O)C(=C)CO)(C)O)O 410.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
[(1R,2E,8S,10R,11S)-10,11-dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-methylprop-2-enoate 11538453 Click to see 394.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
[10,11-Dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-methylprop-2-enoate 72999473 Click to see 394.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.006

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