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Internal ID UUID643fcf089282f117062120
Scientific name Critonia morifolia
Authority (Mill.) R.M.King & H.Rob.
First published in Phytologia 22: 49 (1971)

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Synonyms Top

Scientific name Authority First published in
Eupatorium critonioides Steetz Bot. Voy. Herald 4: 145 (1854)
Eupatorium thyrsigerum Hieron. Bot. Jahrb. Syst. 28(5): 570 (1901)
Eupatorium morifolium Mill. Gard. Dict. ed. 8 n.° 10 (1768)
Critonia thyrsigera (Hieron.) R.M.King & H.Rob. Phytologia 22: 50 (1971)
Eupatorium populifolium Kunth Nov. Gen. Sp. 4(15): 87 (ed. fol.) (1818)
Eupatorium sartorii Sch.Bip. ex Klatt 91 1884

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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 Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil West-central
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000086736
Tropicos 2711373
KEW urn:lsid:ipni.org:names:69558-2
The Plant List gcc-43118
Open Tree Of Life 588536
NCBI Taxonomy 1125402
IUCN Red List 146792809
IPNI 69558-2
iNaturalist 280145
GBIF 5385749

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
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Towards Conservation of the Remarkably High Number of Daisy Trees (Asteraceae) in Mexico Redonda-Martínez R, Pliscoff P, Moreira-Muñoz A, Martínez Salas EM, Samain MS Plants (Basel) 12-Mar-2021
PMCID:PMC8000269
doi:10.3390/plants10030534
PMID:33809003
Natural Compounds as Modulators of Cell Cycle Arrest: Application for Anticancer Chemotherapies Bailon-Moscoso N, Cevallos-Solorzano G, Romero-Benavides JC, Orellana MI Curr Genomics 01-Apr-2017
PMCID:PMC5345333
doi:10.2174/1389202917666160808125645
PMID:28367072
Structure of Two Eudesmanolides, Moriforin A and B Antonio G. Gonz�ez, Antonio Gonz�ez Gonz�ez, Jaime Bermejo Barrera, Angel Yanes Hern�dez, Francisco Est思ez Rosas, Xorge A. Dom地guez The Japan Institute of Heterocyclic Chemistry 19-Feb-2009
doi:10.3987/R-1985-07-1601
Pyrrolizidine alkaloids from critonia morifolia H Wiedenfeld, A.andrade Cetto Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00120-4

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
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 78384682 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1016/S0031-9422(98)00120-4
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 44584035 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/S0031-9422(98)00120-4
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1R)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 101993113 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1016/S0031-9422(98)00120-4
Echinatine 22384 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/S0031-9422(98)00120-4
Rinderine 442758 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/S0031-9422(98)00120-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,5aS,9aR,9bS)-5a,9-dimethyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 101311685 Click to see CC1=CCCC2(C1C3C(CC2)C(=C)C(=O)O3)C 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
(3aS,5aS,9aS,9bS)-5a-methyl-3,9-dimethylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one 101311686 Click to see CC12CCCC(=C)C1C3C(CC2)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
alpha-Cyclocostunolide 442191 Click to see CC1=CCCC2(C1C3C(CC2)C(=C)C(=O)O3)C 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
Arbusculin B 161442 Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.3987/R-1985-07-1601
> Organoheterocyclic compounds / Pyrrolizines
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-1H-pyrrolizin-1-yl]methyl (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 100927179 Click to see CC(C)C(C(C)O)(C(=O)OCC1C=CN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/S0031-9422(98)00120-4

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