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Internal ID UUID643fc6120f371963545043
Scientific name Lepidaploa cotoneaster
Authority (Willd. ex Spreng.) H.Rob.
First published in Proc. Biol. Soc. Washington 103(2): 486 (1990)

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Synonyms Top

Scientific name Authority First published in
Conyza cotoneaster Willd. ex Spreng. Syst. Veg. 3: 509 (1826)
Vernonia debilis Mart. ex DC. Prodr. 5: 54 (1836)
Cacalia cotoneaster (Less.) Kuntze Revis. Gen. Pl. 2: 969 (1891)
Vernonia cotoneaster Less. Linnaea 4: 298 (1829)
Cacalia debilis (Mart. ex DC.) Kuntze Revis. Gen. Pl. 2: 970 (1891)
Vernonia axilliflora Mart. ex Less. Linnaea 4: 297 (1829)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
    • Northern South America
      • Guyana

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000002244
Tropicos 2735848
KEW urn:lsid:ipni.org:names:948500-1
The Plant List gcc-102156
Open Tree Of Life 7052528
NCBI Taxonomy 2067298
IPNI 948500-1
iNaturalist 961831
GBIF 3099787

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
Natürlich vorkommende Terpen‐Derivate, 292. über das erste Sesquiterpenlacton mit einer Allengruppe aus <i>Vernonia cotoneaster</i> Ferdinand Bohlmann, Rajiinder K. Gupta, Jasmin Jakupovic, Robert M. King, Harold Robinson Wiley 19-Jul-2007
doi:10.1002/JLAC.198019801127
Hirsutinolides and other sesquiterpene lactones from Vernonia species Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83168-3

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 / Sesquiterpenoids
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83168-3
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83168-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1,10-Dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl) 2-methylprop-2-enoate 163045855 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
(4,8-diacetyloxy-6,10-dimethyl-2-oxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl)methyl acetate 162853140 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)C(CC(=CC(C1)OC(=O)C)C)OC(=O)C 406.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
[(1R,3S,7R,8S,9Z)-1,10-dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 163045856 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
[(4S,6E,8S,10E,11aR)-4,8-diacetyloxy-6,10-dimethyl-2-oxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl]methyl acetate 162853141 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)C(CC(=CC(C1)OC(=O)C)C)OC(=O)C 406.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
CID 163012586 163012586 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)C(CC(=C=CC1)C)OC(=O)C 346.40 unknown https://doi.org/10.1002/JLAC.198019801127
CID 163188113 163188113 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)C(CC(=C=CC1)C)OC(=O)C 346.40 unknown https://doi.org/10.1002/JLAC.198019801127
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(82)83168-3
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(82)83168-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 163020385 163020385 Click to see CC1=C=CCC(C=C2C(=C(C(=O)O2)OC(=O)C)C(C1)OC(=O)C)(C)O 348.30 unknown https://doi.org/10.1016/0031-9422(82)83168-3
CID 163050266 163050266 Click to see CC1=CCC2C(=C(C(=O)O2)OC(=O)C)C(CC(=C=CC1)C)OC(=O)C 346.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
CID 163050267 163050267 Click to see CC1=CCC2C(=C(C(=O)O2)OC(=O)C)C(CC(=C=CC1)C)OC(=O)C 346.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
CID 163187944 163187944 Click to see CC1=C=CCC(C=C2C(=C(C(=O)O2)OC(=O)C)C(C1)OC(=O)C)(C)O 348.30 unknown https://doi.org/10.1016/0031-9422(82)83168-3
> Organoheterocyclic compounds / Dithiins
3-but-3-en-1-ynyl-6-[(E)-pent-3-en-1-ynyl]dithiine 92036830 Click to see CC=CC#CC1=CC=C(SS1)C#CC=C 230.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
3-But-3-en-1-ynyl-6-pent-3-en-1-ynyldithiine 162859647 Click to see CC=CC#CC1=CC=C(SS1)C#CC=C 230.40 unknown https://doi.org/10.1016/0031-9422(82)83168-3
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
(E)-5-(5-but-3-en-1-ynylthiophen-2-yl)pent-2-en-4-ynal 101415941 Click to see C=CC#CC1=CC=C(S1)C#CC=CC=O 212.27 unknown https://doi.org/10.1016/0031-9422(82)83168-3
2-(3-Buten-1-ynyl)-5-[(E)-3-penten-1-ynyl]thiophene 14550074 Click to see CC=CC#CC1=CC=C(S1)C#CC=C 198.29 unknown https://doi.org/10.1016/0031-9422(82)83168-3
2-But-3-en-1-ynyl-5-pent-3-en-1-ynylthiophene 53440720 Click to see CC=CC#CC1=CC=C(S1)C#CC=C 198.29 unknown https://doi.org/10.1016/0031-9422(82)83168-3
5-(5-But-3-en-1-ynylthiophen-2-yl)pent-2-en-4-ynal 162865918 Click to see C=CC#CC1=CC=C(S1)C#CC=CC=O 212.27 unknown https://doi.org/10.1016/0031-9422(82)83168-3

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