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Ageratina glechonophylla

Ageratina glechonophylla - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcea8eaa16968148338
Scientific name Ageratina glechonophylla
Authority (Less.) R.M.King & H.Rob.
First published in Phytologia 19: 214 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium azangaroense Sch.Bip. Bonplandia 4: 54, nomen (1856)
Eupatorium bartlingianum Steud. Nomencl. Bot. 1: 606 (1840)
Eupatorium azangaroense Sch.Bip. ex Wedd. 217 1857
Eupatorium remyanum Phil. Fl. Atacam. : 29 (1860)
Eupatorium australe Bartl. Index Seminum (GOET, Gottingensis) (1837); et in Linnaea, xii. (1
Kyrstenia glechonophylla Greene Leafl. Bot. Observ. Crit. 1: 9 (1903)
Eupatorium remyanum Philippi Fl. Atacam. 29. 1860.
Eupatorium chilense Bertero Mercurio Chileno 13: 616 (1829)
Ageratina remyana (Phil.) R.M.King & H.Rob. Phytologia 49: 3 (1981)
Ageratina azangaroensis (Sch.Bip. ex Wedd.) R.M.King & H.Rob. Phytologia 19: 212 (1970)
Eupatorium glechonophyllum Less. Linnaea 6: 105 (1831)
Ageratum conspicuum hort. ex K.Koch & Fintelm. Wochenschr. Gärtnerei Pflanzenk. 1: 33 (1858)
Eupatorium inconspicuum Sch.Bip. Linnaea 34: 535 (1866)

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
    • Southern South America
      • Argentina Northwest
      • Chile Central
      • Chile North
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000083352
Tropicos 2712234
KEW urn:lsid:ipni.org:names:6910-2
The Plant List gcc-39838
Open Tree Of Life 1007561
NCBI Taxonomy 176617
IPNI 6910-2
iNaturalist 509342
GBIF 5402753
EOL 6173458

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Accumulation of As, Ag, Cd, Cu, Pb, and Zn by Native Plants Growing in Soils Contaminated by Mining Environmental Liabilities in the Peruvian Andes Cruzado-Tafur E, Bierla K, Torró L, Szpunar J Plants (Basel) 27-Jan-2021
PMCID:PMC7922771
doi:10.3390/plants10020241
PMID:33513684
Leaf traits in Chilean matorral: sclerophylly within, among, and beyond matorral, and its environmental determinants Read J, Sanson G, Pérez Trautmann MF Ecol Evol 03-Feb-2016
PMCID:PMC4739351
doi:10.1002/ece3.1970
PMID:26865953
A chromosomal analysis of four species of Chilean Chrysomelinae (Coleoptera, Chrysomelidae) Petitpierre E, Elgueta M Comp Cytogenet 05-Oct-2012
PMCID:PMC3834574
doi:10.3897/CompCytogen.v6i4.3519
PMID:24260673
Thymol derivatives and a chromene from Ageratina glechonophylla Antonio G. González, Carlos Yanes Hernández, Jaime Bermejo Barrera Elsevier BV 18-Nov-2003
doi:10.1016/0031-9422(92)90072-X
Sesquiterpene lactones, geranylnerol and tremetone derivatives from Ageratina species F Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81124-3
Chromenes and benzofurans from Ageratina glechonophylla Antonio G. González, Jaime Bermejo Barrera, Angel C. Yanes, Jesús G. Díaz, Elsa Ma Rodriguez Pérez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98024-5
Thymol derivatives from Eupatorium glechonophyllum Giuliano Delle Monache, Franco Delle Monache, Josè Becerra, Mario Silva, Francesco Menichini Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84947-X

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
> Benzenoids / Phenol esters
[2-(1-Acetyloxy-2,3-dihydroxypropan-2-yl)-5-methylphenyl] 2-methylpropanoate 162901526 Click to see CC1=CC(=C(C=C1)C(CO)(COC(=O)C)O)OC(=O)C(C)C 310.34 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
[2-[(2R)-1-acetyloxy-2,3-dihydroxypropan-2-yl]-5-methylphenyl] 2-methylpropanoate 162901527 Click to see CC1=CC(=C(C=C1)C(CO)(COC(=O)C)O)OC(=O)C(C)C 310.34 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
[2-[(2R)-2-(acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylpropanoate 163022762 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C)OC(=O)C(C)C 292.33 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
[2-[2-(Acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylpropanoate 14427473 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C)OC(=O)C(C)C 292.33 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
> Benzenoids / Phenols / Cresols / Meta cresols
[(Z)-3-[(Z)-3-acetyloxy-2-(2-hydroxy-4-methylphenyl)prop-1-enoxy]-2-(2-hydroxy-4-methylphenyl)prop-2-enyl] acetate 15138442 Click to see CC1=CC(=C(C=C1)C(=COC=C(COC(=O)C)C2=C(C=C(C=C2)C)O)COC(=O)C)O 426.50 unknown https://doi.org/10.1016/0031-9422(92)90072-X
2-(2-Hydroxy-4-methylphenyl)propane-1,2,3-triol 14543617 Click to see CC1=CC(=C(C=C1)C(CO)(CO)O)O 198.22 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
2-[(4R)-4-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-5-methylphenol 162876331 Click to see CC1=CC(=C(C=C1)C2(COC(O2)(C)C)CO)O 238.28 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
2-[4-(Hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-5-methylphenol 162876330 Click to see CC1=CC(=C(C=C1)C2(COC(O2)(C)C)CO)O 238.28 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 137795506 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
Friedelanol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1016/S0031-9422(00)81124-3
> Organoheterocyclic compounds / Benzofurans
(6-Methylbenzofuran-3-yl)methanol 11084186 Click to see CC1=CC2=C(C=C1)C(=CO2)CO 162.18 unknown https://doi.org/10.1016/S0031-9422(00)98024-5
3-(Acetoxymethyl)-6-methylbenzofuran 14427474 Click to see CC1=CC2=C(C=C1)C(=CO2)COC(=O)C 204.22 unknown https://doi.org/10.1016/S0031-9422(00)98024-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(2,2-Dimethylchromen-6-yl)ethanone 177040 Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C 202.25 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
2-[(Z)-3-hydroxy-1-[1-(7-methoxy-2,2-dimethylchromen-6-yl)ethoxy]prop-1-en-2-yl]-5-methylphenol 15138443 Click to see CC1=CC(=C(C=C1)C(=COC(C)C2=C(C=C3C(=C2)C=CC(O3)(C)C)OC)CO)O 396.50 unknown https://doi.org/10.1016/0031-9422(92)90072-X
Encecalin 114703 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 232.27 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
Encecanescin 5487790 Click to see CC(C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC)OC(C)C3=C(C=C4C(=C3)C=CC(O4)(C)C)OC 450.60 unknown https://doi.org/10.1016/S0031-9422(00)98024-5
Eupatoriochromene 100768 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O 218.25 unknown https://doi.org/10.1016/S0031-9422(00)84947-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)84947-X

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