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Austroeupatorium inulaefolium

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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 UUID643fcbb04fde7605890753
Scientific name Austroeupatorium inulaefolium
Authority (Kunth) R.M.King & H.Rob.
First published in Phytologia 19(7): 434 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium pallidum Hook. & Arn. Companion Bot. Mag. 1: 241 (1836)
Eupatorium entreriense Hieron. Bot. Jahrb. Syst. 22(4-5): 767 (1897)
Eupatorium orgyale DC. Prodr. 5: 174 (1836)
Eupatorium suaveolens Kunth Nov. Gen. Sp. 4(15): 86 (ed. fol.) (1818)
Uncasia pallescens Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)
Eupatorium inulifolium f. suaveolens Hieron. Bot. Jahrb. Syst. 28(5): 572 (1901)
Eupatorium horsfieldii Mig. Fl. Bat. 2027. 1856.
Eupatorium inulaefolium Kunth Nov. Gen. Sp. 4(15): 85 (ed. fol.) (1818)
Austroeupatorium entreriense (Hieron.) R.M.King & H.Rob. Phytologia 19(7): 434 (1970)
Eupatorium duodecimiflorum Sch.Bip. ex Baker Fl. Bras. 6(2): 318 (1876)
Eupatorium paranense Hook. & Arn. Companion Bot. Mag. 1: 241 (1836)
Eupatorium molle Kunth Nov. Gen. Sp. 4(15): 85 (ed. fol.) (1818)
Eupatorium pallescens DC. Prodr. 5: 154 (1836)

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000050339
Open Tree Of Life 7602844
GBIF 5831200

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)!
Title Authors Publication Released IDs
Natürlich vorkommende Terpen‐Derivate, 81. Weitere Inhaltsstoffe aus Vertretern der <i>Eupatorium</i>‐Gruppe Ferdinand Bohlmann, Christa Zdero, Michael Grenz Wiley 29-Jun-2007
doi:10.1002/CBER.19771100324
ent-Norlabdanes and Other Constituents of Four Venezuelan Species Previously Classified in the Genus Eupatorium Jorge Triana, Ali Bahsas, Paulino Delgado, Ramon Jaimes, Carlos O. Trejo American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50119A014
New flavonoids from Eupatorium inulaefolium Graciela E. Ferraro, Virginia S. Martino, Jorge D. Coussio Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(77)84046-6
Ent-norlabdane triols from Austroeupatorium inulaefolium Juan C. Oberti, Virginia E. Sosa, Palaniappan Kulanthaivel, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84958-4
Nor-ent-labdan Derivate aus Austroeupatorium inulaefolium. Bohlmann F, Schmeda-Hirschmann G, Jakupovic J Planta Med 01-Apr-1984
doi:10.1055/S-2007-969675
PMID:17340295

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
(1S,2R,3R,4S,4aR,8aR)-3,4a,8,8-tetramethyl-4-[(2Z)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2,3-triol 70698052 Click to see CC(=CCC1C2(CCCC(C2C(C(C1(C)O)O)O)(C)C)C)C=C 322.50 unknown https://doi.org/10.1002/CBER.19771100324
3,4a,8,8-tetramethyl-4-(3-methylpenta-2,4-dienyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2,3-triol 72975030 Click to see CC(=CCC1C2(CCCC(C2C(C(C1(C)O)O)O)(C)C)C)C=C 322.50 unknown https://doi.org/10.1002/CBER.19771100324
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R,4R,4aR,6R,7S,8R,8aR)-4-[2-(furan-3-yl)-2-oxoethyl]-6,7-dihydroxy-8-(hydroxymethyl)-3,4a-dimethyl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one 101318123 Click to see CC1C(C2(CC(C(C(C2CC1=O)CO)O)O)C)CC(=O)C3=COC=C3 350.40 unknown https://doi.org/10.1016/S0031-9422(00)84958-4
1-(3-Furyl)-2-[(4abeta)-2-methylene-5alpha-(hydroxymethyl)-6alpha,7alpha-dihydroxy-8aalpha-methyldecalin-1alpha-yl]ethanone 15226316 Click to see CC12CC(C(C(C1CCC(=C)C2CC(=O)C3=COC=C3)CO)O)O 334.40 unknown https://doi.org/10.1016/S0031-9422(00)84958-4
2-[6,7-Dihydroxy-5-(hydroxymethyl)-8a-methyl-2-methylidene-1,3,4,4a,5,6,7,8-octahydronaphthalen-1-yl]-1-(furan-3-yl)ethanone 73189500 Click to see CC12CC(C(C(C1CCC(=C)C2CC(=O)C3=COC=C3)CO)O)O 334.40 unknown https://doi.org/10.1016/S0031-9422(00)84958-4
4-[2-(Furan-3-yl)-2-oxoethyl]-6,7-dihydroxy-8-(hydroxymethyl)-3,4a-dimethyl-1,3,4,5,6,7,8,8a-octahydronaphthalen-2-one 162904239 Click to see CC1C(C2(CC(C(C(C2CC1=O)CO)O)O)C)CC(=O)C3=COC=C3 350.40 unknown https://doi.org/10.1016/S0031-9422(00)84958-4
Austroeupatol 15226318 Click to see CC12CC(C(C(C1CCC(=C)C2CCC3=COC=C3)CO)O)O 320.40 unknown https://doi.org/10.1021/NP50119A014
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 139031795 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1055/S-2007-969675
Angeloylgrandifloric acid 6442665 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown https://doi.org/10.1055/S-2007-969675
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1055/S-2007-969675
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969675
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969675
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969675
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969675
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969675
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate 137704689 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1055/S-2007-969675
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1055/S-2007-969675
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1055/S-2007-969675
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/NP50119A014
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Nuchensin 373260 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown https://doi.org/10.1016/0031-9422(77)84046-6
Pedalitin 31161 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(77)84046-6

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