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Eupatorium mikanioides

Eupatorium mikanioides - 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 UUID643fcdbde8e93859785653
Scientific name Eupatorium mikanioides
Authority Chapm.
First published in Fl. South. U.S. : 195 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium crassifolium Shuttlew. ex A.Gray Syn. Fl. N. Amer. 1(2): 97 (1884)
Uncasia mikanioides Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)

Common names Top

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Language Common/alternative name
English semaphore thoroughwort

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000075079
Florida Plant Atlas 1099
USDA Plants EUMI7
Tropicos 2714137
KEW urn:lsid:ipni.org:names:206379-1
The Plant List gcc-31782
Open Tree Of Life 394792
NCBI Taxonomy 102776
Nature Serve 2.146434
IPNI 206379-1
iNaturalist 131156
GBIF 5403162
Freebase /m/04ghwxk
EOL 846626
Wikipedia Eupatorium_mikanioides

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
A thiol-containing ester side chain in a sesquiterpene lactone from Eupatorium mikanioides. Absolute configuration of deacetyleupaserrin and its congeners Werner Herz, Narendra Kumar, John F. Blount American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO01291A023

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 / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,4R,5aR,9bR)-4-hydroxy-3,5a,9-trimethyl-3a,4,5,9b-tetrahydro-3H-benzo[g][1]benzofuran-2,8-dione 162944449 Click to see CC1C2C(CC3(C=CC(=O)C(=C3C2OC1=O)C)C)O 262.30 unknown https://doi.org/10.1021/JO01291A023
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4R,6Z,8S,10Z)-4,8-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one 331147 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/JO01291A023
(3aS,4R,6E,8R,10E,11aR)-4,8-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 162886775 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/JO01291A023
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-(hydroxymethyl)-3-methyloxirane-2-carboxylate 331146 Click to see CC1C(O1)(CO)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 378.40 unknown https://doi.org/10.1021/JO01291A023
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-(hydroxymethyl)but-2-enoate 74036903 Click to see CC=C(CO)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1021/JO01291A023
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-hydroxy-2-(hydroxymethyl)-3-sulfanylbutanoate 433037 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(CO)(C(C)S)O)C(=C)C(=O)O2 412.50 unknown https://doi.org/10.1021/JO01291A023
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2,3-dimethyloxirane-2-carboxylate 433036 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aR,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (3S)-3-hydroxy-2-methylidenebutanoate 162974203 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(=C)C(C)O)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aR,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-(hydroxymethyl)but-2-enoate 163085030 Click to see CC=C(CO)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aR,4R,6E,9R,10E,11aS)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-(hydroxymethyl)but-2-enoate 162946738 Click to see CC=C(CO)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aR,4R,6Z,8R,10E,11aS)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3S)-2-hydroxy-2-(hydroxymethyl)-3-sulfanylbutanoate 162988900 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(CO)(C(C)S)O)C(=C)C(=O)O2 412.50 unknown https://doi.org/10.1021/JO01291A023
[(3aR,4R,6Z,8S,10Z,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R,3R)-2-(hydroxymethyl)-3-methyloxirane-2-carboxylate 162995088 Click to see CC1C(O1)(CO)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 378.40 unknown https://doi.org/10.1021/JO01291A023
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R,3R)-2-(hydroxymethyl)-3-methyloxirane-2-carboxylate 162995091 Click to see CC1C(O1)(CO)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 378.40 unknown https://doi.org/10.1021/JO01291A023
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162987704 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3S)-2-hydroxy-2-(hydroxymethyl)-3-sulfanylbutanoate 162988899 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(CO)(C(C)S)O)C(=C)C(=O)O2 412.50 unknown https://doi.org/10.1021/JO01291A023
[(3aS,4R,6E,8S,10E,11aS)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (3R)-3-hydroxy-2-methylidenebutanoate 162974202 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(=C)C(C)O)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1021/JO01291A023
[(3aS,4S,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 162980140 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1021/JO01291A023

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