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Eupatorium semiserratum

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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 UUID643fc9c55b93b051845933
Scientific name Eupatorium semiserratum
Authority DC.
First published in Prodr. 5: 177 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium ambiguum Hook. Companion Bot. Mag. 1: 96 (1835)
Uncasia semiserrata Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)
Eupatorium cuneifolium var. semiserratum Fernald & Griscom Rhodora 37: 179 (1935)

Common names Top

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Language Common/alternative name
English smallflower 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
  • Northern America
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Louisiana
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000033206
Florida Plant Atlas 1036
Flora of Alabama 739
USDA Plants EUSE
Tropicos 2702490
KEW urn:lsid:ipni.org:names:206905-1
The Plant List gcc-132106
Open Tree Of Life 680346
NCBI Taxonomy 103755
Nature Serve 2.132316
IPNI 206905-1
iNaturalist 162802
GBIF 5403078
Freebase /m/04gw02k
EOL 475575
Wikipedia Eupatorium_semiserratum
CMAUP NPO14553

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
Corrigendum: In silico identification of anti-cancer compounds and plants from traditional Chinese medicine database Dai SX, Li WX, Han FF, Guo YC, Zheng JJ, Liu JQ, Wang Q, Gao YD, Li GH, Huang JF Sci Rep 10-Oct-2016
PMCID:PMC5056451
doi:10.1038/srep34972
PMID:27721399
In silico identification of anti-cancer compounds and plants from traditional Chinese medicine database Dai SX, Li WX, Han FF, Guo YC, Zheng JJ, Liu JQ, Wang Q, Gao YD, Li GH, Huang JF Sci Rep 05-May-2016
PMCID:PMC4857115
doi:10.1038/srep25462
PMID:27145869
Sesquiterpene lactones and other constituents of Eupatorium lancifolium and E. semiserratum Werner Herz, Serengolam V. Govindan, Narendra Kumar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)80035-0

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 / Lappaconitine-type diterpenoid alkaloids
[(2R,3R,5R,6S,8S,9S,13S,17S)-11-ethyl-2,3,8,9-tetrahydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 5316363 Click to see CCN1CC2(CCC(C34C2CC(C31)(C5(CC(C6CC4(C5(C6OC)O)O)OC)O)O)OC)OC(=O)C7=CC=CC=C7N 574.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,4S)-6-[[(4aR,6bS,8R,9R,14aR)-8,9,10-trihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(4S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 6325062 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CC(C9(C8CC(C(C9O)O)(C)C)CO)O)C)C)C)C(=O)O)O)CO)O)O)O)O)O 1137.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(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/10.1016/0031-9422(81)80035-0
[(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/10.1016/0031-9422(81)80035-0
Deacetyleupaserrin 44582751 Click to see CC=C(CO)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown via CMAUP database
Eupatocunin 44444903 Click to see CC=C(C)C(=O)OC1C2C(C=C(C(CC=C(C1O)C)OC(=O)C)C)OC(=O)C2=C 404.50 unknown via CMAUP database
Eupatofolin 54606505 Click to see CC=C(COC(=O)C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 404.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Eupatoriochromene 100768 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O 218.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eupatin 5317287 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O 360.30 unknown via CMAUP database
Eupatoretin 275525 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)O)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
(2S)-5,7-dihydroxy-6-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 163035976 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 316.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
(2s)-5,7,4'-Trihydroxy-6-methoxyflavanone 46893290 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(81)80035-0
5,7-Dihydroxy-6-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 90872794 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 316.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
5,7,4'-Trihydroxy-6-methoxyflavanone 5322074 Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(81)80035-0
Eupatilin 5273755 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-3',5-Dihydroxy-4',6,7-trimethoxyflavanone 44566966 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
(2S)-5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 163066285 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 330.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
5-Hydroxy-6,7,4'-trimethoxyflavanone 14078483 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 330.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
5,3'-Dihydroxy-6,7,4'-trimethoxyflavanone 13871373 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(81)80035-0
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database

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