Eupatorium album - Unknown
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Internal ID UUID643fcc3179790096984770
Scientific name Eupatorium album
Authority L.
First published in Mant. Pl. : 111 (1767)

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Synonyms Top

Scientific name Authority First published in
Eupatorium stigmatosum Bertol. Misc. Bot. v. 15. t. 5
Eupatorium glandulosum Michx. Fl. Bor.-Amer. 2: 98 (1803)
Uncasia alba Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)
Eupatorium petalodium Britton ex Small Bull. Torrey Bot. Club 24: 492. 1897.
Eupatorium glandulosum Michaux Fl. Bor.-Amer. 2: 98. 1803.
Eupatorium album var. album L.
Eupatorium album var. glandulosum (Michx.) DC. Prodr. 5: 178 (1836)

Common names Top

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Language Common/alternative name
English white thoroughwort

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Northern America
    • Northeastern U.S.A.
      • Connecticut
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Delaware
      • Florida
      • Georgia
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000059784
Florida Plant Atlas 3058
Flora of Alabama 717
USDA Plants EUAL2
Tropicos 2710181
KEW urn:lsid:ipni.org:names:99450-2
The Plant List gcc-16856
Open Tree Of Life 971141
NCBI Taxonomy 102768
Nature Serve 2.132636
IPNI 99450-2
iNaturalist 162779
GBIF 5402898
Freebase /m/04glg4r
EPPO EUPAL
EOL 475563
Wikipedia Eupatorium_album
CMAUP NPO27892

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
Trypanocidal and Anti-Inflammatory Effects of Three ent-Kaurane Diterpenoids from Gymnocoronis spilanthoides var. subcordata (Asteraceae) Selener MG, Borgo J, Sarratea MB, Delfino MA, Laurella LC, Cerny N, Gomez J, Coll M, Malchiodi EL, Bivona AE, Barrera P, Redko FC, Catalán CA, Alberti AS, Sülsen VP Pharmaceutics 18-Mar-2024
PMCID:PMC10975076
doi:10.3390/pharmaceutics16030415
PMID:38543309
Tetracyclic analogs of the rosane lactones from Eupatorium album Werner Herz, Serengolam V. Govindan, John F. Blount American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO01331A010
New hydroxylated ent-kauranoic acids from Eupatorium album. Herz W, Sharma RP J Org Chem 19-Mar-1976
doi:10.1021/JO00868A023
PMID:1255283

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
> Alkaloids and derivatives / Aporphines
(6aR)-2,10-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,11-diol 929259 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
Corypalmine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
Jatrorrhizine 72323 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC 338.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1S,14R)-20,21,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-6-ol 5320345 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Oxyacanthine 442333 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9R,10S,11S,13S,14R)-11-hydroxy-5,9,14-trimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162938709 Click to see CC1C2CC(C3C4(CCCC(C4CCC3(C2)C1=O)(C)C(=O)O)C)O 334.40 unknown https://doi.org/10.1021/JO00868A023
(1R,4S,5R,9R,10S,11S,13S,15R)-11,15-dihydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 21593621 Click to see CC12CCCC(C1CCC34C2C(CC(C3)C(=C)C4O)O)(C)C(=O)O 334.40 unknown https://doi.org/10.1021/JO00868A023
11-Hydroxy-5,9,14-trimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162938708 Click to see CC1C2CC(C3C4(CCCC(C4CCC3(C2)C1=O)(C)C(=O)O)C)O 334.40 unknown https://doi.org/10.1021/JO00868A023
11,15-Dihydroxy-16-kauren-19-oic acid 14610549 Click to see CC12CCCC(C1CCC34C2C(CC(C3)C(=C)C4O)O)(C)C(=O)O 334.40 unknown https://doi.org/10.1021/JO00868A023
ent-11|A-Hydroxy-15-oxokaur-16-en-19-oic acid 21593620 Click to see CC12CCCC(C1CCC34C2C(CC(C3)C(=C)C4=O)O)(C)C(=O)O 332.40 unknown https://doi.org/10.1021/JO00868A023
ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid 14610558 Click to see CC12CCCC(C1CCC34C2C(CC(C3)C(=C)C4=O)O)(C)C(=O)O 332.40 unknown https://doi.org/10.1021/JO00868A023
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
methyl 4-[10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate 5317043 Click to see CC(CCC(=O)OC)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C 550.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Encecalin 114703 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 232.27 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(1S,2S,5R,6R,8R,10S,11S,12R)-6,10-dihydroxy-2,6,12-trimethyl-16-oxapentacyclo[10.3.2.15,8.01,11.02,8]octadecan-17-one 101324895 Click to see CC12CCCC3(C1C(CC45C3(CCC(C4)C(C5)(C)O)C)O)OC2=O 334.40 unknown https://doi.org/10.1021/JO01331A010
(1S,2S,5R,6R,8R,9R,11R,12R)-6,9-dihydroxy-2,6,12-trimethyl-16-oxapentacyclo[10.3.2.15,8.01,11.02,8]octadecan-17-one 101324896 Click to see CC12CCCC3(C1CC(C45C3(CCC(C4)C(C5)(C)O)C)O)OC2=O 334.40 unknown https://doi.org/10.1021/JO01331A010
6,10-Dihydroxy-2,6,12-trimethyl-16-oxapentacyclo[10.3.2.15,8.01,11.02,8]octadecan-17-one 162940804 Click to see CC12CCCC3(C1C(CC45C3(CCC(C4)C(C5)(C)O)C)O)OC2=O 334.40 unknown https://doi.org/10.1021/JO01331A010
Eupatalbolide 432738 Click to see CC12CCCC3(C1CC(C45C3(CCC(C4)C(C5)(C)O)C)O)OC2=O 334.40 unknown https://doi.org/10.1021/JO01331A010
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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 https://doi.org/10.1021/JO01331A010

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