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Eupatorium hyssopifolium

Eupatorium hyssopifolium - 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 UUID643fca1858c14207481655
Scientific name Eupatorium hyssopifolium
Authority L.
First published in Sp. Pl. : 836 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium torreyanum Short ex Torr. & A.Gray Fl. N. Amer. 2: 84 (1841)
Eupatorium lecheifolium Greene Pittonia 3(16): 177 (1897)
Eupatorium linearifolium Michaux Fl. Bor.-Amer. 2: 97. 1803.
Uncasia lecheaefolia Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)
Uncasia hyssopifolia Greene Leafl. Bot. Observ. Crit. 1: 13 (1903)
Eupatorium hyssopifolium var. calcaratum Fernald & B.G.Schub. Rhodora 50: 227 (1948)
Eupatorium hyssopifolium var. hyssopifolium L.
Eupatorium linearifolium Michx. Fl. Bor.-Amer. 2: 97, partim (1803)
Eupatorium torreyanum Short & R.Peter Transylvania J. Med. Assoc. Sci. 8(32): 5 (-6) 1836
Eupatorium crassifolium Raf. Fl. Ludov. 62 (sp. falsa). (1817)

Common names Top

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Language Common/alternative name
English hyssopleaf thoroughwort

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Eupatorium hyssopifolium var. laciniatum A.Gray Syn. Fl. N. Amer. 1(2): 98 (1884)

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
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000035601
USDA Plants EUHY
Tropicos 2702479
KEW urn:lsid:ipni.org:names:277025-2
The Plant List gcc-134436
Open Tree Of Life 394784
NCBI Taxonomy 102774
Nature Serve 2.131085
IPNI 277025-2
iNaturalist 136397
GBIF 5403057
Freebase /m/04gpnzc
EPPO EUPHY
EOL 475535
USDA GRIN 454513
Wikipedia Eupatorium_hyssopifolium

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
Effects of season of fire on bee‐flower interaction diversity in a fire‐maintained pine savanna Ulyshen M, Robertson K, Horn S, Dixon C Ecol Evol 21-Aug-2023
PMCID:PMC10441176
doi:10.1002/ece3.10450
PMID:37608923
Digging the New York City Skyline: Soil Fungal Communities in Green Roofs and City Parks McGuire KL, Payne SG, Palmer MI, Gillikin CM, Keefe D, Kim SJ, Gedallovich SM, Discenza J, Rangamannar R, Koshner JA, Massmann AL, Orazi G, Essene A, Leff JW, Fierer N PLoS One 01-Mar-2013
PMCID:PMC3585938
doi:10.1371/journal.pone.0058020
PMID:23469260
Sesquiterpene lactones of Eupatorium hyssopifolium. Germacranolide with an unusual lipid ester side chain Werner Herz, Ram P. Sharma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO00868A022
Neue sesquiterpenlactone und andere inhaltsstoffe aus vertretern der Eupatorium-gruppe Ferdinand Bohlmann, Pradip Kumar Mahanta, Albert Suwita, Antoinette Suwita, Arvind Anant Natu, Christa Zdero, Wolfgang Dorner, Dorothea Ehlers, Michael Grenz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(77)80107-6

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 / Monoterpenoids / Bicyclic monoterpenoids
(3,3,7,9-Tetramethyl-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl) 2-methylbut-2-enoate 163018132 Click to see CC=C(C)C(=O)OC1CCC2(C3C(C2C(=O)C=C3C)C1(C)C)C 316.40 unknown https://doi.org/10.1016/0031-9422(77)80107-6
[(1S,2R,4S,7S,8S)-3,3,7,9-tetramethyl-11-oxo-4-tricyclo[5.4.0.02,8]undec-9-enyl] (Z)-2-methylbut-2-enoate 163018134 Click to see CC=C(C)C(=O)OC1CCC2(C3C(C2C(=O)C=C3C)C1(C)C)C 316.40 unknown https://doi.org/10.1016/0031-9422(77)80107-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(1S,2R,4S,7Z,10R,11R)-4-(hydroxymethyl)-8-methyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162918280 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O3)CO 378.40 unknown https://doi.org/10.1021/JO00868A022
[(1S,2S,4R,7E,10R,11R)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] (E)-4-hydroxy-2-methylbut-2-enoate 124630954 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1021/JO00868A022
[(3aR,4R,11aR)-10-(acetyloxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-methylbut-2-enoate 162870136 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)COC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(77)80107-6
[(3aR,4R,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-methylbut-2-enoate 162988510 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)CO 362.40 unknown https://doi.org/10.1016/0031-9422(77)80107-6
[(3aR,4R,6E,10Z,11aR)-10-(acetyloxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 163194922 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)COC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(77)80107-6
[(E)-4-[[(1S,2R,4S,7Z,10R,11R)-4-(hydroxymethyl)-8-methyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl]oxy]-3-methyl-4-oxobut-2-enyl] (3S)-3-hydroxyoctadecanoate 163053495 Click to see CCCCCCCCCCCCCCCC(CC(=O)OCC=C(C)C(=O)OC1CC(=CCCC2(C(O2)C3C1C(=C)C(=O)O3)CO)C)O 660.90 unknown https://doi.org/10.1021/JO00868A022
[(E)-4-[[(1S,2S,4S,7E,10R,11R)-4-(hydroxymethyl)-8-methyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl]oxy]-3-methyl-4-oxobut-2-enyl] (3R)-3-hydroxyoctadecanoate 163053493 Click to see CCCCCCCCCCCCCCCC(CC(=O)OCC=C(C)C(=O)OC1CC(=CCCC2(C(O2)C3C1C(=C)C(=O)O3)CO)C)O 660.90 unknown https://doi.org/10.1021/JO00868A022
[4-(Hydroxymethyl)-8-methyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] 4-hydroxy-2-methylbut-2-enoate 162837 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O3)CO 378.40 unknown https://doi.org/10.1021/JO00868A022
[4-[[4-(Hydroxymethyl)-8-methyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl]oxy]-3-methyl-4-oxobut-2-enyl] 3-hydroxyoctadecanoate 73823164 Click to see CCCCCCCCCCCCCCCC(CC(=O)OCC=C(C)C(=O)OC1CC(=CCCC2(C(O2)C3C1C(=C)C(=O)O3)CO)C)O 660.90 unknown https://doi.org/10.1021/JO00868A022

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