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Helenium virginicum

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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 UUID643fc8f0b5b86672200520
Scientific name Helenium virginicum
Authority S.F.Blake
First published in Claytonia 3: 13. 1936

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English virginia sneezeweed

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
    • North-central U.S.A.
      • Missouri
    • Southeastern U.S.A.
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000026433
USDA Plants HEVI6
Tropicos 2725567
KEW urn:lsid:ipni.org:names:118807-2
The Plant List gcc-125541
Missouri Botanical Garden 277599
Open Tree Of Life 483911
NCBI Taxonomy 138409
Nature Serve 2.134817
IPNI 118807-2
iNaturalist 163594
GBIF 5401858
Freebase /m/0gkyb6p
EOL 491616
USDA GRIN 416291
Wikipedia Helenium_virginicum
CMAUP NPO28436

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
Using life‐history trait variation to inform ecological risk assessments for threatened and endangered plant species Rueda‐Cediel P, Galic N, Brain R, Pinto‐Ledezma JN, Rico A, Forbes V Integr Environ Assess Manag 24-May-2022
PMCID:PMC10083932
doi:10.1002/ieam.4615
PMID:35373456
Two decades of demography reveals that seed and seedling transitions limit population persistence in a translocated shrub Gross CL, Mackay D Ann Bot 20-May-2014
PMCID:PMC4071100
doi:10.1093/aob/mcu082
PMID:24844983
Life history mediates mate limitation and population viability in self-incompatible plant species Thrall PH, Encinas-Viso F, Hoebee SE, Young AG Ecol Evol 13-Feb-2014
PMCID:PMC3967894
doi:10.1002/ece3.963
PMID:24683451
Constituents of Helenium species. XX. Virginolide, a new guaianolide from Helenium virginicum Werner Herz, Peruvemba Santhanam American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO01288A073

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aR,8aR,9aR)-5,8-dimethyl-1-methylidene-4,8a,9,9a-tetrahydro-3aH-azuleno[6,5-b]furan-2,6-dione 162959664 Click to see CC1=C2C(CC3C(C1)OC(=O)C3=C)C(=CC2=O)C 244.28 unknown https://doi.org/10.1021/JO01288A073
(3aR,8aS,9aR)-5,8-dimethyl-1-methylidene-4,8a,9,9a-tetrahydro-3aH-azuleno[6,5-b]furan-2,6-dione 101286198 Click to see CC1=C2C(CC3C(C1)OC(=O)C3=C)C(=CC2=O)C 244.28 unknown https://doi.org/10.1021/JO01288A073
5,8-dimethyl-1-methylidene-4,8a,9,9a-tetrahydro-3aH-azuleno[6,5-b]furan-2,6-dione 162959663 Click to see CC1=C2C(CC3C(C1)OC(=O)C3=C)C(=CC2=O)C 244.28 unknown https://doi.org/10.1021/JO01288A073
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Erythrinasinate A 101426086 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)OC)O 586.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
6-Prenylapigenin 10382485 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O)C 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1021/JO01288A073
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
5-Hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-f]chromen-10-one 101396889 Click to see CC1(C=CC2=C(O1)C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
Atalantoflavone 14162621 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)C 336.30 unknown via CMAUP database
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Vogelin E 10904337 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)CO 354.40 unknown via CMAUP database
Vogelin F 11143123 Click to see CC(=CCC1=CC(=C(C=C1O)OC)C2=COC3=CC(=CC(=C3C2=O)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
Vogelin D 636894 Click to see CC(=CCC1=C(C=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)OC)C 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
6,8-Diprenylgenistein 480783 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 406.50 unknown via CMAUP database
8-Prenylluteone 471687 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 422.50 unknown via CMAUP database
Auriculasin 5358846 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C 420.50 unknown via CMAUP database
Auriculatin 5358847 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C 420.50 unknown via CMAUP database
Warangalone 5379679 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 404.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Isoderrone 14237660 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)C 336.30 unknown via CMAUP database

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