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Helichrysum thapsus

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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 UUID643fc8f8cf350204273989
Scientific name Helichrysum thapsus
Authority (Kuntze) Moeser
First published in Bot. Jahrb. 44: 263 (1910).

Description Top

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Synonyms Top

Scientific name Authority First published in
Gnaphalium thapsus (O.Hoffm.) Kuntze Revis. Gen. Pl. 3[3]: 154 (1898)
Helichrysum lanatomarginatum Markötter Ann. Univ. Stellenbosch 8(Sect. A, 1): 47. 1930

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000026704
Tropicos 2719567
KEW urn:lsid:ipni.org:names:213427-1
The Plant List gcc-12581
Open Tree Of Life 7601440
IPNI 213427-1
iNaturalist 587042
GBIF 3131429

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)!
Title Authors Publication Released IDs
Flavanones from Helichrysum thapsus Ferdinand Bohlmann, Christa Zdero Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97725-2

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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R,3S)-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 162984698 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
(2r,3s)-3,5,7-Trihydroxy-6-c-geranylflavanone 129710485 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
(2S,3S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,5,7-trihydroxy-2-phenyl-2,3-dihydrochromen-4-one 163031136 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
[(2R,3R)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate 162937917 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)OC(=O)C)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
[(2S,3S)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate 162937916 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)OC(=O)C)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
[5,7-Dihydroxy-6-(3-methylbut-2-enyl)-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate 162937915 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)OC(=O)C)C3=CC=CC=C3)O)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
3,5,7-Trihydroxy-6-c-prenylflavanone 129711202 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
5,7-Dihydroxy-6-prenylflavanone 480763 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
6-(3,7-Dimethylocta-2,6-dienyl)-3,5,7-trihydroxy-2-phenyl-2,3-dihydrochromen-4-one 163031134 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97725-2
6-Prenylpinocembrin 6546086 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)97725-2

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