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Helichrysum athrixiifolium

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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 UUID643fcf0877fdd406145345
Scientific name Helichrysum athrixiifolium
Authority (Kuntze) Moeser
First published in Bot. Jahrb. 44: 281 (1910).

Description Top

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Synonyms Top

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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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No germination or propagation data was added yet.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000086735
Tropicos 2719151
KEW urn:lsid:ipni.org:names:212449-1
The Plant List gcc-43117
Open Tree Of Life 7601053
IPNI 212449-1
iNaturalist 586872
GBIF 3131184
EPPO HECAX
EOL 6230410

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
Three prenylated flavanoids from Helichrysum athrixiifolium Ferdinand Bohlmann, Nezhun Ates Gören Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80458-6

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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-(3-methylbut-2-enoxy)-2,3-dihydrochromen-4-one 162842343 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-7-((3-methyl-2-butenyl)oxy)-2-phenyl-, (S)- 185341 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
5,4'-Dihydroxy-7-O-prenylflavanone 12110170 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
7-O-Prenylpinocembrin 21721815 Click to see CC(=CCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-[2,6-Dihydroxy-4-(3-methylbut-2-enoxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 74819245 Click to see CC(=CCOC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=C(C=C2)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
1-[2,6-Dihydroxy-4-(3-methylbut-2-enoxy)phenyl]-3-phenylprop-2-en-1-one 72729466 Click to see CC(=CCOC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
2',6'-Dihydroxy-4'-prenyloxychalcone 14282634 Click to see CC(=CCOC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
4,2',6'-Trihydroxy-4'-prenyloxychalcone 42607608 Click to see CC(=CCOC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=C(C=C2)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',6'-Trihydroxy-3'-c-prenylchalcone 73171715 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=CC=C2)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6
Desmethylisoxanthohumol 11992148 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=CC=C2)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(00)80458-6

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