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Helichrysum argyrophyllum

Helichrysum argyrophyllum - 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 UUID643fc6e4ac488391896114
Scientific name Helichrysum argyrophyllum
Authority DC.
First published in Prodr. 6: 186 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gnaphalium argyrophyllum Sch.Bip. Bot. Zeitung (Berlin) 3: 171 (1845)

Common names Top

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Language Common/alternative name
Afrikaans gouemuntsewejaartjie

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000010089
Tropicos 2719137
KEW urn:lsid:ipni.org:names:212435-1
The Plant List gcc-10977
Open Tree Of Life 449122
NCBI Taxonomy 112356
IPNI 212435-1
iNaturalist 402442
GBIF 3131909
EPPO HECAG

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
Phylogeny, biogeography, and character evolution of Anaphalis (Gnaphalieae, Asteraceae) Xu XM, Xu H, Yang Z, Wei Z, Gu JY, Liu DH, Liu QR, Zhu SX Front Plant Sci 07-Feb-2024
PMCID:PMC10879626
doi:10.3389/fpls.2024.1336229
PMID:38384761
Twenty-one acylphloroglucinol derivatives and further constituents from south african Helichrysum species J. Jakupovic, C. Zdero, M. Grenz, F. Tsichritzis, L. Lehmann, S.M. Hashemi-Nejad, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80195-5

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 / Acetophenones
1-[(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone 12414274 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(89)80195-5
Ethanone, 1-[2,3-dihydro-2-(1-methylethenyl)-5-benzofuranyl]- 317196 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(89)80195-5
Tremetone 78673 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,2-diacylglycerols
[(2R)-3-hydroxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] 8-methylnonanoate 163029720 Click to see CC=C(C)C(=O)OC(CO)COC(=O)CCCCCCC(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[(2S)-3-hydroxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] decanoate 162915597 Click to see CCCCCCCCCC(=O)OCC(CO)OC(=O)C(=CC)C 328.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[(2S)-3-hydroxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] nonanoate 163024862 Click to see CCCCCCCCC(=O)OCC(CO)OC(=O)C(=CC)C 314.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Hydroxy-2-(2-methylbut-2-enoyloxy)propyl] 8-methylnonanoate 163029719 Click to see CC=C(C)C(=O)OC(CO)COC(=O)CCCCCCC(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Hydroxy-2-(2-methylbut-2-enoyloxy)propyl] decanoate 162915596 Click to see CCCCCCCCCC(=O)OCC(CO)OC(=O)C(=CC)C 328.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Hydroxy-2-(2-methylbut-2-enoyloxy)propyl] nonanoate 163024861 Click to see CCCCCCCCC(=O)OCC(CO)OC(=O)C(=CC)C 314.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
[(2R)-3-acetyloxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] 8-methylnonanoate 162940960 Click to see CC=C(C)C(=O)OC(COC(=O)C)COC(=O)CCCCCCC(C)C 370.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[(2S)-3-acetyloxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] decanoate 163092348 Click to see CCCCCCCCCC(=O)OCC(COC(=O)C)OC(=O)C(=CC)C 370.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[(2S)-3-acetyloxy-2-[(Z)-2-methylbut-2-enoyl]oxypropyl] nonanoate 162912684 Click to see CCCCCCCCC(=O)OCC(COC(=O)C)OC(=O)C(=CC)C 356.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Acetyloxy-2-(2-methylbut-2-enoyloxy)propyl] 8-methylnonanoate 162940959 Click to see CC=C(C)C(=O)OC(COC(=O)C)COC(=O)CCCCCCC(C)C 370.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Acetyloxy-2-(2-methylbut-2-enoyloxy)propyl] decanoate 163092347 Click to see CCCCCCCCCC(=O)OCC(COC(=O)C)OC(=O)C(=CC)C 370.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
[3-Acetyloxy-2-(2-methylbut-2-enoyloxy)propyl] nonanoate 162912683 Click to see CCCCCCCCC(=O)OCC(COC(=O)C)OC(=O)C(=CC)C 356.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1Z,5Z,8R)-1,5-dimethyl-8-(6-methylhepta-1,5-dien-2-yl)cyclodeca-1,5-diene 163042799 Click to see CC1=CCCC(=CCC(CC1)C(=C)CCC=C(C)C)C 272.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
1,5-Dimethyl-8-(6-methylhepta-1,5-dien-2-yl)cyclodeca-1,5-diene 163042798 Click to see CC1=CCCC(=CCC(CC1)C(=C)CCC=C(C)C)C 272.50 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(89)80195-5
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(89)80195-5
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-hydroxyphenyl)-3-methylbutan-1-one 13308867 Click to see CC(C)CC(=O)C1=C(C=CC(=C1)C(=O)C)O 220.26 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(5,7-Dihydroxy-8-methoxy-4-oxo-2-phenylchromen-3-yl) 2-methylbut-2-enoate 72729467 Click to see CC=C(C)C(=O)OC1=C(OC2=C(C1=O)C(=CC(=C2OC)O)O)C3=CC=CC=C3 382.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
3,5,7-Trihydroxy-8-methoxyflavone 3-angelate 14282639 Click to see CC=C(C)C(=O)OC1=C(OC2=C(C1=O)C(=CC(=C2OC)O)O)C3=CC=CC=C3 382.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5

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