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Internal ID UUID643fd1cd77e9f498594482
Scientific name Helichrysum forskahlii
Authority (J.F.Gmel.) Hilliard & B.L.Burtt
First published in Notes Roy. Bot. Gard. Edinburgh 38(1): 146 (1980)

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Synonyms Top

Scientific name Authority First published in
Helichrysum leptothamnus Moeser Bot. Jahrb. Syst. 44(2-3): 258 (1910)
Helichrysum steudneri Schweinf. ex Engl. Abh. Königl. Akad. Wiss. Berlin 1891: 430, in syn. (1892)
Helichrysum helothamnus Moeser Bot. Jahrb. Syst. 44(2-3): 259 (1910)
Helichrysum fruticosum Vatke Linnaea 39: 491 (1875)
Gnaphalium chrysocoma Sch.Bip. Bot. Zeitung (Berlin) 3: 174 (1845)
Helichrysum fruticosum var. chrysocephalum Sch.Bip. ex Vatke
Gnaphalium chrysocephalum Sch.Bip. Bot. Zeitung (Berlin) 3: 174 (1845)
Helichrysum cymosum subsp. helothamnus (Moeser) Hedberg
Gnaphalium forskaolii J.F.Gmel. Syst. Nat. ed. 13[bis] 2(2): 1214 (1792)
Helichrysum fruticosum var. majus Moeser Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 44: 258 1910
Helichrysum helothamnus var. majus (Moeser) Lisowski Fl. Afr. Centr., Spermatophytes, Compos. 2: 92 (1989):.
Gnaphalium fruticosum Forssk. Fl. Aegypt.-Arab. : 218 (1775)
Helichrysum chrysocoma Sch.Bip. ex A.Rich. Tent. Fl. Abyss. 1: 424 (1848)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Helichrysum forskahlii var. compactum (Vatke) Mesfin Compositae Newslett. 22: 13, without full basionym (1992)

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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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000118360
Tropicos 2737031
KEW urn:lsid:ipni.org:names:212761-1
The Plant List gcc-79690
Open Tree Of Life 160105
NCBI Taxonomy 630302
IPNI 212761-1
iNaturalist 963063
GBIF 3131114

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
Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA Molecules 05-Dec-2023
PMCID:PMC10745828
doi:10.3390/molecules28247937
PMID:38138427
Repeatedly Northwards and Upwards: Southern African Grasslands Fuel the Colonization of the African Sky Islands in Helichrysum (Compositae) Blanco-Gavaldà C, Galbany-Casals M, Susanna A, Andrés-Sánchez S, Bayer RJ, Brochmann C, Cron GV, Bergh NG, Garcia-Jacas N, Gizaw A, Kandziora M, Kolář F, López-Alvarado J, Leliaert F, Letsara R, Moreyra LD, Razafimandimbison SG, Schmickl R, Roquet C Plants (Basel) 03-Jun-2023
PMCID:PMC10255704
doi:10.3390/plants12112213
PMID:37299192
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
A Systematic Review of Medicinal Plants of Kenya used in the Management of Bacterial Infections Odongo EA, Mutai PC, Amugune BK, Mungai NN Evid Based Complement Alternat Med 24-Mar-2022
PMCID:PMC8970882
doi:10.1155/2022/9089360
PMID:35368751
Antibacterial and Antifungal Activities of Ethiopian Medicinal Plants: A Systematic Review Nigussie D, Davey G, Tufa TB, Brewster M, Legesse BA, Fekadu A, Makonnen E Front Pharmacol 01-Jun-2021
PMCID:PMC8203926
doi:10.3389/fphar.2021.633921
PMID:34140888
Inhibition of Oxidative Stress and Skin Aging-Related Enzymes by Prenylated Chalcones and Other Flavonoids from Helichrysum teretifolium. Popoola OK, Marnewick JL, Rautenbach F, Ameer F, Iwuoha EI, Hussein AA Molecules 20-Apr-2015
PMCID:PMC6272301
doi:10.3390/MOLECULES20047143
PMID:25903365
An Overview on Cardamonin Gonçalves LM, Valente IM, Rodrigues JA J Med Food 01-Jun-2014
PMCID:PMC4060836
doi:10.1089/jmf.2013.0061
PMID:24433078
Flavonoids and terpenoids from Helichrysum forskahlii. Al-Rehaily AJ, Albishi OA, El-Olemy MM, Mossa JS Phytochemistry 01-Jun-2008
doi:10.1016/J.PHYTOCHEM.2008.03.025
PMID:18485427
12β-hydroxyabieta-7, 13-diene and other constituents from east african Helichrysum species J. Jakupovic, M. Grenz, F. Bohlmann, G.M. Mungai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80127-3

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
Helihumulone 14282633 Click to see CC(=CCC1=C(C(C(=O)C(=C1O)C(=O)CCC2=CC=CC=C2)(CC=C(C)C)OC)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(90)80127-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)80127-3
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)80127-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 928713 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/J.PHYTOCHEM.2008.03.025
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/J.PHYTOCHEM.2008.03.025
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/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
5,7-Dihydroxy-8-prenylflavanone 3144815 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3)C 324.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272301/
Glabranin 124049 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3)C 324.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272301/
https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(90)80127-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
https://doi.org/10.1016/0031-9422(90)80127-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-6-hydroxy-5-methoxy-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 162876365 Click to see CC(=CCOC1=C(C(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
6-Hydroxy-5-methoxy-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 24970588 Click to see CC(=CCOC1=C(C(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
7-Hydroxy-5-methoxy-2-phenylchroman-4-one 4053302 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-Phenyl-1-(2,4,6-trihydroxy-3-methoxyphenyl)propan-1-one 24970524 Click to see COC1=C(C=C(C(=C1O)C(=O)CCC2=CC=CC=C2)O)O 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-(5,7-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)-3-phenylprop-2-en-1-one 58260141 Click to see CC1(CCC2=C(O1)C(=C(C=C2O)O)C(=O)C=CC3=CC=CC=C3)C 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
(E)-1-[3,6-dihydroxy-2-methoxy-4-(3-methylbut-2-enoxy)phenyl]-3-phenylprop-2-en-1-one 24970523 Click to see CC(=CCOC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
(E)-3-phenyl-1-[(3R)-3,5,7-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]prop-2-en-1-one 163068127 Click to see CC1(C(CC2=C(O1)C(=C(C=C2O)O)C(=O)C=CC3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
(E)-3-phenyl-1-[(3S)-3,5,7-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]prop-2-en-1-one 163195222 Click to see CC1(C(CC2=C(O1)C(=C(C=C2O)O)C(=O)C=CC3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
1-(5,7-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)-3-phenylprop-2-en-1-one 76748463 Click to see CC1(CCC2=C(O1)C(=C(C=C2O)O)C(=O)C=CC3=CC=CC=C3)C 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
1-[3,6-Dihydroxy-2-methoxy-4-(3-methylbut-2-enoxy)phenyl]-3-phenylprop-2-en-1-one 74376498 Click to see CC(=CCOC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
3-Phenyl-1-(3,5,7-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)prop-2-en-1-one 163068126 Click to see CC1(C(CC2=C(O1)C(=C(C=C2O)O)C(=O)C=CC3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
CID 460718 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Pinocembrin chalcone 6474295 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',6',4-Tetrahydroxy-3'-prenylchalcone 189267 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=C(C=C2)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025
Desmethylxanthohumol 6443339 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C=CC2=CC=C(C=C2)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.025

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