Helichrysum cymosum - Unknown
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Internal ID UUID643fcf649db62577948928
Scientific name Helichrysum cymosum
Authority (L.) D.Don
First published in in Mem. Wern. Soc. v. (1824) 550; Less. Syn. Comp. 302.

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Helichrysum cymosum subsp. calvum Hilliard Notes Roy. Bot. Gard. Edinburgh 32(3): 346 (1973)
Helichrysum cymosum subsp. cymosum (L.) D.Don

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Zambia
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
    • West-central Tropical Africa
      • Gulf Of Guinea Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000089954
Tropicos 2719232
KEW urn:lsid:ipni.org:names:60464616-2
The Plant List gcc-46253
Open Tree Of Life 906550
NCBI Taxonomy 379243
IPNI 60464616-2
iNaturalist 342438
GBIF 3131345

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
Topsoil and Vegetation Dynamics 14 Years after Eucalyptus grandis Removal in Eastern Cape Province of South Africa Mthethwa K, Ruwanza S Plants (Basel) 24-Aug-2023
PMCID:PMC10490425
doi:10.3390/plants12173047
PMID:37687294
Green-Synthesized Silver Nanoparticles: Antifungal and Cytotoxic Potential for Further Dental Applications Klein W, Ismail E, Maboza E, Hussein AA, Adam RZ J Funct Biomater 20-Jul-2023
PMCID:PMC10381808
doi:10.3390/jfb14070379
PMID:37504874
Elevational distribution of montane Afrotropical butterflies is influenced by seasonality and habitat structure Mtui DT, Ogutu JO, Okick RE, Newmark WD PLoS One 05-Jul-2022
PMCID:PMC9255748
doi:10.1371/journal.pone.0270769
PMID:35789332
Helichrysum Genus and Compound Activities in the Management of Diabetes Mellitus Akinfenwa AO, Sagbo IJ, Makhaba M, Mabusela WT, Hussein AA Plants (Basel) 23-May-2022
PMCID:PMC9143910
doi:10.3390/plants11101386
PMID:35631811
Comparative Study of the Antioxidant Constituents, Activities and the GC-MS Quantification and Identification of Fatty Acids of Four Selected Helichrysum Species Akinyede KA, Hughes GD, Ekpo OE, Oguntibeju OO Plants (Basel) 07-Apr-2022
PMCID:PMC9028396
doi:10.3390/plants11080998
PMID:35448730
Ericaceous vegetation of the Bale Mountains of Ethiopia will prevail in the face of climate change Kidane YO, Hoffmann S, Jaeschke A, Beloiu M, Beierkuhnlein C Sci Rep 03-Feb-2022
PMCID:PMC8813939
doi:10.1038/s41598-022-05846-z
PMID:35115621
Potential Benefits of Antiviral African Medicinal Plants in the Management of Viral Infections: Systematic Review Beressa TB, Deyno S, Mtewa AG, Aidah N, Tuyiringire N, Lukubye B, Weisheit A, Tolo CU, Ogwang PE Front Pharmacol 24-Dec-2021
PMCID:PMC8740180
doi:10.3389/fphar.2021.682794
PMID:35002686
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
A Review on Medicinal Plants Used in the Management of Headache in Africa Frimpong EK, Asong JA, Aremu AO Plants (Basel) 28-Sep-2021
PMCID:PMC8539318
doi:10.3390/plants10102038
PMID:34685845
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Medicinal Properties and In Vitro Biological Activities of Selected Helichrysum Species from South Africa: A Review Akinyede KA, Cupido CN, Hughes GD, Oguntibeju OO, Ekpo OE Plants (Basel) 30-Jul-2021
PMCID:PMC8398148
doi:10.3390/plants10081566
PMID:34451611
Therapeutic Potentials of Antiviral Plants Used in Traditional African Medicine With COVID-19 in Focus: A Nigerian Perspective Attah AF, Fagbemi AA, Olubiyi O, Dada-Adegbola H, Oluwadotun A, Elujoba A, Babalola CP Front Pharmacol 26-Apr-2021
PMCID:PMC8108136
doi:10.3389/fphar.2021.596855
PMID:33981214
The traditional use of southern African medicinal plants in the treatment of viral respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7384428
doi:10.1016/j.jep.2020.113194
PMID:32730880
Medicinal Plants Traded in Informal Herbal Medicine Markets of the Limpopo Province, South Africa Rasethe MT, Semenya SS, Maroyi A Evid Based Complement Alternat Med 16-Apr-2019
PMCID:PMC6500648
doi:10.1155/2019/2609532
PMID:31118951
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986

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
(6S)-3,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-enyl)-2-(3-phenylpropanoyl)cyclohexa-2,4-dien-1-one 163039081 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/S0031-9422(00)91472-9
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/S0031-9422(00)91472-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E)-beta-farnesene 10407 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6Z,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 11975273 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2-Hydroxy-1-(7-methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one 71374358 Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)CO)C 248.27 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> 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/10.1016/0031-9422(89)80195-5
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,4'-Trihydroxy-7,8-dimethoxyflavone 14034221 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)OC 330.29 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,8-dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 162880441 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80195-5
5,8-Dihydroxy-7-methoxyflavanone 13888646 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-5-hydroxy-8-methoxy-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 162876082 Click to see CC(=CCOC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC)C 354.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
8-Methoxypinocembrin 7-O-prenyl ether 14282635 Click to see CC(=CCOC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC)C 354.40 unknown https://doi.org/10.1016/0031-9422(89)80195-5
Dihydrowogonin 11491431 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80195-5
S-Dihydrowogonin 10265977 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80195-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (E)-; Chalcone, 2',6'-dihydroxy-4'-methoxy-; 2',6'-Dihydroxy-4'-methoxychalcone 606469 Click to see COC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
Pinostrobin chalcone 5316793 Click to see COC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,6-Dihydroxy-4-methoxy-3-(3-methylbut-2-enyl)phenyl]-3-phenylprop-2-en-1-one 73194187 Click to see CC(=CCC1=C(C=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)O)OC)C 338.40 unknown https://doi.org/10.1016/S0031-9422(00)91472-9
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)91472-9
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)91472-9
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/10.1016/0031-9422(89)80195-5
Isoxanthohumol(Helichrysum) 15410693 Click to see CC(=CCC1=C(C=C(C(=C1O)C(=O)C=CC2=CC=CC=C2)O)OC)C 338.40 unknown https://doi.org/10.1016/S0031-9422(00)91472-9

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