Pteronia incana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pteronia incana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fc8d18482e126325082
Scientific name Pteronia incana
Authority DC.
First published in Prodr. 5: 358 (1836)

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Synonyms Top

Scientific name Authority First published in
Chrysocoma incana Burm.f. Fl. Ind. Prodr. Fl. Cap.: 23 (1768)
Pteronia xantholepis DC. Prodr. 5: 358 (1836)
Eupatorium cinereum L.f. Suppl. Pl. : 354 (1782)
Athanasia rigida Scop. Introd. : 127
Pteronia rigida P.J.Bergius Descr. Pl. Cap. : 231 (1767)

Common names Top

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Language Common/alternative name
Afrikaans t'kaibebos

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000025449
Tropicos 2718210
KEW urn:lsid:ipni.org:names:240266-1
The Plant List gcc-124582
Open Tree Of Life 1058739
NCBI Taxonomy 72971
IPNI 240266-1
iNaturalist 524304
GBIF 5394765
EPPO PQNIN
Wikipedia Pteronia_incana

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
The role of topographic and soil factors on woody plant encroachment in mountainous rangelands: A mini literature review Gxasheka M, Gajana CS, Dlamini P Heliyon 12-Oct-2023
PMCID:PMC10590860
doi:10.1016/j.heliyon.2023.e20615
PMID:37876417
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
Natural Compounds with Antimicrobial Properties in Cosmetics Rybczyńska-Tkaczyk K, Grenda A, Jakubczyk A, Kiersnowska K, Bik-Małodzińska M Pathogens 15-Feb-2023
PMCID:PMC9959536
doi:10.3390/pathogens12020320
PMID:36839592
Screening of Different Essential Oils Based on Their Physicochemical and Microbiological Properties to Preserve Red Fruits and Improve Their Shelf Life Najmi Z, Scalia AC, De Giglio E, Cometa S, Cochis A, Colasanto A, Locatelli M, Coisson JD, Iriti M, Vallone L, Rimondini L Foods 10-Jan-2023
PMCID:PMC9857945
doi:10.3390/foods12020332
PMID:36673424
Does the landscape functionality approach provide insight into rangeland conditions in the Tanqua Karoo region, South Africa? Saaed M, Jacobs S, Masubelele ML, Khomo L, Samuels I PeerJ 19-May-2022
PMCID:PMC9124461
doi:10.7717/peerj.13305
PMID:35611172
Herbivory and misidentification of target habitat constrain region-wide restoration success of spekboom (Portulacaria afra) in South African subtropical succulent thicket van der Vyver ML, Mills AJ, Difford M, Cowling RM PeerJ 11-Aug-2021
PMCID:PMC8364318
doi:10.7717/peerj.11944
PMID:34447631
Antimicrobial activity of essential plant oils and their major components Mangalagiri NP, Panditi SK, Jeevigunta NL Heliyon 24-Apr-2021
PMCID:PMC8099760
doi:10.1016/j.heliyon.2021.e06835
PMID:33997385
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
Microstructural and histochemical analysis of aboveground organs of Centaurea cyanus used in herbal medicine Haratym W, Weryszko-Chmielewska E, Konarska A Protoplasma 12-Sep-2019
PMCID:PMC6982636
doi:10.1007/s00709-019-01437-4
PMID:31515607
Essential Oils: Sources of Antimicrobials and Food Preservatives Pandey AK, Kumar P, Singh P, Tripathi NN, Bajpai VK Front Microbiol 16-Jan-2017
PMCID:PMC5238431
doi:10.3389/fmicb.2016.02161
PMID:28138324
Trichomes related to an unusual method of water retention and protection of the stem apex in an arid zone perennial species Lusa MG, Cardoso EC, Machado SR, Appezzato-da-Glória B AoB Plants 19-Dec-2014
PMCID:PMC4381741
doi:10.1093/aobpla/plu088
PMID:25527474
Chemical composition and antimicrobial activity of Satureja hortensis and Trachyspermum copticum essential oil Mahboubi M, Kazempour N Iran J Microbiol 01-Dec-2011
PMCID:PMC3330183
PMID:22530088
Antiherpevirus activity of Artemisia arborescens essential oil and inhibition of lateral diffusion in Vero cells Saddi M, Sanna A, Cottiglia F, Chisu L, Casu L, Bonsignore L, De Logu A Ann Clin Microbiol Antimicrob 26-Sep-2007
PMCID:PMC2099429
doi:10.1186/1476-0711-6-10
PMID:17894898
Volatile constituents of <i>Pteronia incana</i> (compositae) K. Bruns, M. Meiertoberens Wiley 04-Nov-2006
doi:10.1002/FFJ.2730020404
Diterpenes and other constituents from Pteronia species C. Zdero, J. Jakupovic, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85434-H

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(2Z,6E,11R)-3,11,15-tris(hydroxymethyl)-7-methylhexadeca-2,6-diene-1,16-diol 162907172 Click to see CC(=CCCC(=CCO)CO)CCCC(CCCC(CO)CO)CO 358.50 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[(1R,3S,5R,6aR,7R,8R,9S,10S,10aR)-1-acetyloxy-10-ethoxy-3,5-dihydroxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-9-yl] decanoate 162890288 Click to see CCCCCCCCCC(=O)OC1C(C(C2CC(C=C3C2(C1OCC)C(OC3O)OC(=O)C)O)(C)CC=C(C)C=C)C 590.80 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020404
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1002/FFJ.2730020404
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020404
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020404
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/FFJ.2730020404
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020404
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6097621 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(90)85434-H
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(90)85434-H
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85434-H
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,4R,6R,8S,9S,12S,14S,16R)-14-(furan-3-yl)-16-hydroxy-8,9,12-trimethyl-3,7,13-trioxapentacyclo[7.6.1.01,12.04,16.06,8]hexadecan-2-one 163020092 Click to see CC12CCC3(C4(C1(C(CC5C2(O5)C)OC4=O)O)CC(O3)C6=COC=C6)C 360.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3R,4R,4aR,5'R,7S,8R,8aR)-5'-(furan-3-yl)-3,4,7,8a-tetrahydroxy-4,4a,7-trimethylspiro[2,3,5,6-tetrahydro-1H-naphthalene-8,3'-oxolane]-2'-one 163034016 Click to see CC12CCC(C3(C1(CCC(C2(C)O)O)O)CC(OC3=O)C4=COC=C4)(C)O 380.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
CID 163106069 163106069 Click to see CC(=O)OC1CCC2(C(C1(C)O)(CCC3(C24CC(OC4=O)C5=COC=C5)CO3)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(90)85434-H
CID 163106554 163106554 Click to see CC=C(C)C(=O)OC1CCC2(C(C1(C)O)(CCC3(C24CC(OC4=O)C5=COC=C5)CO3)C)O 460.50 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[DL-Ala-DL-xiIle-DL-xiIle-DL-Lys-DL-Val-DL-Phe-DL-Leu-DL-xiIle] 133052629 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)C)C(C)CC)CC(C)C)CC2=CC=CC=C2)C(C)C)CCCCN)C(C)CC 898.20 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,2R,3R,5'S,6R,7R)-5'-(furan-3-yl)-3,6,7-trimethylspiro[9-oxatricyclo[5.2.2.01,6]undecane-2,3'-oxolane]-2',8-dione 21680926 Click to see CC1CCC2(C3(CCC2(C14CC(OC4=O)C5=COC=C5)OC3=O)C)C 344.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[4-[(1R,2R,3R)-2,3-dihydroxy-1,2-dimethyl-6-oxocyclohexyl]butan-2-ylidene]-5-(furan-3-yl)oxolan-2-one 163000474 Click to see CC(=C1CC(OC1=O)C2=COC=C2)CCC3(C(=O)CCC(C3(C)O)O)C 362.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
(3R,3aS,5'R,6R,7R)-5'-(furan-3-yl)-3-(hydroxymethyl)-3,3a,6-trimethylspiro[2,4,5,6-tetrahydroindene-7,3'-oxolane]-2'-one 14588970 Click to see CC1CCC2(C(=CCC2(C)CO)C13CC(OC3=O)C4=COC=C4)C 330.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H
5'-(Furan-3-yl)-3-(hydroxymethyl)-3,3a,6-trimethylspiro[2,4,5,6-tetrahydroindene-7,3'-oxolane]-2'-one 14588969 Click to see CC1CCC2(C(=CCC2(C)CO)C13CC(OC3=O)C4=COC=C4)C 330.40 unknown https://doi.org/10.1016/0031-9422(90)85434-H

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