Senecio inaequidens - Unknown
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Details Top

Internal ID UUID643fcc944f817046534310
Scientific name Senecio inaequidens
Authority DC.
First published in Prodr. 6: 401 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio vimineus Harv. Fl. Cap. (Harvey) 3: 401. 1865 [24 Feb-30 Jun 1865]

Common names Top

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Language Common/alternative name
English narrow-leaved ragwort
Czech starček úzkolistý
Welsh creulys gulddail
German schmalblättriges greiskraut
German südafrikanisches greiskraut
Finnish buurivillakko
French seneçon sud-africain
Norwegian Bokmål boersvineblom
Dutch bezemkruiskruid
Norwegian Nynorsk boarsvineblom
Polish starzec nierównozębny
Slovak starček úzkolistý
Chinese 窄叶黄菀
Chinese 窄葉黃菀

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
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland
  • Europe
    • Eastern Europe
      • Belarus
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000064202
USDA Plants SEIN10
Tropicos 2703153
INPN 122630
Flora of Italy 5765
KEW urn:lsid:ipni.org:names:245637-1
The Plant List gcc-21160
Open Tree Of Life 901730
NCBI Taxonomy 58524
NBN Atlas NBNSYS0000004377
IPNI 245637-1
iNaturalist 55607
GBIF 3109086
Freebase /m/0462t_w
EPPO SENIQ
EOL 6189375
USDA GRIN 406768
Wikipedia Senecio_inaequidens

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
Success in restoring native plant communities on kimberlite mining dumps in the Afro‐alpine Drakensberg region of Lesotho Ntloko BR, Mokotjomela TM, Mphafi SP, Siebert SJ Ecol Evol 12-Mar-2024
PMCID:PMC10932747
doi:10.1002/ece3.11022
PMID:38481757
Effects of dietary exposure to plant toxins on bioaccumulation, survival, and growth of black soldier fly (Hermetia illucens) larvae and lesser mealworm (Alphitobius diaperinus) Mulder PP, Mueller-Maatsch JT, Meijer N, Bosch M, Zoet L, Van Der Fels-Klerx HJ Heliyon 16-Feb-2024
PMCID:PMC10884485
doi:10.1016/j.heliyon.2024.e26523
PMID:38404897
Heat Treatment of Seeds to Control Invasive Common Ragweed (Ambrosia artemisiifolia), Narrow-Leaved Ragwort (Senecio inaequidens) and Giant Hogweed (Heracleum mantegazzianum) Hall RM, Urban B, Durec N, Renner-Martin K, Kaul HP, Wagentristl H, Karrer G Plants (Basel) 23-Jan-2024
PMCID:PMC10856870
doi:10.3390/plants13030341
PMID:38337874
Pyrrolizidine alkaloid contamination of food in Africa: A review of current trends and implications Letsyo E, Madilo FK, Effah-Manu L Heliyon 03-Jan-2024
PMCID:PMC10789634
doi:10.1016/j.heliyon.2024.e24055
PMID:38230234
Genome-wide analysis of horizontal transfer in non-model wild species from a natural ecosystem reveals new insights into genetic exchange in plants Aubin E, Llauro C, Garrigue J, Mirouze M, Panaud O, El Baidouri M PLoS Genet 19-Oct-2023
PMCID:PMC10586619
doi:10.1371/journal.pgen.1010964
PMID:37856455
Diet composition of wild columbiform birds: next-generation sequencing of plant and metazoan DNA in faecal samples Schumm YR, Masello JF, Vreugdenhil-Rowlands J, Fischer D, Hillerich K, Quillfeldt P Naturwissenschaften 22-Jul-2023
PMCID:PMC10363069
doi:10.1007/s00114-023-01863-8
PMID:37480393
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Alkaloids in food: a review of toxicity, analytical methods, occurrence and risk assessments Akinboye AJ, Kim K, Choi S, Yang I, Lee JG Food Sci Biotechnol 05-Apr-2023
PMCID:PMC10290023
doi:10.1007/s10068-023-01295-0
PMID:37362815
Native and exotic plants play different roles in urban pollination networks across seasons Zaninotto V, Thebault E, Dajoz I Oecologia 24-Jan-2023
PMCID:PMC9872067
doi:10.1007/s00442-023-05324-x
PMID:36692691
A sensitive LC–MS/MS method for isomer separation and quantitative determination of 51 pyrrolizidine alkaloids and two tropane alkaloids in cow’s milk Klein LM, Gabler AM, Rychlik M, Gottschalk C, Kaltner F Anal Bioanal Chem 01-Oct-2022
PMCID:PMC9613554
doi:10.1007/s00216-022-04344-5
PMID:36183043
Temporal changes in the Swiss flora: implications for flower-visiting insects Abrahamczyk S, Kessler M, Roth T, Heer N BMC Ecol Evol 15-Sep-2022
PMCID:PMC9479241
doi:10.1186/s12862-022-02061-2
PMID:36109688
Diversity and Typology of Land-Use Explain the Occurrence of Alien Plants in a Protected Area Glasnović P, Cernich S, Peroš J, Tišler M, Fišer Ž, Surina B Plants (Basel) 09-Sep-2022
PMCID:PMC9503411
doi:10.3390/plants11182358
PMID:36145760
Metabolic Toxification of 1,2-Unsaturated Pyrrolizidine Alkaloids Causes Human Hepatic Sinusoidal Obstruction Syndrome: The Update Teschke R, Vongdala N, Quan NV, Quy TN, Xuan TD Int J Mol Sci 27-Sep-2021
PMCID:PMC8508847
doi:10.3390/ijms221910419
PMID:34638760
Pyrrolizidine Alkaloids in the Food Chain: Is Horizontal Transfer of Natural Products of Relevance? Chmit MS, Horn G, Dübecke A, Beuerle T Foods 07-Aug-2021
PMCID:PMC8392022
doi:10.3390/foods10081827
PMID:34441604
Anthonomus rubi on Strawberry Fruit: Its Biology, Ecology, Damage, and Control from an IPM Perspective Tonina L, Zanettin G, Miorelli P, Puppato S, Cuthbertson AG, Grassi A Insects 05-Aug-2021
PMCID:PMC8396509
doi:10.3390/insects12080701
PMID:34442268

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
(1S,4E,7R)-4-ethylidene-7-hydroxy-7-methyl-6-methylidene-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 91746605 Click to see CC=C1CC(=C)C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O 333.40 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
Retronecine 10198 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1007/S004250050420
Seneciphylline 5281750 Click to see CC=C1CC(=C)C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O 333.40 unknown https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1021/NP50076A003
Spartioidine 6438237 Click to see CC=C1CC(=C)C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O 333.40 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
(1E,6E)-gamma-humulene 6365330 Click to see CC1=CCCC(=C)C=CC(CCC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
(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)83942-4
2,6,10-Trimethyl-2,6,9,11-dodecatetraene 442368 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
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/S0031-9422(00)83942-4
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
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)83942-4
gamma-Humulene 3015263 Click to see CC1=CCCC(=C)C=CC(CCC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3,4a,5-trimethyl-9-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-8a-yl) 3-methylbutanoate 163036377 Click to see CC1CCCC2(C1(CC3=C(C2=O)OC=C3C)C)OC(=O)CC(C)C 332.40 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
(9-hydroxy-3,4,5-trimethyl-8-oxo-6,7-dihydro-5H-benzo[f][1]benzofuran-7-yl) 2-methylbut-2-enoate 163048267 Click to see CC=C(C)C(=O)OC1CC(C2=C(C1=O)C(=C3C(=C2C)C(=CO3)C)O)C 342.40 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
[(4aR,5S,8aR)-3,4a,5-trimethyl-9-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-8a-yl] 3-methylbutanoate 163036378 Click to see CC1CCCC2(C1(CC3=C(C2=O)OC=C3C)C)OC(=O)CC(C)C 332.40 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
[(5R,6S)-4-(acetyloxymethyl)-9-methoxy-3,5-dimethyl-5,6-dihydrobenzo[f][1]benzofuran-6-yl] (Z)-2-methylbut-2-enoate 163190623 Click to see CC=C(C)C(=O)OC1C=CC2=C(C1C)C(=C3C(=COC3=C2OC)C)COC(=O)C 398.40 unknown https://doi.org/10.1016/S0031-9422(00)81111-5
[(5S,7S)-9-hydroxy-3,4,5-trimethyl-8-oxo-6,7-dihydro-5H-benzo[f][1]benzofuran-7-yl] (Z)-2-methylbut-2-enoate 163195350 Click to see CC=C(C)C(=O)OC1CC(C2=C(C1=O)C(=C3C(=C2C)C(=CO3)C)O)C 342.40 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
[4-(Acetyloxymethyl)-9-methoxy-3,5-dimethyl-5,6-dihydrobenzo[f][1]benzofuran-6-yl] 2-methylbut-2-enoate 162949014 Click to see CC=C(C)C(=O)OC1C=CC2=C(C1C)C(=C3C(=COC3=C2OC)C)COC(=O)C 398.40 unknown https://doi.org/10.1016/S0031-9422(00)81111-5
Bohlmann 183 330226 Click to see CC1CCCC2=C1C(=C3C(=COC3=C2O)C)C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
Cacalol 181105 Click to see CC1CCCC2=C1C(=C3C(=COC3=C2O)C)C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
1-(7-Acetyloxy-4-hydroxy-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-4-yl)ethyl acetate 137796411 Click to see CC1CC(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)(C(C)OC(=O)C)O 483.50 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,4S,6R,7R,11Z)-4-[(1R)-1-chloroethyl]-4-hydroxy-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl] acetate 102523309 Click to see CC1CC(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)(C(C)Cl)O 459.90 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1021/NP50076A003
[(1R,5S,6R,7R)-5,6,7-trimethyl-4-methylidene-3,8,15-trioxo-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadeca-11(17),12-dien-7-yl] acetate 101324857 Click to see CC1C(C(C(=O)OCC2=C3C(CC(=O)N3C=C2)OC(=O)C1=C)(C)OC(=O)C)C 389.40 unknown https://doi.org/10.1016/S0031-9422(00)86705-9
Doronine 5281726 Click to see CC1CC(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)(C(C)Cl)O 459.90 unknown https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1021/NP50076A003
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
Floridanine 139291965 Click to see CC1CC(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)(C(C)O)O 441.50 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
Pterophorine 188464 Click to see CC1C(C(C(=O)OCC2=C3C(CC(=O)N3C=C2)OC(=O)C1=C)(C)OC(=O)C)C 389.40 unknown https://doi.org/10.1016/S0031-9422(00)86705-9
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Trialkylamines
Otonecine 5281740 Click to see CN1CCC(C(=O)C(=CC1)CO)O 185.22 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
> Organoheterocyclic compounds / Azaspirodecane derivatives
Florosenine (neutral) 6441404 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)OC(=O)C)C 423.50 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
Otosenine 6438142 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)O)C 381.40 unknown https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/S0021-9673(00)91299-8
Otosenine 12-acetate 122362136 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)OC(=O)C)C 423.50 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
> Organoheterocyclic compounds / Benzofurans
(1R,11S,12R)-12-hydroxy-1,3-dimethoxy-7,9,11-trimethyl-5,14,15-trioxatetracyclo[9.3.1.02,10.04,8]pentadeca-2(10),3,6,8-tetraen-13-one 162941687 Click to see CC1=COC2=C(C3=C(C(=C12)C)C4(C(C(=O)OC3(O4)OC)O)C)OC 334.30 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
12-Hydroxy-1,3-dimethoxy-7,9,11-trimethyl-5,14,15-trioxatetracyclo[9.3.1.02,10.04,8]pentadeca-2(10),3,6,8-tetraen-13-one 162941685 Click to see CC1=COC2=C(C3=C(C(=C12)C)C4(C(C(=O)OC3(O4)OC)O)C)OC 334.30 unknown https://doi.org/10.1016/S0031-9422(00)83942-4
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6S,7R,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 134714985 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
(1R,6R,7S,17S)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 126968828 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50076A003
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/0165-7992(92)90050-R
(1S,4Z,7S,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 133562009 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50076A003
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/0165-7992(92)90050-R
(5R,10R,11R,12S,15R)-5,10,11,12-tetramethyl-3,8,14-trioxa-18-azatetracyclo[13.5.1.05,10.018,21]henicosa-1(21),19-diene-4,9,13,17-tetrone 163059097 Click to see CC1C(C2(C(=O)OCCC2(C(=O)OCC3=C4C(CC(=O)N4C=C3)OC1=O)C)C)C 403.40 unknown https://doi.org/10.1016/S0031-9422(00)86705-9
5,10,11,12-Tetramethyl-3,8,14-trioxa-18-azatetracyclo[13.5.1.05,10.018,21]henicosa-1(21),19-diene-4,9,13,17-tetrone 163059096 Click to see CC1C(C2(C(=O)OCCC2(C(=O)OCC3=C4C(CC(=O)N4C=C3)OC1=O)C)C)C 403.40 unknown https://doi.org/10.1016/S0031-9422(00)86705-9
Renardine (neutral) (VAN) 102004936 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
Retrorsine 5281743 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1021/NP50076A003
https://doi.org/10.1016/S0021-9673(00)91299-8
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1007/S004250050420
https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1021/NP50076A003
Senecivernine 442764 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1=C)(C)O)C 335.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50076A003
https://doi.org/10.1016/0165-7992(92)90050-R
https://doi.org/10.1021/NP50061A002
Senkirkine 5281752 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
Usaramine 5281756 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1021/NP50076A003
https://doi.org/10.1016/S0021-9673(00)91299-8
https://doi.org/10.1021/NP50061A002
https://doi.org/10.1016/0165-7992(92)90050-R

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