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Jacobaea persoonii

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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 UUID643fccb09eca7609025299
Scientific name Jacobaea persoonii
Authority (De Not.) Pelser
First published in Compositae Newslett. 44: 9 (2006)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio persoonii De Not. Repert. Fl. Ligust. : 229 (1844)
Senecio incanus subsp. italicus (Pers.) Arcang. Arcang.. 1882. 349 1882
Senecio incanus var. italicus Pers. Pers., Syn. Pl. 2. 1807. 435 1807
Senecio incanus subsp. persoonii (De Not.) Nyman Nyman, Consp. Fl. Eur. 1879. 356 1879

Common names Top

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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-0000065259
INPN 610654
Flora of Italy 5762
KEW urn:lsid:ipni.org:names:77073762-1
The Plant List gcc-22185
Open Tree Of Life 469951
NCBI Taxonomy 214902
IPNI 77073762-1
iNaturalist 518192
GBIF 5388608
EPPO JACPN
CMAUP NPO20773

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)!
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Title Authors Publication Released IDs
Pyrrolizidine alkaloids from Senecio persoonii E. Roeder, T. Bourauel, R. Kersten Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85254-O

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
> Alkaloids and derivatives
(12xi,13xi)-12,13-Epoxy-19-hydroxysenecionan-11,16-dione 101621379 Click to see CC=C1CC2(C(O2)(C(=O)OCC3=CCN4C3C(CC4)OC1=O)C)CO 349.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
(9E)-9-ethylidene-7-(hydroxymethyl)-5-methyl-3,6,11-trioxa-15-azatetracyclo[10.5.1.05,7.015,18]octadec-1(17)-ene-4,10-dione 137628476 Click to see CC=C1CC2(C(O2)(C(=O)OCC3=CCN4C3C(CC4)OC1=O)C)CO 349.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
[1,6]Dioxacyclododecino[2,3,4-gh]pyrrolizine-2,7-dione, 3-ethylidene-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-6-methyl-5-methylene-, (3Z,6R,14aR,14bR)- 521227 Click to see CC=C1CC(=C)C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O 333.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
9-Ethylidene-7-(hydroxymethyl)-5-methyl-3,6,11-trioxa-15-azatetracyclo[10.5.1.05,7.015,18]octadec-1(17)-ene-4,10-dione 75092738 Click to see CC=C1CC2(C(O2)(C(=O)OCC3=CCN4C3C(CC4)OC1=O)C)CO 349.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
CID 13258912 13258912 Click to see CC=C1CC(=C)C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(C)O 349.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
erucifoline N-oxide 132282054 Click to see CC=C1CC2(C(O2)(C(=O)OCC3=CC[N+]4(C3C(CC4)OC1=O)[O-])C)CO 365.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
Seneciphylline 5281750 Click to see CC=C1CC(=C)C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O 333.40 unknown https://doi.org/10.1016/0031-9422(93)85254-O
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Friedelane 15559345 Click to see CC1CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 412.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown via CMAUP database
Buchanaxanthone 5481840 Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O 258.23 unknown via CMAUP database
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,5-Trihydroxy-2-prenyl-9H-xanthene-9-one 9995643 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C 312.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
Calabaxanthone 341188 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)OC)C 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown via CMAUP database
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
4-Propyl-6beta,7alpha,10,10-tetramethyl-6,7-dihydro-2H,8H,10H-benzo[1,2-b:3,4-b':5,6-b'']tripyran-2,8-dione 12444385 Click to see CCCC1=CC(=O)OC2=C3C=CC(OC3=C4C(=O)C(C(OC4=C12)C)C)(C)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(10R,11R)-10,11,16,16-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,5,7,13,17-pentaene-4,12-dione 11014914 Click to see CC1C(OC2=C3C(=CC(=O)OC3=C4C=CC(OC4=C2C1=O)(C)C)C5=CC=CC=C5)C 402.40 unknown via CMAUP database

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