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Internal ID UUID643fcc718ef65634482755
Scientific name Senecio macedonicus
Authority Griseb.
First published in Spic. Fl. Rumel. 2(5/6): 221 (1846)

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Language Common/alternative name
Bulgarian македонски спореж

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Senecio macedonicus subsp. barckhausiifolius (Boiss. & Heldr.) J.Calvo Novon 23(2): 140 (2014)
Senecio macedonicus subsp. macedonicus Unknown

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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-0000062799
Tropicos 2701268
KEW urn:lsid:ipni.org:names:246185-1
The Plant List gcc-19794
Open Tree Of Life 688686
Observations.org 132851
NCBI Taxonomy 1268582
IPNI 246185-1
iNaturalist 567058
GBIF 3108351
EPPO SENMK

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
Seco-eremophilanolides from Senecio macedonicus Antoaneta B. Trendafilova, Elena T. Tsankova, Ljuba N. Evstatieva Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00174-6
Alkaloids from the roots of Senecio macedonicus Griseb. Christov V, Mikhova B, Alexandrova R, Dimitrova D, Nikolova E, Evstatieva L Z Naturforsch C J Biosci 01-Sep-2002
doi:10.1515/ZNC-2002-9-1004
PMID:12440711

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
8-Episarracine 91753674 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C=C(C)C 319.40 unknown https://doi.org/10.1515/ZNC-2002-9-1004
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(2-acetyloxy-4-methyl-5-oxo-2H-furan-3-yl)-(2-formyl-1,6-dimethylcyclohex-2-en-1-yl)methyl] 2-methylbut-2-enoate 162907505 Click to see CC=C(C)C(=O)OC(C1=C(C(=O)OC1OC(=O)C)C)C2(C(CCC=C2C=O)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(95)00174-6
[(2-acetyloxy-4-methyl-5-oxo-2H-furan-3-yl)-(2-formyl-1,6-dimethylcyclohex-2-en-1-yl)methyl] 2-methylprop-2-enoate 162997725 Click to see CC1CCC=C(C1(C)C(C2=C(C(=O)OC2OC(=O)C)C)OC(=O)C(=C)C)C=O 390.40 unknown https://doi.org/10.1016/0031-9422(95)00174-6
[(S)-[(2S)-2-acetyloxy-4-methyl-5-oxo-2H-furan-3-yl]-[(1R,6S)-2-formyl-1,6-dimethylcyclohex-2-en-1-yl]methyl] (Z)-2-methylbut-2-enoate 162907506 Click to see CC=C(C)C(=O)OC(C1=C(C(=O)OC1OC(=O)C)C)C2(C(CCC=C2C=O)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(95)00174-6
[(S)-[(2S)-2-acetyloxy-4-methyl-5-oxo-2H-furan-3-yl]-[(1R,6S)-2-formyl-1,6-dimethylcyclohex-2-en-1-yl]methyl] 2-methylprop-2-enoate 162997726 Click to see CC1CCC=C(C1(C)C(C2=C(C(=O)OC2OC(=O)C)C)OC(=O)C(=C)C)C=O 390.40 unknown https://doi.org/10.1016/0031-9422(95)00174-6
> Organoheterocyclic compounds / Pyrrolizidines
[(1R,7S)-7-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl] (Z)-2-methylbut-2-enoate 6428026 Click to see CC=C(C)C(=O)OC1CCN2C1C(CC2)CO 239.31 unknown https://doi.org/10.1515/ZNC-2002-9-1004
[(1S,7R,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl]methyl (E)-2-(hydroxymethyl)but-2-enoate 12315334 Click to see CC=C(C)C(=O)OC1CCN2C1C(CC2)COC(=O)C(=CC)CO 337.40 unknown https://doi.org/10.1515/ZNC-2002-9-1004
[(1S,7R)-7-hydroxy-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl]methyl (Z)-2-methylbut-2-enoate 6428027 Click to see CC=C(C)C(=O)OCC1CCN2C1C(CC2)O 239.31 unknown https://doi.org/10.1515/ZNC-2002-9-1004
Sarracine 5281746 Click to see CC=C(C)C(=O)OC1CCN2C1C(CC2)COC(=O)C(=CC)CO 337.40 unknown https://doi.org/10.1515/ZNC-2002-9-1004

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