Senecio pleistocephalus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID643fc86baaa80319316993
Scientific name Senecio pleistocephalus
Authority S.Moore
First published in J. Bot. 43: 170 (1905)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 多头千里光

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000022258
Tropicos 2721085
KEW urn:lsid:ipni.org:names:246980-1
The Plant List gcc-121518
Open Tree Of Life 7609634
IPNI 246980-1
iNaturalist 556278
GBIF 3109126

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)!
Title Authors Publication Released IDs
Pyrrolizidine alkaloid biosynthesis. Synthesis of N-([4-14C]-4-aminobutyl)-1,2-didehydropyrrolidinium and its incorporation into different pyrrolizidine bases (necines) Alastair A. Denholm, Henry A. Kelly, David J. Robins Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19910002003
Pyrrolizidine alkaloid biosynthesis. Synthesis of 3H-labelled trachelanthamidine and isoretronecanol and their incorporation into three pyrrolizidine bases (necines) Ellen K. Kunec, David J. Robins Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19890001437
Pyrrolizidine alkaloid biosynthesis. Incorporation of 13C-labelled precursors into rosmarinine Henry A. Kelly, David J. Robins Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19870000177
Pyrrolizidine alkaloids. Stereochemistry of the enzymic processes involved in the biosynthesis of rosmarinecine Henry A. Kelly, David J. Robins Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19870002195
Evidence for different 1-hydroxymethylpyrrolizidines as intermediates in the biosynthesis of retronecine and rosmarinecine Ellen K. Kunec, David J. Robins Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39860000250
Evidence for an immonium ion intermediate in pyrrolizidine alkaloid biosynthesis Henry A. Kelly, David J. Robins Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39880000329
Pyrrolizidine alkaloid biosynthesis. Incorporation of 2-aminobutanoic acid labelled with 13C or 2H into the senecic acid portion of rosmarinine and senecionine Iain R. Stirling, Isabel K. A. Freer, David J. Robins Royal Society of Chemistry (RSC) 26-Jul-2002
doi:10.1039/A605623G
Germacrene derivatives and other sesquiterpenes from Senecio species and Lordhowea insularis Ferdinand Bohlmann, Christa Zdero Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)85252-7

Phytochemical Profile Top

Add a new one!
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
Retronecine 10198 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1039/C39880000329
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4,7-Dimethyl-1a-propan-2-yl-2,3,4,4a,5,6-hexahydronaphtho[4a,5-b]oxiren-5-yl) 2-methylbut-2-enoate 162994260 Click to see CC=C(C)C(=O)OC1CC(=CC23C1C(CCC2(O3)C(C)C)C)C 318.40 unknown https://doi.org/10.1016/0031-9422(82)85252-7
[(1aS,4S,4aS,5S,8aS)-4,7-dimethyl-1a-propan-2-yl-2,3,4,4a,5,6-hexahydronaphtho[4a,5-b]oxiren-5-yl] (Z)-2-methylbut-2-enoate 163190028 Click to see CC=C(C)C(=O)OC1CC(=CC23C1C(CCC2(O3)C(C)C)C)C 318.40 unknown https://doi.org/10.1016/0031-9422(82)85252-7
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/10.1016/0031-9422(82)85252-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(82)85252-7
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(82)85252-7
> Organoheterocyclic compounds / Pyrrolizidines
(-)-Rosmarinecine 6452563 Click to see C1CN2CC(C(C2C1O)CO)O 173.21 unknown https://doi.org/10.1039/C39860000250
https://doi.org/10.1039/C39880000329
https://doi.org/10.1039/P19870002195
> Phenylpropanoids and polyketides / Macrolides and analogues
Rosmarinine 5281745 Click to see CC=C1CC(C(C(=O)OCC2C(CN3C2C(CC3)OC1=O)O)(C)O)C 353.40 unknown https://doi.org/10.1039/A605623G
https://doi.org/10.1039/P19870002195
https://doi.org/10.1039/P19870000177
https://doi.org/10.1039/P19890001437
https://doi.org/10.1039/P19910002003
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1039/A605623G

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.