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Senecio latifolius

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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 UUID643fc88189d4f776341519
Scientific name Senecio latifolius
Authority DC.
First published in Prodr. 6: 387 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio sceleratus Schweick. in Onderstepoort Journ. 16: 130. 1941

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000023003
Tropicos 2720974
KEW urn:lsid:ipni.org:names:245958-1
The Plant List gcc-122236
Open Tree Of Life 136437
NCBI Taxonomy 422353
IPNI 245958-1
iNaturalist 405995
GBIF 3106880
EPPO SENLF
USDA GRIN 406967
CMAUP NPO14572

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
Physiologically based kinetic modeling of senecionine N-oxide in rats as a new approach methodology to define the effects of dose and endpoint used on relative potency values of pyrrolizidine alkaloid N-oxides Widjaja F, Zheng L, Wesseling S, Rietjens IM Front Pharmacol 02-Mar-2023
PMCID:PMC10017778
doi:10.3389/fphar.2023.1125146
PMID:36937884
South African Senecio Alkaloids H. L. DE WAAL Springer Science and Business Media LLC 02-Jan-2008
doi:10.1038/146777B0
The senecio alkaloids. Part XIX. The isolation of chlorodeoxysceleratine C. G. Gordon-Gray Royal Society of Chemistry (RSC) 20-Apr-2004
doi:10.1039/J39670000781
Hepatic veno-occlusive disease as a result of a traditional remedy: confirmation of toxic pyrrolizidine alkaloids as the cause, using an in vitro technique Zuckerman M, Steenkamp V, Stewart MJ J Clin Pathol 01-Sep-2002
PMCID:PMC1769740
doi:10.1136/jcp.55.9.676
PMID:12194997
A new pyrrolizidine alkaloid N-oxide and the revised structure of sceleratine Martin W. Bredenkamp, Adriaan Wiechers, Petrus H. van Rooyen Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)80930-8
A new pyrrolizidine alkaloid from Senecio Latifolius DC Martin W. Bredenkamp, Adriaan Wiechers, Petrus H. van Rooyen Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)61967-6

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
(1R,4E,6R,7S,14S,17R)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-14-oxido-2,9-dioxa-14-azoniatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 163194255 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(CO)O)C 367.40 unknown https://doi.org/10.1038/146777B0
Isatidine 5281734 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(CO)O)C 367.40 unknown https://doi.org/10.1038/146777B0
Retrorsine N-oxide 76972338 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(CO)O)C 367.40 unknown https://doi.org/10.1038/146777B0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4,5,6-Trihydroxy-7-methylphthalide 10420195 Click to see CC1=C2C(=C(C(=C1O)O)O)COC2=O 196.16 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives
Flavipin 3083587 Click to see CC1=C(C(=C(C(=C1O)O)O)C=O)C=O 196.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
N-Caffeoyl-L-aspartic acid 23658567 Click to see C1=CC(=C(C=C1C=CC(=O)NC(CC(=O)O)C(=O)O)O)O 295.24 unknown via CMAUP database
N-Coumaroyl-L-aspartic acid 68537088 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC(=O)O)C(=O)O)O 279.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
N-(E)-Caffeoyl-L-tyrosine 10308838 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O 343.30 unknown via CMAUP database
N-Coumaroyl-3-hydroxytyrosine 68540305 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC2=CC(=C(C=C2)O)O)C(=O)O)O 343.30 unknown via CMAUP database
N-p-Coumaroyltyrosine 15825666 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC=C(C=C2)O)O 327.30 unknown via CMAUP database
trans-Clovamide 6506968 Click to see C1=CC(=C(C=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 359.30 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid 90062900 Click to see C1(C(C(OC(C1O)O)C(=O)O)O)O 194.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Epicoccolide A 71732639 Click to see CC1=C(C2=C(C(=C1O)O)OC3C4=C(C(=C(C(=C4C(=O)C2O3)C)O)O)O)C=O 374.30 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see CN1C=NC2=C1C(=O)NC(=O)N2C 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Isocoumarans
4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran 123784052 Click to see CC1=C2COCC2=C(C(=C1O)OC)O 196.20 unknown via CMAUP database
7-Methyl-1,3-dihydro-2-benzofuran-4,5,6-triol 10845133 Click to see CC1=C2COCC2=C(C(=C1O)O)O 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Acetosellin 10883740 Click to see CC=CC=CC=CC1=CC(=C2C3=C1C4=C(COC(C4)CO)C(=O)C3(OC2=O)C)O 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see CC1C2=CC(=C(C=C2CCN1)O)O 179.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Epicoccolide B 11210533 Click to see CC1=C(C2=C(C(=C1O)O)OC(=C2)C3=C(C(=C(C(=C3C=O)O)O)O)C)C=O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-21-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19-tetrol 118731401 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C8=CC(=C(C=C8)O)O)O 738.60 unknown via CMAUP database
Cinnamtannin A2 16130899 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1155.00 unknown via CMAUP database
Cinnamtannin A3 16129741 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=C(C(=CC(=C78)O)O)C9C(C(OC1=CC(=CC(=C91)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1443.30 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
8,8'-Methylenebiscatechin 46182787 Click to see C1C(C(OC2=C1C(=CC(=C2CC3=C(C=C(C4=C3OC(C(C4)O)C5=CC(=C(C=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 592.50 unknown via CMAUP database
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Epicatechin 8-C-beta-D-galactopyranoside 5317057 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(C(C(O3)CO)O)O)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cyanidin 3-arabinoside cation 12137509 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 419.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4S,5R,6R,7R,17R)-4,7-dihydroxy-4-(hydroxymethyl)-5,6,7-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 163025278 Click to see CC1C(C(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1016/S0040-4039(00)61967-6
(1R,4S,5R,6R,7S,17R)-4,7-dihydroxy-7-(hydroxymethyl)-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 162911982 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1039/J39670000781
(1R,5R)-4,7-dihydroxy-7-(hydroxymethyl)-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 5321160 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1016/S0040-4039(01)80930-8
(1R,6S,17R)-4,7-dihydroxy-4-(hydroxymethyl)-5,6,7-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 102004938 Click to see CC1C(C(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1016/S0040-4039(01)80930-8
(1S,4S,5R,6S,7S,17S)-7-(chloromethyl)-4,7-dihydroxy-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 162903450 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1(C)O)(CCl)O)C 387.90 unknown https://doi.org/10.1039/J39670000781
12,18-Dihydroxysenecionan-11,16-dione 267891 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1039/J39670000781
4,7-Dihydroxy-4-(hydroxymethyl)-5,6,7-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 53462821 Click to see CC1C(C(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1016/S0040-4039(00)61967-6
4,7-Dihydroxy-7-(hydroxymethyl)-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 78385457 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1(C)O)(CO)O)C 369.40 unknown https://doi.org/10.1039/J39670000781
7-(Chloromethyl)-4,7-dihydroxy-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 162903449 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1(C)O)(CCl)O)C 387.90 unknown https://doi.org/10.1039/J39670000781
Retrorsine 5281743 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1039/J39670000781

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