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Senecio retrorsus

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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 UUID643fcd95599f3601517944
Scientific name Senecio retrorsus
Authority DC.
First published in Prodr. 6: 387 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio graminicola C.A.Sm. J. S. African Bot. 9: 120 (1943)
Senecio retrorsus var. subedentulus DC.
Senecio latifolius var. retrorsus (DC.) Harv. Fl. Cap. 3: 377 (1865).
Senecio latifolius var. barbellatus (DC.) Harv. Fl. Cap. 3: 377 (1865).
Senecio barbellatus DC. Prodr. 6: 388 (1838)

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
  • Africa
    • South Tropical Africa
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Lesotho

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000073615
Tropicos 2721125
KEW urn:lsid:ipni.org:names:247275-1
The Plant List gcc-30367
Open Tree Of Life 136445
NCBI Taxonomy 422357
IPNI 247275-1
iNaturalist 594361
GBIF 3107538
EPPO SENRT
USDA GRIN 406968
CMAUP NPO21175

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
Exploring African Medicinal Plants for Potential Anti-Diabetic Compounds with the DIA-DB Inverse Virtual Screening Web Server Pereira AS, den Haan H, Peña-García J, Moreno MM, Pérez-Sánchez H, Apostolides Z Molecules 24-May-2019
PMCID:PMC6571761
doi:10.3390/molecules24102002
PMID:31137754
Assessment of Useful Plants in the Catchment Area of the Proposed Ntabelanga Dam in the Eastern Cape Province, South Africa Maroyi A ScientificWorldJournal 30-Jul-2017
PMCID:PMC5554549
doi:10.1155/2017/3763607
PMID:28828397
Contributions of Human Enzymes in Carcinogen Metabolism Rendic S, Guengerich FP Chem Res Toxicol 10-May-2012
PMCID:PMC3398241
doi:10.1021/tx300132k
PMID:22531028
THE ALKALOIDS OF <i>SENECIO</i> SPECIES: I. THE NECINES AND NECIC ACIDS FROM <i>S</i>. <i>RETRORSUS</i> AND <i>S</i>. <i>JACOBAEA</i> Richard H. F. Manske Canadian Science Publishing 24-Apr-2011
doi:10.1139/CJR31-103

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
Antimycin A19 56600064 Click to see CCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C(C)C 548.60 unknown via CMAUP database
Antimycin A20 54764156 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C 506.50 unknown via CMAUP database
Antimycin A2a 447434 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)C 534.60 unknown via CMAUP database
Antimycin A3 245869 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 520.60 unknown via CMAUP database
Antimycin A3a 2'R-epimer 86278330 Click to see CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)C(C)CC 520.60 unknown via CMAUP database
Benzoic acid, 3-(formylamino)-2-hydroxy- 15409159 Click to see C1=CC(=C(C(=C1)NC=O)O)C(=O)O 181.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Methyl-3-hydroxyanthranilic acid 95222 Click to see CC1=C(C(=C(C=C1)C(=O)O)N)O 167.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Virginiae butanolide A 10036830 Click to see CC(C)CCCC(C1C(COC1=O)CO)O 230.30 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
antimycin A1 14957 Click to see CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C 548.60 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Ketomycin 19489 Click to see C1CC(CC=C1)C(=O)C(=O)O 154.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
Oleandomycin 72493 Click to see CC1CC(C(C(O1)OC2C(CC3(CO3)C(=O)C(C(C(C(OC(=O)C(C(C2C)OC4CC(C(C(O4)C)O)OC)C)C)C)O)C)C)O)N(C)C 687.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
9-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]-3H-purin-6-one 21785357 Click to see C1C(C(C(C(O1)N2C=NC3=C2NC=NC3=O)O)O)O 268.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(alphaR,2R)-alpha,5alpha-Dimethyl-6alpha-[(1E,3E,5E,7E,9S)-1,9-diethyl-14-oxo-14-(1H-pyrrole-2-yl)-1,3,5,7-tetradecatetraenyl]tetrahydro-2H-pyran-2beta-acetic acid 101789368 Click to see CCC(CCCCC(=O)C1=CC=CN1)C=CC=CC=CC=C(CC)C2C(CCC(O2)C(C)C(=O)O)C 495.70 unknown via CMAUP database
Indanomycin 10345604 Click to see CCC1CCC2C1C=CC(C2C(=O)C3=CC=CN3)C=CC=C(CC)C4C(CCC(O4)C(C)C(=O)O)C 493.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(2R)-6',10-Dihydroxy-7',9'-dimethoxy-4',5',9-trioxo-4,4',5',9-tetrahydrospiro[benzo[1,2-b:5,4-c']dipyran-2(3H),2'(3'H)-naphtho[1,2-b]furan]-7-carboxylic acid methyl ester 97042233 Click to see COC1=CC(=C(C2=C1C3=C(CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)C(=O)C2=O)O)OC 536.40 unknown via CMAUP database
gamma-Rubromycin 5464075 Click to see COC1=CC(=O)C2=C(C1=O)C(=C3C(=C2O)CC4(O3)CCC5=C(O4)C(=C6C(=C5)C=C(OC6=O)C(=O)OC)O)O 522.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
6-Acetylphenazine-1-carboxylic acid 443635 Click to see CC(=O)C1=C2C(=CC=C1)N=C3C(=N2)C=CC=C3C(=O)O 266.25 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazodiazepines
Pentostatin 439693 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
Vira A deaminase inhibitor 44283251 Click to see C1C(C(OC1N2C=NC3=C2NC=NCC3O)CO)O 268.27 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R,5S)-3-hexyl-4-hydroxy-5-methyloxolan-2-one 11030843 Click to see CCCCCCC1C(C(OC1=O)C)O 200.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Cinerubin B 73593 Click to see CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C=CC(=C4C3=O)O)O)O)OC5CC(C(C(O5)C)OC6CC7C(C(O6)C)OC8C(O7)CC(=O)C(O8)C)N(C)C)O 825.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4Z,6R,7R)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 12311394 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown via CMAUP database
(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/10.1139/CJR31-103
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/10.1139/CJR31-103
Retrorsine 5281743 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1139/CJR31-103

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