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Internal ID UUID643fde5198a2c236964188
Scientific name Crotalaria globifera
Authority E.Mey.
First published in Comm. Pl. Afr. Austr.: 24 (1836)

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Synonyms Top

Scientific name Authority First published in
Crotalaria cinerea Burtt Davy ex I.Verd. Bothalia2: 411 (1928)
Crotalaria pentheri Gand. Bull. Soc. Bot. France60: 459 (1913)
Crotalaria macrostachya Sond. Linnaea23: 27 (1850)
Crotalaria globifera var. glabra E.Mey. Comm. Pl. Afr. Austr.: 24 (1836)
Crotalaria globifera var. pubescens E.Mey. Comm. Pl. Afr. Austr.: 24 (1836)
Crotalaria globifera var. glabra Harv. Fl. Cap. 2: 44 1862

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Varieties (abbr. var.) Top

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Name Authority First published in
Crotalaria globifera var. stenophylla Taub.

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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
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000210668
Tropicos 13029187
KEW urn:lsid:ipni.org:names:488179-1
The Plant List ild-5788
Open Tree Of Life 1093708
NCBI Taxonomy 1132207
IPNI 488179-1
iNaturalist 583039
GBIF 2942923
EOL 691961
USDA GRIN 12323

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Globiferine a pyrrolizidine alkaloid from crotalaria globifera Kenneth Brown, J.Alastair Devlin, David J. Robins Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80352-0

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1R,4R,5R,8S,9S,19R)-9-hydroxy-5,8,9-trimethyl-2,7,11-trioxa-16-azatetracyclo[11.5.1.04,8.016,19]nonadec-13-ene-3,6,10-trione 162896445 Click to see CC1C2C(=O)OC3CCN4C3C(=CC4)COC(=O)C(C2(OC1=O)C)(C)O 365.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
Grantianine 119026130 Click to see CC1C2C(=O)OC3CCN4C3C(=CC4)COC(=O)C(C2(OC1=O)C)(C)O 365.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Penicimarin B 71665535 Click to see CC(CCCC1CC2=C(C(=CC=C2)OC)C(=O)O1)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
> Organoheterocyclic compounds / Pyrrolizines
(1R,4S,5S,6R,16R)-5,6-dihydroxy-5,6-dimethyl-4-propan-2-yl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 101922689 Click to see CC(C)C1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 353.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
5,6-Dihydroxy-4-(2-hydroxypropan-2-yl)-5,6-dimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 163104430 Click to see CC1(C(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)C(C)(C)O)O 369.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
5,6-Dihydroxy-5,6-dimethyl-4-methylidene-7-propan-2-yl-3-oxa-13-azatricyclo[8.5.1.013,16]hexadec-1(15)-en-8-one 5322016 Click to see CC(C)C1C(=O)CC2CCN3C2C(=CC3)COC(=C)C(C1(C)O)(C)O 349.50 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
Dicrotaline 101981705 Click to see CC1(CC(=O)OCC2=CCN3C2C(CC3)OC(=O)C1)O 281.30 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
Globiferine 122201334 Click to see CC1(C(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(C)O)C(C)(C)O)O 369.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
Grantaline 119025712 Click to see CC1(C2C(=O)OC3CCN4C3C(=CC4)COC(=O)C(C2(O1)C)(C)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0
Trichodesmine 119040 Click to see CC(C)C1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 353.40 unknown https://doi.org/10.1016/S0031-9422(00)80352-0

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