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Internal ID UUID643fde6ea9da1030342940
Scientific name Rothia hirsuta
Authority (Guill. & Perr.) Baker
First published in D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 7 (1871)

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Synonyms Top

Scientific name Authority First published in
Xerocarpus hirsutus Guill. & Perr. Fl. Seneg. Tent.: 170 (1832)
Xerocarpus hirsuta Guill. & Perr.
Lotononis desertorum Dümmer Trans. Roy. Soc. South Africa3: 316 (1913)
Amphinomia desertorum (Dümmer) A.Schreib. Mitt. Bot. Staatssamml. München2: 286 (1957)
Westonia hirsuta Kuntze Revis. Gen. Pl.1: 213 (1891)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000211136
Tropicos 13048638
KEW urn:lsid:ipni.org:names:517806-1
The Plant List ild-6222
Open Tree Of Life 552928
NCBI Taxonomy 508216
IPNI 517806-1
iNaturalist 593364
GBIF 5353602
EPPO RTHHI
EOL 695606
USDA GRIN 419243

Genomes (via NCBI) Top

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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
Chemotaxonomic significance of alkaloids in the genus Robynsiophyton Ben-Erik Van Wyk, Gerhard H. Verdoorn Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(91)90086-F
Alkaloids of Rothia trifoliata and Rothia hirsuta. Hussain RA, Kinghorn AD, Molyneux RJ J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A033
PMID:21401151

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 / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/NP50058A033
(1R,2R,4S,9R,10S)-4-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163061089 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O 264.36 unknown https://doi.org/10.1021/NP50058A033
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/NP50058A033
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(91)90086-F
https://doi.org/10.1021/NP50058A033
(1S,2R,4R,5S,9S,10S)-4,5-dihydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 14355510 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(C(C4=O)O)O 280.36 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1R,2S,4S,9R,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] 4-hydroxy-3-methoxybenzoate 162899736 Click to see COC1=C(C=CC(=C1)C(=O)OC2CCN3CC4CC(C3C2)CN5C4CCCC5=O)O 414.50 unknown https://doi.org/10.1021/NP50058A033
[(1S,2R,4R,5S,9S,10S)-5-hydroxy-6-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (Z)-2-methylbut-2-enoate 102437379 Click to see CC=C(C)C(=O)OC1CC2C3CC(CN2C(=O)C1O)C4CCCCN4C3 362.50 unknown https://doi.org/10.1016/0305-1978(91)90086-F
[(1S,2S,4S,9S,10R)-14-Oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-3-phenylprop-2-enoate 6437604 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)OC(=O)C=CC5=CC=CC=C5 394.50 unknown https://doi.org/10.1021/NP50058A033
Isolupanine 15939852 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(91)90086-F
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(91)90086-F
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1016/0305-1978(91)90086-F

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