Brunsvigia orientalis - Unknown
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Internal ID UUID644025671ad9c026504496
Scientific name Brunsvigia orientalis
Authority Ait. ex Eckl.
First published in Topogr. Verz. Pflanzensamml. Ecklon : 7 (1827)

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Synonyms Top

Scientific name Authority First published in
Coburgia multiflora Herb. ex Sims Bot. Mag. 47: sub t. 2113. 1819
Haemanthus orientalis Thunb. Prodr. Pl. Cap. : 59 (1794)
Amaryllis nobilis Salisb. Prodr. Stirp. Chap. Allerton : 235 (1796)
Amaryllis orientalis L. Sp. Pl. : 293 (1753)
Brunsvigia gigantea Heist. Beschr. Neu. Geschl. : 3 (1755)
Brunsvigia multiflora (L.) W.T.Aiton Hortus Kew. 2: 230 (1811)
Brunsvigia rubricaulis M.Roem. Fam. Nat. Syn. Monogr. 4: 57 (1847)
Crinum candelabrum hort. ex M.Roem. Fam. Nat. Syn. Monogr. 4: 57 (1847)

Common names Top

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Language Common/alternative name
English candelabra flower
Afrikaans maartblom
Afrikaans perdespook
Afrikaans lantanter
Afrikaans ajuinbol
Afrikaans kandelaarblom
Afrikaans koningskandelaar
Afrikaans marsblom
Afrikaans rolbossie
Afrikaans seeroogblom,
Chinese 灯台百合
Chinese 灯台花

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000762231
Tropicos 1200953
KEW urn:lsid:ipni.org:names:63511-1
The Plant List kew-301202
Open Tree Of Life 709242
NCBI Taxonomy 379211
IPNI 63511-1
iNaturalist 132796
GBIF 2853381
EOL 1086411

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)!
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Title Authors Publication Released IDs
Environmental pressures on stomatal size may drive plant genome size evolution: evidence from a natural experiment with Cape geophytes Veselý P, Šmarda P, Bureš P, Stirton C, Muasya AM, Mucina L, Horová L, Veselá K, Šilerová A, Šmerda J, Knápek O Ann Bot 31-May-2020
PMCID:PMC7380457
doi:10.1093/aob/mcaa095
PMID:32474609
Does the Prostrate-leaved Geophyte Brunsvigia orientalis Utilize Soil-derived CO2 for Photosynthesis? Cramer MD, Kleizen C, Morrow C Ann Bot 08-Mar-2007
PMCID:PMC2802911
doi:10.1093/aob/mcm019
PMID:17347161
Alkaloids from Brunsvigia orientalis Francesc Viladomat, Giovanna R. Almanza, Carles Codina, Jaume Bastida, William E. Campbell, Shaheed Mathee Elsevier BV 04-Apr-2003
doi:10.1016/S0031-9422(96)00506-7

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Crinamine 118701061 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
(1S,11R,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 12309559 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
(1S,11S,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 162945734 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-15-ol 625708 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene 271606 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Bulphanidine 407581 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Buphanisine 12302149 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Haemanthidine 544807 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Undulatin 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(17-Acetyloxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl) acetate 163046700 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=CC5=C(C=C34)OCO5 373.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
(1S,13S,16S,17R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-triene-16,17-diol 162893619 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
[(1S,13R,16S,17R)-17-acetyloxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 102445642 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=C(C5=C(C=C34)OCO5)OC 403.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
[(1S,13S,16S,17R)-17-acetyloxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 163046701 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=CC5=C(C=C34)OCO5 373.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
[(1S,13S,16S,17R)-17-acetyloxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 163088254 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=C(C5=C(C=C34)OCO5)OC 403.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
1H,6H-5,11b-Ethano[1,3]dioxolo[4,5-j]phenanthridine-1,2-diol, 2,3,4,4a-tetrahydro-7-methoxy- 629204 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7
Bowdensine 541341 Click to see CC(=O)OC1CCC2C3(C1OC(=O)C)CCN2CC4=C(C5=C(C=C34)OCO5)OC 403.40 unknown https://doi.org/10.1016/S0031-9422(96)00506-7

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