Brunsvigia josephinae - Unknown
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Internal ID UUID644025665154c679043298
Scientific name Brunsvigia josephinae
Authority [Ker-Gawl.]
First published in Bot. Reg. 3: t. 192, 193 (1817)

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Synonyms Top

Scientific name Authority First published in
Coburgia josephinae Herb. Bot. Mag. 47: t. 2113 (1819)
Amaryllis gigantea Van Marum Verh. Holl. Maatsch. Weetensch. Haarlem 3: 345 (1806)
Amaryllis josephiniae Redouté Liliac. 7: t. 370 (1812)
Amaryllis josephiniana Herb. Amaryllidaceae : 278 (1837)
Brunsvigia glauca Salisb. Gen. Pl. : 117 (1866)
Brunsvigia gydobergensis D.Müll.-Doblies & U.Müll.-Doblies Feddes Repert. 105: 352 (1994)
Brunsvigia josephiniae var. angutifolia Ker Gawl. Bot. Reg. 3: t. 192. 1817
Amaryllis josephinae Redouté Liliac. 7: t. 370 (1812)

Common names Top

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Language Common/alternative name
English candelabra lily
Spanish amaryllis gigantea
Spanish amaryllis josephiniae
Spanish amaryllis josephiniana
Spanish brunsvigia gigantea
Spanish brunsvigia glauca
Spanish brunsvigia gydobergensis
Spanish coburgia josephinae
Spanish lirio candelabro
Afrikaans lantanter
Chinese 约瑟芬灯台花

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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-0000762214
Tropicos 1200948
KEW urn:lsid:ipni.org:names:63499-1
Open Tree Of Life 6013155
IPNI 63499-1
iNaturalist 581437
GBIF 4013911
Freebase /m/025xrbn
EPPO BSGJO
USDA GRIN 8020
Wikipedia Brunsvigia_josephinae

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)!
Title Authors Publication Released IDs
Further alkaloids from Brunsvigia josephinae Francesc Viladomat, Carles Codina, Jaume Bastida, Shaheed Mathee, William E Campbell Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00375-H
Alkaloids from Brunsvigia josephinæ Francesc Viladomat, Jaume Bastida, Carles Codina, William E. Campbell, Shaheed Mathee Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90611-3

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(00)90611-3
(11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol 5282088 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/0031-9422(95)00375-H
(1R,13R,15R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene 162960780 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/0031-9422(95)00375-H
(1R,13R,15S,18S)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 101683297 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
(9,15-Dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl) acetate 78180690 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 373.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
[(1R,13R,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl] acetate 101682301 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 373.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
[(1R,13R,15R,18S)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl] acetate 145967039 Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 373.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
[(1S,13S,15S,18S)-18-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 162963527 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/0031-9422(95)00375-H
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/0031-9422(95)00375-H
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(00)90611-3
https://doi.org/10.1016/0031-9422(95)00375-H
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/S0031-9422(00)90611-3
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/10.1016/0031-9422(95)00375-H
Ambelline 25092366 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
https://doi.org/10.1016/S0031-9422(00)90611-3
Amberline 494154 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Bulphanidine 407581 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Buphanidrine 338023 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Buphanisin 625225 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Buphanisin 12302149 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Crinan-12-ol, 1,2-didehydro-3alpha,7-dimethoxy- 441585 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)90611-3
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/S0031-9422(00)90611-3
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/0031-9422(95)00375-H
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
[(1S,13R,16S,17S)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 102276357 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5 331.40 unknown https://doi.org/10.1016/S0031-9422(00)90611-3
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown https://doi.org/10.1016/0031-9422(95)00375-H
Sternbergine 178814 Click to see CC(=O)OC1C(C=C2CCN3C2C1C4=CC(=C(C=C4C3)O)OC)O 331.40 unknown https://doi.org/10.1016/S0031-9422(00)90611-3
https://doi.org/10.1016/0031-9422(95)00375-H

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