Cyrtanthus elatus - Unknown
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Internal ID UUID644025c77aa67838786540
Scientific name Cyrtanthus elatus
Authority (Jacq.) Traub
First published in Pl. Life 25: 48 (1969)

Description Top

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Cyrtanthus elatus, also known as the Scarborough lily, is a bulbous flowering plant native to the Cape Province of South Africa. It is also commonly referred to as the fire lily or George lily. The plant produces vibrant flowers in shades of red, orange, yellow, pink, or white and can grow up to 2 feet tall. It is relatively easy to grow in warm, sheltered areas or in pots under glass. The plant requires full sun or slight shade and blooms in late summer or early autumn. Its Latin name, elatus, means "tall" and it has been awarded the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name Authority First published in
Vallota speciosa T.Durand & Schinz Consp. Fl. Afric. 5: 258 (1894)
Vallota purpurea Herb. Appendix : 29 (1821)
Vallota grandiflora Carrière Rev. Hort. (Paris) 42: 50 (1870)
Vallota elata M.Roem. Fam. Nat. Syn. Monogr. 4: 110 (1847)
Amaryllis elata Jacq. Pl. Hort. Schoenbr. 1: 32 (1797)
Amaryllis mexicana hort. ex Savi Fl. Ital. 3: 29 (1824)
Amaryllis purpurea Aiton Hort. Kew. 1: 417 (1789)
Amaryllis speciosa L'Hér. Sert. Angl. : 12 (1789)
Crinum speciosum L.f. Suppl. Pl. : 195 (1782)
Cyrtanthus purpureus Herb. Bot. Mag. 47: 3, t. 2113 (1819)
Cyrtanthus purpureus f. albus Baker ex Traub Pl. Life 25: 48 1969
Cyrtanthus speciosus f. albus (Baker ex Traub) Traub Pl. Life 28: 66 (1972)
Cyrtanthus speciosus f. magnificus (Baker) Traub Pl. Life 28: 66 (1972)
Vallota purpurea var. magnifica Baker Amaryllidaceae 54. 1888
Cyrtanthus purpureus (Ait.) Traub Pl. Life (Stanford) xix. 58 (1963).

Common names Top

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Language Common/alternative name
English george lily, scarborough lily
Afrikaans george-lelie
Afrikaans knysna-lelie
Russian Валлота прекрасная
Chinese 乔治百合
Chinese 红色垂筒花

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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Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
float the seeds until they sprout, then carefully plant just underneath the medium surface

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-0000764910
Tropicos 1201055
KEW urn:lsid:ipni.org:names:64208-1
The Plant List kew-303814
Open Tree Of Life 808523
NCBI Taxonomy 112543
NBN Atlas NBNSYS0200003730
IPNI 64208-1
iNaturalist 401233
GBIF 5325993
Freebase /m/04kvzg
EOL 1087303
USDA GRIN 452437
Wikipedia Cyrtanthus_elatus

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
The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae Danquah CA, Minkah PA, Agana TA, Moyo P, Ofori M, Doe P, Rali S, Osei Duah Junior I, Amankwah KB, Somuah SO, Nugbemado IN, Maharaj VJ, Bhakta S, Gibbons S Molecules 13-Jul-2022
PMCID:PMC9316996
doi:10.3390/molecules27144475
PMID:35889346
Prophyll in Monocots: The Starting Point of Lateral Shoot Phyllotaxis Choob V Front Plant Sci 13-Apr-2022
PMCID:PMC9044502
doi:10.3389/fpls.2022.855146
PMID:35498710
Narcissus Plants: A Melting Pot of Potyviruses Probowati W, Kawakubo S, Ohshima K Viruses 11-Mar-2022
PMCID:PMC8949890
doi:10.3390/v14030582
PMID:35336988
Sequence analyses of RT-PCR products obtained from seven infected leaf samples revealed existence of three potyvirus species in Indian narcissus (Narcissus tazetta L.) Raj R, Kaur C, Srivastava A, Kumar S, Raj SK 3 Biotech 11-Sep-2020
PMCID:PMC7486357
doi:10.1007/s13205-020-02418-8
PMID:32968613
Complete genome sequence analysis of Narcissus yellow stripe virus infecting Narcissus tazetta in India Raj R, Agrawal L, Kumar S, Chauhan PS, Raj SK 3 Biotech 22-Oct-2019
PMCID:PMC6805833
doi:10.1007/s13205-019-1939-6
PMID:31692678
Evolutionary Rates and Phylogeographical Analysis of Odontoglossum Ringspot Virus Based on the 166 Coat Protein Gene Sequences He Z, Dong T, Wu W, Chen W, Liu X, Li L Plant Pathol J 01-Oct-2019
PMCID:PMC6788419
doi:10.5423/PPJ.OA.04.2019.0113
PMID:31632224
Full-length genome sequence of Cyrtanthus elatus virus-A isolated from Narcissus tazetta in India Raj R, Kaur C, Agrawal L, Chauhan PS, Kumar S, Raj SK 3 Biotech 09-Mar-2018
PMCID:PMC5843565
doi:10.1007/s13205-018-1189-z
PMID:29527455
A review of the early stages and host plants of the genera Eumerus and Merodon (Diptera: Syrphidae), with new data on four species Ricarte A, Souba-Dols GJ, Hauser M, Marcos-García MÁ PLoS One 19-Dec-2017
PMCID:PMC5736194
doi:10.1371/journal.pone.0189852
PMID:29261787
The velamen radicum is common among terrestrial monocotyledons Zotz G, Schickenberg N, Albach D Ann Bot 07-Sep-2017
PMCID:PMC5714198
doi:10.1093/aob/mcx097
PMID:28961783
The phylogenetics of the global population of potato virus Y and its necrogenic recombinants Gibbs AJ, Ohshima K, Yasaka R, Mohammadi M, Gibbs MJ, Jones RA Virus Evol 02-Mar-2017
PMCID:PMC5399925
doi:10.1093/ve/vex002
PMID:28458913
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
The pollination niche and its role in the diversification and maintenance of the southern African flora Johnson SD Philos Trans R Soc Lond B Biol Sci 12-Feb-2010
PMCID:PMC2838267
doi:10.1098/rstb.2009.0243
PMID:20047876
Chemistry, Biology and Medicinal Potential of Narciclasine and its Congeners Kornienko A, Evidente A Chem Rev 20-May-2008
PMCID:PMC2856661
doi:10.1021/cr078198u
PMID:18489166
Amaryllidaceae Isocarbostyril Alkaloids and Their Derivatives as Promising Antitumor Agents Ingrassia L, Lefranc F, Mathieu V, Darro F, Kiss R Transl Oncol 01-Mar-2008
PMCID:PMC2510759
doi:10.1593/tlo.08100
PMID:18607503
Alkaloide von <i>Chlidanthus fragrans</i>, <i>Vallota purpurea</i>, <i>Nerine undulata</i> und <i>Hippeastrum vittatum</i> (XI. Mitteil. über Amaryllidaceen‐Alkaloide) Hans‐G. Boit Wiley 20-May-2007
doi:10.1002/CBER.19560890509

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11R,13S,15S,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 162945733 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
(1S,11R,13S,15S,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 49799009 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
(1S,11S,13S,15S,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 154496716 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
https://doi.org/10.1002/CBER.19560890509
(1S,13S,15S,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 5282090 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1002/CBER.19560890509
https://doi.org/10.1016/S0367-326X(00)00313-0
Haemanthamine 441593 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
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/S0367-326X(00)00313-0
https://doi.org/10.1002/CBER.19560890509
Hemanthidine 3002914 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(1S,12S,14R)-9,14-dimethoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene 163050021 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)OC 301.40 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
9,14-Dimethoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene 20589472 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)OC 301.40 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17R,18S)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9-triene-17,18-diol 118701134 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
[(1S,15R,17R,18S,19R)-18-acetyloxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9-trien-17-yl] acetate 56928079 Click to see CC(=O)OC1CC2CCN3C2C(C1OC(=O)C)C4=CC5=C(C=C4C3)OCO5 373.40 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
2,3,3a,4,5,7,12b,12c-Octahydro-1H,10H-[1,3]dioxolo[4,5-j]pyrrolo[3,2,1-de]phenanthridine-1,2-diol 443674 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
Zephyranthine 193339 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(1R,2R)-1-(1,3-benzodioxol-5-yl)-2-[4-[(2R,3S,4R,5S)-5-[4-[(1R,2R)-1-(3,4-dimethoxyphenyl)-1-hydroxypropan-2-yl]oxy-3-methoxyphenyl]-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 158356097 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC(C)C(C3=CC4=C(C=C3)OCO4)O)OC)C5=CC(=C(C=C5)OC(C)C(C6=CC(=C(C=C6)OC)OC)O)OC)C 716.80 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5R,9R,10R,13R,14R,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methyl-5-oxoheptan-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162843958 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
6-Hydroxy-7,8-dimethoxy-2-(2-oxopropyl)-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one 71436822 Click to see CC(=O)CC1CC2C(O1)C3=CC(=C(C(=C3C(=O)O2)O)OC)OC 322.31 unknown https://doi.org/10.1016/S0367-326X(00)00313-0
https://doi.org/10.1002/CBER.19560890509

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