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Clivia nobilis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440259ff19c7847007465
Scientific name Clivia nobilis
Authority Lindl.
First published in Bot. Reg. 14: t. 1182 (1828)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Haemanthus cernuiflorus J.Bell ex Drapiez Herb. Amat. Fl. 4: t. 227 (1830)
Imatophyllum aitonii Hook. Bot. Mag. 55: t. 2856 (1828)
Imatophyllum maximum Guillon Rev. Hort. (Paris) 53: 140 (1881)
Himantophyllum aitonii Duch. Journ. Soc. Imp. Hortic. v. (1859) 626.

Common names Top

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Language Common/alternative name
Spanish haemanthus cernuiflorus
Spanish imatophyllum aitonii
Spanish imatophyllum maximum
Finnish pikkupunasarja
Japanese クンシラン
Swedish kafferlilja
Chinese 垂笑君子兰
Chinese 君子兰
Chinese 垂笑君子蘭

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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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-0000763764
Tropicos 1200888
KEW urn:lsid:ipni.org:names:63634-1
The Plant List kew-302706
Open Tree Of Life 434609
NCBI Taxonomy 112537
IPNI 63634-1
iNaturalist 342535
GBIF 5326276
Freebase /m/03d142l
EOL 1086963
USDA GRIN 10946
Wikipedia Clivia_nobilis

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
Benzoindolizidine Alkaloids Tylophorine and Lycorine and Their Analogues with Antiviral, Anti-Inflammatory, and Anticancer Properties: Promises and Challenges Di Sotto A, Valipour M, Azari A, Di Giacomo S, Irannejad H Biomedicines 24-Sep-2023
PMCID:PMC10603990
doi:10.3390/biomedicines11102619
PMID:37892993
Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin Evidente A Molecules 12-May-2023
PMCID:PMC10224442
doi:10.3390/molecules28104055
PMID:37241796
Amaryllidaceae Alkaloids from Clivia miniata (Lindl.) Bosse (Amaryllidaceae): Isolation, Structural Elucidation, and Biological Activity Šafratová M, Křoustková J, Maafi N, Suchánková D, Vrabec R, Chlebek J, Kuneš J, Opletal L, Bucar F, Cahlíková L Plants (Basel) 10-Nov-2022
PMCID:PMC9692855
doi:10.3390/plants11223034
PMID:36432763
Screening for Plant Volatile Emissions with Allelopathic Activity and the Identification of L-Fenchone and 1,8-Cineole from Star Anise (Illicium verum) Leaves Kang G, Mishyna M, Appiah KS, Yamada M, Takano A, Prokhorov V, Fujii Y Plants (Basel) 28-Oct-2019
PMCID:PMC6918414
doi:10.3390/plants8110457
PMID:31661792
Lycorine: A prospective natural lead for anticancer drug discovery Roy M, Liang L, Xiao X, Feng P, Ye M, Liu J Biomed Pharmacother 14-Aug-2018
PMCID:PMC7127747
doi:10.1016/j.biopha.2018.07.147
PMID:30114645
The Colletotrichum dracaenophilum, C. magnum and C. orchidearum species complexes Damm U, Sato T, Alizadeh A, Groenewald JZ, Crous PW Stud Mycol 07-Apr-2018
PMCID:PMC6030544
doi:10.1016/j.simyco.2018.04.001
PMID:29997400
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
Phytochemical and Biological Investigation of Clivia nobilis Flowers Cultivated in Egypt Shawky E Iran J Pharm Res 01-Jun-2016
PMCID:PMC5149041
PMID:27980589
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
Isolation and Identification of Fourteen Microsatellite Markers in Clivia miniata and Clivia nobilis (Amaryllidaceae) Gao W, Zhao H, Liu Y, Li MR, Nurmamat E, Li LF, Ren YY, Xiao HX Int J Mol Sci 02-Aug-2012
PMCID:PMC3431817
doi:10.3390/ijms13089609
PMID:22949819
Structure of the lycorinine alkaloid nobilisitine A. Schwartz BD, White LV, Banwell MG, Willis AC J Org Chem 21-Oct-2011
doi:10.1021/JO2016899
PMID:21899321
Molecular phylogenetics of Ruscaceae sensu lato and related families (Asparagales) based on plastid and nuclear DNA sequences Kim JH, Kim DK, Forest F, Fay MF, Chase MW Ann Bot 07-Oct-2010
PMCID:PMC2958784
doi:10.1093/aob/mcq167
PMID:20929900
Biological Evaluation of Structurally Diverse Amaryllidaceae Alkaloids and their Synthetic Derivatives: Discovery of Novel Leads for Anticancer Drug Design Evidente A, Kireev AS, Jenkins AR, Romero AE, Steelant WF, Van slambrouck S, Kornienko A Planta Med 23-Feb-2009
PMCID:PMC3125136
doi:10.1055/s-0029-1185340
PMID:19235683
Quantitative analysis of changes in actin microfilament contribution to cell plate development in plant cytokinesis Higaki T, Kutsuna N, Sano T, Hasezawa S BMC Plant Biol 17-Jul-2008
PMCID:PMC2490694
doi:10.1186/1471-2229-8-80
PMID:18637163
Nobilisine, a New Alkaloid from Clivia nobilis Peter W. Jeffs, Luciano Mueller, Amina H. Abou-Donia, Ahmed A. Seif el-Din, Dale Campau American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50057A016

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
9-Azatetracyclo[7.6.1.02,7.012,16]hexadeca-2,4,6-triene 78421824 Click to see C1CC2CCN3C2C(C1)C4=CC=CC=C4C3 213.32 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
Galanthan 6857500 Click to see 213.32 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(2S,3R,7S,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-12-one 12303691 Click to see 317.34 unknown https://doi.org/10.1021/NP50057A016
(3S,7S,9R,10R)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-12-one 162891017 Click to see 317.34 unknown https://doi.org/10.1021/JO2016899
https://doi.org/10.1016/S0031-9422(98)00714-6
(4-Methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl) 3-hydroxybutanoate 14061721 Click to see 403.40 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
[(2S,3R,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] (3R)-3-hydroxybutanoate 14061722 Click to see CC(CC(=O)OC1CC2CCN(C2C3C1OC(=O)C4=CC5=C(C=C34)OCO5)C)O 403.40 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
[(2S,3R,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] (3S)-3-hydroxybutanoate 163022269 Click to see 403.40 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
[(3R,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] 3-hydroxybutanoate 163022268 Click to see CC(CC(=O)OC1CC2CCN(C2C3C1OC(=O)C4=CC5=C(C=C34)OCO5)C)O 403.40 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
Clivatine 3083698 Click to see 403.40 unknown https://doi.org/10.1021/NP50057A016
https://doi.org/10.1016/S0031-9422(98)00714-6
Cliviasine 558132 Click to see CN1CCC2C1C3C(C(C2)O)OC(=O)C4=CC5=C(C=C34)OCO5 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
Nobilisitine A 70698006 Click to see 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
Nobilistine A 12303692 Click to see 317.34 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.1016/S0031-9422(98)00714-6
https://doi.org/10.1021/NP50057A016

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