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Narcissus confusus

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 UUID64401e182e8fa030217651
Scientific name Narcissus confusus
Authority Pugsley
First published in J. Roy. Hort. Soc. 58: 59 (1933)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Narcissus pseudonarcissus subsp. eugeniae (Fern.Casas) Fern.Casas Fontqueria 4: 27 (1983)
Narcissus pseudonarcissus subsp. calcicarpetanus (Fern.Casas) Fern.Casas Fontqueria 4: 27 (1983)
Narcissus pseudonarcissus subsp. radinganorum (Fern.Casas) Mateo & M.B.Crespo Man. Determin. Fl. Valenciana , ed. 2: 450 (2001)
Narcissus pseudonarcissus subsp. pugsleyanus Barra & G.López Anales Jard. Bot. Madrid 39: 298 (1982 publ. 1983)
Narcissus genesii-lopezii Fern.Casas Fontqueria 14: 19 (1987)
Narcissus radinganorum Fern.Casas Fontqueria 6: 41 (1984)
Narcissus eugeniae Fern.Casas Fontqueria 1: 11 (1982)
Narcissus calcicarpetanus Fern.Casas Fontqueria 2: 33 (1982)
Narcissus pseudonarcissus f. stenantha Lange Overs. Kongel. Danske Vidensk. Selsk. Forh. Medlemmers Arbeider 1893: 193 1893
Narcissus portensis var. albidotepaloideus A.Fern., T.Leitão & C.Aguiar Anuário Soc. Brot. 58: 22 (1992)

Common names Top

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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

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000703860
Tropicos 1201282
KEW urn:lsid:ipni.org:names:65976-1
The Plant List kew-282672
Open Tree Of Life 3994385
NCBI Taxonomy 1695117
IPNI 65976-1
iNaturalist 469985
GBIF 2858371
EOL 1115901
USDA GRIN 429123

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
Cytotoxicity and Antiviral Properties of Alkaloids Isolated from Pancratium maritimum Masi M, Di Lecce R, Mérindol N, Girard MP, Berthoux L, Desgagné-Penix I, Calabrò V, Evidente A Toxins (Basel) 07-Apr-2022
PMCID:PMC9029599
doi:10.3390/toxins14040262
PMID:35448871
Transcriptomic and Metabolomic Analyses Reveals That Exogenous Methyl Jasmonate Regulates Galanthamine Biosynthesis in Lycoris longituba Seedlings Li Q, Xu J, Zheng Y, Zhang Y, Cai Y Front Plant Sci 30-Sep-2021
PMCID:PMC8514708
doi:10.3389/fpls.2021.713795
PMID:34659286
Profiles of Secondary Metabolites (Phenolic Acids, Carotenoids, Anthocyanins, and Galantamine) and Primary Metabolites (Carbohydrates, Amino Acids, and Organic Acids) during Flower Development in Lycoris radiata Park CH, Yeo HJ, Kim YJ, Nguyen BV, Park YE, Sathasivam R, Kim JK, Park SU Biomolecules 09-Feb-2021
PMCID:PMC7914633
doi:10.3390/biom11020248
PMID:33572277
Potential Herb–Drug Interactions in the Management of Age-Related Cognitive Dysfunction Auxtero MD, Chalante S, Abade MR, Jorge R, Fernandes AI Pharmaceutics 19-Jan-2021
PMCID:PMC7835864
doi:10.3390/pharmaceutics13010124
PMID:33478035
Biosynthesis and Biological Activities of Newly Discovered Amaryllidaceae Alkaloids Ka S, Koirala M, Mérindol N, Desgagné-Penix I Molecules 23-Oct-2020
PMCID:PMC7660210
doi:10.3390/molecules25214901
PMID:33113950
Recent Progress in Amaryllidaceae Biotechnology Georgiev V, Ivanov I, Pavlov A Molecules 13-Oct-2020
PMCID:PMC7587388
doi:10.3390/molecules25204670
PMID:33066212
Amaryllidaceae alkaloids: identification and partial characterization of montanine production in Rhodophiala bifida plant Reis A, Magne K, Massot S, Tallini LR, Scopel M, Bastida J, Ratet P, Zuanazzi JA Sci Rep 11-Jun-2019
PMCID:PMC6559983
doi:10.1038/s41598-019-44746-7
PMID:31186470
Overview of the Structure–Function Relationships of Mannose-Specific Lectins from Plants, Algae and Fungi Barre A, Bourne Y, Van Damme EJ, Rougé P Int J Mol Sci 10-Jan-2019
PMCID:PMC6359319
doi:10.3390/ijms20020254
PMID:30634645
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
EFFECT OF PPM ON ALKALOID PRODUCTION IN NARCISSUS CONFUSUS SHOOT-CLUMPS R. Colque, F. Viladomat, J. Bastida, C. Codina International Society for Horticultural Science (ISHS) 27-Jul-2015
doi:10.17660/ACTAHORTIC.2001.560.51
Application of hydrostatic CCC–TLC–HPLC–ESI-TOF-MS for the bioguided fractionation of anticholinesterase alkaloids from Argemone mexicana L. roots Kukula-Koch W, Mroczek T Anal Bioanal Chem 25-Jan-2015
PMCID:PMC4365284
doi:10.1007/s00216-015-8468-x
PMID:25618762
Comparative Analysis of Lycorine in Wild Plant and Callus Culture Samples of Hymenocallis littoralis by HPLC-UV Method Subramaniam S, Sundarasekar J, Sahgal G, Murugaiyah V ScientificWorldJournal 06-May-2014
PMCID:PMC4033353
doi:10.1155/2014/408306
PMID:24895650
Influence of plant origin on propagation capacity and alkaloid biosynthesis during long-term in vitro cultivation of Leucojum aestivum L. Bogdanova Y, Stoeva T, Yanev S, Pandova B, Molle E, Burrus M, Stanilova M In Vitro Cell Dev Biol Plant 06-Dec-2008
PMCID:PMC7089496
doi:10.1007/s11627-008-9178-2
PMID:32214772
Effect of galantamine on the human α7 neuronal nicotinic acetylcholine receptor, the Torpedo nicotinic acetylcholine receptor and spontaneous cholinergic synaptic activity Texidó L, Ros E, Martín-Satué M, López S, Aleu J, Marsal J, Solsona C Br J Pharmacol 18-Apr-2005
PMCID:PMC1576175
doi:10.1038/sj.bjp.0706221
PMID:15834443
Narcissus Alkaloids, III. 9-O-Demethylhomolycorine from Narcissus confusus Jaume Bastida, Jose M. Llabrés, Francesc Viladomat, Carles Codina, Mario Rubiralta, Miguel Feliz American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50050A013

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 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(00)81849-X
Hemanthamine 441593 Click to see 301.34 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
https://doi.org/10.1107/S0108270188003853
https://doi.org/10.1002/PCA.660
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
https://doi.org/10.17660/ACTAHORTIC.2001.560.51
https://doi.org/10.1002/PCA.660
(1R,12R,14S)-14-hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-4-carbaldehyde 163038454 Click to see 301.34 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
14-Hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-4-carbaldehyde 18719938 Click to see 301.34 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
Galantamin 3449 Click to see 287.35 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Homolycorine 160473 Click to see 315.40 unknown https://doi.org/10.1021/NP50050A013
https://doi.org/10.1002/PCA.660
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-ol 162894672 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 443682 Click to see 331.40 unknown https://doi.org/10.1002/PCA.660
(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 11873227 Click to see 331.40 unknown https://doi.org/10.1002/PCA.660
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol 419046 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
Pretazettine 73360 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(00)81849-X
> 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/S0031-9422(00)81849-X
https://doi.org/10.1107/S0108270188003853
https://doi.org/10.1002/PCA.660

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