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Narcissus poeticus subsp. radiiflorus

Narcissus poeticus subsp. radiiflorus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644026a0db5c7150963799
Scientific name Narcissus poeticus subsp. radiiflorus
Authority (Salisb.) Baker
First published in Handb. Amaryll. : 12 (1888)

Description Top

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Common names Top

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Language Common/alternative name
Vietnamese narcissus angustifolius

Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000770385
Tropicos 1201775
INPN 137993
KEW urn:lsid:ipni.org:names:77188836-1
The Plant List kew-309106
Open Tree Of Life 625027
Observations.org 139005
NCBI Taxonomy 54856
NBN Atlas NBNSYS0000033501
iNaturalist 61335
GBIF 2858584
EOL 1290696
USDA GRIN 429286

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
Fostering in situ conservation of wild relatives of forage crops Kägi C, Petitpierre B, Meyer P, Lötscher Y, Eggenberg S, Aubry S Front Plant Sci 30-Oct-2023
PMCID:PMC10643147
doi:10.3389/fpls.2023.1287430
PMID:38023832
Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe) Ilić T, Kuzmanović N, Vukojičić S, Lakušić D Plants (Basel) 22-Nov-2022
PMCID:PMC9741231
doi:10.3390/plants11233194
PMID:36501234
Alkaloids from Narcissus angustifolius subsp. transcarpathicus (Amaryllidaceae). Labraña J, Machocho AK, Kricsfalusy V, Brun R, Codina C, Viladomat F, Bastida J Phytochemistry 01-Aug-2002
doi:10.1016/S0031-9422(02)00154-1
PMID:12150811

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
Nangustine 443687 Click to see C1C=C2C3CN(C2C(C1O)O)CC4=CC5=C(C=C34)OCO5 287.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
Pancracine 443688 Click to see C1C(C(C=C2C1N3CC2C4=CC5=C(C=C4C3)OCO5)O)O 287.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(5aR,11bS,11cS)-10-hydroxy-9-methoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one 13877672 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)OC)O 301.34 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
9-Hydroxy-10-methoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one 3844472 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC 301.34 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
9-O-Demethylhomolycorine 388787 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC 301.34 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
> Organoheterocyclic compounds / Benzazepines
(1S,13R,14S,15S)-6,8-dioxa-12-azapentacyclo[10.6.1.02,10.05,9.013,18]nonadeca-2(10),3,5(9),17-tetraene-14,15-diol 163106927 Click to see C1C=C2C3CN(C2C(C1O)O)CC4=C3C=CC5=C4OCO5 287.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
5,7-Dioxa-12-azapentacyclo[10.6.1.02,10.04,8.013,18]nonadeca-2,4(8),9,17-tetraene-14,15-diol 74350017 Click to see C1C=C2C3CN(C2C(C1O)O)CC4=CC5=C(C=C34)OCO5 287.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
Hippagine 625481 Click to see C1C(C(C=C2C1N3CC2C4=CC5=C(C=C4C3)OCO5)O)O 287.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Pseudolycorine 443689 Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O 289.33 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
Vasconine 443690 Click to see COC1=C(C=C2C3=CC=CC4=C3[N+](=CC2=C1)CC4)OC 266.31 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
2-Methyl-4-(4-hydroxyphenyl)-6-methoxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline 618047 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown https://doi.org/10.1016/S0031-9422(02)00154-1
Cherylline 90075 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown https://doi.org/10.1016/S0031-9422(02)00154-1

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