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Narcissus pallidiflorus

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 UUID64401d8fa7545259588774
Scientific name Narcissus pallidiflorus
Authority Pugsley
First published in J. Roy. Hort. Soc. 58: 69 (1933)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Narcissus tortuosus var. pallidiflorus (Pugsley) Nava & Fern.Casado Doc. Jard. Bot. Atlántico 9: 37 (2013)

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000696680
Tropicos 1201280
KEW urn:lsid:ipni.org:names:66144-1
Open Tree Of Life 6013321
NCBI Taxonomy 1695141
IPNI 66144-1
iNaturalist 869229
GBIF 2858403
USDA GRIN 429137

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)!
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Title Authors Publication Released IDs
A heterodimer alkaloid from Narcissus pallidiflorus Carles Codina, Francesc Viladomat, Jaume Bastida, Mario Rubiralta, Jean-Charles Quirion Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85214-Z

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 / Galanthamine-type amaryllidaceae alkaloids
(3aS,6S,7aS)-3a-[6-[[(1R,12S,14S)-14-hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-4-yl]methyl]-1,3-benzodioxol-5-yl]-6-methoxy-1-methyl-2,6,7,7a-tetrahydroindol-3-one 162879277 Click to see CN1CC(=O)C2(C1CC(C=C2)OC)C3=CC4=C(C=C3CN5CCC67CCC(CC6OC8=C(C=CC(=C78)C5)OC)O)OCO4 588.70 unknown https://doi.org/10.1016/0031-9422(90)85214-Z
(3aS,6S)-3a-[6-[[(1S,12S,14S)-14-hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-4-yl]methyl]-1,3-benzodioxol-5-yl]-6-methoxy-1-methyl-2,6,7,7a-tetrahydroindol-3-one 14707484 Click to see CN1CC(=O)C2(C1CC(C=C2)OC)C3=CC4=C(C=C3CN5CCC67CCC(CC6OC8=C(C=CC(=C78)C5)OC)O)OCO4 588.70 unknown https://doi.org/10.1016/0031-9422(90)85214-Z
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Homolycorine 160473 Click to see 315.40 unknown https://doi.org/10.1016/0031-9422(90)85214-Z
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Pretazettine 73360 Click to see 331.40 unknown https://doi.org/10.1016/0031-9422(90)85214-Z

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