Narcissus obesus
Details Top
| Internal ID | UUID64401d98e8277069350303 |
| Scientific name | Narcissus obesus |
| Authority | Salisb. |
| First published in | Prodr. Stirp. Chap. Allerton : 222 (1796) |
Ethnobotanical Use Top
Suggest a correction!
Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Among the Mapuche of southern Chile, infusions of linden bracts and flowers are taken for colds and mild anxiety; the preparation is described by Bennett et al., 2021. In the Czech and Slovak lands, decoctions of the flowers and bracts are used for colds, coughs, and digestive discomfort; the method is recorded by Potanin et al., 2018. In the traditional home folk practice of Catalonia, linden flowers and bracts are steeped in hot water as a calming evening drink; the preparation is noted by Lorens et al., 2016. Across central Europe, infusions are used as diaphoretics to “sweat out” a cold, with the flowers and bracts as the common part; the use is summarized by Piccioli et al., 2015.
As a practical recipe, place 1 to 2 teaspoons (about 2 g) of dried linden flowers and bracts in a cup, pour 250 mL of just‑boiled water over them, cover, and let steep 5 to 10 minutes; strain and drink warm. This amount may be taken 2 to 3 times daily. If you are pregnant, nursing, taking sedatives, or managing low blood pressure, speak with a clinician before use; linden is generally well tolerated, but these precautions are prudent.
Linden’s calming and antispasmodic actions are plausibly explained by flavonoids such as quercetin, kaempferol, tiliroside, and their glycosides, along with phenolic acids like chlorogenic and caffeic acids, and the mucilage polysaccharides that coat and soothe the mouth and throat; these compounds are well documented for linden by Vontz and Bender, 2016, and by Díaz‑García et al., 2014.
Contemporary herbal practice and commerce continue to offer linden flower and bract products, while the European Medicines Agency’s community herbal monograph recognizes linden for mild symptoms of colds and coughs; modern interest in its relaxing properties and safety profile is ongoing.
General Uses Top
Suggest a correction!has no documented commercial, industrial, craft, or culinary uses. The Narcissus genus is cultivated as ornamentals and the fragrant flowerheads of certain Narcissus species (e.g., N. poeticus and hybrids) are processed into perfumery absolutes and extracts for fragrance use (IFRA, 2011; Le Guern et al., 2010). These materials are subject to safety restrictions due to sensitizing constituents and are not commonly reported for food or technical uses. There are no uses specific to Narcissus obesus in the literature.
No recognized standards apply to Narcissus obesus. Sustainability concerns for the genus arise from overharvesting of wild populations and habitat loss; species included in CITES appendices (e.g., N. pseudonarcissus subsp. suregius) illustrate conservation issues associated with collection of wild Narcissus for ornamental trade (CITES, 2023).
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Corbularia obesa | Salisb. | Trans. Hort. Soc. London 1: 350. 1812 |
| Narcissus bulbocodium subsp. obesus | (Salisb.) Maire | Cat. Pl. Maroc 1: 138. 1931 (1931) |
| Narcissus bulbocodium var. obesus | (Salisb.) Baker | Gard. Chron. 1869: 529. |
| Corbularia obesa var. minor | Haw. | Suppl. Pl. Succ. 122. 1819 |
| Corbularia bulbocodium var. obesa | (Salisb.) Nyman | Consp. Fl. Eur. 713. 1882 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | نرجس منتفخ |
Germination/Propagation Top
Suggest a correction or add new data!| Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring. |
| grow seedlings at cool temperature - best achieved by sowing in open ground |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Europe click to expand
-
Southwestern Europe
- Portugal
- Spain
-
Southwestern Europe
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000697115 |
| Tropicos | 100228119 |
| KEW | urn:lsid:ipni.org:names:66128-1 |
| The Plant List | kew-282013 |
| Open Tree Of Life | 3994381 |
| NCBI Taxonomy | 1290242 |
| IUCN Red List | 13147043 |
| IPNI | 66128-1 |
| iNaturalist | 338461 |
| GBIF | 2858709 |
| Freebase | /m/012c142t |
| EOL | 1290700 |
| USDA GRIN | 429260 |
| Wikipedia | Narcissus_obesus |
| CMAUP | NPO23684 |
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.
If you wish to see all the related articles click here.
| Title | Authors | Publication | Released | IDs | ||
|---|---|---|---|---|---|---|
| Narcissus Alkaloids, XVII. Obesine, a Novel Alkaloid from Narcissus, obesus | Francesc Viladomat, Jaume Bastida, Carles Codina, Mario Rubiralta, Jean-Charles Quirion | American Chemical Society (ACS) | 17-Mar-2005 |
|
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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 | |||||
| Hemanthamine | 441593 | Click to see | 301.34 | unknown | https://doi.org/10.1021/NP50084A016 |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids | |||||
| (-)-Galantamine | 9651 | Click to see | 287.35 | unknown | https://doi.org/10.1021/NP50084A016 |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids | |||||
| Pretazettine | 73360 | Click to see | 331.40 | unknown | https://doi.org/10.1021/NP50084A016 |
| > Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines | |||||
| Propylhexedrine | 7558 | Click to see | 155.28 | unknown | https://doi.org/10.1021/NP50084A016 |
| > 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/10.1021/NP50084A016 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| 3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone | 44260067 | Click to see | 376.30 | unknown | via CMAUP database |
| 3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one | 12311234 | Click to see | 376.30 | unknown | via CMAUP database |
| 3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone | 14483219 | Click to see | 362.30 | unknown | via CMAUP database |
| Kaempferol | 5280863 | Click to see | 286.24 | unknown | via CMAUP database |
| Quercetin | 5280343 | Click to see | 302.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides | |||||
| 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one | 13871824 | Click to see | 432.40 | unknown | via CMAUP database |
| 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one | 57511421 | Click to see | 432.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides | |||||
| Orientin | 5281675 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O | 448.40 | unknown | via CMAUP database |
| Vitexin | 5280441 | Click to see | 432.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| Cacticin | 5318644 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O | 478.40 | unknown | via CMAUP database |
| Hyperoside | 5281643 | Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O | 464.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| 2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one | 5386958 | Click to see | 332.26 | unknown | via CMAUP database |
| 3-Methoxyluteolin | 5280681 | Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O | 316.26 | unknown | via CMAUP database |
| 5,7,8,4'-Tetrahydroxy-3-methoxyflavone | 5319442 | Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O | 316.26 | unknown | via CMAUP database |
| Gossypetin 3,3'-dimethyl ether | 21676153 | Click to see | 346.30 | unknown | via CMAUP database |
| Quercetagetin 3-methyl ether | 5320475 | Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O | 332.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids | |||||
| 5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone | 44259895 | Click to see | 390.30 | unknown | via CMAUP database |
| 5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone | 44258045 | Click to see | 390.30 | unknown | via CMAUP database |
| 5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone | 44258041 | Click to see | 376.30 | unknown | via CMAUP database |
| 5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone | 44259884 | Click to see | 362.30 | unknown | via CMAUP database |
| 5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone | 21676156 | Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O | 362.30 | unknown | via CMAUP database |
| 5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone | 44260054 | Click to see | 346.30 | unknown | via CMAUP database |
| 6-Hydroxykaempferol 3,6-dimethyl ether | 5352032 | Click to see | 330.29 | unknown | via CMAUP database |
| Axillarin | 5281603 | Click to see | 346.30 | unknown | via CMAUP database |
| Jaceidin | 5464461 | Click to see | 360.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| Benthamitin | 44259900 | Click to see | 432.40 | unknown | via CMAUP database |
| Casticin | 5315263 | Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O | 374.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids | |||||
| 3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone | 5748553 | Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O | 346.30 | unknown | via CMAUP database |
| 5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone | 44260077 | Click to see | 448.40 | unknown | via CMAUP database |
| 5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone | 44260086 | Click to see | 434.40 | unknown | via CMAUP database |
| 5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone | 369954 | Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O | 404.40 | unknown | via CMAUP database |
| 5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone | 54799 | Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC | 390.30 | unknown | via CMAUP database |
| 5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone | 44260074 | Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O | 420.40 | unknown | via CMAUP database |
| 5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone | 100625 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O | 404.40 | unknown | via CMAUP database |
| 5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone | 44260073 | Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O | 406.30 | unknown | via CMAUP database |
| 5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one | 5386959 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O | 390.30 | unknown | via CMAUP database |
| 5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone | 5386963 | Click to see | 434.40 | unknown | via CMAUP database |
| 5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone | 5487077 | Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC | 420.40 | unknown | via CMAUP database |
| 5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone | 21676158 | Click to see | 406.30 | unknown | via CMAUP database |
| 5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone | 44260043 | Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O | 376.30 | unknown | via CMAUP database |
| 5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone | 44258626 | Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O | 346.30 | unknown | via CMAUP database |
| 5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone | 44260085 | Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O | 406.30 | unknown | via CMAUP database |
| 5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone | 21599528 | Click to see | 390.30 | unknown | via CMAUP database |
| 5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone | 5352085 | Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC | 420.40 | unknown | via CMAUP database |
| 5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone | 5386962 | Click to see | 376.30 | unknown | via CMAUP database |
| 5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone | 44260072 | Click to see | 406.30 | unknown | via CMAUP database |
| 5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone | 11383767 | Click to see | 392.30 | unknown | via CMAUP database |
| 5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone | 44260071 | Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O | 406.30 | unknown | via CMAUP database |
| 5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone | 21676159 | Click to see | 420.40 | unknown | via CMAUP database |
| 5,7,4'-Trihydroxy-3,8-dimethoxyflavone | 13983738 | Click to see | 330.29 | unknown | via CMAUP database |
| Agecorynin D | 14162688 | Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O | 390.30 | unknown | via CMAUP database |
| Calycopterin | 10429470 | Click to see | 374.30 | unknown | via CMAUP database |
| Conyzatin | 13916282 | Click to see | 404.40 | unknown | via CMAUP database |
| Digicitrin | 10071564 | Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC | 434.40 | unknown | via CMAUP database |
| Gossypetin 3,8,3'-trimethyl ether | 5386961 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O | 360.30 | unknown | via CMAUP database |
| Hibiscetin 3,8,4'-trimethyl ether | 44260037 | Click to see | 376.30 | unknown | via CMAUP database |
| Sarothrin | 5386960 | Click to see | 360.30 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |