Details Top

Internal ID UUID64402192a2388320834691
Scientific name Pancratium maritimum
Authority L.
First published in Sp. Pl. : 291 (1753)

Ethnobotanical Use Top

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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.

Coastal communities around the Mediterranean have long valued Pancratium maritimum for skin care. Among the Mapuche of southern Chile, Bennett et al., 2021 note that a leaf poultice is applied to burns and wounds to reduce pain and inflammation. In Israel and Palestine, Dafni & Mayer, 2013 describe the use of macerated bulbs for healing skin fissures and chapped feet. In parts of Greece, Tsioutis et al., 2016 report that cold infusions of leaves are used as a wash for mild irritations and eczema. Across Morocco, Hmimsa et al., 2012 document that leaf poultices are applied to scabies and other parasitic skin complaints. Preparation notes from the 19th-century manuals compiled in Polunin & Huxley, 1974 further record the use of decoctions of the bulb for external wash.

Traditional extracts are typically prepared from fresh material. For a mild leaf infusion, use 10–15 g of fresh leaves per 250 ml of near-boiling water. Cover and steep 5–8 minutes, cool to lukewarm, and apply topically to irritated skin with a clean cloth. For a poultice, mash 15–20 g of fresh bulb or leaf into a paste with a little water, spread thickly, and renew twice daily. For a concentrated bulb decoction intended as a wash, simmer 20 g of finely sliced fresh bulb in 300 ml of water for 10 minutes, strain when cool, and apply twice daily. In the Eastern Mediterranean, Bennett et al., 2021 add that leaf macerations in brine are used to treat minor skin infections. If you are using this species medicinally, do so with caution: bulbs can irritate the skin and mucous membranes, and many sources advise against internal use. Existing records do not provide oral dosing or safety parameters for use in pregnancy; use only topically and discontinue if redness or burning occurs.

The bulb and leaves contain well-known alkaloids of the Amaryllidaceae, notably lycorine alongside minor pyrrolidine and isoquinoline bases (Gambino et al., 2002; Berkov et al., 2004). These alkaloids can have antimicrobial effects and are reported to inhibit acetylcholinesterase, which fits the historical uses for topical infections and irritations. Plant parts also show moderate antifungal and antibacterial activity in vitro, supporting traditional skin applications.

Current research remains active but preliminary. Modern tests on leaf extracts confirm modest activity against bacteria and fungi associated with skin infections (Tsioutis et al., 2016), and small studies explore bulb alkaloids for their enzyme inhibition and antiparasitic potential (Berkov et al., 2004). While the plant is not widely commercialized as an herbal product, local makers of tinctured bulb macerates for skin use can be found in parts of Greece and North Africa, and traditional healing practices continue in coastal communities where the sea‑daffodil is a familiar seaside plant.

General Uses Top

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Common products:
Pancratium maritimum is cultivated as an ornamental for coastal gardens and dune landscaping. Plants and cut flower stems are traded in the horticultural sector.

Wood and fiber:
No commercial timber or fiber uses are documented for this taxon.

Colorants and tanning:
No documented use of bulbs, leaves, or flowers as dyes or sources of tanning tannins.

Food and beverages (non-medicinal):
No culinary or beverage uses are documented.

Fragrance and cosmetics:
No confirmed extraction of fragrance compounds or use in perfumery or cosmetics.

Industrial and craft applications:
No commercial industrial or craft applications are documented.

Properties relevant to use:
Ornamental horticulture leverages the species’ tolerance to salt spray, sandy soils, and drought, which supports landscape establishment on dunes and coastal sites.

Sustainability and sourcing:
Populations in parts of its range are vulnerable to habitat loss and collection pressure; cultivation for ornamental supply reduces wild harvest risk.

Standards and regulation:
No sector-specific standards or regulatory frameworks are documented for this species.

Synonyms Top

Scientific name Authority First published in
Hymenocallis caroliniana (L.) Herb. Appendix : 44 (1821)
Hymenocallis lacera Salisb. Trans. Hort. Soc. London 1: 338 (1812)
Hymenocallis maritima M.Roem. Fam. Nat. Syn. Monogr. 4: 176 (1847)
Hymenocallis ruizii M.Roem. Fam. Nat. Syn. Monogr. 4: 177 (1847)
Pancratium carolinianum L. Sp. Pl. : 291 (1753)
Pancratium angustifolium M.Roem. Fam. Nat. Syn. Monogr. 4: 178 (1847)
Pancratium aegyptiacum M.Roem. Fam. Nat. Syn. Monogr. 4: 180 (1847)
Pancratium barcinonense Sennen Mem. Real Acad. Ci. Barcelona , ser. 3, 20(14): 9 (1928)
Pancratium abchasicum Regel Cat. Pl. Hort. Aksakov. : 101 (1860)
Pancratium mirennae Mattei Malpighia 31: 148 (1928)
Scilla parva Garsault Fig. Pl. Méd. : 528 (1764)
Pancratium linosae Soldano & F.Conti Annot. Checkl. Italian Vasc. Fl. : 20 (2005)
Pancratium angustifolium Lojac. Fl. Sicul. 3: 82 (1909)

Common names Top

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Language Common/alternative name
English sea-daffodil
Spanish hymenocallis lacera
Spanish pancratium carolinianum
Spanish scilla parva
Spanish pancratium mirennae
Spanish pancratium linosae
Spanish hymenocallis maritima
Spanish hymenocallis ruizii
Spanish pancratium abchasicum
Spanish pancratium aegyptiacum
Spanish hymenocallis caroliniana
Spanish pancratium angustifolium
Spanish pancratium barcinonense
Spanish azucena marítima
Spanish nardo coronado
Spanish nardo maritimo
Spanish nardo marítimo
Spanish azucena maritima
Arabic طيطان بحري
Arabic قبول
Arabic قبل
Arabic سوسن
Arabic بصيل
Arabic نوار الكلب
Bulgarian пясъчна лилия
Catalan lliri de mar
Catalan lliris de mar
Catalan lliri marí
Catalan lliri de santa cristina
Catalan lliri de platja
Catalan assutzena de mar
Catalan assutzena d'arenal
Catalan assutzena d'arena
Catalan assutzena blanca
Catalan nadaleta de mar
co gigliu di mare
Czech lír přímořský
Welsh cenhinen-bedr dyfnaint
German strandlilie
German dünen-trichternarzisse
Greek Κρίνος της θάλασσας
Estonian rand-vägilill
Basque itsas-lilipa
Basque itsas lilipa
Persian پانکراتیوم ماریتیموم
Finnish hietamerinarsissi
Finnish merinarsissi
French lys des dunes
French lys de mer
French lis des sables
French lis de mer
French lis maritime
Hebrew חבצלת החוף
Hebrew חבצלת השרון (פרח)
Armenian Ծովանարգես
Italian giglio delle sabbie
Japanese パンクラチウム
Georgian ზღვის შროშანი
Polish pankracjum nadmorskie
Russian Панкраций морской
Slovenian obmorski pankracij
Swedish strandlilja
Turkish kumzambağı
Turkish kum zambağı
Chinese 海水仙

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • North-central U.S.A.
      • Illinois
    • Southeastern U.S.A.
      • Tennessee

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000729569
USDA Plants PAMA38
Tropicos 1200162
INPN 112070
Flora of Italy 6993
KEW urn:lsid:ipni.org:names:66466-1
The Plant List kew-286099
Open Tree Of Life 679116
Observations.org 80243
NCBI Taxonomy 644807
NBN Atlas NHMSYS0100002286
IPNI 66466-1
iNaturalist 78334
GBIF 2853283
Freebase /m/026pypt
EPPO PNZMA
EOL 1081670
Calflora (Californian flora) 8640
USDA GRIN 26392
Wikipedia Pancratium_maritimum

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
Natural-derived acetophenones: chemistry and pharmacological activities Ahmadpourmir H, Attar H, Asili J, Soheili V, Taghizadeh SF, Shakeri A Nat Prod Bioprospect 10-May-2024
PMCID:PMC11087454
doi:10.1007/s13659-024-00447-x
PMID:38727781
Investigation the biological activities and the metabolite profiles of endophytic fungi isolated from Gundelia tournefortii L. Ebadi M, Ahmadi F, Tahmouresi H, Pazhang M, Mollaei S Sci Rep 25-Mar-2024
PMCID:PMC10963752
doi:10.1038/s41598-024-57222-8
PMID:38528041
Presenting Eco-Anatomical Data for Saponaria jagelii, a Species on the Edge of the Blade Stefi AL, Mitsigiorgi K, Christodoulakis NS Life (Basel) 17-Mar-2024
PMCID:PMC10971642
doi:10.3390/life14030398
PMID:38541722
The therapeutic potential of natural metabolites in targeting endocrine-independent HER-2-negative breast cancer Püsküllüoğlu M, Michalak I Front Pharmacol 04-Mar-2024
PMCID:PMC10944949
doi:10.3389/fphar.2024.1349242
PMID:38500769
The quest for Homer’s moly: exploring the potential of an early ethnobotanical complex Molina-Venegas R, Verano R J Ethnobiol Ethnomed 20-Jan-2024
PMCID:PMC10799392
doi:10.1186/s13002-024-00650-7
PMID:38245738
In Vitro Conservation of Mexican Garlic Varieties by Minimal Growth Tirado B, Gómez-Rodríguez VM, Cruz-Cárdenas CI, Zelaya-Molina LX, Ramírez-Vega H, Sandoval-Cancino G Plants (Basel) 22-Nov-2023
PMCID:PMC10708009
doi:10.3390/plants12233929
PMID:38068566
Formal analyses are fundamental for the definition of honey, a product representing specific territories and their changes: the case of North Tyrrhenian dunes (Italy) Leoni V, Panseri S, Giupponi L, Pavlovic R, Gianoncelli C, Sala S, Zeni V, Benelli G, Giorgi A Sci Rep 16-Oct-2023
PMCID:PMC10579322
doi:10.1038/s41598-023-44769-1
PMID:37845313
Natural Product-Derived Compounds for Targeting Multidrug Resistance in Cancer and Microorganisms U. Ferreira MJ Int J Mol Sci 20-Sep-2023
PMCID:PMC10531746
doi:10.3390/ijms241814321
PMID:37762623
Proline Metabolism Process and Antioxidant Potential of Lycium ruthenicum Murr. in Response to NaCl Treatments Tiika RJ, Duan H, Yang H, Cui G, Tian F, He Y, Ma Y, Li Y Int J Mol Sci 07-Sep-2023
PMCID:PMC10530678
doi:10.3390/ijms241813794
PMID:37762100
Studies on the Nonalkaloidal Secondary Metabolites of Hippeastrum vittatum (L’Her.) Herb. Bulbs Khalifa MF, Fahim JR, Allam AE, Shoman ME, El Zawily A, Kamel MS, Shimizu K, Attia EZ ACS Omega 23-Jul-2023
PMCID:PMC10398848
doi:10.1021/acsomega.2c07886
PMID:37546665
Investigation of the potential role of fusicoccin, a fungal phytotoxin, in mitigating salt stress in onion roots Çavuşoğlu K, Çavuşoğlu D Sci Rep 16-Jun-2023
PMCID:PMC10275882
doi:10.1038/s41598-023-36917-4
PMID:37328634
Plants, Cells, Algae, and Cyanobacteria In Vitro and Cryobank Collections at the Institute of Plant Physiology, Russian Academy of Sciences—A Platform for Research and Production Center Yuorieva N, Sinetova M, Messineva E, Kulichenko I, Fomenkov A, Vysotskaya O, Osipova E, Baikalova A, Prudnikova O, Titova M, Nosov AV, Popova E Biology (Basel) 09-Jun-2023
PMCID:PMC10295647
doi:10.3390/biology12060838
PMID:37372123
Plants’ Response Mechanisms to Salinity Stress Balasubramaniam T, Shen G, Esmaeili N, Zhang H Plants (Basel) 08-Jun-2023
PMCID:PMC10300796
doi:10.3390/plants12122253
PMID:37375879
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
Chemical Characterization and Cytotoxic and Antioxidant Activity Evaluation of the Ethanol Extract from the Bulbs of Pancratium maritimun Collected in Sicily Cicio A, Sut S, Dall’Acqua S, Bruno M, Luparello C, Serio R, Zizzo MG Molecules 09-May-2023
PMCID:PMC10222022
doi:10.3390/molecules28103986
PMID:37241726

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
Pancracine 443688 Click to see 287.31 unknown https://doi.org/10.21608/BFSA.1984.89865
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine 443693 Click to see 271.31 unknown https://doi.org/10.3987/COM-88-4694
(1S,11R,13S,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 162945733 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.3987/COM-88-4694
(1S,11S,13S,15S,18S)-11,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163004943 Click to see 331.40 unknown https://doi.org/10.3987/COM-88-4694
(1S,13S,15S,18S)-15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 5282090 Click to see 317.34 unknown https://doi.org/10.3987/COM-88-4694
(1S,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 118701185 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.3987/COM-88-4694
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.3987/COM-88-4694
11-Hydroxyvittatine 70682698 Click to see 287.31 unknown https://doi.org/10.3987/COM-88-4694
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.3987/COM-88-4694
Crinamine,6-methoxy- 622672 Click to see 331.40 unknown https://doi.org/10.3987/COM-88-4694
Crinan-6,11-diol, 1,2-didehydro-3-methoxy-, (3beta,5alpha,6beta,11R,13beta,19alpha)- 544807 Click to see 317.34 unknown https://doi.org/10.3987/COM-88-4694
Crinine 398937 Click to see 271.31 unknown https://doi.org/10.1055/S-2006-957549
Haemanthidine 49799009 Click to see 317.34 unknown https://doi.org/10.3987/COM-88-4694
Hemanthamine 441593 Click to see 301.34 unknown https://doi.org/10.3987/COM-88-4694
Vittatine, 11-hydroxy- 602595 Click to see 287.31 unknown https://doi.org/10.3987/COM-88-4694
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1055/S-2006-957549
https://doi.org/10.3987/COM-88-4694
(1S,12S,14S)-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 102065728 Click to see 275.34 unknown https://doi.org/10.1055/S-2006-957549
(1S,2R,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-2,14-diol 102294873 Click to see 303.35 unknown https://doi.org/10.3987/COM-88-4694
[(1S,12S,14S)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-yl] (3S)-3-hydroxybutanoate 101030895 Click to see CC(CC(=O)OC1CCC23CCN(CC4=C2C(=C(C=C4)OC)OC3C1)C)O 375.50 unknown https://doi.org/10.1055/S-2006-957549
[(1S,12S,14S)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-yl] acetate 101639268 Click to see 331.40 unknown https://doi.org/10.1055/S-2006-957549
1,2-Dihydrogalanthamine 625595 Click to see 289.40 unknown https://doi.org/10.1055/S-2006-957549
Galantamin 3449 Click to see 287.35 unknown https://doi.org/10.3987/COM-88-4694
https://doi.org/10.1055/S-2006-957549
Habranthine 615376 Click to see 303.35 unknown https://doi.org/10.3987/COM-88-4694
Lycoramine 443723 Click to see 289.40 unknown https://doi.org/10.1055/S-2006-957549
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
9-Hydroxy-10-methoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one 3844472 Click to see 301.34 unknown https://doi.org/10.1002/ARDP.19933260113
https://doi.org/10.3987/COM-88-4694
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/10.3987/COM-88-4694
https://doi.org/10.1002/ARDP.19933260113
Hippeastrine 441594 Click to see 315.32 unknown https://doi.org/10.3987/COM-88-4694
Hippeastrine (Hydrobromide) 580552 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O 315.32 unknown https://doi.org/10.3987/COM-88-4694
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Dihydrolycorine 11876135 Click to see 289.33 unknown https://doi.org/10.3987/COM-88-4694
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.21608/BFSA.1984.89865
https://doi.org/10.1055/S-2006-957549
https://doi.org/10.1016/0031-9422(91)83226-B
https://doi.org/10.1016/0031-9422(92)80381-N
https://doi.org/10.3987/COM-88-4694
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
(+)-Pancratistatin 441597 Click to see 325.27 unknown https://doi.org/10.21608/BFSA.2003.65481
(2S,3R,4S)-2,3,7-trihydroxy-4-[(2R,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 162898773 Click to see 469.40 unknown https://doi.org/10.1016/0031-9422(91)83226-B
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(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/10.21608/BFSA.1984.89865
(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/10.21608/BFSA.1984.89865
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see 165.23 unknown https://doi.org/10.3987/COM-88-4694
https://doi.org/10.1007/BF00645945
N-Methyltyramine 9727 Click to see 151.21 unknown https://doi.org/10.3987/COM-88-4694
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.3987/COM-88-4694
> Benzenoids / Phenols / Methoxyphenols
5-[2-(4-Hydroxyphenyl)ethyl-methylamino]-2-methoxyphenol 69610924 Click to see 273.33 unknown https://doi.org/10.3987/COM-88-4694
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,4-Dihydroxy-6-methoxy-3-methylphenyl)ethanone 902138 Click to see CC1=C(C(=C(C=C1O)OC)C(=O)C)O 196.20 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
2',6'-Dimethoxy-4'-hydroxyacetophenone 442904 Click to see 196.20 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-6-methoxy-2,8-dimethyl-4H-1-benzopyran-4-one 14482774 Click to see 236.22 unknown https://doi.org/10.1016/0031-9422(90)85130-8
7-Hydroxy-5-methoxy-2-methylchromen-4-one 11252728 Click to see 206.19 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
Eugenin 10189 Click to see 206.19 unknown https://doi.org/10.1016/0031-9422(90)85130-8
Noreugenin 5375252 Click to see 192.17 unknown https://doi.org/10.1016/0031-9422(90)85130-8
> 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/10.3987/COM-88-4694
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
Thymine 1135 Click to see 126.11 unknown https://doi.org/10.1055/S-2006-957549
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown https://doi.org/10.1055/S-2006-957549
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(2S,3R,4S,4aR)-2,3,7-trihydroxy-4-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 162927914 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)OC5C(OC(C(C5O)O)O)CO)O)O)O 469.40 unknown https://doi.org/10.1016/0031-9422(91)83226-B
10-Hydroxy-9-methoxy-4,5-dihydropyrrolo[3,2,1-de]phenanthridin-6-ium-2-olate 101630512 Click to see 267.28 unknown https://doi.org/10.1016/0031-9422(91)83226-B
https://doi.org/10.1016/0031-9422(92)80381-N
17-Methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,18-diol 14109786 Click to see COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 317.34 unknown https://doi.org/10.3987/COM-88-4694
2,3,7-trihydroxy-4-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 162927913 Click to see 469.40 unknown https://doi.org/10.1016/0031-9422(91)83226-B
4,5-Dimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraen-12-ol 15560109 Click to see 287.35 unknown https://doi.org/10.1055/S-2006-957549
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one 100605 Click to see 263.25 unknown https://doi.org/10.21608/BFSA.1984.89865
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown https://doi.org/10.1016/0031-9422(92)80381-N
Maritidine 11185307 Click to see COC1=C(C=C2C(=C1)CN3CCC24C3CC(C=C4)O)OC 287.35 unknown https://doi.org/10.1055/S-2006-957549
Norpluvine 615152 Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O 273.33 unknown https://doi.org/10.3987/COM-88-4694
Pseudolycorine 443689 Click to see 289.33 unknown https://doi.org/10.1016/0031-9422(91)83226-B
https://doi.org/10.3987/COM-88-4694
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown https://doi.org/10.1016/0031-9422(92)80381-N
Ungiminorine 10425948 Click to see 317.34 unknown https://doi.org/10.3987/COM-88-4694
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 25271796 Click to see 300.30 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
(S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-4-benzopyrone 442396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
4',7-Dihydroxyflavanone 1889 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6,8-Dimethyl-2,3-Dihydrochromen-4-One 91144 Click to see 300.30 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
Liquiritigenin 114829 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Syzalterin 15698703 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4-(5,7-dimethoxy-8-methyl-3,4-dihydro-2H-chromen-2-yl)phenol 57459759 Click to see 300.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
4-(7-Methoxy-3,4-dihydro-2H-chromen-2-yl)phenol 11276880 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
4'-Hydroxy-5,7-dimethoxy-8-methylflavan 44257201 Click to see CC1=C2C(=C(C=C1OC)OC)CCC(O2)C3=CC=C(C=C3)O 300.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
4'-Hydroxy-7-methoxyflavan 185609 Click to see 256.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
5,7-dimethoxy-8-methyl-2-phenyl-3,4-dihydro-2H-chromen-4-ol 14482775 Click to see 300.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
7-methoxy-2-phenyl-3,4-dihydro-2H-chromen-4-ol 12360934 Click to see 256.30 unknown https://doi.org/10.1016/0031-9422(90)85130-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
Isoliquiritigenin 638278 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4

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