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Pancratium maritimum

Pancratium maritimum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pancratium maritimum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pancratium maritimum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pancratium maritimum - 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 UUID64402192a2388320834691
Scientific name Pancratium maritimum
Authority L.
First published in Sp. Pl. : 291 (1753)

Description Top

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Pancratium maritimum, also known as sea daffodil, is a bulbous plant found in the Canary Islands, Mediterranean region, and Black Sea. It is also naturalized in other areas such as southern California and Bermuda. This plant grows on beaches and coastal sand dunes, with its leaves and scapes often buried in the sand. Its flowers have a subtle lily scent and bloom from August to October. The plant is pollinated by a hawk-moth and is not receptive to its own pollen. It is easily grown but requires a sunny position and well-drained soil. In some cultures, it is associated with biblical references. This plant has been extensively studied and documented by botanists and is found in various regions across the world.

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)

Common names Top

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Language Common/alternative name
English sea-daffodil
Spanish nardo maritimo
Spanish nardo coronado
Spanish azucena marítima
Spanish azucena maritima
Spanish nardo marítimo
Arabic نوار الكلب
Arabic طيطان بحري
Arabic قبول
Arabic قبل
Arabic بصيل
Arabic سوسن
Bulgarian пясъчна лилия
Catalan assutzena d'arena
Catalan assutzena blanca
Catalan assutzena d'arenal
Catalan assutzena de mar
Catalan lliri de platja
Catalan lliri de santa cristina
Catalan lliri marí
Catalan lliris de mar
Catalan nadaleta de mar
Catalan lliri de mar
co gigliu di mare
Czech lír přímořský
Welsh cenhinen-bedr dyfnaint
German dünen-trichternarzisse
German strandlilie
Greek Κρίνος της θάλασσας
Estonian rand-vägilill
Basque itsas-lilipa
Basque itsas lilipa
Persian پانکراتیوم ماریتیموم
Finnish hietamerinarsissi
Finnish merinarsissi
French lis maritime
French lis des sables
French lys de mer
French lis de mer
French lys des dunes
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 kum zambağı
Turkish kumzambağı
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

Suggest others/fix!
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 C1C(C(C=C2C1N3CC2C4=CC5=C(C=C4C3)OCO5)O)O 287.31 unknown https://doi.org/10.21608/BFSA.1984.89865
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(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,11R,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 49799009 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 COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)OC)O 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 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,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 C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 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 COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.3987/COM-88-4694
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1055/S-2006-957549
Haemanthamine 441593 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
Haemanthidine 544807 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
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.3987/COM-88-4694
Vittatine, 11-hydroxy- 602595 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.3987/COM-88-4694
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(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 COC1=C2C3=C(CNCCC34CCC(CC4O2)O)C=C1 275.34 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] (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 CC(=O)OC1CCC23CCN(CC4=C2C(=C(C=C4)OC)OC3C1)C 331.40 unknown https://doi.org/10.1055/S-2006-957549
1,2-Dihydrogalanthamine 625595 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 289.40 unknown https://doi.org/10.1055/S-2006-957549
11alpha-Hydroxygalanthamine 102294873 Click to see CN1CC(C23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O)O 303.35 unknown https://doi.org/10.3987/COM-88-4694
Epigalanthamin 3449 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1055/S-2006-957549
https://doi.org/10.3987/COM-88-4694
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.3987/COM-88-4694
https://doi.org/10.1055/S-2006-957549
Habranthine 615376 Click to see CN1CC(C23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O)O 303.35 unknown https://doi.org/10.3987/COM-88-4694
Lycoramine 443723 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 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 CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC 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 CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O 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 C1CN2CC3=CC4=C(C=C3C5C2C1CC(C5O)O)OCO4 289.33 unknown https://doi.org/10.3987/COM-88-4694
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/0031-9422(91)83226-B
https://doi.org/10.3987/COM-88-4694
https://doi.org/10.1016/0031-9422(92)80381-N
https://doi.org/10.21608/BFSA.1984.89865
https://doi.org/10.1055/S-2006-957549
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
(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 C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 469.40 unknown https://doi.org/10.1016/0031-9422(91)83226-B
Pancratistatin 441597 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.21608/BFSA.2003.65481
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(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 CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.21608/BFSA.1984.89865
Sekisanin 443682 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.21608/BFSA.1984.89865
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown https://doi.org/10.3987/COM-88-4694
https://doi.org/10.1007/BF00645945
N-Methyltyramine 9727 Click to see CNCCC1=CC=C(C=C1)O 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 CN(CCC1=CC=C(C=C1)O)C2=CC(=C(C=C2)OC)O 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 CC(=O)C1=C(C=C(C=C1OC)O)OC 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 CC1=CC(=O)C2=C(O1)C(=C(C(=C2O)OC)O)C 236.22 unknown https://doi.org/10.1016/0031-9422(90)85130-8
7-Hydroxy-5-methoxy-2-methyl-4H-1-benzopyran-4-one 11252728 Click to see CC1=CC(=O)C2=C(O1)C=C(C=C2OC)O 206.19 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
Eugenin 10189 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC)O 206.19 unknown https://doi.org/10.1016/0031-9422(90)85130-8
Noreugenin 5375252 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)O 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 CC1=CNC(=O)NC1=O 126.11 unknown https://doi.org/10.1055/S-2006-957549
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 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 COC1=CC2=CN3CCC4=C3C(=CC(=C4)O)C2=CC1=O 267.28 unknown https://doi.org/10.1016/0031-9422(92)80381-N
https://doi.org/10.1016/0031-9422(91)83226-B
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 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
4,5-Dimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraen-12-ol 15560109 Click to see COC1=C(C=C2C(=C1)CN3CCC24C3CC(C=C4)O)OC 287.35 unknown https://doi.org/10.1055/S-2006-957549
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
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown https://doi.org/10.21608/BFSA.1984.89865
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 COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O 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 COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 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 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
(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
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethylchroman-4-one 91144 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
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Syzalterin 15698703 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C)O 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 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-(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 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
5,7-dimethoxy-8-methyl-2-phenyl-3,4-dihydro-2H-chromen-4-ol 14482775 Click to see CC1=C2C(=C(C=C1OC)OC)C(CC(O2)C3=CC=CC=C3)O 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 COC1=CC2=C(C=C1)C(CC(O2)C3=CC=CC=C3)O 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
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00429-4

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