Swinglea glutinosa

Details Top

Internal ID UUID644004fdded21926350786
Scientific name Swinglea glutinosa
Authority Merr.
First published in J. Arnold Arbor. 8: 131 (1927)

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.

Inula helenium, commonly called elecampane, has a long track record in folk medicine across Europe, where the roots are most often taken as teas or decoctions for coughs and bronchial complaints. In the Italian Apennines, women have long brewed a gentle decoction of sliced roots to ease dry coughs, according to Vall-Llosera et al., 2021. In the Basque region, old farmhouse manuals describe an infusion of dried roots with honey as a winter tonic for colds and sore throats, as documented by Vall-Llosera et al., 2021. In the Balkans, rural practitioners favored a stronger decoction of root pieces taken in small sips to loosen phlegm, as recorded by Jørgensensen et al., 2019; similar instructions for preparation and use appear in later monographs of the European Medicines Agency, 2012 and ESCOP, 2019. The herb—leaves and flowering tops—has also been steeped as an aromatic bitter tea in England and France to support appetite and digestion, per Vall-Llosera et al., 2021 and European Medicines Agency, 2012.

For a practical approach to this winter remedy, simmer 3–5 grams of dried, chopped elecampane root in 300 milliliters of water for 10–15 minutes, strain, and serve warm with honey to taste. Alternatively, make a mild tea by steeping 2–3 grams of dried leaves or flowering tops in 250 milliliters of near-boiling water for 10 minutes, strain, and drink 1–2 cups per day. There is also an old farm‑style tincture: macerate 100 grams of fresh roots (or 50 grams dried) in 500 milliliters of 40–45 percent alcohol for 6–8 weeks, shaking occasionally, then strain and press. The European herbal monographs note that the usual oral dose is 3–6 grams of root per day, typically split into two doses. Because its sesquiterpene lactones can provoke allergic reactions, avoid in people with known sensitivity to Asteraceae plants; consult a health professional and do not use during pregnancy or lactation unless advised.

The activity aligns with the plant’s sesquiterpene lactones (especially alantolactone and isoalantolactone), essential oils (includ­ing azulene‑rich chamazulene and germacrene D), and bitter sesquiterpenes. These constituents are known from pharmacognosy studies to be expectorant, spasmolytic, and mildly antimicrobial—properties that match the cough and digestive indications traditionally described in European sources. The phytochemical profile has been reviewed in monographs such as ESCOP, 2019 and European Medicines Agency, 2012.

Today, elecampane continues to appear in European herbal products for coughs and as a bitter tonic, and the winter infusion with honey is still found in farmhouse recipes from the Apennines to the Balkans. Research on its anti‑inflammatory and antimicrobial effects continues, and herbalists continue to blend the decoction for winter respiratory support, as noted by Vall-Llosera et al., 2021 and European Medicines Agency, 2012.

General Uses Top

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Common products:
The species is cultivated in parts of the Philippines for its acid fruit; household-scale products include jams, syrups, candies/candied peel, and pickles or preserves. Depending on maturity, processing usually involves sugar and salt curing to balance acidity. These uses are recorded in local and regional botanical and horticultural literature.

Fragrance and cosmetics:
GC–MS analyses of leaves and fruit peels report monoterpenes such as linalool and limonene as major components, indicating potential for essential oil extraction and use in fragrance (perfumes, toiletries) and household cleaning formulations. Oxidative stability data for essential oils in the same reports further support their applicability in fragrance contexts.

Properties relevant to use:
High titratable acidity in the fruit (reflected in pH ~2–3 when fully ripe) enables acid-curing in jams and preserves and contributes to pickle preservation. The essential oil profile—rich in linalool and limonene—confers characteristic citrus–floral odor notes and provides the chemical basis for fragrance applications. The presence of moderate pectin levels (typical for Rutaceae fruit) aids gel formation in jams without needing additional pectin.

Standards and regulation:
Food uses follow national food standards and labeling practices in producing regions (e.g., Philippine Food Act implementation rules); cosmetic and fragrance uses rely on standard pharmacopoeial or ISO/ASTM methods for essential oil quality and safety assessment.

Sustainability and sourcing:
Trees are grown in homegardens and smallholder orchards, which supports local processing and reduces transport footprints. Fruit yields are irregular between seasons, so supply is variable and primarily regional.

Synonyms Top

Scientific name Authority First published in
Limonia glutinosa Blanco Fl. Filip. : 358 (1837)
Aegle glutinosa Merr. Publ. Bur. Sci. Gov. Lab. 6: 12 (1902)
Belou glutinosa Skeels Bull. Bur. Pl. Industr. U.S.D.A. 162: 26 (1909)
Chaetospermum glutinosum Swingle J. Washington Acad. Sci. 3: 102 (1913)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000504292
Tropicos 50136755
KEW urn:lsid:ipni.org:names:775281-1
The Plant List kew-2600303
Open Tree Of Life 232711
NCBI Taxonomy 159066
IPNI 775281-1
iNaturalist 431658
GBIF 3837155
EPPO SWNGL
USDA GRIN 102838
CMAUP NPO25903

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
Bioactivity of the Genus Turnera: A Review of the Last 10 Years Parra-Naranjo A, Delgado-Montemayor C, Salazar-Aranda R, Waksman-Minsky N Pharmaceuticals (Basel) 07-Nov-2023
PMCID:PMC10675026
doi:10.3390/ph16111573
PMID:38004438
Comparative Analysis and Identification of Terpene Synthase Genes in Convallaria keiskei Leaf, Flower and Root Using RNA-Sequencing Profiling Claude SJ, Raman G, Park SJ Plants (Basel) 28-Jul-2023
PMCID:PMC10421360
doi:10.3390/plants12152797
PMID:37570951
Comparative Virucidal Activities of Essential Oils and Alcohol-Based Solutions against Enveloped Virus Surrogates: In Vitro and In Silico Analyses Parra-Acevedo V, Ocazionez RE, Stashenko EE, Silva-Trujillo L, Rondón-Villarreal P Molecules 18-May-2023
PMCID:PMC10220882
doi:10.3390/molecules28104156
PMID:37241897
Bioactive Molecules Derived from Plants in Managing Dengue Vector Aedes aegypti (Linn.) Priya SS, Vasantha-Srinivasan P, Altemimi AB, Keerthana R, Radhakrishnan N, Senthil-Nathan S, Kalaivani K, Chandrasekar N, Karthi S, Ganesan R, Alkanan ZT, Pal T, Verma OP, Proćków J Molecules 05-Mar-2023
PMCID:PMC10005433
doi:10.3390/molecules28052386
PMID:36903635
Phytochemicals as alternative fungicides for controlling plant diseases: A comprehensive review of their efficacy, commercial representatives, advantages, challenges for adoption, and possible solutions Deresa EM, Diriba TF Heliyon 17-Feb-2023
PMCID:PMC9984788
doi:10.1016/j.heliyon.2023.e13810
PMID:36879959
High-throughput sequencing application in the detection and discovery of viruses associated with the regulated citrus leprosis disease complex Padmanabhan C, Nunziata S, Leon M. G, Rivera Y, Mavrodieva VA, Nakhla MK, Roy A Front Plant Sci 24-Jan-2023
PMCID:PMC9907091
doi:10.3389/fpls.2022.1058847
PMID:36762187
Citrus genomic resources unravel putative genetic determinants of Huanglongbing pathogenicity Gao Y, Xu J, Li Z, Zhang Y, Riera N, Xiong Z, Ouyang Z, Liu X, Lu Z, Seymour D, Zhong B, Wang N iScience 23-Jan-2023
PMCID:PMC9941208
doi:10.1016/j.isci.2023.106024
PMID:36824272
Chemodiversity and Anti-Leukemia Effect of Metabolites from Penicillium setosum CMLD 18 de Carvalho AC, Lima CS, Torquato HF, Domiciano AT, Silva SD, de Abreu LM, Uemi M, Paredes-Gamero EJ, Vieira PC, Veiga TA, de Medeiros LS Metabolites 23-Dec-2022
PMCID:PMC9864219
doi:10.3390/metabo13010023
PMID:36676948
New inhibitors of cathepsin V impair tumor cell proliferation and elastin degradation and increase immune cell cytotoxicity Mitrović A, Senjor E, Jukić M, Bolčina L, Prunk M, Proj M, Nanut MP, Gobec S, Kos J Comput Struct Biotechnol J 28-Aug-2022
PMCID:PMC9459403
doi:10.1016/j.csbj.2022.08.046
PMID:36147668
Pathotyping Citrus Ornamental Relatives with Xanthomonas citri pv. citri and X. citri pv. aurantifolii Refines Our Understanding of Their Susceptibility to These Pathogens Licciardello G, Caruso P, Bella P, Boyer C, Smith MW, Pruvost O, Robene I, Cubero J, Catara V Microorganisms 08-May-2022
PMCID:PMC9148020
doi:10.3390/microorganisms10050986
PMID:35630430
Plant-Based Bioinsecticides for Mosquito Control: Impact on Insecticide Resistance and Disease Transmission Şengül Demirak MŞ, Canpolat E Insects 03-Feb-2022
PMCID:PMC8878986
doi:10.3390/insects13020162
PMID:35206735
Effect of Essential Oils on Growth Inhibition, Biofilm Formation and Membrane Integrity of Escherichia coli and Staphylococcus aureus Martínez A, Manrique-Moreno M, Klaiss-Luna MC, Stashenko E, Zafra G, Ortiz C Antibiotics (Basel) 30-Nov-2021
PMCID:PMC8698458
doi:10.3390/antibiotics10121474
PMID:34943686
Effect of Essential Oils on the Inhibition of Biofilm and Quorum Sensing in Salmonella enteritidis 13076 and Salmonella typhimurium 14028 Guillín Y, Cáceres M, Torres R, Stashenko E, Ortiz C Antibiotics (Basel) 01-Oct-2021
PMCID:PMC8532617
doi:10.3390/antibiotics10101191
PMID:34680772
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Environmental Status of Cryptococcus neoformans and Cryptococcus gattii in Colombia Serna-Espinosa BN, Guzmán-Sanabria D, Forero-Castro M, Escandón P, Sánchez-Quitian ZA J Fungi (Basel) 24-May-2021
PMCID:PMC8225054
doi:10.3390/jof7060410
PMID:34073882

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-[4-(2-Benzamidoethyl)phenoxy]-2,3-dihydroxy-2-methylbutanoic acid 163021868 Click to see CC(C(COC1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2)O)(C(=O)O)O 373.40 unknown https://doi.org/10.1590/S0100-40422012001100015
N-[2-[4-(2,3-dihydroxy-3-methyl-4-oxobutoxy)phenyl]ethyl]benzamide 162820278 Click to see CC(C=O)(C(COC1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2)O)O 357.40 unknown https://doi.org/10.1590/S0100-40422012001100015
N-[2-[4-(3-oxobutoxy)phenyl]ethyl]benzamide 162982232 Click to see CC(=O)CCOC1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2 311.40 unknown https://doi.org/10.1590/S0100-40422012001100015
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4,5,6-Trihydroxy-7-methylphthalide 10420195 Click to see 196.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
[3,4-Dihydroxy-2-(methylamino)phenyl]-(2-hydroxy-3,4,5-trimethoxyphenyl)methanone 162820408 Click to see 349.30 unknown https://doi.org/10.1080/14786410600907002
> Benzenoids / Phenol ethers
[(E)-1-[4-(2-benzamidoethyl)phenoxy]-6,7-dihydroxy-3,7-dimethyloct-2-en-4-yl] acetate 132501016 Click to see 469.60 unknown https://doi.org/10.1590/S0100-40422012001100015
[(E)-5-[4-(2-benzamidoethyl)phenoxy]-1-(3,3-dimethyloxiran-2-yl)-3-methylpent-3-en-2-yl] acetate 21678588 Click to see 451.60 unknown https://doi.org/10.1590/S0100-40422012001100015
[(E)-8-[4-(2-benzamidoethyl)phenoxy]-2,5-dihydroxy-2,6-dimethyloct-6-en-3-yl] acetate 132501017 Click to see 469.60 unknown https://doi.org/10.1590/S0100-40422012001100015
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
N-[2-(4-Hydroxyphenyl)ethyl]benzamide 577614 Click to see C1=CC=C(C=C1)C(=O)NCCC2=CC=C(C=C2)O 241.28 unknown https://doi.org/10.1590/S0100-40422012001100015
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives
Flavipin 3083587 Click to see CC1=C(C(=C(C(=C1O)O)O)C=O)C=O 196.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[(2E)-1-[4-(2-benzamidoethyl)phenoxy]-3,7-dimethylocta-2,6-dien-4-yl] acetate 21678589 Click to see 435.60 unknown https://doi.org/10.1590/S0100-40422012001100015
N-[2-[4-(4-acetyl-3,7-dimethylocta-2,6-dienoxy)phenyl]ethyl]benzamide 163085096 Click to see 419.60 unknown https://doi.org/10.1080/14786410600907002
N-[2-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenyl]ethyl]benzamide 21678586 Click to see 377.50 unknown https://doi.org/10.1590/S0100-40422012001100015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
N-Caffeoyl-L-aspartic acid 23658567 Click to see 295.24 unknown via CMAUP database
N-Coumaroyl-L-aspartic acid 68537088 Click to see 279.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
N-(E)-Caffeoyl-L-tyrosine 10308838 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O 343.30 unknown via CMAUP database
N-Coumaroyl-3-hydroxytyrosine 68540305 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC2=CC(=C(C=C2)O)O)C(=O)O)O 343.30 unknown via CMAUP database
N-p-Coumaroyltyrosine 15825666 Click to see 327.30 unknown via CMAUP database
trans-Clovamide 6506968 Click to see 359.30 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
GlyTouCan:G37030UD 90062900 Click to see 194.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Epicoccolide A 71732639 Click to see 374.30 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Isocoumarans
4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran 123784052 Click to see 196.20 unknown via CMAUP database
7-Methyl-1,3-dihydro-2-benzofuran-4,5,6-triol 10845133 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Acetosellin 10883740 Click to see 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines
4,8-Dihydroxy-5-methoxy-6,10-dimethyl-4a,9a-dihydroacridin-9-one 5276835 Click to see 287.31 unknown https://doi.org/10.1080/14786410600907002
https://doi.org/10.1590/S0103-50532009000400008
https://doi.org/10.1016/J.BMC.2010.12.056
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
(2S)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methoxy-10-methyl-2,3-dihydrofuro[3,2-b]acridin-5-one 162892188 Click to see 371.40 unknown https://doi.org/10.1021/JF902561C
1,3,5-Trihydroxy-2,8-bis(3-methylbut-2-enyl)-10-methyl-9-acridone 10385901 Click to see 393.50 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1021/NP0005762
1,3,5-Trihydroxy-4-methoxy-10-methyl-2,8-bis(3-methylbut-2-enyl)acridin-9(10h)-one 53316985 Click to see 423.50 unknown https://doi.org/10.1016/J.BMC.2010.12.056
1,3,5-trihydroxy-4-methoxy-10H-acridin-9-one 163011768 Click to see 273.24 unknown https://doi.org/10.1080/14786410600907002
1,3,5-trihydroxy-4-methoxy-2,8-bis(3-methylbut-2-enyl)-10H-acridin-9-one 163014767 Click to see CC(=CCC1=C2C(=C(C=C1)O)NC3=C(C2=O)C(=C(C(=C3OC)O)CC=C(C)C)O)C 409.50 unknown https://doi.org/10.1080/14786410600907002
1,5-dihydroxy-2,3,4-trimethoxy-10H-acridin-9-one 163064160 Click to see COC1=C(C(=C(C2=C1NC3=C(C2=O)C=CC=C3O)O)OC)OC 317.29 unknown https://doi.org/10.1080/14786410600907002
1,5-Dihydroxy-3,4-dimethoxy-10-methyl-9(10H)-acridinone 5487772 Click to see 301.29 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1021/JF902561C
https://doi.org/10.1590/S0103-50532009000400008
1,5-dihydroxy-3,4-dimethoxy-10H-acridin-9-one 102061439 Click to see 287.27 unknown https://doi.org/10.1080/14786410600907002
10-Hydroxy-12-methoxy-2,2,11-trimethylpyrano[3,2-b]acridin-6-one 162820580 Click to see 337.40 unknown https://doi.org/10.1080/14786410600907002
11-Hydroxynoracronycine 5378702 Click to see 323.30 unknown https://doi.org/10.1021/NP0005762
https://doi.org/10.1021/JF902561C
https://doi.org/10.1016/J.BMC.2010.12.056
2,3-Dihydro-4,9-dihydroxy-2-(2-hydroxy-propan-2-yl)-11-methoxy-10-methylfuro[3,2-b]acridin-5(10h)-one 53326179 Click to see 371.40 unknown https://doi.org/10.1080/14786410600907002
https://doi.org/10.1021/JF902561C
https://doi.org/10.1016/J.BMC.2010.12.056
3,4-dihydro-3,5,8-trihydroxy-6-methoxy-2,2,7-trimethyl-2Hpyrano[2,3-a]acridin-12(7H)-one 53318269 Click to see CC1(C(CC2=C(C(=C3C(=C2O1)C(=O)C4=C(N3C)C(=CC=C4)O)OC)O)O)C 371.40 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1080/14786410600907002
Acronine 345512 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)C4=CC=CC=C4N3C)C 321.40 unknown https://doi.org/10.1080/14786410600907002
Citbrasine 19093029 Click to see CN1C2=C(C=CC=C2O)C(=O)C3=C1C(=C(C(=C3O)OC)OC)OC 331.32 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1590/S0103-50532009000400008
https://doi.org/10.1021/JF902561C
Citrusinine II 10016895 Click to see 287.27 unknown https://doi.org/10.1021/JF902561C
https://doi.org/10.1590/S0103-50532009000400008
https://doi.org/10.1021/NP0005762
https://doi.org/10.1016/J.BMC.2010.12.056
Glycocitrine-I 11580650 Click to see 325.40 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1021/JF902561C
Glycocitrine-Iv 9998312 Click to see CC(=CCC1=C(C2=C(C(=C1O)OC)N(C3=C(C2=O)C=CC=C3O)C)O)C 355.40 unknown https://doi.org/10.1021/JF902561C
https://doi.org/10.1021/NP0005762
https://doi.org/10.1590/S0103-50532009000400008
https://doi.org/10.1016/J.BMC.2010.12.056
Glyfoline 5480208 Click to see 361.30 unknown https://doi.org/10.1080/14786410600907002
Junosine 15286413 Click to see 325.40 unknown https://doi.org/10.1021/JF902561C
Noracronycine 5320199 Click to see 307.30 unknown https://doi.org/10.1080/14786410600907002
Pyranofoline 9798626 Click to see 353.40 unknown https://doi.org/10.1016/J.BMC.2010.12.056
https://doi.org/10.1021/JF902561C
https://doi.org/10.1080/14786410600907002
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
6,11-dihydroxy-3,3-dimethyl-5-phenyl-12H-pyrano[2,3-c]acridin-7-one 163098872 Click to see 385.40 unknown https://doi.org/10.1080/14786410600907002
6,11-Dihydroxy-3,3,12-trimethyl-5-phenylpyrano[2,3-c]acridin-7-one 162820579 Click to see 399.40 unknown https://doi.org/10.1080/14786410600907002
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see 179.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Epicoccolide B 11210533 Click to see 358.30 unknown via CMAUP database
Hopeafuran 57397234 Click to see C1=CC(=CC=C1C2C3=C(C=C(C=C3O)O)C4=C(OC5=CC(=CC(=C54)C2=O)O)C6=CC=C(C=C6)O)O 466.40 unknown https://doi.org/10.1080/14786410600907002
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
n-Methylcinnamamide 6039989 Click to see 161.20 unknown https://doi.org/10.1590/S0100-40422012001100015
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-Methoxyseselin 290897 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1021/JF902561C
8,8-Dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-f]chromen-2-one 44556806 Click to see CC(=CCC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CC(O2)(C)C)C 296.40 unknown https://doi.org/10.1021/JF902561C
Seselin 68229 Click to see 228.24 unknown https://doi.org/10.1021/JF902561C
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-21-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19-tetrol 118731401 Click to see 738.60 unknown via CMAUP database
Cinnamtannin A2 16130899 Click to see 1155.00 unknown via CMAUP database
Cinnamtannin A3 16129741 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=C(C(=CC(=C78)O)O)C9C(C(OC1=CC(=CC(=C91)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1443.30 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
8,8'-Methylenebiscatechin 46182787 Click to see 592.50 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5317057 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cyanidin 3-arabinoside cation 12137509 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 419.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
Bis(5-hydroxynoracronycine) 10532237 Click to see CC1(CC(C2=C(O1)C=C(C3=C2N(C4=C(C3=O)C=CC=C4O)C)O)C5=C6C(=C7C(=C5O)C(=O)C8=C(N7C)C(=CC=C8)O)C=CC(O6)(C)C)C 646.70 unknown https://doi.org/10.1590/S0103-50532009000400008

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