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Tilia europaea

Tilia europaea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Tilia europaea - 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 UUID643ffee6346bd878073559
Scientific name Tilia europaea
Authority L.
First published in Sp. Pl. : 514 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Tilia pseudobliqua Simonk. Math. Term. Közlem. 22: 300 (1888)
Tilia vulgaris Hill Brit. Herb. 523 (1756); Druce in Rep. Bot. Exch. Cl. Brit. Isles, 1913, iii. 410.
Tilia vulgaris B.Heyne Getreue Darstell. Gew. 3: t. 47 1813
Tilia subparvifolia Borbás Deutsche Bot. Monatsschr. 7: 4 (1889)
Tilia hybrida Behlen Forstbot. , ed. 5: 161 (1843)
Tilia intermedia DC. Prodr. 1: 518 (1824)
Tilia oxycarpa Rchb. ex Bayer Verh. K. K. Zool.-Bot. Ges. Wien 12: 37 (1862)
Tilia officinarum Crantz Stirp. Austr. Fasc. 2: 61 (1763)
Tilia carnuntiae Heinr.Braun Oesterr. Bot. Z. 45: 320 (1895)
Tilia communis Gaterau Desc. Pl. Montauban : 98 (1789)
Tilia banatica Beldie Fl. Republ. Popul. Român. 6: 82 (1958)
Tilia croatica Degen & Heinr.Braun Fl. Veleb. 2: 421 (1937)
Tilia eriostylis Borbás Magyar Orv. Termész. Nagy Gyül. Tört. Vázl. Munk. 23: 384 (1887)
Tilia acuminata Opiz Seznam : 98 (1852)
Tilia cordata f. vulgaris Ig.Vassil.
Tilia platyphyllos subsp. grandifolia Hayek

Common names Top

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Language Common/alternative name
English common linden
English common lime
Spanish tilo híbrido de holanda
Spanish tilo hibrido de holanda
Spanish tilo europeo
Arabic زيزفون أوروبي
Azerbaijani avropa cökəsi
Belarusian ліпа звычайная
Bulgarian европейска липа
Czech lípa obecná
Welsh pisgwydden
Danish kejser-lind
Danish park-lind
German kaiser-linde
German holländische linde
Estonian läänepärn
Persian نمدار معمولی
Finnish puistolehmus
French tilleul intermédiaire
French tilleul commun
Irish teile choiteann
Upper Sorbian nižozemska lipa
Icelandic garðalind
Japanese セイヨウシナノキ
Japanese ティユール
Japanese リンデンバウム
Japanese セイヨウボダイジュ
Norwegian Bokmål parklind
Dutch hollandse linde
Norwegian Nynorsk parklind
os Европæйаг сусхъæд
Russian Липа европейская
Russian Липа обыкновенная
sco lind
Slovak lipa obyčajná
Slovenian navadna lipa
Slovenian tilia × vulgaris
Slovenian evropska lipa
Serbian Европска Липа
Swedish parklind
tt Яурупа юкәсе
udm Европаысь беризь
Chinese 西洋椴
Chinese 欧洲椴

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
  • Europe
    • Eastern Europe
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Ireland
      • Sweden
    • Southeastern Europe
      • Greece
      • Italy
      • Romania
      • Sicilia
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000457539
UNII R43LD7MX6S
Canadensys 17313
USDA Plants TIEU4
Tropicos 32200185
KEW urn:lsid:ipni.org:names:835306-1
The Plant List kew-2518295
Missouri Botanical Garden 287366
Observations.org 336559
NCBI Taxonomy 644191
IPNI 835306-1
iNaturalist 410499
GBIF 3152046
Freebase /m/03gqh2w
EPPO TILVU
EOL 486445
Elurikkus 7943
Elurikkus 365932
USDA GRIN 36679
Wikipedia Tilia_%C3%97_europaea
CMAUP NPO7987
Open Tree Of Life 3942887

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
A comparative study regarding the adulteration detection of honey: Physicochemical parameters vs. impedimetric data Oroian M, Dranca F, Ropciuc S, Pauliuc D Curr Res Food Sci 17-Nov-2023
PMCID:PMC10728335
doi:10.1016/j.crfs.2023.100642
PMID:38115897
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Forensic examination of a fragmentary funerary portrait in the collection of the Harvard art museums Rayner G, Eremin K, Smith K, Cartwright C, Degryse P, Ebbinghaus S Forensic Sci Int Synerg 10-Oct-2023
PMCID:PMC10590840
doi:10.1016/j.fsisyn.2023.100442
PMID:37876377
Cryo-attenuated properties of Tilia miqueliana pericarps and seeds Wu Y, Sun XR, Peng CY, Shen YB, Visscher AM, Pritchard HW, Wang MZ, Deng ZY Front Plant Sci 15-Aug-2023
PMCID:PMC10486270
doi:10.3389/fpls.2023.1228069
PMID:37692432
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Anthropological significance of Tilia trees in Japan Janowski D Ecol Evol 12-Jul-2023
PMCID:PMC10338748
doi:10.1002/ece3.10303
PMID:37456068
Re-Examination of Several Elsinoë Species Reported from Japan Ujat AH, Ono T, Hattori Y, Nakashima C Mycobiology 15-Jun-2023
PMCID:PMC10288934
doi:10.1080/12298093.2023.2219049
PMID:37359956
New Strategies to Increase the Abiotic Stress Tolerance in Woody Ornamental Plants in Mediterranean Climate Leotta L, Toscano S, Ferrante A, Romano D, Francini A Plants (Basel) 18-May-2023
PMCID:PMC10223706
doi:10.3390/plants12102022
PMID:37653939
In Vitro Activity of Farnesol against Malassezia pachydermatis Isolates from Otitis Externa Cases in Dogs Olabode IR, Sachivkina N, Karamyan A, Mannapova R, Kuznetsova O, Bobunova A, Zhabo N, Avdonina M, Gurina R Animals (Basel) 05-Apr-2023
PMCID:PMC10093264
doi:10.3390/ani13071259
PMID:37048514
Breathing Fresh Air in the City: Implementing Avenue Trees as a Sustainable Solution to Reduce Particulate Pollution in Urban Agglomerations Mandal M, Popek R, Przybysz A, Roy A, Das S, Sarkar A Plants (Basel) 03-Apr-2023
PMCID:PMC10097214
doi:10.3390/plants12071545
PMID:37050171
Effect of Silane Coupling Agent Modification on Properties of Brass Powder-Water-Based Acrylic Coating on Tilia europaea Han Y, Yan X Polymers (Basel) 10-Mar-2023
PMCID:PMC10051514
doi:10.3390/polym15061396
PMID:36987177

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 54752972 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=CC(=C(C(=C3C2=O)O)C4=C(C=C5C(=C4O)C(=O)C6=C(C5=O)C(=CC(=C6)C)O)O)O 538.50 unknown via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 54752971 Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
(5aR,10bR)-8,10-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-5a-propan-2-yl-10bH-[1]benzofuro[2,3-b][1]benzofuran-1,3-dione 102521923 Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC3(C2C4=C(O3)C(C(=O)C(C4=O)(C)C)(C)C)C(C)C)O)O 456.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(21R)-Hopa-22(29)-ene-3beta,30-diol 102032092 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5C4(CCC5C(=C)CO)C)C)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5R,8S)-3,8-Dimethyl-5-propan-2-yl-5,6,7,8-tetrahydronaphthalen-2-ol 13368072 Click to see CC1CCC(C2=C1C=C(C(=C2)C)O)C(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(83)85056-0
3,8-Dimethyl-5-propan-2-yl-5,6,7,8-tetrahydronaphthalen-2-ol 3015179 Click to see CC1CCC(C2=C1C=C(C(=C2)C)O)C(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(83)85056-0
cis-5,6,7,8-Tetrahydro-3,8-dimethyl-5-(1-methylethyl)-2-naphthalenol 13368075 Click to see CC1CCC(C2=C1C=C(C(=C2)C)O)C(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(83)85056-0
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
(6Z,10E,14Z,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 25244109 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO 484.80 unknown via CMAUP database
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
3-O-p-Coumaroyloleanolic acid 10579517 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1)C)C(=O)O)C 602.80 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 40884490 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Methyl Betulonate 10766700 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC 468.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNC-1988-3-404
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione 44281346 Click to see CC1(C=C2C(=O)C(C(=O)C(C2(OO1)O)(C)C)(C)C)C 268.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929125 Click to see CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O 688.80 unknown via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 102521922 Click to see CC(C)CC1C2=C(C(=C(C=C2O)O)C(=O)CC(C)C)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 26202536 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Rhodomyrtone 12050020 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Tomentosone A 56929124 Click to see CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O 688.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate 14213589 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 585.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Squamatic acid 5321482 Click to see CC1=CC(=C(C(=C1C(=O)O)O)C)OC(=O)C2=C(C(=C(C=C2C)OC)C(=O)O)O 390.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol 12303802 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)OC)O 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
beta-Pedunculagin 5320441 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database

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