Platanus orientalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Platanus orientalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644002df278cd956833294
Scientific name Platanus orientalis
Authority L.
First published in Sp. Pl. : 999 (1753)

Description Top

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Platanus orientalis, also known as the Old World sycamore or Oriental plane, is a large, deciduous tree that can grow up to 30 meters tall. It is known for its longevity and wide-spreading crown. In autumn, its deep green leaves can change to shades of red, amber, and yellow. The tree's name comes from the fact that it is native to the eastern regions of the Balkans, and it has been cultivated in many parts of Eurasia for centuries. The tree is often found in riverine settings, but it can also thrive in dry soils. It is prized for its shade and coolness during hot summers and is often used for medicinal purposes. The tree has a rich cultural history, with mentions in ancient Greek literature and use in Mughal gardens in Kashmir. It is also featured in music and literature, such as Handel's aria "Ombra mai fu" and Lewis Carol's poem "Jabberwocky." Today, the tree is facing threats from deforestation, but efforts are being made to preserve and protect it.

Synonyms Top

Scientific name Authority First published in
Platanus nana hort. ex K.Koch Dendrologie 2(1): 470 (1872)
Platanus insularis Kotschy ex Koehne Deut. Dendrol. : 206 (1893)
Platanus elongata Steud. Nomencl. Bot. [Steudel] 632. 1821
Platanus laciniata hort. ex K.Koch Dendrologie 2(1): 468 (1872)
Platanus macrophylla Cree ex W.H.Baxter Hort. Brit. , ed. 3: 659 (1839)
Platanus algeriensis hort. ex K.Koch Dendrologie 2(1): 468 (1872)
Platanus cretica Dode Bull. Soc. Dendrol. France 7: 60 (1908)
Platanus digitata Gordon Garden (London 1871-1927) 1: 572 1872
Platanus nepalensis hort. ex W.H.Baxter Suppl. Hort. Brit. [Loudon] 612. 1850 ; third additional suppl. to Loudon's Hortus Britannicus published in new ed. [4], cited in IK as 'Hort. Brit. Suppl. iii.'.
Platanus umbrosa Salisb. Prodr. Stirp. Chap. Allerton 393. 1796 [Nov-Dec 1796]
Platanus pyramidalis Bolle ex Koehne Deut. Dendrol. : 206 (1893)
Platanus orientalior Dode Bull. Soc. Dendrol. France 7: 57 (1908)
Platanus vitifolia Spach ex Dippel Handb. Laubholzk. 3: 276 (1893)
Platanus undulata Steud. Nomencl. Bot. 1: 632 (1821)
Platanus reuteri hort. ex K.Koch Dendrologie 2(1): 468 (1872)
Platanus umbraculifera hort. ex K.Koch Dendrologie 2(1): 468 (1872)
Platanus palmata Moench Methodus : 358 (1794)
Platanus orientalis f. digitata (Gordon) Jankó Bot. Jahrb. Syst. 11: 450 1890
Platanus orientalis var. nepalensis (Morren) Wesm. Bull. Féd. Soc. Hort. Belgique 1867: 315 1868
Platanus digitifolia Palib.
Platanus orientalis var. elongata Aiton Hort. Kew. 3: 364 (1789)
Platanus orientalis var. undulata Aiton Hort. Kew. 3: 364 (1789)

Common names Top

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Language Common/alternative name
English oriental plane
English oriental plane-tree
English chinar
Spanish plátano oriental
Spanish plátanos orientales
Spanish platanos orientales
Spanish platano oriental
Arabic دلب مشرقي
Azerbaijani Şərq çinarı
Bulgarian източен платан
Bulgarian източен чинар
br platan-ar-reter
Catalan plàtan d'orient
Czech platan východní
Welsh pilcoes
Danish orientalsk platan
German orientalische platane
German morgenländische platane
Greek Ανατολικός πλάτανος
Greek Πλάτανος ο Ανατολικός
Estonian idaplaatan
Basque ekialdeko platano
Persian چنار خاوری
Finnish idänplataani
French platane d'orient
French platane d’orient
Galician plátano oriental
Hebrew דולב מזרחי
Croatian azijska platana
Upper Sorbian narańša platana
Hungarian keleti platán
Armenian Չինար
Armenian սոսի
Italian platano orientale
Japanese スズカケノキ
Korean 버즘나무
ks بوٗنؠ
Macedonian чинар
Macedonian источен чинар
Macedonian источен платан
Macedonian платан
Malayalam ചിനാർ
Norwegian Bokmål orientplatan
Dutch oosterse plataan
Norwegian Nynorsk orientplatan
Polish platan wschodni
Punjab چنار
Russian Восточный платан
Russian Платан восточный
Slovak platan východný
Slovenian vzhodna platana
Serbian Азијски платан
Swedish orientalisk platan
Turkish doğu çınarı
Ukrainian Чинар
Ukrainian Платан східний
Ukrainian Чинара
Urdu چنار
Uzbek sharq chinori
Chinese 法国梧桐
Chinese 祛汗树
Chinese 悬铃木
Chinese 净土树
Chinese 法桐
Chinese 三球悬铃木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000487086
UNII T36L9N7Q1H
USDA Plants PLOR6
Tropicos 25300016
INPN 114028
Flora of Italy 1705
KEW urn:lsid:ipni.org:names:685873-1
The Plant List kew-2570462
Plantarium 28656
Missouri Botanical Garden 285139
Open Tree Of Life 787466
Observations.org 9209
NCBI Taxonomy 122832
NBN Atlas NBNSYS0000042166
IUCN Red List 33951
IPNI 685873-1
iNaturalist 181682
GBIF 3152816
Freebase /m/01z200
EPPO PLTOR
EOL 596130
Calflora (Californian flora) 9389
USDA GRIN 28803
Wikipedia Platanus_orientalis
PaleoBotany 97993

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_025762735.1 ASM2576273v1 Scaffold Iridian Genomes 2022-10-19 95.0x 1.39 Gb

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
Pest categorisation of Crisicoccus seruratus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Antonatos S, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 22-Apr-2024
PMCID:PMC11033835
doi:10.2903/j.efsa.2024.8740
PMID:38650611
High Trunk Truncation as a Potential Sustainable Management Option for Asian Longhorned Beetle on Salix babylonica Huang C, Wang H, Hai X, Wang Z, Lyu F Insects 16-Apr-2024
PMCID:PMC11050171
doi:10.3390/insects15040278
PMID:38667408
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Green biosourced composite for efficient reactive dye decontamination: immobilized Gibberella fujikuroi on maize tassel biomatrix Celik S, Kurtulus Tas S, Sayin F, Akar T, Tunali Akar S Environ Sci Pollut Res Int 15-Mar-2024
PMCID:PMC11023956
doi:10.1007/s11356-024-32809-w
PMID:38488918
Evaluation of Free Radical Scavenging and Antimicrobial Activity of Coleus amboinicus-Mediated Iron Oxide Nanoparticles Kunjan F, Shanmugam R, Govindharaj S Cureus 04-Mar-2024
PMCID:PMC10988995
doi:10.7759/cureus.55472
PMID:38571817
Removing Heavy Metals: Cutting-Edge Strategies and Advancements in Biosorption Technology Staszak K, Regel-Rosocka M Materials (Basel) 01-Mar-2024
PMCID:PMC10934587
doi:10.3390/ma17051155
PMID:38473626
Extraction of Lightweight Platanus orientalis L. Fruit’s Stem Fiber and Determination of Its Mechanical and Physico-Chemical Properties and Potential of Its Use in Composites Kaya AI Polymers (Basel) 28-Feb-2024
PMCID:PMC10935309
doi:10.3390/polym16050657
PMID:38475338
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Dietary phenolic compounds as promising therapeutic agents for diabetes and its complications: A comprehensive review Aryal D, Joshi S, Thapa NK, Chaudhary P, Basaula S, Joshi U, Bhandari D, Rogers HM, Bhattarai S, Sharma KR, Regmi BP, Parajuli N Food Sci Nutr 30-Jan-2024
PMCID:PMC11077226
doi:10.1002/fsn3.3983
PMID:38726403
Assessment of an effective quantitative model with multi-criteria decision-making method for sustainable campus Aksoy O, Demir S, Ersoz ND, Gokkaya MD Environ Sci Pollut Res Int 20-Jan-2024
PMCID:PMC10881700
doi:10.1007/s11356-024-32040-7
PMID:38243028
Levels and sources of polycyclic aromatic hydrocarbons (PAHs) near hospitals and schools using leaves and barks of Sambucus nigra and Acacia melanoxylon Alexandrino K, Sánchez NE, Viteri F Environ Geochem Health 16-Jan-2024
PMCID:PMC10791842
doi:10.1007/s10653-023-01825-z
PMID:38227159
Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G Plants (Basel) 26-Dec-2023
PMCID:PMC10780482
doi:10.3390/plants13010077
PMID:38202385
Safety evaluation of the food enzyme endo‐polygalacturonase from the non‐genetically modified Aspergillus tubingensis strain MUCL 55013 Lambré C, Barat Baviera JM, Bolognesi C, Cocconcelli PS, Crebelli R, Gott DM, Grob K, Lampi E, Mengelers M, Mortensen A, Rivière G, Steffensen I, Tlustos C, Van Loveren H, Vernis L, Zorn H, Herman L, Roos Y, Andryszkiewicz M, Fernàndez‐Fraguas C, Kovalkovičová N, Liu Y, Lunardi S, Nielsen E, di Piazza G, Chesson A EFSA J 20-Nov-2023
PMCID:PMC10659768
doi:10.2903/j.efsa.2023.8397
PMID:38027442

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1055/S-0028-1097634
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Octadecanoic acid, hexacosyl ester 3085149 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC 649.20 unknown https://doi.org/10.1055/S-0028-1097634
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hentriacontanol 68345 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 452.80 unknown https://doi.org/10.1055/S-0028-1097634
12-Tricosanol 3084429 Click to see CCCCCCCCCCCC(CCCCCCCCCCC)O 340.60 unknown https://doi.org/10.1055/S-0028-1097634
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds
[2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydrochromen-6-yl] hexadecanoate 13691242 Click to see CCCCCCCCCCCCCCCC(=O)OC1=C(C2=C(C(=C1C)C)OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C 669.10 unknown https://doi.org/10.1007/BF00629969
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see CCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCC 450.80 unknown https://doi.org/10.1055/S-0028-1097634
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(2-Hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl) dodecanoate 162848969 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCC)C)C)C 613.00 unknown https://doi.org/10.1007/BF00629969
(2-Hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl) hexadec-15-enoate 162850818 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCCCC=C)C)C)C 667.10 unknown https://doi.org/10.1007/BF00629969
(2-Hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl) tetradec-13-enoate 162875727 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCC=C)C)C)C 639.00 unknown https://doi.org/10.1007/BF00629969
(2-Hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl) tetradecanoate 163035983 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCCC)C)C)C 641.10 unknown https://doi.org/10.1007/BF00629969
[(2S)-2-hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl] dodecanoate 163191397 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCC)C)C)C 613.00 unknown https://doi.org/10.1007/BF00629969
[(2S)-2-hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl] hexadec-15-enoate 162850819 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCCCC=C)C)C)C 667.10 unknown https://doi.org/10.1007/BF00629969
[(2S)-2-hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl] hexadecanoate 163188960 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCCCCC)C)C)C 669.10 unknown https://doi.org/10.1007/BF00629969
[(2S)-2-hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl] tetradec-13-enoate 162875728 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCC=C)C)C)C 639.00 unknown https://doi.org/10.1007/BF00629969
[(2S)-2-hexadecyl-2,5,7,8-tetramethyl-3,4-dihydrochromen-6-yl] tetradecanoate 163035984 Click to see CCCCCCCCCCCCCCCCC1(CCC2=C(O1)C(=C(C(=C2C)OC(=O)CCCCCCCCCCCCC)C)C)C 641.10 unknown https://doi.org/10.1007/BF00629969
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2006-959751
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162900437 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)OC7C(C(C(C(O7)CO)O)O)O)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1181.00 unknown https://doi.org/10.1007/S10600-010-9616-3
[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162900436 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)OC7C(C(C(C(O7)CO)O)O)O)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1181.00 unknown https://doi.org/10.1007/S10600-010-9616-3
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 130556 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 https://doi.org/10.1023/B:CONC.0000025479.07578.5D
Epicatechin-(4beta->8)-epigallocatechin 3'-gallate 11513300 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)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
Epicatechin(4b->8)epigallocatechin 3-O-gallate 14521001 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)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
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 https://doi.org/10.1023/B:CONC.0000025479.07578.5D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
(+)-Catechin gallate 5276454 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 367141 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
Flavan-3,3',4',5,5',7-hexol 1249 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1023/B:CONC.0000025479.07578.5D
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1006/PHRS.1999.0562
https://doi.org/10.1055/S-2006-959751
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol 3-(2'',3''-di-(E)-p-coumaroylrhamnoside) 44258960 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown https://doi.org/10.1006/PHRS.1999.0562
Platanoside 6451113 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown https://doi.org/10.1006/PHRS.1999.0562
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162872444 Click to see CC(C)(CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 534.50 unknown https://doi.org/10.1055/S-0028-1097634
Amurensin 5318156 Click to see CC(C)(CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 534.50 unknown https://doi.org/10.1055/S-0028-1097634

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