Geranium sylvaticum - Unknown
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Details Top

Internal ID UUID64401df4cafb2356480280
Scientific name Geranium sylvaticum
Authority L.
First published in Sp. Pl. : 681 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Geranium alpestre Schur Enum. Pl. Transsilv. 135. 1866 [Apr-Jun 1866]
Geranium angulatum Curtis Bot. Mag. 6: t. 203 (1792)
Geranium argenteum Geners. ex Wahlenb. Fl. Carpat. Princ. 208 1814
Geranium batrachioides Cav. Diss. 4: 211 (1787)
Geranium caeruleopurpureum Gilib. Fl. Lit. Inch. ii. 175. 1782
Geranium caroli-principis Pantu Analele Acad. Române , ser. 2, 29(3): 51 (1907)
Geranium eglandulosum Dalla Torre Alpenfl. : 147 (1899)
Geranium fastigiatum Gliem. ex Bab. J. Linn. Soc., Bot. 11: 800 (1871)
Geranium lemanianum Briq. Annuaire Conserv. Jard. Bot. Genève 3: 83 (1899)
Geranium purpureocaeruleum Ledeb. Fl. Ross. 1: 465 (1842)
Geranium ranunculifolium Schur ex Nyman Consp. Fl. Eur. : 137 (1878)
Geranium sylvaticum var. glanduligerum Petrova & Kožuharov Fl. Narodna Republ. Bulg. 7: 492. 1979
Geranium sylvestre Olaf. & Pov. ex Bab. J. Linn. Soc., Bot. 11: 300 (1870)
Geranium transsylvanicum Schott & Kotschy ex R.Knuth Pflanzenr. , IV, 129: 140 (1912)
Geranium venosum Pers. Syn. Pl. 2: 235 (1806)

Common names Top

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Language Common/alternative name
English wood crane's-bill
English wood cranesbill
Azerbaijani meşəlik ətirşahı
azb مئشهلیک اتیرشاهی
Belarusian герань лясная
Bulgarian горски здравец
Czech kakost lesní
Welsh pig-yr-aran y coed
Danish skov-storkenæb
German wald-storchschnabel
German waldstorchschnabel
Estonian mets-kurereha
Persian شمعدانی جنگلی
Finnish metsäkurjenpolvi
French géranium des bois
Irish crobh coille
Croatian Šumska iglica
Upper Sorbian lěsna pyskawa
Hungarian erdei gólyaorr
Icelandic blágresi
Icelandic storkablágresi
Icelandic litunargras
Italian geranio selvatico
Italian geranio dei prati
Japanese ウッドクレインズビル
Kazakh Орман қазтамағы
Lithuanian miškinis snaputis
Latvian meža gandrene
Norwegian Bokmål skogstorkenebb
Dutch bosooievaarsbek
Norwegian Nynorsk skogstorkenebb
os Кæлдæф
Polish bodziszek leśny
Russian герань лесная
se boaresgállarássi
Slovak pakost lesný
Slovenian gozdna krvomočnica
Swedish alpnäva
Swedish midsommarblomster
Swedish skogsnäva
Turkish orman turnagagası
Ukrainian Герань лісова
Ukrainian журавець лісовий
Ukrainian герань лісова
Chinese 林地老鹳草
Chinese 森林老鹳草

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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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
      • Irkutsk
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Québec
    • North-central U.S.A.
      • Illinois
    • Subarctic America
      • Greenland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000701427
Canadensys 6052
USDA Plants GESY
Tropicos 13900049
INPN 100160
Flora of Italy 2812
KEW urn:lsid:ipni.org:names:322492-2
The Plant List kew-2824138
Plantarium 17528
Open Tree Of Life 628152
NCBI Taxonomy 379956
NBN Atlas NBNSYS0000003148
Nature Serve 2.158981
IPNI 322492-2
iNaturalist 85429
GBIF 2891147
Freebase /m/0cxyr1
EPPO GERSY
EOL 130445
Elurikkus 4899
USDA GRIN 419400
Wikipedia Geranium_sylvaticum
CMAUP NPO4073

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
Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J Ecol Evol 07-Mar-2024
PMCID:PMC10918743
doi:10.1002/ece3.11061
PMID:38455145
Exploring Cereal Metagenomics: Unravelling Microbial Communities for Improved Food Security Masenya K, Manganyi MC, Dikobe TB Microorganisms 02-Mar-2024
PMCID:PMC10974370
doi:10.3390/microorganisms12030510
PMID:38543562
Effects of leaf herbivory and autumn seasonality on plant secondary metabolites: A meta‐analysis Skovmand L, O'Dea RE, Greig KA, Amato KR, Hendry AP Ecol Evol 13-Feb-2024
PMCID:PMC10864732
doi:10.1002/ece3.10912
PMID:38357594
Root litter decomposition is suppressed in species mixtures and in the presence of living roots Heredia‐Acuña C, Semchenko M, De Vries FT J Ecol 13-Oct-2023
PMCID:PMC10976660
doi:10.1111/1365-2745.14207
PMID:38550391
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Epigenetic Control of Plant Response to Heavy Metals Fasani E, Giannelli G, Varotto S, Visioli G, Bellin D, Furini A, DalCorso G Plants (Basel) 07-Sep-2023
PMCID:PMC10537915
doi:10.3390/plants12183195
PMID:37765359
Mass Spectrometric Fingerprint Mapping Reveals Species-Specific Differences in Plant Polyphenols and Related Bioactivities Vanhakylä S, Salminen JP Molecules 31-Aug-2023
PMCID:PMC10490256
doi:10.3390/molecules28176388
PMID:37687216
Affinity of Tannins to Cellulose: A Chromatographic Tool for Revealing Structure-Activity Patterns Suominen E, Savila S, Sillanpää M, Damlin P, Karonen M Molecules 13-Jul-2023
PMCID:PMC10384774
doi:10.3390/molecules28145370
PMID:37513244
Hydrolyzable tannins are incorporated into the endocarp during sclerification of the water caltrop Trapa natans Huss JC, Antreich SJ, Felhofer M, Mayer K, Eder M, Vieira Dias dos Santos AC, Ramer G, Lendl B, Gierlinger N Plant Physiol 10-Jul-2023
PMCID:PMC10762508
doi:10.1093/plphys/kiad408
PMID:37427803
The monoaminergic system is a bilaterian innovation Goulty M, Botton-Amiot G, Rosato E, Sprecher SG, Feuda R Nat Commun 06-Jun-2023
PMCID:PMC10244343
doi:10.1038/s41467-023-39030-2
PMID:37280201
Enhancing Attention and Interest in Plants to Mitigate Plant Awareness Disparity Prokop P, Fančovičová J Plants (Basel) 02-Jun-2023
PMCID:PMC10255336
doi:10.3390/plants12112201
PMID:37299180
Oligomeric Proanthocyanidins: An Updated Review of Their Natural Sources, Synthesis, and Potentials Nie F, Liu L, Cui J, Zhao Y, Zhang D, Zhou D, Wu J, Li B, Wang T, Li M, Yan M Antioxidants (Basel) 26-Apr-2023
PMCID:PMC10215713
doi:10.3390/antiox12051004
PMID:37237870
Inoculum source dependent effects of ericoid, mycorrhizal fungi on flowering and reproductive success in highbush blueberry (Vaccinium corymbosum) O’Neill E, Brody AK, Ricketts T PLoS One 19-Apr-2023
PMCID:PMC10115346
doi:10.1371/journal.pone.0284631
PMID:37075057
Geranium sylvaticum increases pollination probability by sexually dimorphic flowers Soininen JO, Kytöviita M Ecol Evol 28-Dec-2022
PMCID:PMC9797467
doi:10.1002/ece3.9670
PMID:36590340
Intensive grassland management disrupts below-ground multi-trophic resource transfer in response to drought Chomel M, Lavallee JM, Alvarez-Segura N, Baggs EM, Caruso T, de Castro F, Emmerson MC, Magilton M, Rhymes JM, de Vries FT, Johnson D, Bardgett RD Nat Commun 16-Nov-2022
PMCID:PMC9668848
doi:10.1038/s41467-022-34449-5
PMID:36385003

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3-Galloylshikimic acid 10449030 Click to see C1C(C(C(C=C1C(=O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 326.25 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
Fisheacid 139583718 Click to see C1C(C(=CC2=CC=CC=C21)C3=CC4=CC=CC=C4CC3C(=O)O)C(=O)O 346.40 unknown https://doi.org/10.1016/0031-9422(94)00898-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1016/0031-9422(94)00898-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3-dihydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 13270012 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
3,4-Di-O-galloylquinic acid 460895 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
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
Neochlorogenic acid 5280633 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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101228664 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=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)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 1155.00 unknown via CMAUP database
Procyanidin B3 146798 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 C2 11182062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Leucocianidol 440833 Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 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 https://doi.org/10.1016/0031-9422(94)00898-4
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown https://doi.org/10.1016/0031-9422(94)00898-4
Kuromanin 441667 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 https://doi.org/10.1016/0031-9422(94)00898-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 154496409 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/0031-9422(94)00898-4
(2S,3R,4S,5S,6S)-2-[7-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 154496973 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 655.60 unknown https://doi.org/10.1016/0031-9422(94)00898-4
3',5'-Dimethoxy-4',7-dihydroxy-5-(beta-D-glucopyranosyloxy)-3-[(6-O-acetyl-beta-D-glucopyranosyl)oxy]flavylium 101918997 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C([O+]=C3C=C(C=C(C3=C2)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O 697.60 unknown via CMAUP database
Cyanin 441688 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/0031-9422(94)00898-4
Malvin 441765 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 655.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12304323 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
delphinidin 3-O-beta-D-glucoside betaine 165559 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=O)C=C3O2)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(94)00898-4
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside 5491814 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-glucopyranoside 9830456 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(2R,3R,4S,5R,6R)-6-(((3,4,5-Trihydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrakis(3,4,5-trihydroxybenzoate) 9876301 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1,2-Di-O-galloyl-4,6-O-(S)-hexahydroxydiphenoyl-beta-D-glucopyranose 101259865 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
3-O-digalloyl-1,2,4,6-tetra-O-beta-D-galloylglucose 16164119 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 1092.80 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O 1110.80 unknown via CMAUP database

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