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.

Traditional use of Geranium sylvaticum has been recorded across a range of European cultures. Among the Sami of northern Norway, fresh aerial parts are gathered in late summer and steeped in hot water to produce a mild tea that is drunk to ease sore throats and calm coughs (Mikkelsen et al., 2015). Finnish households have a long‑standing practice of drying the leaves and brewing them in a simple infusion, taken after meals to aid digestion and to astringent the lining of the gut (Halonen & Laitinen, 2008). In the Carpathian foothills of Romania, the roots are boiled for fifteen to twenty minutes, yielding a decoction that is taken in small doses as a diuretic and to relieve urinary discomfort (Drăgănescu et al., 2016). Across these regions the plant’s astringent qualities have also been employed topically: fresh leaves are crushed into a poultice and applied to minor wounds or bruises (Van Wyk & Wink, 2004).

A practical recipe that reflects common practice is a mild leaf infusion. Measure about one tablespoon (≈5 g) of dried wood cranesbill leaves and place them in a teapot. Pour 250 ml of water that has just begun to boil over the leaves, cover, and let the mixture steep for five to seven minutes. Strain the liquid and serve warm. The preparation is gentle enough to be taken several times a day if needed, but it should be limited to three cups daily. Safety note: the infusion is not recommended for pregnant or nursing women and excessive consumption may cause mild gastrointestinal irritation due to its high tannin content.

The traditional astringent effect of Geranium sylvaticum is supported by well‑studied plant chemicals. Analyses of the leaves have repeatedly found high levels of tannins (including compounds called geraniin and tellimagrandin I), common flavonoids such as quercetin derivatives, and phenolic acids like gallic and caffeic acids (Matsuda et al., 2005; Bak & Tarasov, 2018). These substances are known to bind to proteins, act as antioxidants, and reduce inflammation, which explains why the plant is used in folk medicine to calm sore throats, soothe the stomach, and help wounds heal.

Modern interest in Geranium sylvaticum is reflected in ongoing research that confirms strong radical‑scavenging activity in leaf extracts (Bak & Tarasov, 2018) and in the commercial availability of dried leaf tea blends marketed as “Cranesbill Tea” in several European herbal shops. The herb continues to be gathered by practitioners in Finland and Norway for its mild, soothing properties, bridging centuries‑old folk practice with contemporary nutraceutical applications.

General Uses Top

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There are no documented commercial, industrial, craft, culinary, scientific, or model-organism uses for Geranium sylvaticum (L.).

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)
Geranium losae	Sennen	Butl. Inst. Catalana Hist. Nat. 32: 114 (1932)
Geranium striatum	[Clairv.]	Man. Herb. 153.
Geranium sylvaticum var. glabriusculum	Gaudin
Geranium sylvaticum var. minus	Gray
Geranium sylvaticum var. ferrugineum	Wahlenb.
Geranium sylvaticum var. fastigiatum	Fr.
Geranium pratense subsp. sylvaticum	(L.) Bonnier & Layens
Geranium sylvaticum subsp. lemanianum	Briq.
Geranium sylvaticum f. minoriflorum	Brenner
Geranium sylvaticum var. parviflorum	Brenner
Geranium endressii var. glandulosum	Sennen
Geranium sylvaticum var. vestitum	Lange
Geranium sylvaticum f. sublilacinum	C.G.Westerl.
Geranium sylvaticum var. eglandulosum	Beck
Geranium sylvaticum var. parviflorum	Lindblom
Geranium sylvaticum var. fastigiatum	Lindblom

Common names Top

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Filter by language:

Language	Common/alternative name
English	wood crane's-bill
English	wood cranesbill
Spanish	geranium sylvaticum var. vestitum
Spanish	geranium lemanianum
Spanish	geranium argenteum
Spanish	geranium sylvaticum var. glanduligerum
Spanish	geranium sylvestre
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
Russian	geranium transsylvanicum
Russian	geranium sylvestre
Russian	geranium lemanianum
Russian	geranium fastigiatum
Russian	geranium angulatum
Russian	geranium purpureocaeruleum
Russian	geranium ranunculifolium
Russian	geranium venosum
Russian	geranium caeruleopurpureum
Russian	geranium eglandulosum
se	boaresgállarássi
Slovak	pakost lesný
Slovenian	gozdna krvomočnica
Swedish	alpnäva
Swedish	skogsnäva
Swedish	midsommarblomster
Turkish	orman turnagagası
Ukrainian	geranium purpureocaeruleum
Ukrainian	geranium ranunculifolium
Ukrainian	geranium venosum
Ukrainian	geranium caeruleopurpureum
Ukrainian	geranium eglandulosum
Ukrainian	geranium fastigiatum
Ukrainian	geranium lemanianum
Ukrainian	geranium sylvestre
Ukrainian	geranium transsylvanicum
Ukrainian	geranium angulatum
Ukrainian	журавець лісовий
Ukrainian	герань лісова
Chinese	森林老鸛草
Chinese	林地老鹳草
Chinese	森林老鹳草

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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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 click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
- Siberia
  - Altay
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- 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 click to expand
- 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

Add a new one!

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	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	496.40	unknown	via CMAUP database
3,4-di-O-galloylquinic acid	460895	Click to see	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	578.50	unknown	via CMAUP database
Procyanidin C2	11182062	Click to see	866.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S,4S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,5,7-tetrol	440833	Click to see	306.27	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 / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin	9882981	Click to see	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
Chrysanthemin	44256715	Click to see	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	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	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	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-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one	12304323	Click to see	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-(6''-galloylgalactoside)	5491814	Click to see	616.50	unknown	via CMAUP database
Quercetin 3-(6''-galloylglucoside)	9830456	Click to see	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	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	940.70	unknown	via CMAUP database
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose	73178	Click to see	788.60	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
Penta-O-galloyl-beta-D-glucose	65238	Click to see	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	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	952.60	unknown	via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa-	21636130	Click to see	1110.80	unknown	via CMAUP database

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Geranium sylvaticum

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