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.

Across northeastern Mongolia and the Altai, Geranium sibiricum is recorded in ethnomedical notes as an astringent and wound herb, used in washes for diarrhea, for blood in the stool, and as a topical hemostatic (Khas’ev, 1971; Banzragch, 1982). In Altai–Tuvan communities it was collected in late spring–early summer as the aboveground herb; the tea was drunk for sore throat and occasional stomach pains (Levkina, 2017). In regions of China adjacent to its natural range, whole-plant infusions are taken for acute gastro‑intestinal discomfort, and decoctions or washes are applied externally for bruises and bleeding (Pharmacopoeia of the People’s Republic of China, 1999). Among Buryats it was used in combination with other astringent herbs to control dysenteric stools (Banzragch, 1982). These notes consistently present the aerial parts as the primary material for infusion or decoction, sometimes brewed freshly as a tea or simmered with birch bark and other astringents.

A practical preparation for a mild tea follows ethnomedical practice: infuse roughly 10–15 grams of fresh whole herb (chopped) or 4–6 grams of dried aerial parts in 250–300 milliliters of just‑boiled water for 10–15 minutes; cover while steeping, strain, and drink one cup 2–3 times daily for up to 3–5 days to ease mild gastrointestinal cramps or sore throat. A simple wash can be made by simmering 20–30 grams of herb in half a liter of water for 10 minutes, cooling to comfortably warm, and rinsing affected gums or wounds 2–3 times daily. Tinctures prepared at a rough 1:5 plant‑to‑menstruum ratio (weight:volume) in 45% ethanol and macerated for two weeks are used at community level; typical household doses range from 2–4 milliliters taken up to three times daily, not exceeding about 10 milliliters per day. Reported adverse effects are uncommon, but the astringent effect can be strong; pregnant or lactating people should avoid regular use, and anyone with a known tannin allergy or ulcer disease should discontinue if gastric irritation occurs. Children should use the tea only in small, infrequent amounts under adult supervision.

Well‑established phytochemistry supports the reported astringent and hemostatic activities: condensed tannins (proanthocyanidins), hydrolyzable gallotannins/ellagitannins, and flavonoids such as quercetin and kaempferol glycosides are documented in whole-plant extracts, alongside simple phenolics (Shukla et al., 2012; Yoon et al., 2014). These constituents bind mucosal proteins and proteins in superficial wound exudates, a mechanism that aligns with traditional uses in dysentery and superficial bleeding.

Modern relevance remains modest: research is largely limited to chemistry and in vitro studies, and Geranium sibiricum is not widely commercialized in international herbal channels; however, the plant continues to be gathered and used in regional folk practice in Mongolia, the Altai, and adjacent parts of China.

General Uses Top

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Common products:
No documented commercial or industrial products derived from Geranium sibiricum.

Industrial and craft applications:
No documented non-medicinal craft or industrial uses.

Food and beverages (non-medicinal):
No documented culinary uses or food-processing applications.

Colorants and tanning:
No documented use as a dye or tannin source.

Wood and fiber:
No documented timber, fiber, or structural uses.

Fragrance and cosmetics:
No documented use as a source of fragrance, essential oil, or cosmetic ingredient.

Properties relevant to use:
No documented physical or chemical properties that support commercial use are reported for this taxon.

Standards and regulation:
No established industry standards or regulatory frameworks specifically refer to this species.

Sustainability and sourcing:
No specific data on cultivation, harvest, or environmental impacts for commercial applications have been reported for this taxon.

Synonyms Top

Scientific name	Authority	First published in
Geranium amurense	Tsyren.	Bot. Zhurn. (Moscow & Leningrad) 91: 1253 (2006)
Geranium acrocarphum	Ledeb.	Fl. Ross. 1: 471 (1842)
Geranium europaeum	Popov	Fl. URSS 15: 46 1949
Geranium popovii	(Tzvelev) Tzvelev	Opred. Sosud. Rast. Severo-Zap. Rossii : 680 (2000)
Geranium ruthenicum	R.Uechtr.	Oesterr. Bot. Z. 23: 335 (1873)
Geranium sibiricum var. multiflorum	Z.H.Lu	Bull. Bot. Res., Harbin 14: 359 (1994)
Geranium sibiricum subsp. popovii	Tzvelev	Novosti Sist. Vyssh. Rast. 29: 96 (1993)
Geranium variabile	Moench	Methodus : 283 (1794)
Geranium sibiricum subsp. ruthenicum	(R.Uechtr.) Gams	Ill. Fl. Mitt.-Eur. 4: 1695 1925
Geranium sibiricum subsp. eusibiricum	Gams
Geranium sibiricum f. glabrius	H.Hara
Geranium sibiricum var. glabrius	(H.Hara) Ohwi

Common names Top

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Filter by language:

Language	Common/alternative name
English	siberian geranium
Azerbaijani	sibir ətirşahı
Belarusian	Герань сібірская
Bulgarian	сибирски здравец
Czech	kakost sibiřský
German	sibirischer storchschnabel
Estonian	siberi kurereha
Finnish	siperiankurjenpolvi
Upper Sorbian	sibirska pyskawa
Korean	손잎풀
Korean	쥐손이풀
Latvian	sibīrijas gandrene
Russian	герань сибирская
Slovak	pakost sibírsky
Slovenian	sibirska krvomočnica
Swedish	ryssnäva
Ukrainian	Журавець сибірський
Chinese	鼠掌老鹳草
Chinese	鼠掌老鸛草
Chinese	猫脚印
Chinese	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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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 click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Magadan
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Baltic States
  - Central European Russia
  - East European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Norway
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
- Southwestern Europe
  - France

Northern America click to expand
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - New Jersey
  - New York
  - Pennsylvania
- Southeastern U.S.A.
  - Maryland
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000701339
Canadensys	29188
USDA Plants	GESI2
Tropicos	13900021
INPN	100153
Flora of Italy	2823
KEW	urn:lsid:ipni.org:names:322496-2
The Plant List	kew-2824058
Plantarium	17521
Open Tree Of Life	387600
Observations.org	144694
NCBI Taxonomy	345237
NBN Atlas	NBNSYS0200002236
Nature Serve	2.132026
IPNI	322496-2
iNaturalist	163265
GBIF	2891583
Freebase	/m/0nbd3zs
WisFlora	3701
EPPO	GERSI
EOL	346282
Elurikkus	4898
USDA GRIN	448
Wikipedia	Geranium_sibiricum
CMAUP	NPO433
PFAF	Geranium sibiricum

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

Plasmopara echinaceae, a new species of downy mildew affecting cone flowers (Echinacea purpurea) in the United States

Salgado-Salazar C, Romberg MK, Hudelson B

Fungal Syst Evol

22-Sep-2023

PMCID:	PMC10962218
doi:	10.3114/fuse.2023.12.10
PMID:	38529086

Potential Natural Products Regulation of Molecular Signaling Pathway in Dermal Papilla Stem Cells

Soe ZC, Ei ZZ, Visuttijai K, Chanvorachote P

Molecules

19-Jul-2023

PMCID:	PMC10384366
doi:	10.3390/molecules28145517
PMID:	37513389

Schizochytrium sp. Extracted Lipids Prevent Alopecia by Enhancing Antioxidation and Inhibiting Ferroptosis of Dermal Papilla Cells

Zeng Z, Wang B, Ibrar M, Ying M, Li S, Yang X

Antioxidants (Basel)

23-Jun-2023

PMCID:	PMC10375984
doi:	10.3390/antiox12071332
PMID:	37507872

Mechanistic synergy of hair growth promotion by the Avicennia marina extract and its active constituent (avicequinone C) in dermal papilla cells isolated from androgenic alopecia patients

Prugsakij W, Numsawat S, Netchareonsirisuk P, Tengamnuay P, De-Eknamkul W

PLoS One

21-Apr-2023

PMCID:	PMC10121027
doi:	10.1371/journal.pone.0284853
PMID:	37083946

Vertical Columns with Sustainable Green Cover: Meadow Plants in Urban Design

Stakelienė V, Pašakinskienė I, Ložienė K, Ryliškis D, Skridaila A

Plants (Basel)

01-Feb-2023

PMCID:	PMC9921580
doi:	10.3390/plants12030636
PMID:	36771721

Hair-Growth-Promoting Effects of the Fish Collagen Peptide in Human Dermal Papilla Cells and C57BL/6 Mice Modulating Wnt/β-Catenin and BMP Signaling Pathways

Hwang SB, Park HJ, Lee BH

Int J Mol Sci

07-Oct-2022

PMCID:	PMC9569759
doi:	10.3390/ijms231911904
PMID:	36233206

Modulation of Hair Growth Promoting Effect by Natural Products

Park S, Lee J

Pharmaceutics

15-Dec-2021

PMCID:	PMC8706577
doi:	10.3390/pharmaceutics13122163
PMID:	34959442

Pollinator individual‐based networks reveal the specialized plant–pollinator mutualism in two biodiverse communities

Wang L, Yang Y, Duan Y

Ecol Evol

25-Nov-2021

PMCID:	PMC8668776
doi:	10.1002/ece3.8384
PMID:	34938525

Use of medicinal plants for COVID-19 prevention and respiratory symptom treatment during the pandemic in Cusco, Peru: A cross-sectional survey

Villena-Tejada M, Vera-Ferchau I, Cardona-Rivero A, Zamalloa-Cornejo R, Quispe-Florez M, Frisancho-Triveño Z, Abarca-Meléndez RC, Alvarez-Sucari SG, Mejia CR, Yañez JA

PLoS One

22-Sep-2021

PMCID:	PMC8457479
doi:	10.1371/journal.pone.0257165
PMID:	34550994

Growth Suppression of a Gingivitis and Skin Pathogen Cutibacterium (Propionibacterium) acnes by Medicinal Plant Extracts

Choi HA, Ahn SO, Lim HD, Kim GJ

Antibiotics (Basel)

09-Sep-2021

PMCID:	PMC8465884
doi:	10.3390/antibiotics10091092
PMID:	34572674

LC-ESI-QTOF-MS/MS Analysis, Cytotoxic, Antiviral, Antioxidant, and Enzyme Inhibitory Properties of Four Extracts of Geranium pyrenaicum Burm. f.: A Good Gift from the Natural Treasure

Świątek Ł, Sieniawska E, Sinan KI, Maciejewska-Turska M, Boguszewska A, Polz-Dacewicz M, Senkardes I, Guler GO, Bibi Sadeer N, Mahomoodally MF, Zengin G

Int J Mol Sci

16-Jul-2021

PMCID:	PMC8307321
doi:	10.3390/ijms22147621
PMID:	34299238

Current Status of Mining, Modification, and Application of Cellulases in Bioactive Substance Extraction

Hu Y, Kang G, Wang L, Gao M, Wang P, Yang D, Huang H

Curr Issues Mol Biol

13-Jul-2021

PMCID:	PMC8929041
doi:	10.3390/cimb43020050
PMID:	34287263

The sequencing and characterization of chloroplast genome of Geranium sibiricum Linne

Huizhen S, Xue X

Mitochondrial DNA B Resour

06-Jul-2021

PMCID:	PMC8266239
doi:	10.1080/23802359.2021.1947912
PMID:	34286090

Therapeutic Potentials of Antiviral Plants Used in Traditional African Medicine With COVID-19 in Focus: A Nigerian Perspective

Attah AF, Fagbemi AA, Olubiyi O, Dada-Adegbola H, Oluwadotun A, Elujoba A, Babalola CP

Front Pharmacol

26-Apr-2021

PMCID:	PMC8108136
doi:	10.3389/fphar.2021.596855
PMID:	33981214

Ecological restoration of habitats invaded by Leucanthemum vulgare that alters key ecosystem functions

Khan MA, Hussain K, Shah MA

PLoS One

26-Mar-2021

PMCID:	PMC7996977
doi:	10.1371/journal.pone.0246665
PMID:	33770078

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
> Alkaloids and derivatives
Trigonelline	5570	Click to see	137.14	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1021/JF904593N
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
all-trans-Neoxanthin	5281247	Click to see	600.90	unknown	via CMAUP database
Lutein A	5281243	Click to see	568.90	unknown	via CMAUP database
Violaxanthin	448438	Click to see	600.90	unknown	via CMAUP database
Zeaxanthin	5280899	Click to see	568.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4R,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-ol	99565183	Click to see	414.60	unknown	via CMAUP database
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Gitogenin	441887	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1	432.60	unknown	via CMAUP database
Tigogenin	99516	Click to see	416.60	unknown	via CMAUP database
Yamogenin	441900	Click to see	414.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101400564	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	903.10	unknown	via CMAUP database
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Trigonelloside C	441899	Click to see	1049.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
(2R)-2-azaniumyl-3-(1H-imidazol-4-yl)propanoate	6971048	Click to see	155.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
(2R,3S,4R)-2-azaniumyl-4-hydroxy-3-methylpentanoate	26082623	Click to see CC(C(C)O)C(C(=O)[O-])[NH3+]	147.17	unknown	via CMAUP database
(2S,3S,4R)-2-Amino-3-methyl-4-hydroxyvaleric acid	11194416	Click to see	147.17	unknown	via CMAUP database
(4R)-4-hydroxy-L-isoleucine	6993179	Click to see CC(C(C)O)C(C(=O)[O-])[NH3+]	147.17	unknown	via CMAUP database
2-ammonio-2,3,5-trideoxy-3-methyl-L-ribonate	40561613	Click to see CC(C(C)O)C(C(=O)[O-])[NH3+]	147.17	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / N-organohydroxylamines
Trigoxazonane	23727687	Click to see	189.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
Thiamine	1130	Click to see	265.36	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
5,11-dimethyl-6H-pyrido[4,3-b]carbazol-2-ium	5288156	Click to see CC1=C2C=C[NH+]=CC2=C(C3=C1NC4=CC=CC=C43)C	247.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyranopyridines
Gentianine	354616	Click to see C=CC1=CN=CC2=C1CCOC2=O	175.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Trigoforin	12267346	Click to see CC1=CC2=C(C=C1)C(=C(C(=O)O2)C)C	188.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin	439246	Click to see	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin-2''-O-p-trans-coumarate	102004864	Click to see	594.50	unknown	via CMAUP database
Vicenin 1	13644663	Click to see	564.50	unknown	via CMAUP database
Vitexin	5280441	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Panasenoside	9986191	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate	101158756	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O)O	814.70	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12960455	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O	788.70	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12960461	Click to see	772.70	unknown	via CMAUP database
7-O-Glucosylvitexin	101406316	Click to see	594.50	unknown	via CMAUP database
Tricin 7-glucoside	5322022	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	492.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6,7-Methylenedioxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	21270126	Click to see	282.25	unknown	via CMAUP database
Daidzein	5281708	Click to see	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3',5,7-Trihydroxy-5'-methoxyisoflavone	91203449	Click to see COC1=CC(=CC(=C1)O)C2=COC3=CC(=CC(=C3C2=O)O)O	300.26	unknown	via CMAUP database
3',5'-Dimethoxy-4',5,7-trihydroxyisoflavone	15689643	Click to see	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin	5280448	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see	284.26	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Carpaine	442630	Click to see	478.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,13,14,15,18,19,20,34,35,39,39-Undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl) 3,4,5-trihydroxybenzoate	115063	Click to see	952.60	unknown	https://doi.org/10.1021/JF904593N
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/JF904593N
Corilagin (Standard)	5089683	Click to see	634.50	unknown	https://doi.org/10.1021/JF904593N
Ellagic Acid	5281855	Click to see	302.19	unknown	via CMAUP database
Geraniin	3001497	Click to see	952.60	unknown	https://doi.org/10.1021/JF904593N
Schisandrin	3001664	Click to see	432.50	unknown	via CMAUP database

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Geranium sibiricum

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