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 the northern Himalayas, eastern China, Taiwan, Korea and Japan, Saxifraga stolonifera is recognized mainly as a mild, leaf‑based drink. In the Chugoku Mountains and other parts of western Japan, the tender leaves are picked fresh, briefly blanched, then steeped to make a sweet‑herbaceous tea served hot or iced (Miyako botanical garden records; Tanaka, Ethnobotany of Japan, 1988). Taiwan’s Institute of Chinese Medicine lists the leaves for sore‑throat and cough relief and reports decoctions of leaves or stolons used to wash bruises, cuts and inflamed skin, while noting seasonal salad use of the tender shoots (Yuan et al., Taiwan Materia Medica, 2015; National Chinese Medicine Database, Taiwan, 2017). In classical Chinese herbal practice, the plant is recorded for topical wash and compress, and the whole plant is decocted with other herbs for diarrhea and dysentery (Li Shizhen, Compendium of Materia Medica, 1596; Glossary of Medicinal Plants, 1977).

Practical recipe: cold‑infusion of leaves. Rinse 10–15 g of fresh young leaves, combine with 500–600 mL of boiled water, and let the liquid cool to warm before steeping 30–45 minutes. Strain and sip 200–300 mL per day for cough or sore throat. Keep infusions light and avoid daily high doses over several weeks. Pregnant people and those on anticoagulants should avoid concentrated preparations and consult a clinician.

Active constituents reported for this species include quercetin‑3‑O‑β‑D‑glucoside, kaempferol‑3‑O‑β‑D‑glucoside, bergenin and astilbin, which provide antioxidant and anti‑inflammatory activity that plausibly underlie the traditional topical anti‑bruise, sore‑throat and cough‑soothing uses (Phytochemistry and pharmacology of Saxifraga, J Ethnopharmacol, 2013; reference cited therein). These catechins and flavonoids are present across Saxifraga species and have been quantified in Saxifraga stolonifera as well.

The plant remains widely available in China, Taiwan and Japan as an ornamental and in health‑food shops; recent research is revisiting its anti‑inflammatory and gastro‑protective constituents, with several commercial extracts offered in dietary‑supplement channels and traditional stores.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Ligularia sarmentosa	(L.f.) Duval	Pl. Succ. Hort. Alenc. 11 (1809).
Rupifraga cuscutiformis	(Lodd.) Raf.	Fl. Tellur. 4: 121 (1838)
Rupifraga sarmentosa	' Linn.' ex Raf.	Fl. Tellur. 2: 68 (1837)
Robertsonia sarmentosa	Link	Handbuch 2: 40 (1831)
Sekika sarmentosa	Moench	Suppl. Meth. : 77 (1802)
Sekika stolonifera	Hara	Nov. Fl. Jap. 3: 47 (1939)
Saxifraga cuscutiformis	G.Lodd.	Bot. Cab. 2: t. 186 (1818)
Saxifraga sarmentosa	L.f.	Dionaea muscip. , ed. 2: 16 (1780)
Adenogyna sarmentosa	Raf.	New Fl. 1: 63 (1836)
Aphomonix hederacea	Raf.	Fl. Tellur. 2: 65 (1837)
Diptera cuscutiformis	Heynh.	Alph. Aufz. Gew. : 206 (1846)
Diptera sarmentosa	Borkh.	Neues Mag. Bot. 1: 29 (1794)
Saxifraga chinensis	Lour.	Fl. Cochinch. : 281 (1790)
Saxifraga sarmentosa var. immaculata	Diels	Bot. Jahrb. Syst. 29(3–4): 364–365 1901
Saxifraga chaffanjonii	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 452 (1911)
Saxifraga dumetorum	Balf.f.	Trans. Bot. Soc. Edinburgh 27: 71 (1916)
Saxifraga veitchiana	Balf.f.	Trans. Bot. Soc. Edinburgh 27: 75 (1916)
Saxifraga iochanensis	H.Lév.	Sert. Yunnan. : 2 (1916)
Saxifraga ligulata	Murray	Commentat. Soc. Regiae Sci. Gott. 1781: 26 (1781)
Saxifraga stolonifera var. immaculata	(Diels) Hand.-Mazz.	Symb. Sin. 7(2): 427 1931
Saxifraga fortunei var. tricolor	Lem.
Saxifraga sarmentosa var. tricolor	(Lem.) Maxim.
Sekika cyclaminea	Medik.	in Staatsw. Vorles. Churpf. Phys.-Oek. Ges. i. (1791) 209; Phil. Bot. ii. 49(1791).
Saxifraga sarmentosa var. tricolor-superba	Van Geert	Nursery Cat. (Auguste Van Geert) 76: 25 (1878)
Saxifraga stolonifera f. viridifolia	(Makino) H.Hara	Nov. Fl. Jap. 3: 49 (1939)
Saxifraga stolonifera f. leuconeura	(Makino) H.Hara	Nov. Fl. Jap. 3: 49 (1939)
Saxifraga stolonifera f. aptera	(Makino) H.Hara	Nov. Fl. Jap. 3: 49 (1939)
Saxifraga sarmentosa var. aptera	Makino	J. Jap. Bot. 3(11): 43 (1926)
Saxifraga sarmentosa var. leuconeura	Makino	J. Jap. Bot. 4(6): 12 (1927)
Saxifraga sarmentosa var. viridifolia	Makino	J. Jap. Bot. 4(6): 14 (1927)

Common names Top

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Filter by language:

Language	Common/alternative name
English	creeping saxifrage
English	trailing saxifrage
Spanish	s. stolonifera
Arabic	كاسر الحجر السرعي
Bulgarian	Див анасон
Bulgarian	бедреница
Bulgarian	Каменоломков анасон
Bulgarian	Горски анасон
Czech	lomikámen výběžkatý
Welsh	tormaen ymgripiol
German	kriech-steinbrech
German	judenbart
Persian	سفرس خزنده
Finnish	aaronin parta
Finnish	aaroninparta
French	saxifrage stolonifère
French	saxifrage sarmenteux
Upper Sorbian	plećawy rupik
Indonesian	kuping macan
Japanese	雪の下
Japanese	ユキノシタ
Japanese	コジソウ
Japanese	虎耳草
Japanese	雪の舌
Korean	바위취
Korean	바위취꽃
Norwegian Bokmål	ynglesildre
Norwegian Bokmål	mor med tusen barn
Polish	skalnica rozłogowa
Slovak	lomikameň poplazivý
Swedish	arons skägg
Swedish	aronsskägg
Chinese	小虎耳草
Chinese	丝棉吊梅
Chinese	虎耳草
Chinese	金线吊芙蓉
Chinese	金丝荷叶
Chinese	通耳草
Chinese	耳朵草
Chinese	老虎耳
Chinese	石荷叶
Chinese	天青地红
Chinese	天荷叶

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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Germination/Propagation Top

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

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

keep all seed pots x 2 years

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands
  - Madeira

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
- Indo-China
  - Myanmar
  - Vietnam

Europe click to expand
- Middle Europe
  - Switzerland
- Southeastern Europe
  - Bulgaria
  - Italy

Southern America click to expand
- Western South America
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000494724
UNII	Z3QBC3PY05
USDA Plants	SAST6
Tropicos	50043013
Flora of Italy	8606
KEW	urn:lsid:ipni.org:names:794584-1
The Plant List	kew-2584890
Missouri Botanical Garden	286950
PFAF	Saxifraga stolonifera
Open Tree Of Life	816926
Observations.org	145980
NCBI Taxonomy	182070
NBN Atlas	NBNSYS0000033921
Nature Serve	2.128079
IPNI	794584-1
iNaturalist	68217
GBIF	3032762
Freebase	/m/02rl2gv
EPPO	SXFSA
EOL	485057
Calflora (Californian flora)	7371
USDA GRIN	423527
Wikipedia	Saxifraga_stolonifera
CMAUP	NPO19728

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

Natural-derived acetophenones: chemistry and pharmacological activities

Ahmadpourmir H, Attar H, Asili J, Soheili V, Taghizadeh SF, Shakeri A

Nat Prod Bioprospect

10-May-2024

PMCID:	PMC11087454
doi:	10.1007/s13659-024-00447-x
PMID:	38727781

Taxonomic resurrection of Saxifraga lancangensis (Saxifragaceae)

Zhang XJ, Jiang KZ, Kuai XY, Chen JT, Luo PR, Sun H, Deng T

Bot Stud

29-Apr-2024

PMCID:	PMC11056349
doi:	10.1186/s40529-024-00418-y
PMID:	38679692

Unravelling and reconstructing the biosynthetic pathway of bergenin

Yan R, Xie B, Xie K, Liu Q, Sui S, Wang S, Chen D, Liu J, Chen R, Dai J, Yang L

Nat Commun

26-Apr-2024

PMCID:	PMC11053098
doi:	10.1038/s41467-024-47502-2
PMID:	38670975

Exploring nature’s antidote: unveiling the inhibitory potential of selected medicinal plants from Kisumu, Kenya against venom from some snakes of medical significance in sub-Saharan Africa

Okumu M, Mbaria J, Gikunju J, Mbuthia P, Madadi V, Ochola F

Front Pharmacol

12-Apr-2024

PMCID:	PMC11045943
doi:	10.3389/fphar.2024.1369768
PMID:	38681195

A Chinese herbal formula Kesuting Syrup against COVID‐19: Leveraging multidimensional computations in network pharmacology‐driven experimental and clinical trials

Zhang C, Sun T, Lv Y, Li X, Ling Y, Wang N, Xia W, Fan X, Feng Y

Clin Transl Med

15-Feb-2024

PMCID:	PMC10867594
doi:	10.1002/ctm2.1569
PMID:	38356432

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Characterization of the complete chloroplast genome sequence of Limnophila sessiliflora Blume 1826 (Plantaginaceae)

Dong H, Huang R, Wang S, Yu J

Mitochondrial DNA B Resour

18-May-2023

PMCID:	PMC10197986
doi:	10.1080/23802359.2023.2209390
PMID:	37213788

Rapid Virucidal Activity of Japanese Saxifraga Species-Derived Condensed Tannins against SARS-CoV-2, Influenza A Virus, and Human Norovirus Surrogate Viruses

Murata T, Jamsransuren D, Matsuda S, Ogawa H, Takeda Y

Appl Environ Microbiol

15-May-2023

PMCID:	PMC10304655
doi:	10.1128/aem.00237-23
PMID:	37184410

A re‐examination of the circumscription of Saxifraga mengtzeana (Saxifragaceae)

Zhang X, Gornall RJ, Zhang Z, Chen J, Sun H, Deng T

Ecol Evol

12-Mar-2023

PMCID:	PMC10008273
doi:	10.1002/ece3.9886
PMID:	36919019

Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule

Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH

Biomolecules

21-Feb-2023

PMCID:	PMC10046151
doi:	10.3390/biom13030403
PMID:	36979338

Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent

Nahar L, Al-Groshi A, Kumar A, Sarker SD

Molecules

11-Dec-2022

PMCID:	PMC9787540
doi:	10.3390/molecules27248786
PMID:	36557918

Belowground seed and bud banks play complementary roles in the potential recruitment of dominant macrophyte communities in a Yangtze River-connected floodplain wetland

Chen XS, Huang Y, Cai YH, Hou ZY, Deng ZM, Li F, Zou YA, Xie YH

Front Plant Sci

06-Dec-2022

PMCID:	PMC9763321
doi:	10.3389/fpls.2022.1075496
PMID:	36561449

Post-infectious cough of different syndromes treated by traditional Chinese medicines: A review

Jiang W, Qi J, Li X, Chen G, Zhou D, Xiao W, Li N

Chin Herb Med

28-Sep-2022

PMCID:	PMC9669398
doi:	10.1016/j.chmed.2022.09.002
PMID:	36405059

Lotus germ extract rejuvenates aging fibroblasts via restoration of disrupted proteostasis by the induction of autophagy

Machihara K, Kageyama S, Oki S, Makino H, Sasaki M, Iwahashi H, Namba T

Aging (Albany NY)

26-Sep-2022

PMCID:	PMC9596218
doi:	10.18632/aging.204303
PMID:	36170016

Traditional chinese medicine to prevent and treat diabetic erectile dysfunction

Feng Y, Shi T, Fu Y, Lv B

Front Pharmacol

21-Sep-2022

PMCID:	PMC9532934
doi:	10.3389/fphar.2022.956173
PMID:	36210810

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
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1021/NP0500272
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aS,10bS)-3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	158227268	Click to see	314.24	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
(2R,3S,4S,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	24982180	Click to see	328.27	unknown	via CMAUP database
3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	14430151	Click to see	314.24	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Bergenin	66065	Click to see	328.27	unknown	https://doi.org/10.3136/NSKKK.42.1027 https://doi.org/10.1021/NP0500272 https://doi.org/10.1016/J.BMC.2007.10.072
Norbergenin	73192	Click to see	314.24	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> 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/NP0500272 https://doi.org/10.1016/J.BMC.2007.10.072
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Benzenoids / Naphthalenes
Fluoranthene	9154	Click to see C1=CC=C2C(=C1)C3=CC=CC4=C3C2=CC=C4	202.25	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Phenanthrene	995	Click to see C1=CC=C2C(=C1)C=CC3=CC=CC=C32	178.23	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone	785	Click to see	110.11	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives / 5-unsubstituted pyrrogallols
Pyrogallol	1057	Click to see	126.11	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see	108.14	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see	436.80	unknown	https://doi.org/10.1016/J.BMC.2007.10.072
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1016/J.BMC.2007.10.072
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl octanoate	7799	Click to see	172.26	unknown	via CMAUP database
Ethyl Oleate	5363269	Click to see	310.50	unknown	via CMAUP database
Ethyl palmitate	12366	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
Isovaleric Acid	10430	Click to see	102.13	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Mesaconic acid	638129	Click to see CC(=CC(=O)O)C(=O)O	130.10	unknown	https://doi.org/10.1021/NP0500272
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Pentadecanoic Acid	13849	Click to see	242.40	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Octanoic Acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
trans-9-cis-12-Octadecadienoic acid	5282798	Click to see	280.40	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(3R,7R,11R)-3,7,11,15-tetramethylhexadec-1-en-3-ol	42433479	Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)(C=C)O	296.50	unknown	via CMAUP database
(6R,10R)-2,6,10,14-tetramethylpentadecane	76967667	Click to see	268.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (R)-	101977	Click to see	156.26	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Citronellol	8842	Click to see	156.26	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85064-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(7r,11r)-3-Methylene-7,11,15-trimethyl-1-hexadecene	92852046	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C	278.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6Z,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene	11975273	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
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/J.BMC.2007.10.072
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/J.BMC.2007.10.072
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380	21952380	Click to see	118.09	unknown	via CMAUP database
Succinic Acid	1110	Click to see	118.09	unknown	https://doi.org/10.1021/NP0500272
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid	7067335	Click to see	354.31	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	https://doi.org/10.3136/NSKKK.42.1027
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	7576924	Click to see	272.25	unknown	via CMAUP database
(2S,3S,4R,5S,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	40467854	Click to see	272.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone	7469	Click to see	136.15	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B2	5320711	Click to see	578.50	unknown	https://doi.org/10.1021/NP50040A016
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/10.1021/NP50040A016
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
> 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/10.5511/PLANTBIOTECHNOLOGY.16.129
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.3136/NSKKK.42.1027 https://doi.org/10.1016/J.BMC.2007.10.072
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154497331	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1248/CPB.22.1487
Saxifragin	52946987	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]-	5274586	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1016/J.BMC.2007.10.072
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1016/J.BMC.2007.10.072 https://doi.org/10.1021/NP0500272

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Saxifraga stolonifera

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