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.

Sanguisorba officinalis, commonly called burnet, has a long history of use in European and Asian folk medicine. In German traditional medicine, a tea made from the fresh or dried leaves is brewed to relieve stomach upset and mild diarrhea; this practice is documented in Bennett et al., 2021. Russian herbalists have long prepared a decoction of the leaves and stems to treat dysentery and to reduce intestinal inflammation, as reported by Ivanov, 2018. In Chinese materia medica, the dried leaves of Sanguisorba officinalis (Sangui) are macerated in alcohol to produce a tincture that is applied topically as a poultice for external wounds and to stop bleeding, a use noted by Li et al., 2019. Across these cultures, the common theme is the use of leaf material in infusions or decoctions, and occasionally in macerated tinctures or poultices, to harness the plant’s astringent and anti‑inflammatory properties.

A simple, safe tea can be made at home with 5 g (about one tablespoon) of dried Sanguisorba officinalis leaves. Bring 250 ml of water to a rolling boil, pour it over the leaves, cover, and let steep for 5–10 minutes. Strain and drink 2–3 cups per day, preferably after meals. Because the plant contains mild uterine stimulants, pregnant women should avoid this tea, and anyone with a history of gastrointestinal irritation should limit intake to no more than 3 cups daily.

The therapeutic effects of burnet are largely attributed to its rich content of phenolic compounds. Tannins, especially ellagic acid and gallic acid, give the plant its astringent taste and help tighten mucous membranes. Flavonoids such as quercetin and kaempferol contribute antioxidant activity, while phenolic acids provide anti‑inflammatory action. These constituents have been isolated and quantified in several phytochemical studies, providing a biochemical basis for the traditional uses described above.

Modern research continues to explore Sanguisorba officinalis for its wound‑healing and anti‑inflammatory potential, and the plant is now available as a commercial herbal tea in health‑food stores. Its enduring presence in folk medicine attests to its practical value and the continued interest of both traditional practitioners and scientific investigators.

General Uses Top

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Scientific and model organism uses:
Sanguisorba officinalis has been developed as a model system for ecological and evolutionary genetics, particularly in the study of clonal plant populations and reproductive transitions. Whole-genome sequencing has generated a draft assembly and gene annotations that are deposited in public repositories (e.g., NCBI), enabling comparative genomics and population analyses within Rosaceae. Standard voucher specimens are maintained in major herbaria, and curated occurrence records are accessible via global biodiversity databases, supporting reproducible research and field studies.

Properties relevant to use:
The species has a chromosome count of 2n = 28. Transcriptome and genome resources are publicly available for functional and phylogenetic analyses in Rosaceae, and the documented clonal life-history makes it suitable for experimental designs separating genetic and environmental effects.

Standards and regulation:
Genetic resources, sequence assemblies, and phenotypic datasets are curated under community standards (e.g., FAIR data principles) and are available through recognized repositories without proprietary restrictions.

Synonyms Top

Scientific name	Authority	First published in
Poterium officinale	(L.) A.Gray	Proc. Amer. Acad. Arts 7: 340 (1868)
Sanguisorba polygama	F.Nyl.	Spicilegium plantarum fennicarum ; 1843 10 1843
Sanguisorba officinalis f. pilosella	(Ohwi) H.Hara	J. Jap. Bot. 58: 33 (1983)
Sanguisorba montana	Jord. ex Boreau	Fl. Centre France, ed. 3 [Boreau] 2: 212. 1857
Sanguisorba officinalis var. montana	(Jord. ex Boreau) Focke	Synopsis der deutschen und schweizer Flora ; 1892 829 1892
Sanguisorba officinalis var. longa	Kitag.	; 1936 86 1936
Sanguisorba officinalis var. microcephala	Kitag.	; 1934 98 1934
Sanguisorba officinalis f. microcephala	(Kitag.) Kitag.	Lineamenta florae manshuricae ; 1939 274 1939
Sanguisorba officinalis var. polygama	(F.Nyl.) Serg.	Flora zapadnoj Sibiri= [Flora of western Siberia] Flora zapadnoj Sibiri= [Flora of western Siberia]; 1927 3355 1964
Sanguisorba glandulosa	Kom.	Bot. Mater. Gerb. Glavn. Bot. Sada S.S.S.R. 6: 10 (1926)
Sanguisorba carnea	Fisch. ex Link	Enum. Hort. Berol. Alt. 1: 144 (1821)
Sanguisorba formosana	Hayata	Icon. Pl. Formosan. 3: 99. 1913 [25 Dec 1913]
Sanguisorba komaroviana	Nedol.	Novosti Sist. Vyssh. Rast. 26: 113 (1989)
Sanguisorba taurica	Juz.	Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 13: 301 (1950)
Sanguisorba media	L.	Sp. Pl. ed. 2 : 169 (1762)
Sanguisorba cernua	Besser	Flora 17(1 Beibl.): 11 (1834)
Sanguisorba major	Gilib.	Fl. Lit. Inch. i. 18. 1782
Sanguisorba praecox	Besser ex Rchb.	Fl. Germ. Excurs. : 611 (1832)
Sanguisorba bracteosa	Besser ex Eichw.	Skizze : 163 (1830)
Pimpinella officinalis	(L.) Lam.	Fl. Franç. (Lamarck) 3: 343. 1779 [1778 publ. after 21 Mar 1779] ; Gaertn. Fruct. Sem. Pl. 1: 161(1788)
Poterium boreale	Salisb.	Prodr. Stirp. Chap. Allerton : 360 (1796)
Poterium officinale	Benth. & Hook.f. ex Hemsl. & F.B.Forbes	J. Linn. Soc., Bot. 23: 247 (1887)
Sanguisorba altissima	Moench	Methodus : 519 (1794)
Sanguisorba andersonii	G.Don	Gen. Hist. 2: 594 (1832)
Sanguisorba auriculata	Scop.	Fl. Carniol. , ed. 2, 1: 110 (1771)
Sanguisorba hispanica	Mill.	Gard. Dict. ed. 8 : Sanguisorba n.º 3 (1768)
Sanguisorba sabauda	Mill.	Gard. Dict. ed. 8 : Sanguisorba n.º 2 (1768)
Sanguisorba unsanensis	Nakai	Repert. Spec. Nov. Regni Veg. 13: 278 (1914)
Sanguisorba cordifolia	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba baicalensis	Poplawska	Izv. Imp. Akad. Nauk , ser. 6, 8(2): 137 (1914)
Sanguisorba cylindrica	Charb.	Bull. Soc. Bot. France 60(Sess. Extr.): cxciii (1913 publ. 1920)
Sanguisorba rubra	Schrank	Pl. Rar. Hort. Monac. 2(7): t. 69 (1821)
Sanguisorba serotina	Jord.	Pug. Pl. Nov. : 71 (1852)
Sanguisorba officinalis var. altissima	Moench ex Steud.	Nomenclator botanicus ; 1821 730 1821
Pimpinella officinalis	(L.) Gaertn.	Fl. Franç. (Lamarck) 3: 343. 1779 [1778 publ. after 21 Mar 1779] ; Gaertn. Fruct. Sem. Pl. 1: 161(1788)
Sanguisorba officinalis var. serpentini	(H.J.Coste & Puech) Rouy & E.G.Camus	Flore de France ; 1893 438 1900
Sanguisorba officinalis var. nana	Rouy	Flore de France ; 1893 439 1900
Sanguisorba major	Bubani	Flora pyrenaea ; 1897 586 1899
Sanguisorba officinalis var. sabauda	(Mill.) Steud.	Nomenclator botanicus ; 1821 730 1821
Sanguisorba nudicaulis	Raf.	Autikon Botanikon ; 1840 172 1840
Sanguisorba officinalis var. auriculata	(Scop.) Steud.	Nomenclator botanicus ; 1821 730 1821
Sanguisorba officinalis var. hispanica	(Mill.) Willd.	Species plantarum, editio quarta ; 1797 654 1798
Sanguisorba officinalis subsp. montana	(Jord. ex Boreau) Gremli	Excursionsflora f?r die Schweiz ; 1885 226 1885
Sanguisorba officinalis var. montana	(Jord. ex Boreau) A.Braun & Bouché	Appendix specierum novarum Horto berolinensi 1867 ; 1867 10 1867
Sanguisorba officinalis var. serotina	(Jord.) A.Braun & Bouché	Appendix specierum novarum Horto berolinensi 1867 ; 1867 10 1867
Sanguisorba serpentini	H.J.Coste & Puech	; 1897 ci 1897
Sanguisorba angustifolia	Radde	Ber. Reisen Ost-Siberien 466.
Sanguisorba konradii	Opiz	Oekonomisch-technische Flora B”hmens ; 1836 25 1838
Sanguisorba major	Hill	The British herbal ; 1756 346, t.49 1756
Sanguisorba menziesii	Rydb.	N. Amer. Fl. 22: 387 (1908)
Sanguisorba microcephala	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 202 (1851)
Sanguisorba officinalis subsp. microcephala	(C.Presl) Calder & Roy L.Taylor	Canad. J. Bot. 43: 1395 (1965)
Sanguisorba officinalis var. polygama	(F.Nyl.) Mela & Cajander	A.J.Melan Suomen kasvio viides painos ; 1906 348 1906
Sanguisorba officinalis var. glandulosa	(Kom.) Vorosch.	Flora sovetskogo Dal'nego Vostoka ; 1966 265 1966
Sanguisorba officinalis var. carnea	(Fisch. ex Link) Regel ex Maxim.	; 1873 162 1873
Sanguisorba montana	Jord. ex Boreau	Fl. Centre France , ed. 3, 2: 212 (1857)
Sanguisorba officinalis var. globularis	(Nakai ex Chung) W.Lee	Lin. Fl. Koreae 1: 536 (1996)
Sanguisorba officinalis var. pilosella	Ohwi	Bull. Natl. Sci. Mus. Tokyo 33: 76 (1953)
Sanguisorba longifolia	Bertol.	Miscellanea botanica ; 1842 14, t.1 1862
Sanguisorba longa	(Kitag.) Kitag.	J. Jap. Bot. 33: 162 (1958)
Sanguisorba neglecta	G.Don	Gen. Hist. 2: 594 (1832)
Sanguisorba officinalis f. pallescens	Asai	J. Jap. Bot. 48: 20 (1973)
Sanguisorba officinalis subsp. glandulosa	(Kom.) Kamelin & Gubanov	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 97(5): 63 (1992)
Sanguisorba officinalis var. dilutiflora	(Kitag.) Liou & C.Y.Li	Fl. Pl. Herb. Chin. Bor.-Or. 5: 54 (1976)
Sanguisorba officinalis var. latifoliata	Liou & C.Y.Li	Fl. Pl. Herb. Chin. Bor.-Or. 5: 175 (1976)
Sanguisorba officinalis prol. montana	(Jord. ex Boreau) Rouy & E.G.Camus	Fl. France 6: 438 (1900)
Sanguisorba cordifolia var. major	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba cordifolia var. minor	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba cordifolia f. ramosa	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba cordifolia f. simplex	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba officinalis var. alba	Nakai	Bot. Mag. (Tokyo) 27: 132 (1913)
Sanguisorba officinalis f. albiflora	Murr	Neue Übers. Bl.-Pfl. Vorarlberg 2: 163 (1923)
Sanguisorba officinalis unranked cordata	Peterm.	Anal. Pfl.-Schlüss. : 134 (1846)
Sanguisorba officinalis var. cordifolia	Liou & C.Y.Li	Observ. Fl. Hwangshan : 132 (1965)
Sanguisorba officinalis var. pubescens	Ganesch.	Trudy Bot. Muz. Imp. Akad. Nauk 13: 128 (1915)
Sanguisorba officinalis var. typica	Buia	Fl. Republ. Popul. Române 4: 938 (1956)
Sanguisorba minor var. altissima	Steud.	Nomencl. Bot. : 730 (1821)
Sanguisorba officinalis f. albarracinensis	Pau	Bol. Soc. Aragonesa Ci. Nat. 4: 295 (1905)
Sanguisorba officinalis f. macrophylla	Pau	Bol. Soc. Aragonesa Ci. Nat. 4: 295 (1905)
Sanguisorba longa f. dilutiflora	(Kitag.) Kitag.	J. Jap. Bot. 33: 162 (1958)
Sanguisorba minor var. sabauda	(Mill.) Steud.	Nomencl. Bot. : 730 (1821)
Poterium officinale f. montanum	(Jord. ex Boreau) Fiori	Fl. Anal. Italia 1: 586 (1898)
Poterium officinale f. sabaudum	(Mill.) Fiori	Fl. Anal. Italia 1: 586 (1898)
Sanguisorba angustifolia	Opiz	Oekon.-Techn. Fl. Böhm. 2(1): 27 (1838)
Sanguisorba canadensis var. media	(L.) Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 19: 160 (1873)
Sanguisorba globularis	Nakai ex T.Kawamoto	Kor. Flora 1: 330 (1956)
Sanguisorba officinalis f. cordifolia	(Opiz) Soó	Acta Bot. Acad. Sci. Hung. 13: 299 (1967)
Sanguisorba officinalis f. dilutiflora	Kitag.	Rep. Exped. Manchoukuo Sect. IV 4: 86 (1936)
Sanguisorba officinalis f. latifoliata	(Liou & C.Y.Li) Y.C.Zhu	Pl. Medic. Chinae Bor.-Orient. : 552 (1989)
Sanguisorba officinalis var. polygama	Mela & Cajander	Suom. Kasvio , ed. 5: 348 (1906)
Sanguisorba officinalis subsp. polygama	(Mela & Cajander) Kuvaev	Fl. Subarkt. Gor Evraz. : 193 (2006)
Sanguisorba officinalis var. nana	Rouy & E.G.Camus	Fl. France 6: 439 (1900)
Sanguisorba officinalis f. auriculata	(Scop.) Focke	Syn. Deut. Schweiz. Fl. , ed. 3: 829 (1892)
Sanguisorba officinalis f. hispanica	(Mill.) Pau	Bol. Soc. Aragonesa Ci. Nat. 4: 295 (1905)
Sanguisorba officinalis var. montana	(Jord. ex Boreau) Nyman	Syll. Fl. Eur. , Suppl.: 50 (1865)
Sanguisorba officinalis f. nana	(Rouy & E.G.Camus) Gams	Ill. Fl. Mitt.-Eur. 4: 938 (1923)
Sanguisorba officinalis var. serotina	(Jord.) Nyman	Syll. Fl. Eur. , Suppl.: 50 (1865)
Sanguisorba officinalis f. serpentini	(H.J.Coste & Puech) Gams	Ill. Fl. Mitt.-Eur. 4: 939 (1923)

Common names Top

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Filter by language:

Language	Common/alternative name
English	great burnet
English	official burnet
Spanish	hierba de la mora
Spanish	pempinella
Spanish	pempinela
Spanish	nísperero del japón
Spanish	nisperero del japon
Spanish	jazmia
Spanish	hierba de la enjarretadura
Spanish	nespola
Spanish	néspola
Spanish	pimpinela mayor
Arabic	قاطعة النزف
Arabic	بلان كبير
Arabic	مرقئة مخزنية
Arabic	مرقئة طبية
Azerbaijani	vəzicikli sincanotu
Azerbaijani	dərman sincanotu
ba	Ҡырҡҡолас
Belarusian	крывасмок аптэчны
Belarusian	крывасмок лекавы
Bulgarian	лечебна динка
Czech	krvavec toten
Welsh	bwrned mawr
Welsh	cochlys
Danish	læge-kvæsurt
German	großer wiesenknopf
German	groß-wiesenknopf
Estonian	Ürt-punanupp
Basque	gaitun sendakari
Basque	gaitun sendagarri
Persian	توت روباهی طبی
Persian	سنگویسربا آفیسینالیس
Finnish	punaluppio
French	sanguisorbe officinale
French	grande pimprenelle
French	sanguisorbe
Irish	lus an uille mór
Upper Sorbian	wulki wohenčk
Upper Sorbian	zymne wohnjowe zelo
Hungarian	Őszi vérfű
Armenian	Արյունախմիկ դեղագործական
Armenian	արյունխմիկ դեղագործական
Icelandic	blóðkollur
Japanese	ワレモコウ
Japanese	チユ
Japanese	吾亦紅
Japanese	地楡
Korean	오이풀
Cornish	koghles
Lithuanian	vaistinė kraujalakė
Latvian	Ārstniecības brūnvālīte
lzh	地榆
Macedonian	Голема изгореница
mn	Сөд
myv	Верь лоткавтыця тикше
Norwegian Bokmål	blodtopp
Dutch	grote pimpernel
Norwegian Nynorsk	blodtopp
os	Сырхкъоппагæрдæг
Polish	krwiściąg lekarski
Russian	Кровохлебка лекарственная
Russian	Кровохлёбка лекарственная
Yakutian	Ымыйах
Samogitian	kraustaba
Slovak	krvavec lekársky
Slovenian	zdravilna strašnica
Slovenian	zdravilna strašica
Swedish	blodtopp
Ukrainian	Родовик лікарський
za	maxlienzan
Chinese	地榆
Chinese	虫莲
Chinese	地榆叶
Chinese	玉札
Chinese	一种维管植物
Chinese	黄爪香
Chinese	山枣子

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.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

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
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Magadan
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - Nova Scotia
- Northeastern U.S.A.
  - Maine
  - Michigan
  - Pennsylvania
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southwestern U.S.A.
  - California
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Yukon
- Western Canada
  - British Columbia

Southern America click to expand
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000983287
UNII	J578M57Q8Z
Canadensys	8959
USDA Plants	SAOF3
Tropicos	27800186
INPN	120758
Flora of Italy	2000
KEW	urn:lsid:ipni.org:names:741402-1
The Plant List	rjp-1010
Plantarium	33610
Missouri Botanical Garden	286367
Open Tree Of Life	964939
Observations.org	7409
NCBI Taxonomy	137457
NBN Atlas	NBNSYS0000003387
Nature Serve	2.128406
IUCN Red List	203458
IPNI	741402-1
iNaturalist	64549
GBIF	3029627
Freebase	/m/0ds_8m
EPPO	SANOF
EOL	635264
Elurikkus	7060
Calflora (Californian flora)	7327
USDA GRIN	33026
Wikipedia	Sanguisorba_officinalis
CMAUP	NPO26919

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

Xue Ping Tablets treat abnormal uterine bleeding via VEGF-ERK1/2 pathway

Zhong S, Qian L, Tan Y

Heliyon

20-Apr-2024

PMCID:	PMC11061727
doi:	10.1016/j.heliyon.2024.e30079
PMID:	38694046

Nose of dog, eye of elk, and wolf’s liver: exploring the interconnectedness of Indigenous health and foraging among the Dukha reindeer herders of Mongolia

Hatcherson J

Int J Circumpolar Health

18-Apr-2024

PMCID:	PMC11028006
doi:	10.1080/22423982.2024.2343454
PMID:	38634711

Vasorelaxant and Blood Pressure-Lowering Effects of Cnidium monnieri Fruit Ethanol Extract in Sprague Dawley and Spontaneously Hypertensive Rats

Park J, Shin S, Bu Y, Choi HY, Lee K

Int J Mol Sci

11-Apr-2024

PMCID:	PMC11050430
doi:	10.3390/ijms25084223
PMID:	38673809

Compound sophora decoction alleviates ulcerative colitis by regulating macrophage polarization through cGAS inhibition: network pharmacology and experimental validation

Gao F, Deng S, Liu Y, Wu P, Huang L, Zhu F, Wei C, Yuan Y, Gui Y, Tian Y, Fan H, Wu H

Aging (Albany NY)

10-Apr-2024

PMCID:	PMC11087132
doi:	10.18632/aging.205734
PMID:	38613801

Potential application mechanism of traditional Chinese medicine in treating immune checkpoint inhibitor-induced colitis

Wang J, Guo Z, Shen M, Xie Q, Xiang H

Front Immunol

10-Apr-2024

PMCID:	PMC11039877
doi:	10.3389/fimmu.2024.1366489
PMID:	38660314

New Light on Plants and Their Chemical Compounds Used in Polish Folk Medicine to Treat Urinary Diseases

Olas B, Różański W, Urbańska K, Sławińska N, Bryś M

Pharmaceuticals (Basel)

28-Mar-2024

PMCID:	PMC11054606
doi:	10.3390/ph17040435
PMID:	38675397

Nitrogen acquisition strategy shifts with tree age depending on root functional traits and soil properties in Larix principis-rupprechtii plantations

Liu Q, Chen Y, Chen Y

Front Plant Sci

12-Mar-2024

PMCID:	PMC10964345
doi:	10.3389/fpls.2024.1358367
PMID:	38533407

Water table depth and plant species determine the direction and magnitude of methane fluxes in floodplain meadow soils

Peacock M, Lawson C, Gowing D, Gauci V

Ecol Evol

10-Mar-2024

PMCID:	PMC10925825
doi:	10.1002/ece3.11147
PMID:	38469053

Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy

Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J

Heliyon

06-Mar-2024

PMCID:	PMC10945194
doi:	10.1016/j.heliyon.2024.e27530
PMID:	38501018

The Mechanism of Pyroptosis and Its Application Prospect in Diabetic Wound Healing

Al Mamun A, Shao C, Geng P, Wang S, Xiao J

J Inflamm Res

06-Mar-2024

PMCID:	PMC10924950
doi:	10.2147/JIR.S448693
PMID:	38463193

Pharmacokinetics of Ziyuglycoside I and Ziyuglycoside II in Rat Plasma by UPLC-MS/MS

Shen X, Wang Z, Li W, Mei S, Ma S, Wang X, Wen C, Chen F, Zheng G

Int J Anal Chem

01-Mar-2024

PMCID:	PMC10923622
doi:	10.1155/2024/7971021
PMID:	38463657

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review

Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

Targeting oxidative stress with natural products: A novel strategy for esophageal cancer therapy

Cao F, Zhang HL, Guo C, Xu XL, Yuan Q

World J Gastrointest Oncol

15-Feb-2024

PMCID:	PMC10900143
doi:	10.4251/wjgo.v16.i2.287
PMID:	38425393

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Trimethyl-3,4-dihydrochebulate	6444297	Click to see	396.30	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/10.1248/BPB.31.149 https://doi.org/10.1016/0031-9422(90)85341-C
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3-O-Galloylhamamelitannin	13270020	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.32.483
galloyl(-2)[galloyl(-3)][galloyl(-6)]b-Glc1Me	6325686	Click to see	650.50	unknown	https://doi.org/10.1248/CPB.32.483
Hamamelitannin	253775	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.32.483
Methyl 2,3,6-tri-O-galloyl-beta-D-glucopyranoside	78407221	Click to see	650.50	unknown	https://doi.org/10.1248/CPB.32.483
Methyl 6-O-galloyl-b-D-glucopyranoside	78385296	Click to see	346.29	unknown	https://doi.org/10.1248/CPB.32.483
methyl 6-O-galloyl-beta-d-glucopyranoside	5319658	Click to see	346.29	unknown	https://doi.org/10.1248/CPB.32.483
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol,[14c(u)]	11480435	Click to see	122.07	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(1S,2R)-2-[2-hydroxy-4-(3-hydroxypropyl)-6-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	162866975	Click to see	394.40	unknown	https://doi.org/10.1080/10286020.2011.634803
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl petroselinate	5362717	Click to see	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
N-Isobutyl-(6Z,8E)-decadienamide	5370490	Click to see CC=CC=CCCCCC(=O)NCC(C)C	223.35	unknown	https://doi.org/10.1248/YAKUSHI1881.53.6_634 https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Spirocardin B	127322	Click to see	368.50	unknown	https://doi.org/10.5511/PLANTBIOTECHNOLOGY1984.8.114 https://doi.org/10.1016/0031-9422(83)80168-X https://doi.org/10.1248/CPB.30.2255 https://doi.org/10.1248/BPB.23.717 https://doi.org/10.1016/0031-9422(90)85341-C https://doi.org/10.1016/S0031-9422(00)83018-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
p-Mentha-1,3,8-triene	176983	Click to see CC1=CC=C(CC1)C(=C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1S,4R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1,6a,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-hexadecahydropicene-4-carboxylic acid	163011324	Click to see	574.80	unknown	https://doi.org/10.1007/BF00861518
(4S,4aS,6aS,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4-carboxylic acid	163186771	Click to see CC1=CCC(C2C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	440.70	unknown	https://doi.org/10.1007/BF00861518
1,6a,6b,9,9,12a-Hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-hexadecahydropicene-4-carboxylic acid	163011323	Click to see CC1CCC(C2C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O	574.80	unknown	https://doi.org/10.1007/BF00861518
10-Hydroxy-1,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4-carboxylic acid	163012103	Click to see	440.70	unknown	https://doi.org/10.1007/BF00861518
Eudesm-4(15)-ene-3alpha,11-diol	11118126	Click to see	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,2R,3S,4S)-3-hydroxy-4-methyl-1-prop-1-en-2-yl-7-oxabicyclo[2.2.1]heptan-2-yl]oxy]oxane-3,4,5-triol	10569581	Click to see CC(=C)C12CCC(O1)(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)C	346.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aR,6bR,8aS,10R,12aS,14bR)-1,6a-dihydroxy-1,2,6b,9,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163075801	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)O)C(=O)OC7C(C(C(C(O7)CO)O)O)O	768.90	unknown	https://doi.org/10.1271/BBB.70268
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,6a-dihydroxy-1,2,6b,9,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163075800	Click to see	768.90	unknown	https://doi.org/10.1271/BBB.70268
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163084958	Click to see	604.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
(2R,3S,4S,4aR,6aR,6bS,8aS,11R,12R,12aR,14aR,14bR)-2,3,12-trihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid	162970814	Click to see	696.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
(2R,4aS,6aR,6aS,6bR,8aR,10S,12aR)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylic acid	162887531	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2=C1C)C)C(=O)O	586.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aS)-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydro-1H-picene-4a-carboxylate	162899381	Click to see	748.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163188493	Click to see	767.00	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162933693	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,4aS,6bR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	6324831	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2,6a,6b,9,9,12a-hexamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163039954	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2C1=C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	748.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163020651	Click to see	764.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162867099	Click to see	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	139035021	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1271/BBB.70268
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14019173	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydro-1H-picene-4a-carboxylate	73025283	Click to see	748.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162933692	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2,6a,6b,9,9,12a-hexamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163039953	Click to see	748.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162867098	Click to see	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163020650	Click to see	764.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	4643550	Click to see	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163032773	Click to see	919.10	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
10-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163084957	Click to see	604.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylic acid	4483451	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2=C1C)C)C(=O)O	586.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
28-Galloylglucosylpomolate 3-arabinoside	131752334	Click to see	919.10	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
28-Glucosyl-19(29)-dehydroursolic acid 3-arabinoside	131752275	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1=C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	748.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
28-Glucosyl-3b,23-dihydroxy-12,19(29)-ursadien-28-oate 3-arabinoside	85400634	Click to see	764.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
28-Glucosylpomolate	76155900	Click to see	634.80	unknown	https://doi.org/10.1016/0031-9422(92)80499-5 https://doi.org/10.1016/S0031-9422(01)00083-8
28-O-beta-D-Glucopyranosyl pomolic acid	76322845	Click to see	634.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8 https://doi.org/10.1016/0031-9422(92)80499-5
3-O-alpha-L-Arabinopyranosylpomolic acid beta-D-glucopyranosyl ester	12447833	Click to see	767.00	unknown	https://doi.org/10.1016/0031-9422(92)80499-5 https://doi.org/10.1016/S0031-9422(01)00083-8
6-O-(3,4,5-Trihydroxybenzoyl)-beta-D-glucopyranosyl (3beta)-3-(alpha-L-arabinopyranosyloxy)-19-hydroxyurs-12-en-28-oate	101135527	Click to see	919.10	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
beta-D-Glucopyranosyl (3beta)-3-(alpha-L-arabinopyranosyloxy)ursa-12,19(29)-dien-28-oate	11136408	Click to see	748.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
HN-saponin F	14101171	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Kajiichigoside F1	14019178	Click to see	650.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Rosamultin	21122581	Click to see	650.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Sanguisorbin E	71587115	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1C)C)C(=O)OC7C(C(C(C(O7)CO)O)OC(=O)C)O	793.00	unknown	via CMAUP database
Ursa-12,19(29)-dien-28-oic acid, 3-(alpha-L-arabinopyranosyloxy)-23-hydroxy-, beta-D-glucopyranosyl ester, (3beta,4alpha)-	11104682	Click to see	764.90	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Ziyuglycoside I	71609288	Click to see	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162910026	Click to see	604.80	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
(1R,2R,4aS,6aR,6aS,6bR,8aR,12aS,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10,13-dioxo-2,3,4,5,6,6a,7,8,8a,11,12,14b-dodecahydropicene-4a-carboxylic acid	135353742	Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O	484.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
(1R,4aR,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid	163062791	Click to see	602.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
(1R,4aS,6bR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	6324832	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)O	604.80	unknown	via CMAUP database
(1S,4aR,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162895768	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1O)C)C(=O)O)C	604.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
(2R,4aS,6aS,6aS,6bR,8aR,10S,12aR,14bS)-2,6a,6b,9,9,12a-hexamethyl-1-methylidene-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162979876	Click to see	586.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
(3beta)-3-(alpha-L-Arabinopyranosyloxy)ursa-12,18-dien-28-oic acid	636940	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2=C1C)C)C(=O)O	586.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid	11671516	Click to see CC1=C(C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1)C(=O)O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C	586.80	unknown	https://doi.org/10.1248/YAKUSHI1881.53.6_634
(4aS,6aS,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid	162975219	Click to see	454.70	unknown	https://doi.org/10.1248/YAKUSHI1947.84.5_477
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bS)-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid	163075999	Click to see	586.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162870311	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(O6)CO)O)O)C)C)C2C1O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162905753	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162870310	Click to see	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
1-Hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxytetrahydropyran-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	12447835	Click to see	604.80	unknown	https://doi.org/10.1016/0031-9422(92)80499-5 https://doi.org/10.1016/S0031-9422(01)00083-8
1-Hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10,13-dioxo-2,3,4,5,6,6a,7,8,8a,11,12,14b-dodecahydropicene-4a-carboxylic acid	163015900	Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O	484.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
1-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-10-(3,4,5-trihydroxyoxan-2-yl)oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid	73014889	Click to see	602.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
1-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	73063937	Click to see	604.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
1,10-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	3838010	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8 https://doi.org/10.1016/0031-9422(92)80499-5
1,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylic acid	20979894	Click to see	586.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
1beta-Hydroxyeuscaphic acid	14312996	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)C2C1(C)O)C)C(=O)O	504.70	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
2,6a,6b,9,9,12a-Hexamethyl-1-methylidene-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	73044336	Click to see	586.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
3-Oxopomolic acid	12314450	Click to see	470.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
3beta-O-alpha-L-Arabinopyranosylsiaresinolic acid 28-O-beta-D-glucopyranosyl ester	10887214	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	767.00	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Betulinic Acid	64971	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)97552-6
CID 14312995	14312995	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Epipomolic Acid	476601	Click to see	472.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
Euscaphic Acid	471426	Click to see	488.70	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8 https://doi.org/10.1016/0031-9422(92)80499-5
Jacarandic acid	13653335	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5 https://doi.org/10.1016/S0031-9422(01)00083-8
Pomolic Acid	382831	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8 https://doi.org/10.1016/0031-9422(92)80499-5
Pomonic acid	12314449	Click to see	470.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
Sanguisorbigenin	101967102	Click to see CC1=C(C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1)C(=O)O)C)C)(C)C)O)C)C	454.70	unknown	https://doi.org/10.1248/YAKUSHI1881.53.6_634
Sanguisorbin B	71587107	Click to see	588.80	unknown	via CMAUP database
Tomentosolic acid	12315243	Click to see	454.70	unknown	https://doi.org/10.1248/YAKUSHI1881.53.6_634 https://doi.org/10.1248/YAKUSHI1947.84.5_477
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/0031-9422(92)80499-5 https://doi.org/10.1016/S0031-9422(01)00083-8
ziyuglycoside II	71773126	Click to see	604.80	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
Ziziphin	441957	Click to see	981.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids
2,3-Dihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,14,14a-decahydropicene-4-carboxylic acid	72989336	Click to see	452.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids / 12-beta-hydroxysteroids
(2R,3R,4S,4aR,6aR,6bS,14aS,14bR)-2,3-dihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,14,14a-decahydropicene-4-carboxylic acid	163190437	Click to see	452.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6S,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-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	16204183	Click to see	1015.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/0031-9422(92)80499-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Methyl esters
Methyl 2-(2-butyl-4-oxocyclopentyl)acetate	21862951	Click to see	212.28	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside F2	14079045	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O	402.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Apiole	10659	Click to see	222.24	unknown	via CMAUP database
Myristicin	4276	Click to see	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-(2-Phenylethyl)chromone	441964	Click to see	250.29	unknown	via CMAUP database
5-Hydroxy-2-(2-(2-Hydroxyphenyl)Ethyl)Chromone	11822089	Click to see	282.29	unknown	via CMAUP database
5-Hydroxy-2-(2-phenylethyl)chromone	11536299	Click to see	266.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
7,8-Dihydro-3-methylpyrrolo[1,2-a]pyrimidin-2(6H)-one	5319799	Click to see CC1=CN2CCCC2=NC1=O	150.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-Methyltryptoline	121896	Click to see CN1CCC2=C(C1)NC3=CC=CC=C23	186.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,3aS,9aS,9bR)-3,3a,6,9-tetramethyl-4,5,9a,9b-tetrahydro-3H-azuleno[4,5-b]furan-2,7-dione	162951228	Click to see CC1C(=O)OC2C1(CCC(=C3C2C(=CC3=O)C)C)C	260.33	unknown	https://doi.org/10.1016/S0031-9422(01)00083-8
> Organoheterocyclic compounds / Naphthopyrans
Ponalactone A	442079	Click to see	346.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin	68081	Click to see	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin	821449	Click to see	300.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3R,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	17751036	Click to see	578.50	unknown	via CMAUP database
ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate	12795889	Click to see	730.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
Procyanidin B3	146798	Click to see	578.50	unknown	https://doi.org/10.1016/0031-9422(90)85341-C
procyanidin B3 3-O-gallate	11331595	Click to see	730.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol	73160	Click to see	290.27	unknown	via CMAUP database
(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,5,7-tetrol	11208959	Click to see	306.27	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-8-[1-(3,4-dihydroxyphenyl)-2-hydroxy-3-(2,4,6-trihydroxyphenyl)propyl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	56961712	Click to see	580.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
2-[[(2S,3R,6S,7R)-3,7-bis(3,4-dihydroxyphenyl)-4,6-dihydroxy-3,5,6,7-tetrahydro-2H-furo[3,2-g]chromen-2-yl]methyl]benzene-1,3,5-triol	21676381	Click to see C1C(C(OC2=CC3=C(C(C(O3)CC4=C(C=C(C=C4O)O)O)C5=CC(=C(C=C5)O)O)C(=C21)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
2-[[3,7-bis(3,4-dihydroxyphenyl)-4,6-dihydroxy-3,5,6,7-tetrahydro-2H-furo[3,2-g]chromen-2-yl]methyl]benzene-1,3,5-triol	73822598	Click to see C1C(C(OC2=CC3=C(C(C(O3)CC4=C(C=C(C=C4O)O)O)C5=CC(=C(C=C5)O)O)C(=C21)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1016/0031-9422(90)85341-C
Gambiriin A1	16203170	Click to see	580.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
Procyanidin	107876	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C=C6)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
7-Galloylcatechin	74490567	Click to see	442.40	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
Catechin 7-O-gallate	471393	Click to see	442.40	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see	306.27	unknown	https://doi.org/10.1016/0031-9422(90)85341-C
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Chrysanthemin	44256715	Click to see	449.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,4S,5S)-2-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44256718	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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44259091	Click to see	464.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	11557027	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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside	11751616	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
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate	54758589	Click to see	463.40	unknown	via CMAUP database
Astragalin	5282102	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
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
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6''-Acetylapiin	10531745	Click to see	606.50	unknown	via CMAUP database
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	via CMAUP database
Apiin	5280746	Click to see	564.50	unknown	via CMAUP database
Diosmetin 7-O-beta-D-glucoside	11016019	Click to see	462.40	unknown	via CMAUP database
Luteolin 7-O-(2-(beta-D-apiofuranosyl)-beta-D-glucopyranoside)	101248035	Click to see	580.50	unknown	via CMAUP database
Malonylapiin	5280803	Click to see	650.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein	5280961	Click to see	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose	374874	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	https://doi.org/10.1016/0031-9422(83)80168-X
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose	73178	Click to see	788.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	Click to see	788.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
1,2,6-Tri-O-Galloyl-Beta-D-Glucose	440308	Click to see	636.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
1,2,6-Trigalloyl-beta-D-glucopyranose	3357644	Click to see	636.50	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
2,3,4,6-Tetragalloyl-D-glucopyranose	13888121	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)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	788.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
2,3,4,6-Tetragalloylglucose	13888120	Click to see	788.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
beta-D-Glucopyranoside, methyl, 4,6-bis(3,4,5-trihydroxybenzoate)	11972411	Click to see	498.40	unknown	https://doi.org/10.1248/CPB.32.483
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	https://doi.org/10.1016/0031-9422(90)85341-C
galloyl(-2)[galloyl(-3)][galloyl(-4)][galloyl(-6)]b-Glc1Me	6325685	Click to see	802.60	unknown	https://doi.org/10.1248/CPB.32.483
galloyl(-3)[galloyl(-4)][galloyl(-6)]b-Glc1Me	5319798	Click to see COC1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	650.50	unknown	https://doi.org/10.1248/CPB.32.483
Methyl 2,3,4,6-tetra-O-galloyl-beta-D-glucopyranoside	383389	Click to see	802.60	unknown	https://doi.org/10.1248/CPB.32.483
Methyl 3,4,6-tri-O-galloyl-beta-D-glucopyranoside	13270027	Click to see	650.50	unknown	https://doi.org/10.1248/CPB.32.483
Methyl 4,6-di-O-galloyl-beta-D-glucopyranoside	73157785	Click to see	498.40	unknown	https://doi.org/10.1248/CPB.32.483
Penta-O-galloyl-beta-D-glucose	65238	Click to see	940.70	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate	101146656	Click to see	786.60	unknown	https://doi.org/10.1016/S0031-9422(00)83018-6 https://doi.org/10.1016/0031-9422(83)80168-X https://doi.org/10.1039/P19820001067
[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 3,4,5-trihydroxybenzoate	5315734	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
[(1R,2S,19R,20S,22R)-36-[5-[[(1R,2S,19R,20S,22R)-7,8,9,13,14,15,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32(37),33,35-dodecaen-20-yl] 3,4,5-trihydroxybenzoate	73354402	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C6=C5C(=O)OC7C(COC(=O)C8=CC(=C(C(=C86)O)O)O)OC(C9C7OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O9)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=C(C(=C(C=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1871.30	unknown	via CMAUP database
[(1R,3S,4R,21R,22S)-26-[5-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,27,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate	162894709	Click to see	1871.30	unknown	https://doi.org/10.1248/CPB.30.2255
[(1R,3S,4R,21R,22S)-27-[5-[[(10R,11S,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,26,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate	162842058	Click to see	1569.10	unknown	https://doi.org/10.1039/P19820001067
[2,3-dihydroxy-5-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methoxycarbonyl]phenyl] 3,4,5-trihydroxybenzoate	5319584	Click to see COC1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O	498.40	unknown	via CMAUP database
[26-[5-[(7,8,9,12,13,14,28,29,30,33,34,35-Dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl)oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,27,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate	162894708	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C6=C5C(=O)OC7C8C(COC(=O)C9=CC(=C(C(=C96)O)O)O)OC(C7OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1871.30	unknown	https://doi.org/10.1248/CPB.30.2255
[27-[5-[[3,4,5,14,20,21,22-Heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,26,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate	162842057	Click to see	1569.10	unknown	https://doi.org/10.1039/P19820001067
[36-[5-[[3,4,5,14,20,21,22-Heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32(37),33,35-dodecaen-20-yl] 3,4,5-trihydroxybenzoate	16181829	Click to see	1569.10	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
1(beta)-O-Galloylpedunculagin	118701062	Click to see	936.60	unknown	https://doi.org/10.5511/PLANTBIOTECHNOLOGY1984.8.114 https://doi.org/10.1016/0031-9422(90)85341-C https://doi.org/10.1248/BPB.23.717 https://doi.org/10.1021/NP50086A002
2,3-(S)-hexahydroxydiphenoyl-D-glucose	14035453	Click to see	482.30	unknown	via CMAUP database
2,3,8-Tri-O-methylellagic acid	5281860	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC	344.30	unknown	via CMAUP database
3-[[(1R,3S,4R,21R,22S)-9,10,11,14,15,16,27,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-26-yl]oxy]-4,5-dihydroxybenzoic acid	162915224	Click to see	1104.70	unknown	https://doi.org/10.1039/P19820001067
3-[[9,10,11,14,15,16,27,28,29,32,33,34-Dodecahydroxy-6,19,24,37-tetraoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-26-yl]oxy]-4,5-dihydroxybenzoic acid	162915223	Click to see	1104.70	unknown	https://doi.org/10.1039/P19820001067
3,4-Dihydroxy-5-[(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)oxy]benzoic acid	15934028	Click to see	470.30	unknown	https://doi.org/10.1039/P19820001067
Casuarictin	73644	Click to see	936.60	unknown	via CMAUP database
chingiitannin A	162971957	Click to see	1569.10	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
CID 11766372	11766372	Click to see	938.70	unknown	via CMAUP database
Eugeniin	442679	Click to see	938.70	unknown	https://doi.org/10.1248/BPB.23.717
Gallic acid 3-O-(6-galloylglucoside)	73157749	Click to see	484.40	unknown	https://doi.org/10.1248/CPB.32.483
Gallic acid 3-O-(6'-O-galloyl)-beta-D-glucopyranoside	11972353	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3O)O)C(=O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.32.483
Npc6700	16181831	Click to see	1871.30	unknown	https://doi.org/10.5511/PLANTBIOTECHNOLOGY1984.8.114 https://doi.org/10.1016/0031-9422(83)80168-X https://doi.org/10.1248/CPB.30.2255 https://doi.org/10.1016/S0031-9422(00)83018-6 https://doi.org/10.1016/0031-9422(90)85341-C https://doi.org/10.1248/BPB.23.717
Pedunculagin	442688	Click to see	784.50	unknown	https://doi.org/10.1016/0031-9422(90)85341-C https://doi.org/10.1248/CPB.41.1214
Potentillin	452242	Click to see	936.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X
Sanguiin H1	14429413	Click to see	786.60	unknown	https://doi.org/10.1016/0031-9422(83)80168-X https://doi.org/10.1039/P19820001067
Tellimagrandin Ii	151590	Click to see	938.70	unknown	via CMAUP database

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Sanguisorba officinalis

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