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.

In European folk medicine the above‑ground parts of Scutellaria galericulata are steeped as a mild nervine tea. British herbalists recorded a “weak infusion” of the herb used for gentle relaxation and occasional insomnia, noting that the plants gathered along riverbanks were most favored for a calmer cup (Grieve, 1931). Across Finland and the Nordic countries, rural healers and nature‑herb entrepreneurs similarly prepared a light infusion of the leaves and tops as a calming after‑supper drink, a practice recognized in early‑century pharmacognosy texts (Madaus, 1938). In the Soviet Union the herb was regarded as a safe sedative and poured as a domestic infusion—often alongside honey—for night‑time use, as summarized in a standard Soviet herbal reference (Turova and Sapozhnikov, 1976). A concise recipe for this soothing tea follows. Place 1–2 teaspoons (about 2–4 g) of the dried aerial parts into a teapot or cup, pour 250 ml of just‑boiled water, cover and steep 10–12 minutes, then strain. If too bitter, add a little honey. Use 1–2 cups after dinner or before bed; avoid use in pregnancy and discontinue if drowsiness interferes with safety‑critical tasks. If you take sedatives, check with a clinician first because skullcaps can potentiate GABAergic effects.

Throughout these regions the preparation is understood as a mild relaxant rather than a strong anesthetic. The taste is grassy with a gentle, slightly minty‑bitter edge that drinkers often find “settling” when used consistently for a few weeks. Older British sources list skullcap as a “nervine tonic” and emphasize that a light infusion is best for regular use, with stronger decoctions reserved for acute conditions (Grieve, 1931).

The leaves and flowering tops contain flavonoids such as scutellarin, baicalin, and wogonin together with phenolic acids that have known sedative, anti‑inflammatory, and antioxidant properties. These constituents are well documented for Scutellaria and have been isolated from S. galericulata as well, providing a plausible basis for the calming tea (Turova and Sapozhnikov, 1976).

In the present day, S. galericulata remains a minor ingredient in regional herbal blends for stress and sleep, and several small producers market dried “riverbank skullcap” for nightly infusions. Contemporary research continues to probe scutellaria flavonoids for neuroactive and anti‑inflammatory effects, though most studies focus on the better‑studied S. baicalensis and S. lateriflora rather than S. galericulata itself.

General Uses Top

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Common products:
No established commercial, industrial, or craft products derived from Scutellaria galericulata are documented in the sources consulted.

Industrial and craft applications:
None are documented.

Food and beverages (non-medicinal):
None are documented.

Colorants and tanning:
None are documented.

Wood and fiber:
None are documented.

Fragrance and cosmetics:
None are documented.

Properties relevant to use:
No specific physical/chemical properties relevant to commercial applications are documented.

Standards and regulation:
No standards or regulatory frameworks applying to S. galericulata use are documented.

Sustainability and sourcing:
No sourcing or sustainability data specific to S. galericulata are documented.

Scientific/model-organism use:
S. galericulata is represented in open biodiversity data resources used for mapping and ecological modeling (e.g., GBIF; USDA PLANTS) and in community science platforms (e.g., iNaturalist). These repositories provide occurrence records, taxonomy, and distribution information supporting scientific analyses and research on wetland and riparian plant communities. No established laboratory protocols, reference genomes, or cultivar resources specific to S. galericulata are reported.

Synonyms Top

Scientific name	Authority	First published in
Scutellaria adamsii	Spreng.	Syst. Veg. 2: 701 (1825)
Scutellaria epilobiifolia	A.Ham.	Esq. Monogr. Scutellaria : 32 (1832)
Scutellaria epilobiifolia f. albiflora	Fernald	Rhodora 23: 86 (1921)
Scutellaria epilobiifolia f. rosea	Fernald	Rhodora 23: 86 (1921)
Scutellaria galericulata f. albiflora	Millsp.	Prelim. Cat. Fl. W. Virginia : 428 (1892)
Scutellaria galericulata var. epilobiifolia	(Ham.) Jordal	Rhodora 53: 158 (1951)
Scutellaria galericulata var. glaberrima	Benth.	Labiat. Gen. Spec. : 437 (1834)
Scutellaria galericulata f. rosea	E.L.Rand & Redfield	Fl. Mt. Desert Isl. : 137 (1894)
Scutellaria pauciflora	Pant.	Oesterr. Bot. Z. 23: 266 (1873)
Scutellaria galericulata var. pauciflora	(Pant.) Nyman	Consp. Fl. Eur. 573. 1881
Scutellaria galericulata var. humilis	Tinant	Fl. Luxemb. 313. 1836
Scutellaria galericulata var. pubens	Crép.	Man. Fl. Belgique ed. 2: 180. 1866
Cassida galericulata	Scop.	Fl. Carniol. , ed. 2, 1: 430 (1771)
Cassida major	Gilib.	Fl. Lit. Inch. 1: 90 (1782)
Scutellaria galericulata var. vulgaris	Benth.	Labiat. Gen. Spec. : 437 (1834)
Scutellaria galericulata f. uberrima	C.G.Westerl.	Bot. Not. 1906: 13 (1906)
Scutellaria galericulata var. pubescens	Mutel	Fl. Franç. Herbor. 3: 53 (1836)

Common names Top

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Filter by language:

Language	Common/alternative name
English	marsh skullcap
English	hooded skullcap
English	common scullcap
English	skullcap
Spanish	yerba de la celada
Spanish	cassida galericulata
Spanish	scutellaria pauciflora
Spanish	escutelaria comun
Spanish	terciaria
Spanish	scutellaria epilobiifolia
Spanish	cassida major
Spanish	canina
Spanish	casida
Spanish	escutelaria
Spanish	escutelaria común
Spanish	hierba de la celada
Spanish	tercianaria
Arabic	قصيده
Arabic	هربون مقلنس
Belarusian	Шлемнік каўпаканосны
Belarusian	Шлёмнік звычайны
Bulgarian	обикновена превара
Catalan	escutel·lària
Czech	šišák vroubkovaný
Welsh	cycyllog
Danish	almindelig skjolddrager
German	gewöhnliches helmkraut
German	sumpf-helmkraut
German	sumpfhelmkraut
Estonian	harilik tihashein
Persian	بشقابی معمولی
Finnish	vuohennokka
Finnish	luhtavuohennokka
French	scutellaire toque
French	scutellaire à casque
French	scutellaire a casque
French	grande toque
Upper Sorbian	wšědny šišak
Italian	scutellaia comune
Lithuanian	pelkinė kalpokė
Latvian	bruņu ķiverene
Norwegian Bokmål	skjoldbærer
Dutch	blauw glidkruid
Norwegian Nynorsk	skjoldberar
Polish	tarczyca pospolita
Romanian	mirgău
Russian	шлемник обыкновенный
Russian	шлемник колпачковый
Russian	шлемник колпаковидный
Russian	сердечная трава
Russian	маточник
Russian	лихорадочная трава
Russian	Шлемник обыкновенный
Slovak	šišak vrúbkovaný
Slovenian	navadna čeladnica
Swedish	getnos
Swedish	frossört
Ukrainian	шоломниця звичайна
Ukrainian	Шоломниця звичайна
Chinese	盔状黄芩
Chinese	兜冠黄芩
Chinese	岩藿香

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
  - Inner Mongolia
  - Xinjiang
- Eastern Asia
  - Japan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Iran
  - Palestine
  - Turkey

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

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

Northern America click to expand
- Eastern Canada
  - Labrador
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Delaware
  - Florida
  - Georgia
  - Maryland
  - North Carolina
- Southwestern U.S.A.
  - Arizona
  - California
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Yukon
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000307828
UNII	UF7PNA775L
Canadensys	6455
USDA Plants	SCGA
Tropicos	17600337
INPN	122069
Flora of Italy	4454
KEW	urn:lsid:ipni.org:names:458280-1
The Plant List	kew-189114
Plantarium	34718
Open Tree Of Life	907313
Observations.org	7433
NCBI Taxonomy	53169
NBN Atlas	NBNSYS0000004259
Nature Serve	2.135492
IUCN Red List	19210380
IPNI	458280-1
iNaturalist	79016
GBIF	2926759
Freebase	/m/02qsspx
WisFlora	5013
EPPO	SCDGA
EOL	578026
Elurikkus	7189
Calflora (Californian flora)	7433
USDA GRIN	449354
Wikipedia	Scutellaria_galericulata

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_946896805.1	daScuGale1.1	Chromosome	WELLCOME SANGER INSTITUTE	2022-09-21	53	312.48 Mb

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

A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

Novel insight into the therapeutical potential of flavonoids from traditional Chinese medicine against cerebral ischemia/reperfusion injury

Zhou J, Sun F, Zhang W, Feng Z, Yang Y, Mei Z

Front Pharmacol

29-Feb-2024

PMCID:	PMC10937431
doi:	10.3389/fphar.2024.1352760
PMID:	38487170

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Adaptive Relationships in Hemi-Boreal Forests: Tree Species Responses to Competition, Stress, and Disturbance

Petrokas R, Manton M

Plants (Basel)

13-Sep-2023

PMCID:	PMC10535793
doi:	10.3390/plants12183256
PMID:	37765418

Lakeshore vegetation: More resilient towards human recreation than we think?

Meyer N, Swiatloch A, Dittrich S, von Oheimb G

Ecol Evol

08-Jul-2023

PMCID:	PMC10329258
doi:	10.1002/ece3.10268
PMID:	37424934

Protective effects of Chinese herbal monomers against ischemia-reperfusion injury

Abudurexiti A, Feng B, Nong Q, Zhang Y, Xu Z, He C, Huang H, Chen J, Gao H

Am J Transl Res

15-May-2023

PMCID:	PMC10250973
PMID:	37303663

Long-Term Vegetation Changes and Socioeconomic Effects of River Engineering in Industrialized Areas (Southern Poland)

Rahmonov O, Dragan W, Cabała J, Krzysztofik R

Int J Environ Res Public Health

27-Jan-2023

PMCID:	PMC9915360
doi:	10.3390/ijerph20032255
PMID:	36767623

Investigation of Chemical Composition and Biological Activities of Ajuga pyramidalis—Isolation of Iridoids and Phenylethanoid Glycosides

Gori A, Boucherle B, Rey A, Rome M, Barette C, Soleilhac E, Philouze C, Fauvarque MO, Fuzzati N, Peuchmaur M

Metabolites

14-Jan-2023

PMCID:	PMC9860644
doi:	10.3390/metabo13010128
PMID:	36677053

Targeting the Interplay of Autophagy and ROS for Cancer Therapy: An Updated Overview on Phytochemicals

Dong L, He J, Luo L, Wang K

Pharmaceuticals (Basel)

08-Jan-2023

PMCID:	PMC9865312
doi:	10.3390/ph16010092
PMID:	36678588

A Background Search on the Potential Role of Scutellaria and Its Essential Oils

Zehravi M, Karthika C, Azad AK, Ahmad Z, Khan FS, Rahman MS, Akter R, Rahman MH

Biomed Res Int

27-Jul-2022

PMCID:	PMC9365597
doi:	10.1155/2022/7265445
PMID:	35968239

Phytochemical Profiling and Bio-Potentiality of Genus Scutellaria: Biomedical Approach

Shah M, Mubin S, Hassan SS, Tagde P, Ullah O, Rahman MH, Al-Harrasi A, Rehman NU, Murad W

Biomolecules

04-Jul-2022

PMCID:	PMC9313281
doi:	10.3390/biom12070936
PMID:	35883492

Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change

Caven AJ, Wiese JD

Heliyon

03-Jun-2022

PMCID:	PMC9192816
doi:	10.1016/j.heliyon.2022.e09640
PMID:	35711997

Specific Flavonoids and Their Biosynthetic Pathway in Scutellaria baicalensis

Pei T, Yan M, Huang Y, Wei Y, Martin C, Zhao Q

Front Plant Sci

03-Mar-2022

PMCID:	PMC8928390
doi:	10.3389/fpls.2022.866282
PMID:	35310641

The effect of a static magnetic field and baicalin or baicalein interactions on amelanotic melanoma cell cultures (C32)

Synowiec-Wojtarowicz A, Pawłowska-Góral K, Krawczyk A, Gawron S, Kimsa-Dudek M

Mol Biol Rep

20-Jan-2022

PMCID:	PMC8924135
doi:	10.1007/s11033-022-07148-z
PMID:	35059971

An overview of pharmacological activities of baicalin and its aglycone baicalein: New insights into molecular mechanisms and signaling pathways

Hu Z, Guan Y, Hu W, Xu Z, Ishfaq M

Iran J Basic Med Sci

01-Jan-2022

PMCID:	PMC9118284
doi:	10.22038/IJBMS.2022.60380.13381
PMID:	35656442

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(1R,2R,3R,4S,5R,6R,8R,10R,11R)-2-acetyloxy-3-hydroxy-5-[2-[(3S)-2-hydroxyoxolan-3-yl]ethyl]-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-10-yl] (E)-2-methylbut-2-enoate	100936352	Click to see CC=C(C)C(=O)OC1C23C(CC(O1)CC24CO4)C(C(C(C3OC(=O)C)O)C)(C)CCC5CCOC5O	508.60	unknown	https://doi.org/10.1016/0031-9422(93)85509-P
[(1R,2S,4R,5S,6R,8R,10R,11R)-2-acetyloxy-5-[2-[(3S)-2-hydroxyoxolan-3-yl]ethyl]-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-10-yl] (E)-2-methylbut-2-enoate	101688135	Click to see CC=C(C)C(=O)OC1C23C(CC(O1)CC24CO4)C(C(CC3OC(=O)C)C)(C)CCC5CCOC5O	492.60	unknown	https://doi.org/10.1016/0031-9422(95)00521-8
[(1R,2S,4R,5S,6R,8R,10S,11R)-2-acetyloxy-5-[2-[(2S,3S)-2-hydroxyoxolan-3-yl]ethyl]-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-10-yl] (E)-2-methylbut-2-enoate	163036551	Click to see	492.60	unknown	https://doi.org/10.1016/0031-9422(95)00521-8
[2-Acetyloxy-5-[2-(2-hydroxyoxolan-3-yl)ethyl]-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-10-yl] 2-methylbut-2-enoate	163036549	Click to see CC=C(C)C(=O)OC1C23C(CC(O1)CC24CO4)C(C(CC3OC(=O)C)C)(C)CCC5CCOC5O	492.60	unknown	https://doi.org/10.1016/0031-9422(95)00521-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/S10600-014-1015-8
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/10.1007/S10600-014-1015-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2R,3R,4S,5S,6R,8R,10R,11R)-2-acetyloxy-5-[2-[(3S)-2-hydroxyoxolan-3-yl]ethyl]-4,5-dimethyl-10-[(E)-2-methylbut-2-enoyl]oxyspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-3-yl] (E)-2-methylbut-2-enoate	101688134	Click to see	590.70	unknown	https://doi.org/10.1016/0031-9422(95)00521-8
[(1R,2S,3R,4aR,5S,6R,8S,8aR)-5-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (E)-2-methylbut-2-enoate	102056500	Click to see	548.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
[(1R,2S,4R,5S,6R,7S,8S,10R,11R)-5-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-2,10-diacetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-7-yl] (E)-2-methylbut-2-enoate	102056205	Click to see CC=C(C)C(=O)OC1C2CC3(CO3)C4(C1C(C(CC4OC(=O)C)C)(C)C5CC6CCOC6O5)C(O2)OC(=O)C	548.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
[(1R,2S,4R,5S,6R,7S,8S,10R,11R)-5-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-2,10-diacetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-7-yl] (E)-2-methylbut-2-enoate	102056204	Click to see	546.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B https://doi.org/10.1016/0031-9422(93)85509-P
[5-(2,3,3a,4,5,6a-Hexahydrofuro[2,3-b]furan-5-yl)-2,10-diacetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-7-yl] 2-methylbut-2-enoate	162879319	Click to see	548.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
[5-(3a,4,5,6a-Tetrahydrofuro[2,3-b]furan-5-yl)-2,10-diacetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-7-yl] 2-methylbut-2-enoate	163022756	Click to see	546.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
[5-(3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl)-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] 2-methylbut-2-enoate	78410219	Click to see	548.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Catalpol	91520	Click to see	362.33	unknown	https://doi.org/10.1016/0305-1978(91)90023-S
> Organoheterocyclic compounds / Furofurans
[(1R,4S,5S,10R)-5-(3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl)-2-acetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-10-yl] 2-methylpropanoate	101606383	Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3OC(=O)C(C)C)OC(=O)C	476.60	unknown	https://doi.org/10.1016/0031-9422(90)85018-B
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,6,7-trihydroxy-2-phenyl-2,3-dihydrochromen-4-one	26248749	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=CC=C3	272.25	unknown	https://doi.org/10.1007/BF00567050
Dihydrobaicalein	9816931	Click to see	272.25	unknown	https://doi.org/10.1007/BF00567050
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1007/BF00567050
Baicalein	5281605	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O	270.24	unknown	https://doi.org/10.1007/BF00565313 https://doi.org/10.1007/BF00567050
Scutellarein	5281697	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O	286.24	unknown	https://doi.org/10.1007/BF00567050
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(5-hydroxy-6-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid	162849017	Click to see	460.40	unknown	https://doi.org/10.1007/BF00567050
(2R,3R,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	124708143	Click to see	462.40	unknown	https://doi.org/10.1007/BF00567050
3,4,5-Trihydroxy-6-(5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl)oxyoxane-2-carboxylic acid	5387370	Click to see	446.40	unknown	https://doi.org/10.1007/BF00567050
3,4,5-Trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid	12004622	Click to see	460.40	unknown	https://doi.org/10.1007/BF00567050
6-(5,6-Dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	3807559	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1007/BF00567050
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1007/BF00567050
Baicalin	64982	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1007/BF00565313 https://doi.org/10.1007/BF00567050
Dihydrobaicalein 7-O-glucuronide	14135324	Click to see C1C(OC2=CC(=C(C(=C2C1=O)O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC=CC=C4	448.40	unknown	https://doi.org/10.1007/BF00567050
Dihydrobaicalin	14135325	Click to see	448.40	unknown	https://doi.org/10.1007/BF00567050
Luteolin-7-O-glucuronide	13607752	Click to see	462.40	unknown	https://doi.org/10.1007/BF00567050
Npc60669	44257628	Click to see	430.40	unknown	https://doi.org/10.1007/BF00567050
Oroxindin	3084961	Click to see	460.40	unknown	https://doi.org/10.1007/BF00567050
Oroxylin A glucoronide	14655552	Click to see	460.40	unknown	https://doi.org/10.1007/BF00567050
Oroxylin A-7-o-beta-D-glucuronide	14655551	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC4C(C(C(C(O4)C(=O)O)O)O)O	460.40	unknown	https://doi.org/10.1007/BF00567050
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3S,4R,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-5,6-dihydroxy-2-phenylchromen-4-one	162897856	Click to see	416.40	unknown	https://doi.org/10.1007/BF00565313
7-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-5,6-dihydroxy-2-phenylchromen-4-one	72615939	Click to see	416.40	unknown	https://doi.org/10.1007/BF00565313
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A	5320315	Click to see	284.26	unknown	https://doi.org/10.1007/BF00567050
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin	5281703	Click to see	284.26	unknown	https://doi.org/10.1007/BF00567050

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Scutellaria galericulata

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