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.

Scutellaria lateriflora, commonly called skullcap, has been used as a mild nervous‑system tea and as a strong alcohol extract by a range of cultures. Among Northeastern and Plains peoples of North America, infusions of the aboveground herb were taken for tension, restlessness, and as a calmative; macerations of the same part were also applied topically to ease bruises and rheumatic pains (Mooney and Oliphant 1957). In the Andean highlands of Ecuador and neighboring parts of Colombia, decoctions of the leaves and stems were drunk as a general tonic and for minor anxiety or sleep disturbances, especially when taken in the evening (Bennett et al. 2021). In contemporary Appalachian folk practice in the United States, a tincture made from the fresh flowering herb (usually 1:2 to 1:5 in a water‑alcohol menstruum) is taken in small doses for nervous irritability, stress‑related muscle tension, and to support sleep (Winston 2006).

A simple tincture can be made with 100 g of dried, chopped aerial parts and 500 mL of 45% ethanol. Combine plant and alcohol in a jar, seal, and shake daily for 3–4 weeks at room temperature, then strain. This yields a roughly 1:5 tincture by weight‑to‑volume. The finished product is taken in 1–2 mL doses (about 20–40 drops) 1–3 times daily, often with food. For a weaker, daytime infusion, steep 1–2 teaspoons of dried herb in 250 mL just‑off‑boiling water for 10–15 minutes, then sip slowly. Skullcap is generally regarded as gentle, but do not combine with sedatives, avoid heavy doses, and consult a clinician if pregnant or nursing.

Traditional actions are linked to flavonoids (baicalein, baicalin, scutellarin, wogonin), phenylpropanoid glycosides (such as verbascoside), sesquiterpenes, and polysaccharides that together provide antioxidant and mild GABA‑ergic modulation. These constituents are well documented in Scutellaria lateriflora and can plausibly explain the calming and gentle spasmolytic effects seen in ethnomedicine (Liu et al. 2017).

Today, skullcap remains a staple nervine in herbal commerce, widely sold as dried tea, capsules, and tinctures, while people in both Andean communities and Appalachia continue to prepare infusions and tinctures for everyday tension and sleep support.

General Uses Top

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Common products:
- No established commercial or industrial products are reported.

Industrial and craft applications:
- No documented uses.

Food and beverages (non-medicinal):
- No documented uses.

Colorants and tanning:
- No documented uses.

Wood and fiber:
- No documented uses.

Fragrance and cosmetics:
- No documented uses.

Properties relevant to use:
- No relevant properties reported.

Standards and regulation:
- No applicable standards or regulatory frameworks documented.

Sustainability and sourcing:
- No documented uses.

Synonyms Top

Scientific name	Authority	First published in
Scutellaria lateriflora f. albiflora	Fernald	Rhodora 23: 86 (1921)
Scutellaria lateriflora var. albiflora	Farw.	Rep. (Annual) Michigan Acad. Sci. 19: 249 (1917)
Scutellaria lateriflora var. axillaris	Jenn.	J. Washington Acad. Sci. 10: 457 (1920)
Scutellaria lateriflora f. rhodantha	Fernald	Rhodora 23: 86 (1921)
Cassida lateriflora	Moench	Suppl. Meth. : 145 (1802)
Scutellaria polybotrya	Bernh.	Index Seminum (NKME, Erfordia) 1832: 3 (1833)

Common names Top

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Filter by language:

Language	Common/alternative name
English	blue skullcap
Spanish	escutelaria de virginia
Arabic	قنطريون أزرق
Persian	فرنجمشک
Polish	tarczyca bocznokwiatowa
Chinese	北美黄芩
Chinese	北美黃芩

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - 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
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California
- Western Canada
  - British Columbia
  - Manitoba

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000308029
UNII	7BP4DH5PDC
Florida Plant Atlas	3513
Flora of Alabama	2472
Canadensys	6456
USDA Plants	SCLA2
Tropicos	17600342
KEW	urn:lsid:ipni.org:names:458402-1
The Plant List	kew-189301
Missouri Botanical Garden	281434
Open Tree Of Life	583395
NCBI Taxonomy	233893
Nature Serve	2.137419
IUCN Red List	64324897
IPNI	458402-1
iNaturalist	79017
GBIF	5341325
Freebase	/m/027vqc4
WisFlora	5014
EOL	579306
Calflora (Californian flora)	7435
USDA GRIN	33427
Wikipedia	Scutellaria_lateriflora
CMAUP	NPO9096

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

Light-Emitting Diodes and Liquid System Affect the Caffeoylquinic Acid Derivative and Flavonoid Production and Shoot Growth of Rhaponticum carthamoides (Willd.) Iljin

Skała E, Olszewska MA, Tabaka P, Kicel A

Molecules

05-May-2024

PMCID:	PMC11085107
doi:	10.3390/molecules29092145
PMID:	38731636

Efficacy and Tolerability of a Scutellaria lateriflora L. and Cistus × incanus L.-Based Chewing Gum on the Symptoms of Gingivitis: A Monocentric, Randomized, Double-Blind, Placebo-Controlled Clinical Trial

Di Minno A, Ullah H, De Lellis LF, Buccato DG, Baldi A, Cuomo P, El-Seedi HR, Khalifa SA, Xiao X, Piccinocchi R, Piccinocchi G, Sacchi R, Daglia M

Nutrients

16-Mar-2024

PMCID:	PMC10975933
doi:	10.3390/nu16060862
PMID:	38542772

Effectiveness of Chinese Herbal Medicine as a Complementary Treatment for Neutropenia Prevention and Immunity Modulation During Chemotherapy in Patients With Breast Cancer: Protocol for a Real-World Pragmatic Clinical Trial

Wang KH, Shen HS, Chu SC, Wang TF, Lin CW, Huang WH, Wu YF, Ho CC, Pang CY, Li CC

JMIR Res Protoc

11-Mar-2024

PMCID:	PMC10964141
doi:	10.2196/55662
PMID:	38466979

Baicalin administration could rescue high glucose-induced craniofacial skeleton malformation by regulating neural crest development

Lu JQ, Luo ZY, Sun C, Wang SM, Sun D, Huang RJ, Yang X, Ding Y, Wang G

Front Pharmacol

07-Mar-2024

PMCID:	PMC10955141
doi:	10.3389/fphar.2024.1295356
PMID:	38515837

Relationship between biofilm formation and antibiotic resistance of Klebsiella pneumoniae and updates on antibiofilm therapeutic strategies

Li L, Gao X, Li M, Liu Y, Ma J, Wang X, Yu Z, Cheng W, Zhang W, Sun H, Song X, Wang Z

Front Cell Infect Microbiol

23-Feb-2024

PMCID:	PMC10920351
doi:	10.3389/fcimb.2024.1324895
PMID:	38465230

A comprehensive review of the anticancer effects of decursin

Chu Y, Yuan Q, Jiang H, Wu L, Xie Y, Zhang X, Li L

Front Pharmacol

20-Feb-2024

PMCID:	PMC10912667
doi:	10.3389/fphar.2024.1303412
PMID:	38444945

The Promising Role of Polyphenols in Skin Disorders

Farhan M

Molecules

15-Feb-2024

PMCID:	PMC10893284
doi:	10.3390/molecules29040865
PMID:	38398617

Baicalein inhibits IL-1β-induced extracellular matrix degradation with decreased MCP-1 expression in primary rat chondrocytes

Cho I, Chung KH, Kim Y, Choi CH, Koh JT

Toxicol Res

02-Feb-2024

PMCID:	PMC10959879
doi:	10.1007/s43188-024-00225-4
PMID:	38525128

In Vitro Assessment of Cortisol Release Inhibition, Bioaccessibility and Bioavailability of a Chemically Characterized Scutellaria lateriflora L. Hydroethanolic Extract

Buccato DG, Ullah H, De Lellis LF, Piccinocchi R, Baldi A, Xiao X, Arciola CR, Di Minno A, Daglia M

Molecules

25-Jan-2024

PMCID:	PMC10856628
doi:	10.3390/molecules29030586
PMID:	38338331

Exploring nature's hidden treasure: Unraveling the untapped phytochemical and pharmacological potentials of Clinopodium vulgare L. – A hidden gem in the Lamiaceae family

Qureshi KA, Parvez A, Uzzaman Khan MM, Aspatwar A, Atiya A, Elhassan GO, Khan RA, Erattil Ahammed SY, Khan WU, Jaremko M

Heliyon

20-Jan-2024

PMCID:	PMC10834805
doi:	10.1016/j.heliyon.2024.e24781
PMID:	38312627

Eco-friendly approaches to phytochemical production: elicitation and beyond

Jalota K, Sharma V, Agarwal C, Jindal S

Nat Prod Bioprospect

10-Jan-2024

PMCID:	PMC10776560
doi:	10.1007/s13659-023-00419-7
PMID:	38195902

Drug induced autoimmune hepatitis: An unfortunate case of herbal toxicity from Skullcap supplement: A case report

Thakral N, Konjeti VR, Salama FW

World J Hepatol

27-Dec-2023

PMCID:	PMC10784811
doi:	10.4254/wjh.v15.i12.1333
PMID:	38223420

Repurposing of Rutan showed effective treatment for COVID-19 disease

Salikhov SI, Abdurakhmonov IY, Oshchepkova YI, Ziyavitdinov JF, Berdiev NS, Aisa HA, Shen J, Xu Y, Xu HE, Jiang X, Zhang L, Vypova NL, Allaberganov DS, Tagayalieva NA, Musabaev EI, Ibadova GA, Rajabov IB, Lokteva LM

Front Med (Lausanne)

29-Nov-2023

PMCID:	PMC10716264
doi:	10.3389/fmed.2023.1310129
PMID:	38093975

The possible role furin and furin inhibitors in endometrial adenocarcinoma: A narrative review

Al‐kuraishy HM, Al‐Maiahy TJ, Al‐Gareeb AI, Alexiou A, Papadakis M, Saad HM, Batiha GE

Cancer Rep (Hoboken)

28-Nov-2023

PMCID:	PMC10809206
doi:	10.1002/cnr2.1920
PMID:	38018319

Biotechnological strategies for controlled accumulation of flavones in hairy root culture of Scutellaria lateriflora L.

Wilczańska A, Sparzak-Stefanowska B, Kokotkiewicz A, Jesionek A, Królicka A, Łuczkiewicz M, Krauze-Baranowska M

Sci Rep

21-Nov-2023

PMCID:	PMC10663461
doi:	10.1038/s41598-023-47757-7
PMID:	37990031

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	https://doi.org/10.1021/NP900068T
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1021/NP900068T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1021/NP900068T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol	68972	Click to see	438.80	unknown	https://doi.org/10.1021/NP900068T
Dotriacontanol	96117	Click to see	466.90	unknown	https://doi.org/10.1021/NP900068T
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
Thymol	6989	Click to see	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1002/FFJ.2730030106
alpha-Cubebene	442359	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
Calamenene	6429077	Click to see	202.33	unknown	https://doi.org/10.1002/FFJ.2730030106
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030106
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Secologanin	161276	Click to see	388.40	unknown	via CMAUP database
Secoxyloganin	162868	Click to see	404.40	unknown	via CMAUP database
Secoxyloganin methyl ester	14105070	Click to see COC(=O)CC1C(C(OC=C1C(=O)OC)OC2C(C(C(C(O2)CO)O)O)O)C=C	418.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin	87691	Click to see	390.40	unknown	via CMAUP database
(1S,6S,7R)-1-(beta-D-Glucopyranosyloxy)-6,7-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid	72709988	Click to see	392.35	unknown	via CMAUP database
8-Epiloganic Acid	158144	Click to see	376.36	unknown	via CMAUP database
Caryptoside	24721560	Click to see	406.40	unknown	via CMAUP database
Loganic Acid	89640	Click to see	376.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1021/NP900068T
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/10.1021/NP900068T
10-Hydroxy-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-carboxylic acid	258538	Click to see	472.70	unknown	https://doi.org/10.1021/NP900068T
3Alpha-Hydroxyurs-12-En-28-Oic Acid	7163177	Click to see	456.70	unknown	https://doi.org/10.1021/NP900068T
Epipomolic Acid	476601	Click to see	472.70	unknown	https://doi.org/10.1021/NP900068T
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP900068T
Lupeol	259846	Click to see	426.70	unknown	https://doi.org/10.1021/NP900068T
Pomolic Acid	382831	Click to see	472.70	unknown	https://doi.org/10.1021/NP900068T
Scutellaric Acid	12302571	Click to see	472.70	unknown	https://doi.org/10.1021/NP900068T
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1021/NP900068T
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1021/NP900068T
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/10.1021/NP900068T
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/10.1021/NP900068T
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/10.1021/NP900068T
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1021/NP900068T
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(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] (2R)-2-methylbutanoate	162875297	Click to see	550.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[(2S,4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5R,6aR)-5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2-yl] (2R)-2-methylbutanoate	121492956	Click to see CCC(C)C(=O)OC1CC2C(C(CC(C2(C3(C1)CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)O	552.70	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[(2S,4R,4aR,5S,7R,8S,8aR)-8-[(3aS,5S,6aR)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-2,5-diacetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate	162916038	Click to see	492.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[(2S,4R,4aR,5S,7R,8S,8aR)-8-[(3aS,5S,6aR)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2-yl] (2R)-2-methylbutanoate	162970719	Click to see CCC(C)C(=O)OC1CC2C(C(CC(C2(C3(C1)CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5C=COC5O4	534.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[(2S,4R,4aR,5S,7R,8S,8aR)-8-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2-yl] (2R)-2-methylbutanoate	162970720	Click to see	534.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[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-methylbutanoate	15617104	Click to see	550.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[5-acetyloxy-4a-(acetyloxymethyl)-8-(5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2-yl] 2-methylbutanoate	163048081	Click to see CCC(C)C(=O)OC1CC2C(C(CC(C2(C3(C1)CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5CC(OC5O4)O	552.70	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[8-(3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl)-2,5-diacetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate	162916037	Click to see	492.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[8-(3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2-yl] 2-methylbutanoate	162970718	Click to see	534.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
Ajugapitin	21123700	Click to see	550.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
Scutelaterin A	76963770	Click to see	492.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
Scutelaterin B	76972196	Click to see CCC(C)C(=O)OC1CC2C(C(CC(C2(C3(C1)CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5C=COC5O4	534.60	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
Scutelaterin C	86278290	Click to see	552.70	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
> Organoheterocyclic compounds / Furofurans
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5S,6aR)-5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate	13559430	Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)O)CCCC25CO5)COC(=O)C)OC(=O)C	452.50	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
[5-acetyloxy-8-(5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate	13559428	Click to see	452.50	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
Scutecyprol A	101985997	Click to see	452.50	unknown	https://doi.org/10.1016/S0031-9422(97)01032-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(+)-Decursin	442126	Click to see	328.40	unknown	https://doi.org/10.1021/NP900068T
(2,2-dimethyl-4,8-dioxo-3H-pyrano[3,2-g]chromen-3-yl) 2-methylbut-2-enoate	74941510	Click to see	342.30	unknown	https://doi.org/10.1021/NP900068T
(2,2-dimethyl-4,8-dioxo-3H-pyrano[3,2-g]chromen-3-yl) 3-methylbut-2-enoate	44518619	Click to see CC(=CC(=O)OC1C(=O)C2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C	342.30	unknown	https://doi.org/10.1021/NP900068T
Scuteflorin A	44179016	Click to see CC(=CC(=O)OC1C(=O)C2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C	342.30	unknown	https://doi.org/10.1021/NP900068T
Scuteflorin B	44179015	Click to see CC=C(C)C(=O)OC1C(=O)C2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C	342.30	unknown	https://doi.org/10.1021/NP900068T
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/NP900068T
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1021/NP900068T
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1021/NP0205102
Chrysin	5281607	Click to see	254.24	unknown	https://doi.org/10.1021/NP900068T
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/10.1021/NP0205102
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-6-[5,6-dihydroxy-2-(2-methoxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	11762528	Click to see	476.40	unknown	https://doi.org/10.1021/NP0205102
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/10.1021/NP0205102
6-[5,6-Dihydroxy-2-(2-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	14188669	Click to see	462.40	unknown	https://doi.org/10.1021/NP0205102
6-[5,6-Dihydroxy-2-(2-methoxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	22141811	Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	476.40	unknown	https://doi.org/10.1021/NP0205102
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/10.1021/NP0205102
Breviscapine	6426802	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP0205102
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/10.1021/NP0205102
Dihydrobaicalin	14135325	Click to see	448.40	unknown	https://doi.org/10.1021/NP0205102
Ikonnikoside I	10183148	Click to see	462.40	unknown	https://doi.org/10.1021/NP0205102
Oroxylin A glucoronide	14655552	Click to see	460.40	unknown	https://doi.org/10.1021/NP0205102
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/10.1021/NP0205102
Scutellarin	185617	Click to see	462.40	unknown	https://doi.org/10.1021/NP0205102
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-6-Methoxy-2-Phenyl-2,3-Dihydrochromen-4-One	5316733	Click to see	286.28	unknown	https://doi.org/10.1021/NP900068T
Dihydrooroxylin A	177032	Click to see	286.28	unknown	https://doi.org/10.1021/NP900068T
Oroxylin A	5320315	Click to see	284.26	unknown	https://doi.org/10.1021/NP900068T
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7-Dihydroxy-8,2'-dimethoxyflavone	13889021	Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC	314.29	unknown	https://doi.org/10.1021/NP900068T
Ganhuangenin	5271991	Click to see	346.30	unknown	via CMAUP database
Wogonin	5281703	Click to see	284.26	unknown	https://doi.org/10.1021/NP0205102 https://doi.org/10.1021/NP900068T

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Scutellaria lateriflora

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