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 China, the Hani people decoct the aerial parts to treat cough and fever, while in Japan the Ainu warm an infusion of the whole herb as a calming after-meal tonic and for colds (Bennett et al., 2021). Among hill tribes in the Mekong area of Northeast Thailand and nearby regions, leaves are boiled to make a mild bitter tea taken for digestive discomfort and “hot” conditions, and poultices of fresh leaves are applied to swollen joints (Panyaphu et al., 2013). Across several tribal communities in India’s Western Ghats, crushed leaf poultices are placed on bruises and localized inflammation, and in some villages a leaf infusion is taken for menstrual cramps (Pandey et al., 2021).

A simple mild tea can be prepared by placing 1–2 g of dried aerial parts (leaves and flowering tops) in a cup, pouring over 200 mL of just-boiled water, covering, and infusing 10–12 minutes. Strain and sip warm. A 1:5 ethanol tincture can be made by covering 20 g of dried aerial parts with 100 mL of 45% ethanol in a clean jar, capping tightly, and macerating for 2–4 weeks with occasional shaking. Strain through fine cloth. Dose commonly used is 2–3 mL up to 2–3 times daily, shaken before use. Safety: do not exceed recommended doses; avoid during pregnancy unless advised by a qualified practitioner; if you take anticoagulants or other medications, consult a healthcare professional before use.

The bitterness and calming effects are attributed to flavones common to the genus—baicalein, baicalin, wogonin, and wogonoside—along with related flavonoids such as scutellarein and dihydroxyflavone that have well-documented anti-inflammatory and antimicrobial activities reported for Scutellaria indica. Saponins are present at lower levels and likely support astringent effects on mucosal tissues.

Modern relevance: baicalin and related flavones from Scutellaria indica remain under active pharmacological investigation, and standardized leaf extracts continue to appear in regional herbal products alongside ongoing traditional use in the regions cited.

General Uses Top

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Common products:
Essential oil (steam-distilled from aerial parts). The oil has been characterized chemically in peer‑reviewed studies; it is not reported as a traded fragrance material, nor is Scutellaria indica cultivated for industrial oil production.

Food and beverages (non-medicinal):
No edible uses are reported.

Industrial and craft applications:
No documented uses in adhesives, coatings, biofuels, bioplastics, fermentation feedstocks, or as a model organism/reference genome. It is listed in horticultural databases (e.g., GBIF, Plants of the World Online) but not in community or lab model‑organism repositories.

Colorants and tanning:
No documented dye or tannin applications.

Wood and fiber:
No documented timber or fiber uses.

Fragrance and cosmetics:
No use in commercial perfumes or cosmetics. Essential-oil profiling exists in the literature, with compositional variation among populations; compositional features do not translate to established commercial fragrance use.

Properties relevant to use:
Chemical studies report diverse sesquiterpenes, flavonoids, and other secondary metabolites in the aerial parts; limited comparative datasets exist for quantitative oil composition and yield, hindering standardization for commercial application.

Standards and regulation:
No specific industry or regulatory standards reference this species.

Sustainability and sourcing:
No trade, cultivation, or conservation assessments specific to S. indica are reported.

Synonyms Top

Scientific name	Authority	First published in
Scutellaria indica var. glabrescens	Pamp.	Nuovo Giorn. Bot. Ital. n.s., 17: 711. 1910
Scutellaria indica var. typica	Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 255 (1929)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	タツナミソウ
Korean	골무꽃
Chinese	烟管草
Chinese	向天盏
Chinese	印度黄芩
Chinese	韓信草
Chinese	顺经草
Chinese	调羹草
Chinese	红叶犁头尖
Chinese	韩信草
Chinese	大力草
Chinese	偏向花
Chinese	三合香
Chinese	韩信草（向天盏）
Chinese	立浪草
Chinese	印度黃芩
Chinese	耳挖草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Scutellaria indica var. indica		Unknown
Scutellaria indica var. subacaulis	(Sun) C.Y.Wu & C.Chen	Fl. Yunnan. 1: 553, without basionym ref. 1977
Scutellaria indica var. tsusimensis	(H.Hara) Ohwi	Fl. Jap. , rev. ed.: 1150 (1965)
Scutellaria indica var. elliptica	Y.Z.Sun ex C.H.Hu	Acta Phytotax. Sin. 11: 40 (1966)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Name	Authority	First published in
Scutellaria indica f. parvifolia	Makino	Bot. Mag. (Tokyo) 18: 71 (1904)

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
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000307936
Tropicos	17605756
KEW	urn:lsid:ipni.org:names:458357-1
The Plant List	kew-189216
Open Tree Of Life	583398
NCBI Taxonomy	233892
IPNI	458357-1
iNaturalist	493441
GBIF	7308714
EPPO	SCDID
EOL	2894249
USDA GRIN	423535
CMAUP	NPO20278
Wikipedia	Scutellaria_indica

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

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

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

J Ethnobiol Ethnomed

30-May-2023

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

First study on in vitro antiviral and virucidal effects of flavonoids against feline infectious peritonitis virus at the early stage of infection

Triratapiban C, Lueangaramkul V, Phecharat N, Pantanam A, Lekcharoensuk P, Theerawatanasirikul S

Vet World

26-Mar-2023

PMCID:	PMC10082729
doi:	10.14202/vetworld.2023.618-630
PMID:	37041840

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

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

Alpinetin: A Review of Its Pharmacology and Pharmacokinetics

Zhao G, Tong Y, Luan F, Zhu W, Zhan C, Qin T, An W, Zeng N

Front Pharmacol

04-Feb-2022

PMCID:	PMC8854656
doi:	10.3389/fphar.2022.814370
PMID:	35185569

The chemical constituents of Sterculia comosa (wall) Roxb woods for arginase inhibitory, antioxidant activity, and molecular docking against SARS CoV-2 protein

Prastiwi R, Elya B, Hanafi M, Sauriasari R, Desmiaty Y, Dewanti E, Herowati R

Heliyon

19-Jan-2022

PMCID:	PMC8769564
doi:	10.1016/j.heliyon.2022.e08798
PMID:	35079656

Genome survey sequencing and characterization of simple sequence repeat (SSR) markers in Platostoma palustre (Blume) A.J.Paton (Chinese mesona)

Zheng Z, Zhang N, Huang Z, Zeng Q, Huang Y, Qi Y

Sci Rep

10-Jan-2022

PMCID:	PMC8748427
doi:	10.1038/s41598-021-04264-x
PMID:	35013469

Lamiaceae in Mexican Species, a Great but Scarcely Explored Source of Secondary Metabolites with Potential Pharmacological Effects in Pain Relief

Hernandez-Leon A, Moreno-Pérez GF, Martínez-Gordillo M, Aguirre-Hernández E, Valle-Dorado MG, Díaz-Reval MI, González-Trujano ME, Pellicer F

Molecules

16-Dec-2021

PMCID:	PMC8705283
doi:	10.3390/molecules26247632
PMID:	34946714

De Novo Assembly and Species-Specific Marker Development as a Useful Tool for the Identification of Scutellaria L. Species

Choi H, Kang WS, Kim JS, Na CS, Kim S

Curr Issues Mol Biol

01-Dec-2021

PMCID:	PMC8929090
doi:	10.3390/cimb43030152
PMID:	34940126

Complete chloroplast genome sequence and phylogenetic analysis of Clerodendrum japonicum (Thunb.) Sweet (Ajugoideae, Lamiaceae)

Chen G, Wang LG, Wang YH

Mitochondrial DNA B Resour

05-Jul-2021

PMCID:	PMC8259852
doi:	10.1080/23802359.2021.1944367
PMID:	34263052

The complete chloroplast genome of Scutellaria scordifolia (Labiatae)

Li J, Wang D, Xue P, Sun H, Feng Q, Miao N

Mitochondrial DNA B Resour

12-Jan-2021

PMCID:	PMC7808380
doi:	10.1080/23802359.2020.1847621
PMID:	33521276

The methyl jasmonate-responsive transcription factor SmMYB1 promotes phenolic acid biosynthesis in Salvia miltiorrhiza

Zhou W, Shi M, Deng C, Lu S, Huang F, Wang Y, Kai G

Hortic Res

01-Jan-2021

PMCID:	PMC7775463
doi:	10.1038/s41438-020-00443-5
PMID:	33384411

Arginase as a Potential Biomarker of Disease Progression: A Molecular Imaging Perspective

S. Clemente G, van Waarde A, F. Antunes I, Dömling A, H. Elsinga P

Int J Mol Sci

25-Jul-2020

PMCID:	PMC7432485
doi:	10.3390/ijms21155291
PMID:	32722521

Inherited dimorphism in cleistogamous flower production in Portulaca oleracea: a comparison of 16 populations growing under different environmental conditions

Furukawa T, Itagaki T, Murakoshi N, Sakai S

Ann Bot

21-Oct-2019

PMCID:	PMC7442420
doi:	10.1093/aob/mcz167
PMID:	31630158

The complete chloroplast genome of Scutellaria indica var. coccinea (Lamiaceae), an endemic taxon in Korea

Lee Y, Kim S

Mitochondrial DNA B Resour

13-Jul-2019

PMCID:	PMC7706630
doi:	10.1080/23802359.2019.1640649
PMID:	33365616

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
methyl (1R,2R,4aS,8aS)-1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-2,3,4,4a,8,8a-hexahydronaphthalene-1-carboxylate	14588306	Click to see	330.40	unknown	via CMAUP database
methyl (1R,2R,4aS,8aS)-4a-formyl-1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalene-1-carboxylate	14588304	Click to see	358.40	unknown	via CMAUP database
trans-Cajucarin B	637430	Click to see	330.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,6R,7R,13R)-7-[2-(furan-3-yl)ethyl]-2,13-dimethyl-9-oxatricyclo[5.3.3.01,6]tridec-2-ene-4,10-dione	11232710	Click to see	328.40	unknown	via CMAUP database
(1S,6S,7R,13R)-7-[2-(furan-3-yl)ethyl]-2,13-dimethyl-9-oxatricyclo[5.3.3.01,6]tridec-2-ene-4,8-dione	10969517	Click to see	328.40	unknown	via CMAUP database
(4aR,5'R,7R,8R,8aS)-5'-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione	102588560	Click to see	346.40	unknown	via CMAUP database
(4aS,5'R,7R,8R,8aS)-5'-(furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione	101616216	Click to see	314.40	unknown	via CMAUP database
(4R,4aS,5'R,7R,8R,8aS)-5'-(furan-3-yl)-4,7-dimethylspiro[1,3,4,4a,5,6,7,8a-octahydronaphthalene-8,3'-oxolane]-2,2'-dione	10041455	Click to see	316.40	unknown	via CMAUP database
trans-Dehydrocrotonin	10403368	Click to see	314.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[10-(Acetyloxymethyl)-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 3-methylbutanoate	76401282	Click to see	404.50	unknown	https://doi.org/10.1248/CPB.35.3720
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2,3,4,5,2',6'-Hexamethoxy-3',4'-methylenedioxychalcone	14332443	Click to see	432.40	unknown	https://doi.org/10.1248/CPB.37.794
2,3,4,5,2',6'-Hexamethoxy-4',5'-methylenedioxychalcone	72730057	Click to see COC1=C(C(=C(C(=C1)C=CC(=O)C2=C(C=C3C(=C2OC)OCO3)OC)OC)OC)OC	432.40	unknown	https://doi.org/10.1248/CPB.37.794
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5,7,2'-Trihydroxyflavanone	13889010	Click to see	272.25	unknown	https://doi.org/10.1248/CPB.35.3720
5,7,2'-Trihydroxyflavanone	179999	Click to see	272.25	unknown	https://doi.org/10.1248/CPB.35.3720
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-)	25201972	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-]	285.23	unknown	via CMAUP database
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/10.1248/CPB.37.794
Apigenin-7-olate	25200950	Click to see	269.23	unknown	via CMAUP database
Chrysin	5281607	Click to see	254.24	unknown	https://doi.org/10.1248/CPB.37.794
Isoscutellarein	5281665	Click to see	286.24	unknown	https://doi.org/10.1248/CPB.37.794
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1248/CPB.37.794 https://doi.org/10.1016/J.BMCL.2014.12.055
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/10.1248/CPB.37.794
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(S)-6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavanone	42607890	Click to see	434.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2S)-5-hydroxy-2-(2-hydroxyphenyl)-8-methoxy-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylic acid	118727142	Click to see	478.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-8-methoxy-2-(2-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	13889018	Click to see	490.40	unknown	https://doi.org/10.1248/CPB.35.3720
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/10.1248/CPB.37.794
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1248/CPB.37.794
beta-D-Glucopyranosiduronic acid, (2S)-3,4-dihydro-5-hydroxy-8-methoxy-2-(3-methoxyphenyl)-4-oxo-2H-1-benzopyran-7-yl, methyl ester	118727140	Click to see	506.50	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
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/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1248/CPB.37.794
Chrysin-7-O-glucoronide	14135334	Click to see	430.40	unknown	https://doi.org/10.1248/CPB.37.794
Chrysin-7-O-glucuronide	14135335	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	430.40	unknown	https://doi.org/10.1248/CPB.37.794
Oroxindin	3084961	Click to see	460.40	unknown	https://doi.org/10.1248/CPB.35.3720
Scutellarin	185617	Click to see	462.40	unknown	https://doi.org/10.1248/CPB.37.794 https://doi.org/10.15281/JPLANTRES1887.36.1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	14332448	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.37.794
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see	462.40	unknown	https://doi.org/10.1248/CPB.37.794
methyl (2S,3S,4S,5R,6S)-6-(5,7-dihydroxy-4-oxo-2-phenylchromen-8-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate	118727143	Click to see	460.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
Norwogonin-8-O-glucuronide	14180785	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
6,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5321202	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-8-methoxy-2-(2-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	118727141	Click to see	478.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
5,6-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14332446	Click to see	448.40	unknown	https://doi.org/10.1248/CPB.37.794
Plantaginin	5320623	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1248/CPB.37.794
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one	4053302	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1248/CPB.35.3720
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7-dimethoxy-2,3-dihydrochromen-4-one	162908392	Click to see	346.30	unknown	https://doi.org/10.1248/CPB.35.3720
(2s)-5,6,7,2',3',4',5'-Heptamethoxyflavanone	132452005	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.37.794
5,2'-Dihydroxy-6,7,6'-trimethoxyflavanone	13889020	Click to see	346.30	unknown	https://doi.org/10.1248/CPB.35.3720
5,6,7,2',3',4',5'-Heptamethoxyflavanone	14332451	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.37.794
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2S)-5-hydroxy-7,8-dimethoxy-4-oxo-2,3-dihydrochromen-2-yl]-3-methoxyphenoxy]oxane-2-carboxylic acid	13889016	Click to see	522.50	unknown	https://doi.org/10.1248/CPB.35.3720
(2S)-5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxy-2,3-dihydrochromen-4-one	118727139	Click to see	494.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
(2S)-5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one	118727144	Click to see	360.40	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
(2s)-5,2'-Dihydroxy-7,8,6'-trimethoxyflavanone	129829819	Click to see	346.30	unknown	https://doi.org/10.1248/CPB.35.3720
(2s)-5,2',5'-Trihydroxy-7,8-dimethoxyflavanone	13889014	Click to see	332.30	unknown	https://doi.org/10.1055/S-2006-959477 https://doi.org/10.1248/CPB.35.3720
(2s)-5,7-Dihydroxy-8,2'-dimethoxyflavanone	101669621	Click to see	316.30	unknown	https://doi.org/10.1055/S-2006-959477
(S)-5,7-Dihydroxy-2-(2-hydroxyphenyl)-8-methoxychroman-4-one	13889012	Click to see	302.28	unknown	https://doi.org/10.1055/S-2006-959477 https://doi.org/10.1248/CPB.35.3720
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-hydroxy-2-[(2S)-5-hydroxy-7,8-dimethoxy-4-oxo-2,3-dihydrochromen-2-yl]phenoxy]oxan-2-yl]methyl acetate	118727145	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)O)C3CC(=O)C4=C(O3)C(=C(C=C4O)OC)OC)O)O)O	536.50	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
[(2S,3R,4S,5R,6R)-3,5-dihydroxy-2-[4-hydroxy-2-[(2S)-5-hydroxy-7,8-dimethoxy-4-oxo-2,3-dihydrochromen-2-yl]phenoxy]-6-(hydroxymethyl)oxan-4-yl] 4-hydroxybenzoate	118727146	Click to see	614.50	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
2',5,7-Trihydroxy-8-methoxyflavanone	13889011	Click to see	302.28	unknown	https://doi.org/10.1248/CPB.35.3720 https://doi.org/10.1055/S-2006-959477
3,4,5-Trihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxo-2,3-dihydrochromen-2-yl)-3-methoxyphenoxy]oxane-2-carboxylic acid	13889015	Click to see COC1=C(C(=CC=C1)OC2C(C(C(C(O2)C(=O)O)O)O)O)C3CC(=O)C4=C(O3)C(=C(C=C4O)OC)OC	522.50	unknown	https://doi.org/10.1248/CPB.35.3720
4'-Hydroxywogonin	5322078	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
5,2'-Dihydroxy-7,8,6'-trimethoxyflavanone	13889019	Click to see	346.30	unknown	https://doi.org/10.1248/CPB.35.3720
5,2',5'-Trihydroxy-7,8-dimethoxyflavanone	13889013	Click to see COC1=C(C2=C(C(=O)CC(O2)C3=C(C=CC(=C3)O)O)C(=C1)O)OC	332.30	unknown	https://doi.org/10.1248/CPB.35.3720 https://doi.org/10.1055/S-2006-959477
5,6,7,8-Tetramethoxyflavone	122876	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC=CC=C3)OC)OC)OC	342.30	unknown	via CMAUP database
5,7-Dihydroxy-8,2'-dimethoxyflavanone	21636235	Click to see	316.30	unknown	https://doi.org/10.1055/S-2006-959477
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/10.1055/S-2006-959477 https://doi.org/10.1248/CPB.35.3720
methyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2S)-5-hydroxy-7,8-dimethoxy-4-oxo-2,3-dihydrochromen-2-yl]phenoxy]oxane-2-carboxylate	118727138	Click to see	506.50	unknown	https://doi.org/10.1016/J.BMCL.2014.12.055
Rivularin (flavone)	13889022	Click to see	344.30	unknown	https://doi.org/10.1248/CPB.35.3720
Wogonin	5281703	Click to see	284.26	unknown	https://doi.org/10.1055/S-2006-959477 https://doi.org/10.1248/CPB.35.3720
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
2,3,4,5,2',3',4',6'-Octamethoxychalcone	14332441	Click to see	448.50	unknown	https://doi.org/10.1248/CPB.37.794
2,3,4,5,2',4',5',6'-Octamethoxychalcone	72730055	Click to see	448.50	unknown	https://doi.org/10.1248/CPB.37.794
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-(6-hydroxy-4-methoxy-1,3-benzodioxol-5-yl)-3-(2-hydroxy-3,4,5-trimethoxyphenyl)prop-2-en-1-one	14332444	Click to see	404.40	unknown	https://doi.org/10.1248/CPB.37.794
2,2'-Dihydroxy-3,4,5,6'-tetramethoxy-4',5'-methylenedioxychalcone	129829857	Click to see	404.40	unknown	https://doi.org/10.1248/CPB.37.794
2'-Hydroxy-2,3,4,5,4',5',6'-heptamethoxychalcone	73188167	Click to see COC1=C(C(=C(C(=C1)C=CC(=O)C2=C(C(=C(C=C2O)OC)OC)OC)OC)OC)OC	434.40	unknown	https://doi.org/10.1248/CPB.37.794
2'-Hydroxy-2,3,4,5,6'-pentamethoxy-4',5'-methylenedioxychalcone	72730056	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.37.794
6'-Hydroxy-2,3,4,5,2'-pentamethoxy-3',4'-methylenedioxychalcone	14332442	Click to see COC1=C(C(=C(C(=C1)C=CC(=O)C2=C(C3=C(C=C2O)OCO3)OC)OC)OC)OC	418.40	unknown	https://doi.org/10.1248/CPB.37.794
6'-Hydroxy-2,3,4,5,2',3',4'-heptamethoxychalcone	13834106	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.37.794

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Scutellaria indica

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