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 baicalensis, known as Baikal skullcap, has a long history of use in East Asian traditional medicine. In Chinese practice the dried root is boiled as a decoction to treat fever, sore throat, and upper‑respiratory infections; the same root is macerated in alcohol to produce a tincture for its anti‑inflammatory and antiviral properties (Chinese Pharmacopoeia, 2020). Korean traditional medicine records the root as a decoction for cough, bronchitis, and as a poultice for skin inflammation (Korean Pharmacopoeia, 2015). In Japanese Kampo, the root is also prepared as a decoction for “heat” symptoms such as fever and sore throat, and a tincture is used externally for skin irritations (Japanese Pharmacopoeia, 2019). Across these cultures the root is the primary part used, with bark and leaves occasionally added in small amounts for specific formulations.

A simple, safe tincture can be made at home. Take 10 g of dried Scutellaria baicalensis root and place it in a clean glass jar. Add 100 ml of 70 % ethanol (or a 1:5 ratio of root to solvent). Seal the jar and let it steep for 24 hours at room temperature, shaking gently once a day. After steeping, strain the liquid through a fine mesh or cheesecloth into a dark‑glass bottle. Store the tincture in a cool, dark place; it will keep for up to a year. Use 1–2 ml (≈ 5–10 drops) diluted in water or tea once or twice daily. Pregnant or nursing women should avoid this tincture, and individuals with liver or kidney disease should consult a healthcare professional before use.

The therapeutic effects of Scutellaria baicalensis are largely attributed to its flavone constituents. Baicalin, the most abundant compound, is a glycoside that is hydrolyzed to baicalein in the body; both exhibit strong anti‑inflammatory, antioxidant, and antiviral activities. Wogonin and chrysin, other flavones present in the root, also contribute to the plant’s anti‑cancer and neuroprotective properties. These well‑established phytochemicals provide a biochemical basis for the traditional uses described above.

Today, baicalin‑rich extracts are sold as dietary supplements and are the subject of ongoing pharmacological research, including studies on their potential to inhibit influenza virus replication and to modulate immune responses. The continued use of Scutellaria baicalensis in both traditional and modern contexts underscores its relevance as a natural source of bioactive compounds.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Scutellaria adamsii	A.Ham.	Esq. Monogr. Scutellaria : 34 (1832)
Scutellaria baicalensis f. albiflora	H.W.Jen & Y.J.Chang	J. Beijing Forest. Univ. 13(3): 3 (1991)
Scutellaria davurica	Pall. ex Ledeb.	Fl. Ross. 3: 397 (1849)
Scutellaria lanceolaria	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 110 (1865)
Scutellaria macrantha	Fisch. ex Rchb.	Iconogr. Bot. Pl. Crit. 5: 52 (1827)
Scutellaria speciosa	Fisch. ex Turcz.	Bull. Soc. Imp. Naturalistes Moscou 24(II): 389 (1851)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	baikal skullcap
Azerbaijani	baykal başlıqotu
Belarusian	Шлёмнік байкальскі
Bulgarian	Шлемник байкалски
Bulgarian	байкалски шлемник
Czech	šišák bajkalský
German	baikalhelmkraut
German	baikal-helmkraut
Esperanto	bajkala skutelario
Estonian	baikali tihashein
French	scutellaire du baïkal
Japanese	黄岑
Japanese	黄苓
Japanese	コガネバナ
Japanese	オウゴン
Korean	황금
lzh	黃芩
Polish	tarczyca bajkalska
Russian	Шлемник байкальский
Thai	อึ่งงิ้ม
Vietnamese	hoàng cầm
Vietnamese	hoàng cầm (cây)
Chinese	黃芩
Chinese	黄岑
Chinese	黄芩子
Chinese	黄芩
Chinese	香水水草

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Buryatiya
  - Chita
  - Irkutsk

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000307642
UNII	6YF0M477I5
Tropicos	17604355
KEW	urn:lsid:ipni.org:names:458155-1
The Plant List	kew-188938
Open Tree Of Life	795166
Observations.org	122062
NCBI Taxonomy	65409
IPNI	458155-1
iNaturalist	565882
GBIF	7309014
Freebase	/m/03qcbsm
EPPO	SCDBA
Elurikkus	586527
USDA GRIN	33424
Wikipedia	Scutellaria_baicalensis
CMAUP	NPO28877
Plantarium	34695

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_005771605.1	ASM577160v1	Chromosome	Shanghai Chen Shan Botanical Garden	2019-05-29	173.37	368.76 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

Baicalin nanodelivery system based on functionalized metal-organic framework for targeted therapy of osteoarthritis by modulating macrophage polarization

Huang L, Yao Y, Ruan Z, Zhang S, Feng X, Lu C, Zhao J, Yin F, Cao C, Zheng L

J Nanobiotechnology

09-May-2024

PMCID:	PMC11080297
doi:	10.1186/s12951-024-02494-5
PMID:	38724958

Efficacy and safety of herbal medicine combined with acupuncture in pediatric epilepsy treatment: A meta-analysis of randomized controlled trials

Su HW, Chen HT, Kao CL, Hung KC, Lin YT, Liu PH, Lin CM, Chen IW

PLoS One

09-May-2024

PMCID:	PMC11081325
doi:	10.1371/journal.pone.0303201
PMID:	38723054

Baicalin and baicalein from Scutellaria baicalensis Georgi alleviate aberrant neuronal suppression mediated by GABA from reactive astrocytes

Cho J, Hong E, Kim Y, Song J, Ju YH, Kim H, Lee H, Kim H, Nam M

CNS Neurosci Ther

07-May-2024

PMCID:	PMC11076983
doi:	10.1111/cns.14740
PMID:	38715318

Baicalin alleviates angiotensin II‐induced cardiomyocyte apoptosis and autophagy and modulates the AMPK/mTOR pathway

Cheng Y, Yan M, He S, Xie Y, Wei L, Xuan B, Shang Z, Wu M, Zheng H, Chen Y, Yuan M, Peng J, Shen A

J Cell Mol Med

07-May-2024

PMCID:	PMC11075640
doi:	10.1111/jcmm.18321
PMID:	38712979

An Overview on Atopic Dermatitis, Oxidative Stress, and Psychological Stress: Possible Role of Nutraceuticals as an Additional Therapeutic Strategy

Alessandrello C, Sanfilippo S, Minciullo PL, Gangemi S

Int J Mol Sci

04-May-2024

PMCID:	PMC11084351
doi:	10.3390/ijms25095020
PMID:	38732239

On the mechanism of wogonin against acute monocytic leukemia using network pharmacology and experimental validation

Wang X, Wang Y, Chen J, Wang Q, Liu Z, Yin Y, Yang T, Shen T, Sa Y

Sci Rep

02-May-2024

PMCID:	PMC11065882
doi:	10.1038/s41598-024-60859-0
PMID:	38698063

Network Pharmacology and Molecular Docking Identify the Potential Mechanism and Therapeutic Role of Scutellaria baicalensis in Alzheimer’s Disease [Letter]

Yulion R, Andriani L, Aliyah SH

Drug Des Devel Ther

02-May-2024

PMCID:	PMC11073132
doi:	10.2147/DDDT.S475021
PMID:	38712308

Huaier Polysaccharide Alleviates Dextran Sulphate Sodium Salt-Induced Colitis by Inhibiting Inflammation and Oxidative Stress, Maintaining the Intestinal Barrier, and Modulating Gut Microbiota

Tang YF, Xie WY, Wu HY, Guo HX, Wei FH, Ren WZ, Gao W, Yuan B

Nutrients

30-Apr-2024

PMCID:	PMC11085394
doi:	10.3390/nu16091368
PMID:	38732614

Target Cell Extraction and Spectrum–Effect Relationship Coupled with BP Neural Network Classification for Screening Potential Bioactive Components in Ginseng Extract with a Protective Effect against Myocardial Damage

Li J, Lin M, Xie Z, Chen L, Qi J, Yu B

Molecules

28-Apr-2024

PMCID:	PMC11085743
doi:	10.3390/molecules29092028
PMID:	38731522

Research progress on the role of macrophages in acne and regulation by natural plant products

Zhao D, Wang Y, Wu S, Ji X, Gong K, Zheng H, Zhu M

Front Immunol

26-Apr-2024

PMCID:	PMC11082307
doi:	10.3389/fimmu.2024.1383263
PMID:	38736879

Potential Targets of Natural Products for Improving Cardiac Ischemic Injury: The Role of Nrf2 Signaling Transduction

Wang H, Han J, Dmitrii G, Zhang XA

Molecules

26-Apr-2024

PMCID:	PMC11085255
doi:	10.3390/molecules29092005
PMID:	38731496

Pharmacotherapy for Keloids and Hypertrophic Scars

Murakami T, Shigeki S

Int J Mol Sci

25-Apr-2024

PMCID:	PMC11083137
doi:	10.3390/ijms25094674
PMID:	38731893

Regulation of Microtubule Stability in Pulmonary Microvascular Endothelial Cells in Rats with Severe Acute Pancreatitis: Qingyi Decoction is a Potential CDK5 Inhibitor

Cao Y, Li F, Sun Z, Liu J, Liu J, Yang Q, Ge P, Luo Y, Chen H

J Inflamm Res

24-Apr-2024

PMCID:	PMC11063490
doi:	10.2147/JIR.S451755
PMID:	38699595

Research advances on molecular mechanism and natural product therapy of iron metabolism in heart failure

Zhang T, Luo L, He Q, Xiao S, Li Y, Chen J, Qin T, Xiao Z, Ge Q

Eur J Med Res

24-Apr-2024

PMCID:	PMC11044586
doi:	10.1186/s40001-024-01809-4
PMID:	38659000

TCM targets ferroptosis: potential treatments for cancer

Qin L, Zhong Y, Li Y, Yang Y

Front Pharmacol

22-Apr-2024

PMCID:	PMC11082647
doi:	10.3389/fphar.2024.1360030
PMID:	38738174

Phytochemical Profile Top

Add a new one!

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

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives
3-Phenylfuran	518802	Click to see	144.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
di-N-Octyl Phthalate	8346	Click to see	390.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Di(2-ethylhexyl) phthalate	8343	Click to see	390.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Dibutyl Phthalate	3026	Click to see	278.34	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see	122.12	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
3-Methoxybenzaldehyde	11569	Click to see COC1=CC=CC(=C1)C=O	136.15	unknown	via CMAUP database
4-Methoxybenzaldehyde	31244	Click to see	136.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
2-Methylbenzyl alcohol	6994	Click to see	122.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
2,4-Dimethoxy-1-(1-propenyl)benzene	5314067	Click to see	178.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Benzene and substituted derivatives / Styrenes
Benzylideneacetone	637759	Click to see CC(=O)C=CC1=CC=CC=C1	146.19	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see	208.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol	996	Click to see	94.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Cresols / Ortho cresols
O-Cresol	335	Click to see	108.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see	108.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Methoxyphenols
4-Vinylguaiacol	332	Click to see	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
5-Ethenyl-2-methoxyphenol	10441857	Click to see COC1=C(C=C(C=C1)C=C)O	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1271/BBB1961.51.1449
Guaiacol	460	Click to see	124.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
Isoeugenol	853433	Click to see	164.20	unknown	https://doi.org/10.1271/BBB1961.51.1449
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Benzenoids / Phenols / Methoxyphenols / Gingerdiols
CID 5318276	5318276	Click to see	268.35	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane	12405	Click to see CCCCCCCCCCCCCCCCCCCCCC	310.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Dodecane	8182	Click to see	170.33	unknown	https://doi.org/10.1271/BBB1961.51.1449
Eicosane	8222	Click to see	282.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heneicosane	12403	Click to see	296.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptacosane	11636	Click to see	380.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1271/BBB1961.51.1449
Nonadecane	12401	Click to see	268.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pentacosane	12406	Click to see	352.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pentadecane	12391	Click to see	212.41	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1271/BBB1961.51.1449
Tridecane	12388	Click to see	184.36	unknown	https://doi.org/10.1271/BBB1961.51.1449
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate	8181	Click to see	270.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1271/BBB1961.51.1449
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1271/BBB1961.51.1449
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1271/BBB1961.51.1449
Heptanoic Acid	8094	Click to see	130.18	unknown	https://doi.org/10.1271/BBB1961.51.1449
Nonanoic Acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
Octanoic Acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see	302.50	unknown	via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene	44268166	Click to see	254.40	unknown	via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol	101586702	Click to see	286.50	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	via CMAUP database
Abietatriene	6432211	Click to see	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
Isopimara-7,15-diene	13969536	Click to see	272.50	unknown	via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate	11290126	Click to see	318.50	unknown	via CMAUP database
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradiene	443469	Click to see	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1S,4S,5R,6R,9S,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxo-7-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl]methyl hexadecanoate	5318035	Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC2C3C(C3(C)C)CC(C4(C2=O)C=C(C(C4(C1O)O)O)C)C	586.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geranylacetone	1549778	Click to see	194.31	unknown	https://doi.org/10.1271/BBB1961.51.1449
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see	136.23	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
(4-(Prop-1-en-2-yl)cyclohexyl)methanol	519954	Click to see	154.25	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
d-beta-Phellandrene	442484	Click to see	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
(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/10.1271/BBB1961.51.1449
6-Methoxygossypol	3085061	Click to see	532.60	unknown	via CMAUP database
6,10,14-Trimethylpentadecan-2-one	10408	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C	268.50	unknown	https://doi.org/10.1271/BBB1961.51.1449
alpha-Cubebene	442359	Click to see	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol	91457	Click to see	222.37	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1S,3Z,6S,7E,11R,12R,13S,17S)-1,4,8,14,14,17-hexamethyltricyclo[9.8.0.012,17]nonadeca-3,7-diene-6,13-diol	163189028	Click to see	374.60	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,2S,3R,4R,4aS,8aR)-2-benzoyloxy-3-hydroxy-3,4,8a-trimethyl-8-methylidene-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-1,2,4a,5,6,7-hexahydronaphthalen-1-yl] benzoate	102247117	Click to see	558.70	unknown	https://doi.org/10.1016/0031-9422(96)00380-9
[2-benzoyloxy-3-hydroxy-3,4,8a-trimethyl-8-methylidene-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-1,2,4a,5,6,7-hexahydronaphthalen-1-yl] benzoate	162905592	Click to see	558.70	unknown	https://doi.org/10.1016/0031-9422(96)00380-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	101280203	Click to see	456.70	unknown	via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one	101280208	Click to see	456.70	unknown	via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	21672660	Click to see	456.70	unknown	via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene	101280202	Click to see	470.80	unknown	via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	51051617	Click to see	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
Campesteryl Ferulate	15056832	Click to see	576.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(10R,13S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-[1-[5-methyl-6-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]ethyl]-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	11968816	Click to see	887.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-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	636741	Click to see	414.70	unknown	via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see	410.70	unknown	via CMAUP database
Npc196776	50930798	Click to see	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
2-Butenedioic acid	723	Click to see	116.07	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Fumaric Acid	444972	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Malonic acid	867	Click to see C(C(=O)O)C(=O)O	104.06	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Succinic Acid	1110	Click to see	118.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid	311	Click to see	192.12	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
L-Malic Acid	222656	Click to see	134.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Malic Acid	525	Click to see	134.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5S)-3-((E)-3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylic Acid	12310830	Click to see	354.31	unknown	via CMAUP database
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
cis-Chlorogenic acid	1794425	Click to see	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol	4961358	Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O	300.30	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
GlyTouCan:G20812UT	53301851	Click to see	342.30	unknown	via CMAUP database
Salidroside	159278	Click to see	300.30	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-2-one	10172008	Click to see	326.34	unknown	via CMAUP database
Npc66700	9986231	Click to see	612.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
(3R,4R,5R)-2-[(3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyperoxy-5-(hydroxymethyl)oxolane-3,4-diol	91884769	Click to see	314.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
2,3-Dihydroxybutanedioic Acid	875	Click to see	150.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
Mesotartaric acid	447315	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	https://doi.org/10.1007/S10600-008-0023-Y
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Methylfurfural	12097	Click to see CC1=CC=C(O1)C=O	110.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
Pyrrole-2-carboxaldehyde	13854	Click to see	95.10	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Sebacaldehyde	3016433	Click to see C(CCCCC=O)CCCC=O	170.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(E)-beta-Damascone	5374527	Click to see CC=CC(=O)C1=C(CCCC1(C)C)C	192.30	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylpyrrole	14079	Click to see	109.13	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-Hydroxyacetophenone	68490	Click to see C1=CC=C(C=C1)C(=O)CO	136.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
4'-Methoxyacetophenone	7476	Click to see CC(=O)C1=CC=C(C=C1)OC	150.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
Benzoylacetone	7166	Click to see	162.18	unknown	via CMAUP database
Paeonol	11092	Click to see CC(=O)C1=C(C=C(C=C1)OC)O	166.17	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Butylphthalide	61361	Click to see	190.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3,8-Dihydroxy-2,4,6-trimethoxyxanthone	5316837	Click to see	318.28	unknown	via CMAUP database
6,8-Dihydroxy-9-oxoxanthen-4-olate	25200626	Click to see	243.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Mellein	28516	Click to see	178.18	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran	19602	Click to see	138.21	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see	117.15	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3alpha-Dihydrocadambine	162138	Click to see	546.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
3-N-Butyl-4,5-dihydrophthalide	173843	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
3-N-butyl-4,5-dihydrophthalide, (S)-	3085257	Click to see	192.25	unknown	https://doi.org/10.1271/BBB1961.51.1449
Cnidilide	160710	Click to see	194.27	unknown	https://doi.org/10.1271/BBB1961.51.1449
Ligustilide	5319022	Click to see	190.24	unknown	https://doi.org/10.1271/BBB1961.51.1449
Sedanolide	5018391	Click to see CCCCC1C2CCCC=C2C(=O)O1	194.27	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones
1(3H)-Isobenzofuranone, 3-butylidene-	62368	Click to see CCCC=C1C2=CC=CC=C2C(=O)O1	188.22	unknown	https://doi.org/10.1271/BBB1961.51.1449
Butylidenephthalide	5352899	Click to see	188.22	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
gamma-Caprolactone	12756	Click to see CCC1CCC(=O)O1	114.14	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene	102594798	Click to see	276.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
beta-Skytanthine	442552	Click to see CC1CCC2C1CN(CC2C)C	167.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see	126.11	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Phenylpropanoids and polyketides / Aurone flavonoids
(2Z)-2-benzylidene-4,5,6-trihydroxy-1-benzofuran-3-one	5322048	Click to see C1=CC=C(C=C1)C=C2C(=O)C3=C(O2)C=C(C(=C3O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenylprop-2-Enal	307	Click to see	132.16	unknown	https://doi.org/10.1271/BBB1961.51.1449
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2R,3R,4R,5R,6R)-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	73157771	Click to see	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	74027662	Click to see	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside	132274946	Click to see	624.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0031-9422(99)00306-4
Acteoside;Kusaginin;TJC160	354009	Click to see	624.60	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0031-9422(96)00443-8
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-	72725940	Click to see	652.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Jionoside D	9895632	Click to see	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Leucosceptoside A	10394343	Click to see	638.60	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
Martynoside	5319292	Click to see	652.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/S0031-9422(99)00306-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid	445858	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Cupressuflavone	5281609	Click to see	538.50	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(2R,3S)-2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	163014180	Click to see	290.27	unknown	https://doi.org/10.1248/CPB.33.2411
2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	163014179	Click to see	290.27	unknown	https://doi.org/10.1248/CPB.33.2411
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol	11095	Click to see	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
(2R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-4-oxo-2,3-dihydrochromen-5-olate	25200419	Click to see	287.24	unknown	via CMAUP database
(2S)-dihydrotricetin	440836	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)O)O)O	304.25	unknown	via CMAUP database
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see	270.28	unknown	via CMAUP database
2,3,3,5,6-Pentahydroxy-2-phenylchromen-4-one	54231395	Click to see	304.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857833/
2',5,6',7-Tetrahydroxyflavanone	42607849	Click to see	288.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.30.1792 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2S)-	157671	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=CC=C3O)O	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1007/BF00630621 https://doi.org/10.1248/CPB.30.1792 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
Carthamidin	188308	Click to see	288.25	unknown	via CMAUP database
Dihydrobaicalein	9816931	Click to see	272.25	unknown	via CMAUP database
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
Strobopinin	442520	Click to see	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one	86311089	Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
2-(2,6-Dihydroxyphenyl)-3,5,7-trihydroxychroman-4-one	71307292	Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/0031-9422(95)00200-Q
2',3,5,6',7-Pentahydroxyflavanone	157633	Click to see	304.25	unknown	https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
2',3,5,7-Tetrahydroxyflavanone	3082330	Click to see	288.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(2,6-Dihydroxyphenyl)-5,6,7,8-tetrahydroxychromen-4-one	141059302	Click to see	318.23	unknown	https://doi.org/10.1248/CPB.33.2411
5,7-Dihydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	74977417	Click to see	448.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5,7,2'-Trihydroxyflavone	5322064	Click to see	270.24	unknown	https://doi.org/10.1248/CPB.40.531
5,7,2',3'-Tetrahydroxyflavone	5321864	Click to see	286.24	unknown	https://doi.org/10.1248/CPB.40.531
5,7,2',5'-Tetrahydroxyflavone	5487756	Click to see C1=CC(=C(C=C1O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X
5,7,2',6'-Tetrahydroxyflavone	5321865	Click to see C1=CC(=C(C(=C1)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	286.24	unknown	https://doi.org/10.1007/BF00630621 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
5,7,6'-trihydroxyflavone 2'-O-beta-D-glucopyranoside	102445445	Click to see	448.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
7-Hydroxy-4-oxo-2-phenylchromen-5-olate	25200543	Click to see	253.23	unknown	via CMAUP database
7,3',4'-Trihydroxyflavone	5322065	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	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/YAKUSHI1947.104.5_529
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/10.1006/JMCC.1999.1021 https://doi.org/10.1252/KAKORONBUNSHU.22.287 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1055/S-2004-815489 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1021/NP980163P https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1248/BPB.21.1067 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1016/S0039-9140(00)00514-2 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1055/S-0029-1243111
Chrysin	5281607	Click to see	254.24	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/YAKUSHI1947.104.5_529 https://doi.org/10.1007/BF02976430 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1248/YAKUSHI1947.105.2_148
Isoscutellarein	5281665	Click to see	286.24	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Norwogonin	5281674	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/10.1248/YAKUSHI1947.103.6_607 https://doi.org/10.1016/S0176-1617(00)80282-5
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/YAKUSHI1947.104.5_529 https://doi.org/10.1055/S-0029-1243121
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,4',7-Trihydroxyflavone	5281611	Click to see	270.24	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1016/S0039-9140(00)00514-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)-6-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one	13644660	Click to see	564.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one	44257699	Click to see	564.50	unknown	via CMAUP database
5,7-Dihydroxy-2-phenyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-YL]-8-(3,4,5-trihydroxyoxan-2-YL)chromen-4-one	44715843	Click to see	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-2-phenyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one	73829976	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=CC=C4)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Chrysin 6-C-arabinoside 8-C-glucoside	21722008	Click to see	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Chrysin 6-C-glucoside 8-C-arabinoside	21722007	Click to see	548.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8 https://doi.org/10.1016/S0031-9422(96)00443-8
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(00)82692-8
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3R,4S,5R,6S)-6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	69717682	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/10.1016/S0031-9422(96)00443-8
(3S,4S,6S)-6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	44258403	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	via CMAUP database
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/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1078/0944711041495173 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M
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/10.1016/J.JPBA.2010.04.019 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1055/S-2006-958036
apigenin-7-O-glucuronide	12912214	Click to see	446.40	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
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/10.1055/S-2001-15810 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/0306-3623(95)02143-4 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1055/S-2006-961769 https://doi.org/10.1055/S-2004-815489 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0039-9140(00)00514-2 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1111/J.1600-0609.2009.01365.X https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.1252/KAKORONBUNSHU.22.287 https://doi.org/10.1078/0944711041495173 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1055/S-0029-1243121 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1248/CPB.35.3494
Baicalin methyl ester	15223582	Click to see	460.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
Dihydrobaicalin	14135325	Click to see	448.40	unknown	https://doi.org/10.1248/YAKUSHI1947.103.6_607
Glychionide A	11597485	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	446.40	unknown	via CMAUP database
Methyl 6-(5,6-dihydroxy-4-oxo-2-phenylchromen-7-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylate	72747690	Click to see	460.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
Npc60669	44257628	Click to see	430.40	unknown	via CMAUP database
Oroxindin	3084961	Click to see	460.40	unknown	https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1002/PTR.1216 https://doi.org/10.1078/0944711041495173 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1248/YAKUSHI1947.105.2_148
Oroxylin A glucoronide	14655552	Click to see	460.40	unknown	https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1248/YAKUSHI1947.105.2_148
oroxylin A glucuronide	44567248	Click to see	460.40	unknown	https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1078/0944711041495173
Scutellarin	185617	Click to see	462.40	unknown	via CMAUP database
Scutellarin(1-)	29927686	Click to see	461.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
ISOSCUTELLAREIN 8-O-beta-D-GLUCURONIDE	14332450	Click to see	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
8-methoxy-2-phenyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5319440	Click to see	430.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-3,7-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,3-dihydrochromen-4-one	5317187	Click to see	628.50	unknown	via CMAUP database
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	5353588	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
7-[(4,8-Dihydroxy-7-oxo-2,6-dioxabicyclo[3.2.1]octan-3-yl)oxy]-5,6-dihydroxy-2-phenylchromen-4-one	69755698	Click to see	428.30	unknown	https://doi.org/10.1248/CPB.33.2411
7-[[(1S,3S,4R,5S,8R)-4,8-dihydroxy-7-oxo-2,6-dioxabicyclo[3.2.1]octan-3-yl]oxy]-5,6-dihydroxy-2-phenylchromen-4-one	162921922	Click to see	428.30	unknown	https://doi.org/10.1248/CPB.33.2411
Oroxin A	5320313	Click to see	432.40	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1248/YAKUSHI1947.105.2_148
wogonin 7-O-glucoside	51136398	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)CO)O)O)O	446.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2R)-2-(2,6-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol	124708188	Click to see C1CC2=C(C=C(C=C2OC1C3=C(C=CC=C3O)O)O)O	274.27	unknown	https://doi.org/10.1248/CPB.33.2411
2',5,6',7-Tetrahydroxyflavane	92043131	Click to see	274.27	unknown	https://doi.org/10.1248/CPB.33.2411
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 2-O-methylated flavonoids
5-Hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethylchromen-4-one	162904250	Click to see	326.30	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-)	25203524	Click to see	299.25	unknown	via CMAUP database
Geraldone	5281618	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Quercetagetin 3-methyl ether	5320475	Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O	332.26	unknown	via CMAUP database
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see	284.26	unknown	via CMAUP database
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	https://doi.org/10.1111/J.1600-0609.2009.01365.X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7,2',6'-Trihydroxy-5-methoxyflavanone	5322075	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=C(C=CC=C3O)O)O	302.28	unknown	via CMAUP database
> 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/10.1248/YAKUSHI1947.105.2_148
5,7,4'-Trihydroxy-6-methoxyflavanone	5322074	Click to see	302.28	unknown	via CMAUP database
6-Methoxynaringenin	46893290	Click to see COC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
Oroxylin A	5320315	Click to see	284.26	unknown	https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1007/BF00630621 https://doi.org/10.5586/ASBP.1999.015 https://doi.org/10.1002/MC.20570 https://doi.org/10.1002/PTR.1216 https://doi.org/10.1021/NP9003036 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1007/BF02277510 https://doi.org/10.1248/CPB.51.339 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1016/S0006-2952(03)00233-8
Tenaxin II	5322076	Click to see	300.26	unknown	https://doi.org/10.1248/CPB.40.531
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(2,6-dimethoxyphenyl)-3,5,7-trimethoxy-2,3-dihydrochromen-4-one	162958441	Click to see COC1C(OC2=C(C1=O)C(=CC(=C2)OC)OC)C3=C(C=CC=C3OC)OC	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
2-(2,6-Dimethoxyphenyl)-3,5,7-trimethoxy-2,3-dihydrochromen-4-one	162958440	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7
2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4H-chromene-3,4-diol	5316834	Click to see COC1=C(C=C(C=C1)C2=C(C(C3=CC(=C(C=C3O2)OC)OC)O)O)OC	360.40	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 5,8-dihydroxy-2-(2-hydroxyphenyl)-6,7-dimethoxy-	156993	Click to see	330.29	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	102445447	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)OC	492.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	163049058	Click to see	492.40	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7-dimethoxychromen-4-one	74977825	Click to see	492.40	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1016/S0031-9422(96)00443-8
5,8-Dihydroxy-6,7-dimethoxyflavone	153441	Click to see	314.29	unknown	via CMAUP database
5,8,2'-Trihydroxy-7-methoxyflavone	156992	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3O)O	300.26	unknown	https://doi.org/10.1248/YAKUSHI1947.100.12_1220
Chrysosplenetin	5281608	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1111/J.1600-0609.2009.01365.X
Salvigenin	161271	Click to see	328.30	unknown	https://doi.org/10.1248/YAKUSHI1947.104.5_529
Tectochrysin	5281954	Click to see	268.26	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-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)-3-methoxyphenoxy]oxane-2-carboxylic acid	14825641	Click to see	520.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl) (2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoate	163052805	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC(=O)C(C(C(C(C=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.33.2411
(5-Hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl) 2,3,4,5-tetrahydroxy-6-oxohexanoate	163052804	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC(=O)C(C(C(C(C=O)O)O)O)O	460.40	unknown	https://doi.org/10.1248/CPB.33.2411
2-C-(5-Hydroxy-8-methoxy-4-oxo-2-phenyl-4H-1-benzopyran-7-YL)-D-glucuronic acid	29927693	Click to see	460.40	unknown	via CMAUP database
3,4,5-Trihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)-3-methoxyphenoxy]oxane-2-carboxylic acid	14825640	Click to see COC1=C(C(=CC=C1)OC2C(C(C(C(O2)C(=O)O)O)O)O)C3=CC(=O)C4=C(O3)C(=C(C=C4O)OC)OC	520.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
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/10.1248/CPB.38.3488
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7,8-trimethoxychromen-4-one	162869198	Click to see	522.50	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/0031-9422(95)00200-Q
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one	101932172	Click to see	492.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5-hydroxy-2-[2-hydroxy-6-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7,8-trimethoxychromen-4-one	162869199	Click to see	522.50	unknown	https://doi.org/10.1016/0031-9422(95)00200-Q
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one	133561455	Click to see	492.40	unknown	https://doi.org/10.1016/S0031-9422(96)00443-8
5-Hydroxy-7,8-dimethoxyflavone	188316	Click to see	298.29	unknown	via CMAUP database
5,2'-Dihydroxy-6,7,8,3'-tetramethoxy flavone	15896301	Click to see	374.30	unknown	https://doi.org/10.1016/S0031-9422(99)00306-4
5,2',5'-Trihydroxy-6,7,8-trimethoxyflavone	21721900	Click to see	360.30	unknown	via CMAUP database
5,2',5'-Trihydroxy-7,8-dimethoxyflavone	21122623	Click to see	330.29	unknown	https://doi.org/10.1248/CPB.40.531
5,7-dihydroxy-2-[3-hydroxy-2-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-methoxychromen-4-one	102445446	Click to see COC1=C(C=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O	508.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-2-[3-hydroxy-2-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-methoxychromen-4-one	74977898	Click to see	508.40	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1016/S0031-9422(96)00443-8
5,7-Dihydroxy-6,8-dimethoxyflavone	11609345	Click to see	314.29	unknown	via CMAUP database
5,7-Dihydroxy-6,8,2',3'-tetramethoxyflavone	5316833	Click to see	374.30	unknown	via CMAUP database
5,7,2'-Trihydroxy-6,8-dimethoxyflavone	9818878	Click to see	330.29	unknown	https://doi.org/10.1055/S-2002-36357
5,7,2'-Trihydroxy-8,6'-dimethoxyflavone	5322060	Click to see	330.29	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531
5,7,2',3'-Tetrahydroxy-8,6'-dimethoxyflavone	21718608	Click to see	346.30	unknown	https://doi.org/10.1055/S-2007-969712
5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone	5321859	Click to see	346.30	unknown	via CMAUP database
6,2'-Dihydroxy-5,7,8,6'-tetramethoxyflavone	10872445	Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)O)OC)OC)O	374.30	unknown	https://doi.org/10.1055/S-2002-36357
Ganhuangenin	5271991	Click to see	346.30	unknown	https://doi.org/10.1055/S-0029-1243111 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/0031-9422(95)00200-Q https://doi.org/10.1007/BF00630621 https://doi.org/10.1002/(SICI)1099-1573(199808)12:5<340::AID-PTR316>3.0.CO;2-U https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1248/CPB.33.3982
Rivularin (flavone)	13889022	Click to see	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1016/S0031-9422(96)00443-8
Scutevulin	5321205	Click to see	300.26	unknown	via CMAUP database
Skullcapflavone I	5320399	Click to see	314.29	unknown	https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/YAKUSHI1947.107.10_827 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1006/JMCC.1999.1021
Skullcapflavone Ii	124211	Click to see	374.30	unknown	https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1007/BF02976430 https://doi.org/10.1016/J.ETAP.2014.12.002 https://doi.org/10.1016/0031-9422(95)00200-Q https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1352373/ https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1055/S-2006-957517 https://doi.org/10.1006/JMCC.1999.1021 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1248/YAKUSHI1947.105.2_148
Tenaxin I	159029	Click to see	344.30	unknown	https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1016/S0031-9422(96)00443-8
Viscidulin II	5322059	Click to see	330.29	unknown	https://doi.org/10.1248/CPB.40.531
Wogonin	5281703	Click to see	284.26	unknown	https://doi.org/10.5586/ASBP.1999.015 https://doi.org/10.1248/YAKUSHI1947.105.2_148 https://doi.org/10.1007/BF02277510 https://doi.org/10.15281/JPLANTRES1887.36.1 https://doi.org/10.1002/CHIN.200333219 https://doi.org/10.1006/JMCC.1999.1021 https://doi.org/10.1007/BF00040133 https://doi.org/10.1016/S0031-9422(96)00443-8 https://doi.org/10.1016/J.JPBA.2010.04.019 https://doi.org/10.1016/S0031-9422(00)94792-7 https://doi.org/10.1055/S-2007-969712 https://doi.org/10.1248/CPB.40.531 https://doi.org/10.1248/CPB.51.339 https://doi.org/10.1055/S-2007-969517 https://doi.org/10.1016/S0006-2952(02)01347-3 https://doi.org/10.1002/(SICI)1099-1573(199808)12:5<340::AID-PTR316>3.0.CO;2-U https://doi.org/10.1248/YAKUSHI1947.104.5_529 https://doi.org/10.1248/CPB.33.4894 https://doi.org/10.1016/S0031-9422(99)00306-4 https://doi.org/10.1016/S0176-1617(00)80282-5 https://doi.org/10.1248/CPB.35.3494 https://doi.org/10.1055/S-2001-15810 https://doi.org/10.1016/S0378-8741(97)00045-7 https://doi.org/10.1248/CPB.50.896 https://doi.org/10.1016/S0304-4165(99)00152-X https://doi.org/10.1158/1078-0432.CCR-04-1974 https://doi.org/10.1007/BF02980087 https://doi.org/10.1515/ZNC-1997-11-1215 https://doi.org/10.1016/S0021-9673(01)87399-4 https://doi.org/10.1055/S-2006-961769 https://doi.org/10.1007/BF02976430 https://doi.org/10.1002/(SICI)1099-1573(199909)13:6<479::AID-PTR484>3.0.CO;2-M https://doi.org/10.1016/0003-2670(94)80134-7 https://doi.org/10.1016/S0021-9673(98)00906-6 https://doi.org/10.1055/S-2006-958036 https://doi.org/10.1248/CPB.33.2411 https://doi.org/10.1248/BPB.31.838 https://doi.org/10.1248/YAKUSHI1947.107.4_315 https://doi.org/10.1111/J.2042-7158.1997.TB06119.X https://doi.org/10.1248/CPB.32.5051 https://doi.org/10.1055/S-0029-1243121
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257269	Click to see	594.50	unknown	via CMAUP database
Puerarin	5281807	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O	416.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Iridin	5281777	Click to see COC1=CC(=CC(=C1OC)O)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2',7-Dihydroxy-4',5'-dimethoxyisoflavone	5316763	Click to see COC1=C(C=C(C(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)OC	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-(2,6-dihydroxyphenyl)-2-propen-1-one	5321869	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=C(C=CC=C2O)O)O)O	302.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Combretastatin A4	5351344	Click to see	316.30	unknown	via CMAUP database
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien	192694	Click to see	330.29	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Scutellaria baicalensis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top