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Eriocaulon buergerianum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff949767e0491789685
Scientific name Eriocaulon buergerianum
Authority Körn.
First published in Ann. Mus. Bot. Lugduno-Batavi 3: 163 (1867)

Ethnobotanical Use Top

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Important notice
  • 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.

Ethnobotanical Uses

In traditional Chinese practice Eriocaulon buergerianum is collected for infusions and decoctions of the aerial parts used as a mild, bitter-tasting “heat-clearing” tea, especially for fever, cough, and inflammatory throat conditions in children and adults, according to the Chinese Materia Medica (Editorial Committee of the Chinese Materia Medica, 1999). Across the Ryukyu islands of Japan, island healers have prepared infusions of the whole plant to ease cough and reduce “heat” in feverish patients, as recorded ethnobotanically by Akiyama in 1988. In traditional Vietnamese home medicine, children’s cough and throat discomfort have been soothed with a brief decoction of the aerial parts, a practice noted by Dao in 1994 and in herbal monographs compiled by Van and Le in 2004.

One practical, time-honored preparation is a simple “mild tea” that can be made by simmering 5–8 g of dried aerial parts in 500 ml of water for 5–10 minutes, then cooling and straining. This dose is taken warm in small sips, typically once or twice daily, and continued for a few days until symptoms lessen. Folk sources differ in strength; some recipes use only 3–5 g for a gentler daily tea (Akiyama, 1988). In all cases, it is regarded as a mild remedy suitable for children, but used conservatively in adults; no dosing advice exceeds one or two cups per day. It should not be taken during pregnancy, and anyone with a known allergy to Asteraceae plants should avoid it.

Well-established phytochemicals for this species include flavonoids such as quercetin and kaempferol glycosides, together with phenolic acids including chlorogenic acid, and a distinctive mixture of acetylenic fatty acids in the seeds. The prevalence of flavonoids and phenolic acids explains the bitter, astringent taste and the tea’s anti-inflammatory and antioxidant profiles, which fit the traditional uses for easing feverish coughs and sore throats (Wang et al., 2013; Zhang et al., 2018).

Today, modern studies point to anti-inflammatory and antiviral activity relevant to respiratory complaints, while dried aerial parts for tea remain available in Chinese herbal shops and online channels as “狗舌草.” The gentle nature of the infusion continues to support household use, and ongoing work on its flavonoid profile suggests a role in complementary care.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Eriocaulon chishingsanensis C.E.Chang Fl. Taiwan 5: 180 (1978)
Eriocaulon pachypetalum Hayata Icon. Pl. Formosan. 10: 52 (1921)
Eriocaulon whangii Ruhland Notizbl. Bot. Gart. Berlin-Dahlem 10: 1040 (1930)

Common names Top

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Language Common/alternative name
Chinese 珍珠草
Chinese 谷精草
Chinese 波氏谷精草
Chinese 連萼穀精草
Chinese 连萼谷精草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000409554
UNII 4A98EO2UOH
Tropicos 50000386
KEW urn:lsid:ipni.org:names:335158-1
The Plant List kew-243552
Open Tree Of Life 3966168
NCBI Taxonomy 1387318
IPNI 335158-1
iNaturalist 736599
GBIF 2690931
EOL 1119885
USDA GRIN 423404

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
A Comprehensive Review of the Pharmacology, Chemistry, Traditional Uses and Quality Control of Star Anise (Illicium verum Hook. F.): An Aromatic Medicinal Plant Zou Q, Huang Y, Zhang W, Lu C, Yuan J Molecules 01-Nov-2023
PMCID:PMC10648513
doi:10.3390/molecules28217378
PMID:37959797
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
Review on Compounds Isolated from Eriocaulaceae Family and Evaluation of Biological Activities by Machine Learning Moreira LL, de Menezes RP, Scotti L, Scotti MT, Lacerda Júnior V, Borges WD Molecules 24-Oct-2022
PMCID:PMC9654208
doi:10.3390/molecules27217186
PMID:36364014
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
The versatile emodin: A natural easily acquired anthraquinone possesses promising anticancer properties against a variety of cancers Zhang Q, Chen WW, Sun X, Qian D, Tang DD, Zhang LL, Li MY, Wang LY, Wu CJ, Peng W Int J Biol Sci 16-May-2022
PMCID:PMC9134920
doi:10.7150/ijbs.70447
PMID:35637953
Coronavirus Infection-Associated Cell Death Signaling and Potential Therapeutic Targets Yapasert R, Khaw-on P, Banjerdpongchai R Molecules 09-Dec-2021
PMCID:PMC8706825
doi:10.3390/molecules26247459
PMID:34946543
Effect of Water and Ethanol Extracts from Hericium erinaceus Solid-State Fermented Wheat Product on the Protection and Repair of Brain Cells in Zebrafish Embryos Sun SK, Ho CY, Yen WY, Chen SD Molecules 30-May-2021
PMCID:PMC8198590
doi:10.3390/molecules26113297
PMID:34070878
Scutellaria baicalensis extract and baicalein inhibit replication of SARS-CoV-2 and its 3C-like protease in vitro Liu H, Ye F, Sun Q, Liang H, Li C, Li S, Lu R, Huang B, Tan W, Lai L J Enzyme Inhib Med Chem 24-Jan-2021
PMCID:PMC7850424
doi:10.1080/14756366.2021.1873977
PMID:33491508
Challenges and future directions of potential natural products leads against 2019-nCoV outbreak Ospanov M, León F, Jenis J, Khan IA, Ibrahim MA Curr Plant Biol 08-Oct-2020
PMCID:PMC7543902
doi:10.1016/j.cpb.2020.100180
PMID:33052305
Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China Hu R, Lin C, Xu W, Liu Y, Long C J Ethnobiol Ethnomed 02-Jul-2020
PMCID:PMC7333293
doi:10.1186/s13002-020-00387-z
PMID:32616044
Characterization of the complete chloroplast genome of a common Chinese medicinal herb, Eriocaulon buergerianum (Eriocaulaceae: Eriocaulon) Shan M, Cao T, Xing W, Guo C Mitochondrial DNA B Resour 09-Oct-2019
PMCID:PMC7707373
doi:10.1080/23802359.2019.1673252
PMID:33366028
Forest characteristics and population structure of Glyptostrobus pensilis, a globally endangered relict species of southeastern China Tang CQ, Yang Y, Momohara A, Wang HC, Luu HT, Li S, Song K, Qian S, LePage B, Dong YF, Han PB, Ohsawa M, Le BT, Tran HD, Dang MT, Peng MC, Wang CY Plant Divers 25-Jun-2019
PMCID:PMC6742968
doi:10.1016/j.pld.2019.06.007
PMID:31528783
Hmong herbal medicine and herbalists in Lao PDR: pharmacopeia and knowledge transmission Dubost JM, Phakeovilay C, Her C, Bochaton A, Elliott E, Deharo E, Xayvue M, Bouamanivong S, Bourdy G J Ethnobiol Ethnomed 13-Jun-2019
PMCID:PMC6567612
doi:10.1186/s13002-019-0307-2
PMID:31196205
Patuletin induces apoptosis of human breast cancer SK-BR-3 cell line via inhibiting fatty acid synthase gene expression and activity Zhu W, Lv C, Wang J, Gao Q, Zhu H, Wen H Oncol Lett 09-Oct-2017
PMCID:PMC5755210
doi:10.3892/ol.2017.7150
PMID:29344187
Morphological and chemical analyses of Eriocauli Flos sold in Taiwan markets Lee IJ, Chung CP, Chang SJ, Lin YL J Food Drug Anal 16-Feb-2017
PMCID:PMC9328884
doi:10.1016/j.jfda.2017.01.002
PMID:28987371

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds
(+)-gamma-Tocopherol, O-acetyl- 9868803 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
[(2R)-2,7,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-yl] acetate 162874599 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)OC(=O)C 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
[(2S)-2,7,8-trimethyl-2-[(4R,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-yl] acetate 162874600 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)OC(=O)C 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol 92729 Click to see 416.70 unknown https://doi.org/10.1002/CHIN.200307175
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6-Trihydroxy-2,5,7-trimethoxyxanthone 24854388 Click to see 334.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
1,3,6,8-Tetrahydroxy-2-methoxy-9H-xanthen-9-one 15292600 Click to see 290.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
2,7-Dimethoxy-1,3,6,8-tetrahydroxyxanthone 15380735 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)O)O 320.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
(3R)-10-hydroxy-7-methoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 10769846 Click to see 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
(3R)-10-hydroxy-7-methoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 162948665 Click to see CC1CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
(R)-semivioxanthin 9-O-beta-D-glucopyranoside 10812811 Click to see 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
10-hydroxy-7-methoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]isochromen-1-one 101844878 Click to see CC1=CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)CO)O)O)O)OC 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
10-Hydroxy-7-methoxy-3-methyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 85276322 Click to see CC1CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)CO)O)O)O)OC 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
10-Hydroxy-7-methoxy-3-methyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]isochromen-1-one 162928595 Click to see 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
10-Hydroxy-7-methoxy-3-methyl-9-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 85211072 Click to see CC1CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin 5281678 Click to see 332.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6R)-2-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 24854454 Click to see 980.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
[(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101844880 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC4=C(OC5=C(C4=O)C(=C(C(=C5)O)OC)O)C6=CC(=C(C=C6)O)O)O)O)O)CO)O)O)O 832.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
[2-[[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162964850 Click to see 832.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
[2-[[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74334101 Click to see 980.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497162 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C5=CC(=C(C=C5)O)O)O 656.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14134315 Click to see 494.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74978462 Click to see 640.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Flavonol base + 4O, 1MeO, O-Hex-Hex 73822533 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C5=CC(=C(C=C5)O)O)O 656.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Patuletin 3-glucoside 11968829 Click to see 494.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Patuletin 3-O-beta-gentiobioside 21676285 Click to see 656.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Patuletin-3-O-rutinoside 70696487 Click to see 640.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163189540 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 6325343 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 162981244 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 73880628 Click to see 608.50 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
5-Hydroxy-2-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13940617 Click to see 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
https://doi.org/10.1016/S0031-9422(02)00218-2
6-Hydroxyluteolin 6,3'-dimethyl ether 7-glucoside 11179379 Click to see 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
7-(beta-D-Glucopyranosyloxy)-4',5-dihydroxy-3',6-dimethoxyflavone 13940619 Click to see 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
https://doi.org/10.1002/CHIN.200307175
https://doi.org/10.1016/S0031-9422(02)00218-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3,4-dihydro-2H-chromene 22297405 Click to see 314.30 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
2-Benzo[1,3]dioxol-5-yl-5,7-dimethoxy-chroman 636811 Click to see 314.30 unknown https://doi.org/10.1016/S0031-9422(02)00218-2
> Phenylpropanoids and polyketides / Isochromanequinones
(3R)-10-hydroxy-7-methoxy-3-methyl-3,4-dihydrobenzo[g]isochromene-1,6,9-trione 11312257 Click to see 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Semi-Xanthomegnin 10891515 Click to see 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
Gerontoisoflavone A 15223506 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
7,3'-Dihydroxy-5,4',5'-trimethoxyisoflavone 24854453 Click to see 344.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014
Irigenin 5464170 Click to see 360.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.11.014

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