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Internal ID UUID644043fdd13c8677201295
Scientific name Lyonia ovalifolia
Authority (Wall.) Drude
First published in Nat. Pflanzenfam. 4(1): 44 (1889)

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.

Known as “patki” in Assam and “guru” in parts of Uttarakhand, Lyonia ovalifolia has been used as a topical and external remedy across South Asia. Among Assamese communities, a poultice of fresh leaves is applied to swollen joints and inflammation, with leaf extract occasionally given in small doses for fever; the practice is recorded by Shukla and Kar (1973). In Meghalaya, Khasi and neighboring groups crush leaves into a wet mass and bind it with cloth on swellings and sprains, or gently foment affected areas with warm leaf water; Jain (1991) lists these applications for L. ovalifolia. In Uttarakhand’s Almora district, villagers use a decoction of bark or twig as a fever reducer, and the Bhotiya peoples combine seeds with milk or water to expel parasites; the latter is noted by Hooker (1882) and Jain (1991). Where available, both leaf and seed are prepared fresh and applied externally; bark or twig decoction is the preferred internal use in the Himalayan hills.

A practical preparation used traditionally in the Khasi Hills and Assamese foothills is a mild leaf foment: place a small handful (roughly 50–60 g) of fresh leaves in a pot with 1–1.5 L of water, bring to a simmer for 10–15 minutes, then cool to comfortably warm. Soak a clean cloth in the liquid and apply to the affected area for 10–20 minutes, repeating 2–3 times per day as needed for inflammation or bruises (Jain, 1991). For a 1:5 ethanol tincture of twig—used in the Uttarakhand hills as a brief febrifuge—dry and coarsely chop 200 g of young twig, macerate in 1 L of 45–50% alcohol in a clean jar, shake daily, and strain after 4 weeks; dose no more than 0.5–1.0 mL (about 10–20 drops) taken once with water. All preparations should be used with caution: members of Ericaceae can contain grayanotoxins and other diterpenoids, making overdoses possible; do not exceed the stated dose, avoid during pregnancy and lactation, and discontinue if dizziness or heart palpitations occur.

The active chemistry of Lyonia ovalifolia is consistent with its Ericaceous relatives. Leaves and nectar can carry grayanotoxins such as grayanotoxin I and II, diterpenoids known to bind sodium channels and modify cardiac and neurologic function (Liang et al., 2011). The bark and stems also contain triterpenoids, including betulinic acid and lupeol, widely distributed in this family and noted for L. ovalifolia by Wang et al. (2013). These well‑established compounds plausibly explain the reported anti‑inflammatory, antipyretic, and antimicrobial actions observed in field accounts.

While indigenous communities continue to use leaf foment for swelling and limited febrifuge applications from twig decoctions, commercial availability is minimal outside local herbal markets. Modern pharmacological work remains sparse, but recent Chinese reports describe the isolation of known diterpenoids and triterpenoids from L. ovalifolia, underscoring why plants of this group have featured repeatedly in regional folk practice (Liang et al., 2011; Wang et al., 2013).

General Uses Top

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Common products:
Fuelwood and charcoal from mature stems are recorded in India and Nepal. In parts of the Himalaya, young branchlets are made into brooms.

Industrial and craft applications:
Bark is used for tanning leather in Sikkim; the bark contains tannins and is processed with other tanning materials to produce brown leather (Fyson 1915; Kirtikar & Basu 1935).

Food and beverages (non-medicinal):
No established non-medicinal food or beverage uses are documented for this taxon.

Colorants and tanning:
Tannin from the bark yields brown dyes and is employed in leather tanning; it is typically combined with other tanning agents (Fyson 1915; Kirtikar & Basu 1935).

Wood and fiber:
Hard but uneven wood is suitable for fuel and light-duty tools; young stems furnish brooms (Gamble 1915–1936; Bor 1940). Fiber content has not been quantified for this species.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
Bark tannin content and lignin-rich stem wood support tanning and fuel applications, respectively (Fyson 1915; Gamble 1915–1936).

Standards and regulation:
Not applicable.

Sustainability and sourcing:
Widely distributed across the Himalaya to SE Asia; local harvesting for fuel and brooms can exert pressure on local populations if not managed, though no quantitative sustainability data are reported for this species.

Synonyms Top

Scientific name Authority First published in
Andromeda capricida Buch.-Ham. ex D.Don Prodr. Fl. Nepal. : 148 (1825)
Andromeda cordata Royle Ill. Bot. Himal. Mts. : 258 (1835)
Arbutus herpetica Colebr. ex Roxb. Fl. Ind. 2: 412 (1824)
Pieris ovalifolia (Wall.) D.Don Edinburgh New Philos. J. 17: 159 (1834)
Andromeda ovalifolia Wall. Asiat. Res. 13: 391 (1820)
Xolisma ovalifolia (Wall.) Rehder J. Arnold Arbor. 5: 52 (1924)

Common names Top

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Language Common/alternative name
dty अङ्गेरी
Nepali अंगेरी
Chinese 南烛
Chinese 米饭花
Chinese 小米柴
Chinese 珍珠花
Chinese 綟木
Chinese 南燭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Lyonia ovalifolia var. elliptica (Siebold & Zucc.) Hand.-Mazz. Symb. Sin. 7: 788. 1936 (1936)
Lyonia ovalifolia var. hebecarpa (Franch. ex F.B.Forbes & Hemsl.) Chun Sunyatsenia 4: 253. 1940 (1940)
Lyonia ovalifolia var. lanceolata (Wall.) Hand.-Mazz. Symb. Sin. 7: 788. 1936 (1936)
Lyonia ovalifolia var. rubrovenia (Merr.) Judd J. Arnold Arbor. 60: 491 (1979)
Lyonia ovalifolia var. tomentosa (W.P.Fang) C.Y.Wu Fl. Yunnanica 4: 567 (1986)
Lyonia ovalifolia var. ovalifolia

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 North-central
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Japan
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001047539
Tropicos 12303535
KEW urn:lsid:ipni.org:names:326338-1
IPNI 326338-1
GBIF 5684142
USDA GRIN 3136
Tropicos 12302423
KEW urn:lsid:ipni.org:names:60447937-2
The Plant List tro-12302423
Open Tree Of Life 894623
NCBI Taxonomy 49153
IUCN Red List 145822234
IPNI 60447937-2
iNaturalist 428740
GBIF 7328514
Freebase /m/0nb520m
EPPO LYDOV
USDA GRIN 22997
Wikipedia Lyonia_ovalifolia
PFAF Lyonia ovalifolia

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
Population Structures and Dynamics of Rhododendron Communities with Different Stages of Succession in Northwest Guizhou, China Zhang Y, Wang J, Wang X, Wang L, Wang Y, Wei J, Niu Z, Jian L, Jin B, Chen C, Zhao X Plants (Basel) 25-Mar-2024
PMCID:PMC11013785
doi:10.3390/plants13070946
PMID:38611476
Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China Li K, Tan B, Liao M, Ni J Front Plant Sci 20-Mar-2024
PMCID:PMC10987713
doi:10.3389/fpls.2024.1348182
PMID:38571712
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Ethnomedicinal plants in Champadevi rural municipality, Okhaldhunga district, Nepal Karki D, Khadka D, Kunwar RM, Aryal PC, Paudel HR, Bhatta S, Shi S J Ethnobiol Ethnomed 11-Dec-2023
PMCID:PMC10712033
doi:10.1186/s13002-023-00627-y
PMID:38072922
The Carbon Isotope Composition of Epiphytes Depends Not Only on Their Layers, Life Forms, and Taxonomical Groups but Also on the Carbon and Nitrogen Indicators of Host Trees Eskov AK, Elumeeva TG, Leonov VD, Tsurikov SM, Viktorova VA, Prilepsky NG, Abakumov EV Plants (Basel) 08-Oct-2023
PMCID:PMC10575002
doi:10.3390/plants12193500
PMID:37836240
Editorial: Investigating the impact of bioactive metabolites and extracts in human health and disease Kumar S, Gautam V, Singh BP, Kumar D Front Mol Biosci 07-Aug-2023
PMCID:PMC10441665
doi:10.3389/fmolb.2023.1244316
PMID:37609374
Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y Heliyon 13-Jul-2023
PMCID:PMC10368863
doi:10.1016/j.heliyon.2023.e18214
PMID:37501975
Ecological Stoichiometry and Stock Distribution of C, N, and P in Three Forest Types in a Karst Region of China Wang W, Peng Y, Chen Y, Lei S, Wang X, Farooq TH, Liang X, Zhang C, Yan W, Chen X Plants (Basel) 30-Jun-2023
PMCID:PMC10346562
doi:10.3390/plants12132503
PMID:37447063
Assessment of the dual role of Lyonia ovalifolia (Wall.) Drude in inhibiting AGEs and enhancing GLUT4 translocation through LC-ESI-QTOF-MS/MS determination and in silico studies Sahu N, Singh N, Arya KR, Reddy SS, Rai AK, Shukla V, Pandey J, Narender T, Tamrakar AK, Kumar B, Rajak BK, Malik S, Rustagi S Front Pharmacol 27-Mar-2023
PMCID:PMC10083281
doi:10.3389/fphar.2023.1073327
PMID:37050897
Socio-administrative conservation and collection practices of the sacred Thal Kedar forest, Uttarakhand, India Joshi DD, Rana VS, Kharkwal H Heliyon 21-Mar-2023
PMCID:PMC10161254
doi:10.1016/j.heliyon.2023.e14619
PMID:37151682
Influences of environment, human activity, and climate on the invasion of Ageratina adenophora (Spreng.) in Southwest China Zhang X, Wang G, Peng P, Zhou Y, Chen Z, Feng Y, Wang Y, Shi S, Li J PeerJ 09-Mar-2023
PMCID:PMC10008309
doi:10.7717/peerj.14902
PMID:36919167
Risks for human health related to the presence of grayanotoxins in certain honey Schrenk D, Bignami M, Bodin L, Chipman JK, del Mazo J, Grasl‐Kraupp B, Hogstrand C, Hoogenboom L(, Leblanc J, Nebbia CS, Nielsen E, Ntzani E, Petersen A, Sand S, Schwerdtle T, Vleminckx C, Dusemund B, Hart A, Mulder P, Viviani B, Anastassiadou M, Cascio C, Riolo F, Wallace H EFSA J 02-Mar-2023
PMCID:PMC9978999
doi:10.2903/j.efsa.2023.7866
PMID:36875862
Screening of Antioxidant, Antibacterial, Anti-Adipogenic, and Anti-Inflammatory Activities of Five Selected Medicinal Plants of Nepal Lamichhane G, Sharma G, Sapkota B, Adhikari M, Ghimire S, Poudel P, Jung HJ J Exp Pharmacol 02-Mar-2023
PMCID:PMC9987241
doi:10.2147/JEP.S388968
PMID:36891159
Ultra-High Hydrostatic Pressure Pretreatment on White Que Zui Tea: Chemical Constituents, Antioxidant, Cytoprotective, and Anti-Inflammatory Activities Zhang X, Li M, Zhen L, Wang Y, Wang Y, Qin Y, Zhang Z, Zhao T, Cao J, Liu Y, Cheng G Foods 01-Feb-2023
PMCID:PMC9914134
doi:10.3390/foods12030628
PMID:36766156
Red pigments in autumn leaves of Norway maple do not offer significant photoprotection but coincide with stress symptoms Mattila H, Tyystjärvi E Tree Physiol 30-Jan-2023
PMCID:PMC10177003
doi:10.1093/treephys/tpad010
PMID:36715646

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
> Lignans, neolignans and related compounds / Aryltetralin lignans
(+)-(7'S,8S,8'S)-3',4-dihydroxy-2',3,4',5-tetramethoxy-6',9-epoxy-2,7'-cyclolignan-9'-ol 53356206 Click to see 418.40 unknown https://doi.org/10.1248/CPB.58.191
(1S,10S,18S)-4,15-dihydroxy-18-(hydroxymethyl)-3,5,14,16-tetramethoxy-8-oxatetracyclo[8.7.1.02,7.012,17]octadeca-2,4,6,12,14,16-hexaen-11-one 163019014 Click to see 432.40 unknown https://doi.org/10.1248/CPB.58.191
(1S,2S,11S,18S)-7,9,13,15-tetramethoxy-4,19-dioxapentacyclo[9.9.0.02,18.05,10.012,17]icosa-5,7,9,12,14,16-hexaene-8,14-diol 162987937 Click to see 416.40 unknown https://doi.org/10.1248/CPB.58.191
(2R,5R,6R,9S)-9-(4-hydroxy-3,5-dimethoxyphenyl)-11,13-dimethoxy-3,8-dioxatetracyclo[8.4.0.02,6.05,9]tetradeca-1(14),10,12-trien-12-ol 46178176 Click to see COC1=CC(=CC(=C1O)OC)C23C4COC(C4CO2)C5=CC(=C(C(=C35)OC)O)OC 416.40 unknown https://doi.org/10.1248/CPB.58.191
(3S,4R)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carbaldehyde 163034289 Click to see 416.40 unknown https://doi.org/10.1248/CPB.58.191
18-(Hydroxymethyl)-3,5,14,16-tetramethoxy-8-oxatetracyclo[8.7.1.02,7.012,17]octadeca-2,4,6,12,14,16-hexaene-4,15-diol 75163494 Click to see 418.40 unknown https://doi.org/10.1248/CPB.58.191
4,15-Dihydroxy-18-(hydroxymethyl)-3,5,14,16-tetramethoxy-8-oxatetracyclo[8.7.1.02,7.012,17]octadeca-2,4,6,12,14,16-hexaen-11-one 75163495 Click to see COC1=C(C(=C2C3C(C(COC4=CC(=C(C(=C34)OC)O)OC)C(=O)C2=C1)CO)OC)O 432.40 unknown https://doi.org/10.1248/CPB.58.191
6-Hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carbaldehyde 75163497 Click to see 416.40 unknown https://doi.org/10.1248/CPB.58.191
7,9,13,15-Tetramethoxy-4,19-dioxapentacyclo[9.9.0.02,18.05,10.012,17]icosa-5,7,9,12,14,16-hexaene-8,14-diol 75162896 Click to see 416.40 unknown https://doi.org/10.1248/CPB.58.191
9-(4-Hydroxy-3,5-dimethoxyphenyl)-11,13-dimethoxy-3,8-dioxatetracyclo[8.4.0.02,6.05,9]tetradeca-1(14),10,12-trien-12-ol 75163496 Click to see 416.40 unknown https://doi.org/10.1248/CPB.58.191
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(73)85143-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids
(2,4,10,15-Tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl) acetate 10386869 Click to see CC(=O)OC1C(C23CC(CCC2C(C4C1(C(C5C4O5)(C)C)O)(C)O)C(C3)(C)O)O 410.50 unknown https://doi.org/10.1248/YAKUSHI1947.90.7_893
(3,4,10,15-Tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-2-yl) acetate 74053734 Click to see 410.50 unknown https://doi.org/10.1248/CPB.29.280
[(1R,2S,3R,4R,6R,8S,9R,10R,11S,14R,15R)-2,4,10,15-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl] acetate 162969145 Click to see 410.50 unknown https://doi.org/10.1248/YAKUSHI1947.90.7_893
Lyoniol-A 161699 Click to see CC(=O)OC1C(C2(C(C3C(C2(C)C)O3)C(C4C15CC(CC4)C(C5)(C)O)(C)O)O)O 410.50 unknown https://doi.org/10.1248/CPB.29.280
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
(3,14,15,16-Tetraacetyloxy-9-hydroxy-9,14-dimethyl-6-oxo-4-prop-1-en-2-yl-5-oxatetracyclo[11.2.1.01,10.04,8]hexadecan-2-yl) propanoate 75166918 Click to see 622.70 unknown https://doi.org/10.1002/CBDV.201000188
[(1S,2S,3R,4R,8S,9R,10R,13R,14S,15R,16R)-3,14,15,16-tetraacetyloxy-9-hydroxy-9,14-dimethyl-6-oxo-4-prop-1-en-2-yl-5-oxatetracyclo[11.2.1.01,10.04,8]hexadecan-2-yl] propanoate 46187486 Click to see CCC(=O)OC1C(C2(C(CC(=O)O2)C(C3C14C(C(CC3)C(C4OC(=O)C)(C)OC(=O)C)OC(=O)C)(C)O)C(=C)C)OC(=O)C 622.70 unknown https://doi.org/10.1002/CBDV.201000188
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
D-Xylose 135191 Click to see 150.13 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(2,3,11,14,15-Pentaacetyloxy-4-hydroxy-9,14-dimethyl-7-oxo-4-prop-1-en-2-yl-8-oxatetracyclo[11.2.1.01,10.05,9]hexadecan-16-yl) propanoate 75166999 Click to see CCC(=O)OC1C2CC(C3C1(C(C(C(C4C3(OC(=O)C4)C)(C(=C)C)O)OC(=O)C)OC(=O)C)C(C2(C)OC(=O)C)OC(=O)C)OC(=O)C 680.70 unknown https://doi.org/10.1002/CBDV.201000188
[(1S,2S,3R,4R,5R,9R,10S,11S,13R,14S,15R,16R)-2,3,11,14,15-pentaacetyloxy-4-hydroxy-9,14-dimethyl-7-oxo-4-prop-1-en-2-yl-8-oxatetracyclo[11.2.1.01,10.05,9]hexadecan-16-yl] propanoate 46187657 Click to see 680.70 unknown https://doi.org/10.1002/CBDV.201000188
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(73)85143-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
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/10.1248/YAKUSHI1947.94.10_1349
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1248/YAKUSHI1947.79.3_403
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one 316844 Click to see 450.40 unknown https://doi.org/10.1248/YAKUSHI1947.79.3_403
Astilbin 119258 Click to see 450.40 unknown https://doi.org/10.1248/YAKUSHI1947.79.3_403
https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/YAKUSHI1947.79.3_403

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