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

Description Top

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Lyonia ovalifolia is a plant species belonging to the Ericaceae family. It is found in various countries such as Himalaya, Nepal, China, Japan, Cambodia, Myanmar, Thailand, Vietnam, and Malaysia. In India, it is known as Anyaar, while in Nepal it is called Angeri.

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)

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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No subspecies added yet.

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)

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 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

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
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
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
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
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
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
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
Chloroplast genome assemblies and comparative analyses of commercially important Vaccinium berry crops Fahrenkrog AM, Matsumoto GO, Toth K, Jokipii-Lukkari S, Salo HM, Häggman H, Benevenuto J, Munoz PR Sci Rep 14-Dec-2022
PMCID:PMC9751094
doi:10.1038/s41598-022-25434-5
PMID:36517490
Pestalotiopsis Diversity: Species, Dispositions, Secondary Metabolites, and Bioactivities Wu C, Wang Y, Yang Y Molecules 21-Nov-2022
PMCID:PMC9695833
doi:10.3390/molecules27228088
PMID:36432188

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 COC1=C(C(=C2C3C(C(CC2=C1)COC4=CC(=C(C(=C34)OC)O)OC)CO)OC)O 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 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
(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 COC1=C(C(=C2C3C4COC(C4COC5=CC(=C(C(=C35)OC)O)OC)C2=C1)OC)O 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 COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C=O)CO 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 COC1=C(C(=C2C3C(C(CC2=C1)COC4=CC(=C(C(=C34)OC)O)OC)CO)OC)O 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 COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C=O)CO 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 COC1=C(C(=C2C3C4COC(C4COC5=CC(=C(C(=C35)OC)O)OC)C2=C1)OC)O 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 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
> 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 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
[(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 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
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
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.10_1349
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 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 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
[(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 C1C(C(C(C(O1)O)O)O)O 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
Secorhodomollolide D 46187657 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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 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-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 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
Isoastilbin 316844 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1248/YAKUSHI1947.79.3_403

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