Pyrola japonica - Unknown
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Internal ID UUID64404d168baf3802614368
Scientific name Pyrola japonica
Authority Klenze ex Alef.
First published in Linnaea 28: 57 (1856)

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Synonyms Top

Scientific name Authority First published in
Pyrola coreana Andres Bull. Jard. Bot. Buitenzorg , sér. 3, 14: 5 (1936)
Pyrola asarifolia var. japonica (Klenze ex Alef.) Miq. Ann. Mus. Bot. Lugduno-Batavi 2:166. 1866
Pyrola rotundifolia var. albiflora Maxim. Bull. Acad. Imp. Sci. Saint-Petersbourg 18(1): 52–53 1872
Pyrola incarnata var. japonica (Klenze ex Alef.) Koidz. Fl. Symb. Orient.-Asiat. 74 1930
Pyrola rotundifolia f. subaphylla (Maxim.) Makino Bot. Mag. (Tokyo) 27(314): 24 1913

Common names Top

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Language Common/alternative name
Japanese イチヤクソウ
Korean 노루발
Korean 노루발풀
Chinese 鹿衔草
Chinese 日本鹿蹄草

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Khabarovsk
      • Kuril Islands
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001128988
Tropicos 26800187
KEW urn:lsid:ipni.org:names:60463201-2
The Plant List tro-26800187
Open Tree Of Life 755277
Observations.org 129692
NCBI Taxonomy 642532
IPNI 60463201-2
iNaturalist 701722
GBIF 4936689
Freebase /m/0nbcqlm
EPPO PYWJA
EOL 2891099
Elurikkus 6659
USDA GRIN 30422
CMAUP NPO13524

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
Effects of Pieris japonica (Ericaceae) dominance on cool temperate forest altered-understory environments and soil microbiomes in Southern Japan Tokumoto Y, Katayama A PLoS One 11-Jan-2024
PMCID:PMC10783712
doi:10.1371/journal.pone.0296692
PMID:38206984
Belowground carbon transfer across mycorrhizal networks among trees: Facts, not fantasy Klein T, Rog I, Livne-Luzon S, van der Heijden MG, Körner C Open Res Eur 03-Oct-2023
PMCID:PMC10751480
doi:10.12688/openreseurope.16594.1
PMID:38152158
Mass spectrometry data on specialized metabolome of medicinal plants used in East Asian traditional medicine Kang KB, Jeong E, Son S, Lee E, Lee S, Choi SY, Kim HW, Yang H, Shim SH Sci Data 27-Aug-2022
PMCID:PMC9420114
doi:10.1038/s41597-022-01662-2
PMID:36030263
Japanese “nameko” mushrooms (Pholiota microspora) produced via sawdust-based cultivation exhibit severe genetic bottleneck associated with a single founder S. Hirao A, Kumata A, Takagi T, Sasaki Y, Shigihara T, Kimura E, Kaneko S Mycoscience 31-May-2022
PMCID:PMC10012341
doi:10.47371/mycosci.2022.03.002
PMID:37089630
Transformation of Long-Lived Albino Epipremnum aureum ‘Golden Pothos’ and Restoring Chloroplast Development Hung CY, Zhang J, Bhattacharya C, Li H, Kittur FS, Oldham CE, Wei X, Burkey KO, Chen J, Xie J Front Plant Sci 12-May-2021
PMCID:PMC8149757
doi:10.3389/fpls.2021.647507
PMID:34054894
Identification and Quantification of Phenolic Compounds from Mexican Oregano (Lippia graveolens HBK) Hydroethanolic Extracts and Evaluation of Its Antioxidant Capacity Cortés-Chitala MD, Flores-Martínez H, Orozco-Ávila I, León-Campos C, Suárez-Jacobo Á, Estarrón-Espinosa M, López-Muraira I Molecules 29-Jan-2021
PMCID:PMC7866295
doi:10.3390/molecules26030702
PMID:33572779
Evidence for newly discovered albino mutants in a pyroloid: implication for the nutritional mode in the genus Pyrola Shutoh K, Tajima Y, Matsubayashi J, Tayasu I, Kato S, Shiga T, Suetsugu K Am J Bot 17-Apr-2020
PMCID:PMC7216931
doi:10.1002/ajb2.1462
PMID:32304099
A Review on the Phytochemistry, Pharmacology, Pharmacokinetics and Toxicology of Geniposide, a Natural Product Shan M, Yu S, Yan H, Guo S, Xiao W, Wang Z, Zhang L, Ding A, Wu Q, Li SF Molecules 10-Oct-2017
PMCID:PMC6151614
doi:10.3390/molecules22101689
PMID:28994736
Root-associated fungal communities in three Pyroleae species and their mycobiont sharing with surrounding trees in subalpine coniferous forests on Mount Fuji, Japan Jia S, Nakano T, Hattori M, Nara K Mycorrhiza 13-Jul-2017
PMCID:PMC5645451
doi:10.1007/s00572-017-0788-6
PMID:28707027
Mixotrophy in Pyroleae (Ericaceae) from Estonian boreal forests does not vary with light or tissue age Lallemand F, Puttsepp Ü, Lang M, Luud A, Courty PE, Palancade C, Selosse MA Ann Bot 31-May-2017
PMCID:PMC5591414
doi:10.1093/aob/mcx054
PMID:28575199
Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi Hynson NA, Schiebold JM, Gebauer G Ann Bot 24-Jul-2016
PMCID:PMC4998980
doi:10.1093/aob/mcw119
PMID:27451987
Synthesis of New Hydrated Geranylphenols and in Vitro Antifungal Activity against Botrytis cinerea Soto M, Espinoza L, Chávez MI, Díaz K, Olea AF, Taborga L Int J Mol Sci 03-Jun-2016
PMCID:PMC4926374
doi:10.3390/ijms17060840
PMID:27271604
Chemical constituents of volatile oil from Pyrolae herba and antiproliferative activity against SW1353 human chondrosarcoma cells. Cai L, Ye H, Li X, Lin Y, Yu F, Chen J, Li H, Liu X Int J Oncol 01-Apr-2013
doi:10.3892/IJO.2013.1816
PMID:23404045
Screening of Korean Medicinal Plant Extracts for α-Glucosidase Inhibitory Activities Sancheti S, Sancheti S, Lee SH, Lee JE, Seo SY Iran J Pharm Res 01-Mar-2011
PMCID:PMC3828923
PMID:24250352
Phenolic glycosides from Pyrola japonica. Kim JS, Shim SH, Xu YN, Kang SS, Son KH, Chang HW, Kim HP, Bae K Chem Pharm Bull (Tokyo) 01-Jun-2004
doi:10.1248/CPB.52.714
PMID:15187393

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
> Alkaloids and derivatives
Ethyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate 34167 Click to see CCOC(=O)C1=CCCN(C1)C 169.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Diisobutyl phthalate 6782 Click to see CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C 278.34 unknown https://doi.org/10.3892/IJO.2013.1816
> Benzenoids / Naphthalenes / Naphthoquinones
Chimaphilin 101211 Click to see CC1=CC2=C(C=C1)C(=O)C=C(C2=O)C 186.21 unknown https://doi.org/10.1007/BF02975157
https://doi.org/10.1248/CPB.52.714
> Benzenoids / Phenols / Benzenediols / Catechols
Urushiol III 5281862 Click to see CCCC=CCC=CCCCCCCCC1=C(C(=CC=C1)O)O 316.50 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
Propane 6334 Click to see CCC 44.10 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Acanthoside D 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.52.714
Syringaresinol-di-O-glucoside 442830 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.52.714
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see CCCCCCCCCCCCCCCC(=O)OCC 284.50 unknown https://doi.org/10.3892/IJO.2013.1816
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Octacosanoate 5461029 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)[O-] 423.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
6-Hentriacontanol 5318007 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(CCCCC)O 452.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Benzoicacidcyanomethylester 5320547 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
cis-Phytol 6430833 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Isophytol 10453 Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)(C=C)O 296.50 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Phytol [FHFI] 9018 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2Z,6E)-8-[5-hydroxy-4-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,6-dimethylocta-2,6-dienoxy]oxane-3,4,5-triol 11192700 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)COC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 600.70 unknown https://doi.org/10.1248/CPB.52.714
2-(Hydroxymethyl)-6-[8-[5-hydroxy-4-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,6-dimethylocta-2,6-dienoxy]oxane-3,4,5-triol 85430392 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)COC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 600.70 unknown https://doi.org/10.1248/CPB.52.714
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 154497023 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.52.714
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 3488508 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.52.714
7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 11574644 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown via CMAUP database
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.52.714
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10416408 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 618.80 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
Ziyuglycoside I 71609288 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O 767.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 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 via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
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 via CMAUP database
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 via CMAUP database
Oleanolic Acid (Caryophyllin) 49867939 Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C 456.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
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 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 7576924 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[4-hydroxy-2-[(2Z,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienyl]-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163010518 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 438.50 unknown https://doi.org/10.1248/CPB.52.714
(2S,3R,4S,5S,6R)-2-[(4-hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 21577106 Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O 484.50 unknown https://doi.org/10.1248/CPB.52.714
(2S,3R,4S,5S,6R)-2-[4-hydroxy-2-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienyl]-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 12314350 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 438.50 unknown https://doi.org/10.1016/S0031-9422(00)82573-X
(2S,3R,4S,5S,6R)-2-[4-hydroxy-2-[(E)-4-hydroxy-3-methylbut-2-enyl]-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11417365 Click to see CC1=CC(=C(C=C1O)CC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 370.40 unknown https://doi.org/10.1248/CPB.52.714
1-[3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 12306788 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 328.31 unknown https://doi.org/10.1248/CPB.52.714
2-[(4-Hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 73802915 Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O 484.50 unknown https://doi.org/10.1248/CPB.52.714
2-[4-Hydroxy-2-(3-hydroxy-3-methylbutyl)-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72962288 Click to see CC1=CC(=C(C=C1O)CCC(C)(C)O)OC2C(C(C(C(O2)CO)O)O)O 372.40 unknown https://doi.org/10.1248/CPB.52.714
2-[4-Hydroxy-2-(4-hydroxy-3-methylbut-2-enyl)-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72953409 Click to see CC1=CC(=C(C=C1O)CC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 370.40 unknown https://doi.org/10.1248/CPB.52.714
2-[4-Hydroxy-2-(8-hydroxy-3,7-dimethylocta-2,6-dienyl)-5-methylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73802914 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 438.50 unknown https://doi.org/10.1248/CPB.52.714
2-Methyl-4-(beta-D-glucopyranosyloxy)-5-(3-hydroxy-3-methylbutyl)phenol 11440184 Click to see CC1=CC(=C(C=C1O)CCC(C)(C)O)OC2C(C(C(C(O2)CO)O)O)O 372.40 unknown https://doi.org/10.1248/CPB.52.714
Androsin 164648 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 328.31 unknown https://doi.org/10.1248/CPB.52.714
CID 5318079 5318079 Click to see CC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.52.714
Homoarbutin 324796 Click to see CC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.52.714
methyl 2-[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetate 11256426 Click to see COC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 344.31 unknown https://doi.org/10.1248/CPB.52.714
Methyl 2-[5-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetate 72771925 Click to see COC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 344.31 unknown https://doi.org/10.1248/CPB.52.714
Pyrolatin 21577105 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CO)OC2C(C(C(C(O2)CO)O)O)O 438.50 unknown https://doi.org/10.1248/CPB.52.714
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Chimonanthine 3083909 Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C 346.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate 46906036 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O 301.23 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-chromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl] 3,4,5-trihydroxybenzoate 5480249 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
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/CPB.52.714
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51521831 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/CPB.52.714
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 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 via CMAUP database
2'-O-galloylhyperin 6453359 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 46217100 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)CO)O)O)O)O 624.50 unknown via CMAUP database
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/CPB.52.714
Isoquercetin 5280804 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 via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown via CMAUP database

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