Pieris japonica - Unknown
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Details Top

Internal ID UUID6440440df275a555914567
Scientific name Pieris japonica
Authority (Thunb.) D.Don ex G.Don
First published in Gen. Hist. 3: 832 (1834)

Description Top

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Pieris japonica, also known as Japanese andromeda or Japanese pieris, is a flowering plant in the heath family that is native to eastern China, Taiwan, and Japan. It is a medium-sized evergreen shrub or tree that is widely cultivated in gardens. The plant produces small urn-shaped flowers in white or pink, which contrast beautifully against the young red leaves in early spring. However, it is important to note that the plant is poisonous if consumed due to the presence of grayanotoxins. It is typically grown in partially shaded, acidic soil and is often paired with other lime-hating plants. There are several cultivars of Pieris japonica that have received the Royal Horticultural Society's Award of Garden Merit for their beautiful flowers and foliage.

Synonyms Top

Scientific name Authority First published in
Pieris taiwanensis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 169 (1911)
Pieris polita W.W.Sm. & Jeffrey Notes Roy. Bot. Gard. Edinburgh 9: 117 (1916)
Lyonia polita (W.W.Sm. & Jeffrey) Chun Sunyatsenia 4: 253 (1940)
Lyonia popowii (Palib.) Chun Sunyatsenia 4: 253 (1940)
Pieris japonica var. taiwanensis (Hayata) Kitam. Acta Phytotax. Geobot. 25(2-3): 36. 1972 [25 Jul 1972]

Common names Top

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Language Common/alternative name
English japanese andromeda
English japanese pieris
Bulgarian японски пиерис
German japanische lavendelheide
Esperanto japana andromedo
Persian خلنگ ژاپنی
Finnish japaninkellovaivero
Japanese アシビ
Japanese あせび
Japanese アセビ
lzh 馬醉木
Dutch rotsheide
Russian Пиерис японская
Russian Пиерис японский
Turkish japon lavanta fundası
Chinese 馬醉木
Chinese 梫木
Chinese 日本马醉木
Chinese 台湾马醉木
Chinese 马醉木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001047846
Cornell Woody Plants 174
USDA Plants PIJA3
UConn 318
Tropicos 12303159
INPN 113506
KEW urn:lsid:ipni.org:names:331662-1
The Plant List tro-12303159
Missouri Botanical Garden 280045
Open Tree Of Life 238775
Observations.org 188698
NCBI Taxonomy 317406
NBN Atlas NHMSYS0000461267
IUCN Red List 147632270
IPNI 331662-1
iNaturalist 127181
GBIF 2882631
Freebase /m/03gr472
EPPO PIRJA
EOL 180252
Elurikkus 323798
USDA GRIN 28355
Wikipedia Pieris_japonica
PaleoBotany 34256

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
A Review on the Pharmacological Aspects of Engeletin as Natural Compound Zhong X, Huang R, Chen X, Lei Y Drug Des Devel Ther 23-Dec-2023
PMCID:PMC10752015
doi:10.2147/DDDT.S437703
PMID:38152488
DNA barcoding as new diagnostic tool to lethal plant poisoning in herbivorous mammals Schweikle S, Häser A, Wetters S, Raisin M, Greiner M, Rigbers K, Fischer U, Pietsch K, Suntz M, Nick P PLoS One 15-Nov-2023
PMCID:PMC10650979
doi:10.1371/journal.pone.0292275
PMID:37967132
Appendage-Bearing Sordariomycetes from Dipterocarpus alatus Leaf Litter in Thailand Samaradiwakara NP, de Farias AR, Tennakoon DS, Aluthmuhandiram JV, Bhunjun CS, Chethana KW, Kumla J, Lumyong S J Fungi (Basel) 29-May-2023
PMCID:PMC10299658
doi:10.3390/jof9060625
PMID:37367561
An Overview of Phytophthora Species on Woody Plants in Sweden and Other Nordic Countries Matsiakh I, Menkis A Microorganisms 17-May-2023
PMCID:PMC10221925
doi:10.3390/microorganisms11051309
PMID:37317283
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
Adapting small jumping robots to compliant environments Divi S, Reynaga C, Azizi E, Bergbreiter S J R Soc Interface 01-Mar-2023
PMCID:PMC9974292
doi:10.1098/rsif.2022.0778
PMID:36854379
Pupal Warning Coloration of Three Species of Cystidia (Lepidoptera: Geometridae: Ennominae) in Relation to Their Pupation Sites Tsubuki M, Hayashi F Insects 31-Dec-2022
PMCID:PMC9865983
doi:10.3390/insects14010038
PMID:36661966
Morphology and Phylogeny of Pestalotiopsis (Sporocadaceae, Amphisphaeriales) from Fagaceae Leaves in China Jiang N, Voglmayr H, Xue H, Piao CG, Li Y Microbiol Spectr 10-Nov-2022
PMCID:PMC9769744
doi:10.1128/spectrum.03272-22
PMID:36354327
Forest characteristics, population structure and growth trends of threatened relict Pseudotsuga forrestii in China Tang CQ, Yao SQ, Han PB, Wen JR, Li S, Peng MC, Wang CY, Matsui T, Li YP, Lu S, He Y Plant Divers 07-Nov-2022
PMCID:PMC10435900
doi:10.1016/j.pld.2022.10.005
PMID:37601542
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Morphology, Phylogeny, and Pathogenicity of Pestalotioid Species on Camellia oleifera in China Li L, Yang Q, Li H J Fungi (Basel) 15-Dec-2021
PMCID:PMC8705482
doi:10.3390/jof7121080
PMID:34947061
Multiplex LAMP Detection of the Genus Phytophthora and Four Phytophthora Species P. ramorum, P. lateralis, P. kernoviae, and P. nicotianae, with a Plant Internal Control Hieno A, Li M, Otsubo K, Suga H, Kageyama K Microbes Environ 10-Jun-2021
PMCID:PMC8209452
doi:10.1264/jsme2.ME21019
PMID:34108359
Phytochemical Investigation of New Algerian Lichen Species: Physcia Mediterranea Nimis Kerboua M, Ahmed MA, Samba N, Aitfella-Lahlou R, Silva L, Boyero JF, Raposo C, Lopez Rodilla JM Molecules 20-Feb-2021
PMCID:PMC7924039
doi:10.3390/molecules26041121
PMID:33672591
UPLC-PDA-Q Exactive Orbitrap-MS profiling of the lipophilic compounds product isolated from Eucalyptus viminalis plants Ossipov V, Koivuniemi A, Mizina P, Salminen JP Heliyon 23-Dec-2020
PMCID:PMC7772544
doi:10.1016/j.heliyon.2020.e05768
PMID:33385084

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids
(1R,2S,3R,4R,6R,8S,9S,10R,11R,14R,15R,17R)-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecane-2,3,4,10,15,17-hexol 162971970 Click to see CC1(C2C(O2)C3C1(C(C(C45CC(C(C4O)CCC5C3(C)O)(C)O)O)O)O)C 384.50 unknown https://doi.org/10.1248/CPB.28.3124
(2,4,10,11,15,17-Hexahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl) acetate 162849844 Click to see CC(=O)OC1C(C23CC(C(C2O)CCC3(C(C4C1(C(C5C4O5)(C)C)O)(C)O)O)(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
(3-Acetyloxy-2,4,10,11,15-pentahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-17-yl) propanoate 162881916 Click to see CCC(=O)OC1C2CCC3(C1(CC2(C)O)C(C(C4(C(C3(C)O)C5C(C4(C)C)O5)O)OC(=O)C)O)O 498.60 unknown https://doi.org/10.1248/CPB.28.3124
(3-Acetyloxy-4,10,11,15,17-pentahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-2-yl) propanoate 162867760 Click to see CCC(=O)OC1C(C2(C(C3C(C2(C)C)O3)C(C4(C15CC(C(C5O)CC4)(C)O)O)(C)O)O)OC(=O)C 498.60 unknown https://doi.org/10.1248/CPB.28.3124
[(1R,2S,3R,4R,6R,8S,9R,10S,11S,14R,15R,17R)-3-acetyloxy-4,10,11,15,17-pentahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-2-yl] propanoate 162867761 Click to see CCC(=O)OC1C(C2(C(C3C(C2(C)C)O3)C(C4(C15CC(C(C5O)CC4)(C)O)O)(C)O)O)OC(=O)C 498.60 unknown https://doi.org/10.1248/CPB.28.3124
[(1S,2S,3R,4R,6R,8S,9R,10S,11S,14R,15R,17R)-3-acetyloxy-2,4,10,11,15-pentahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-17-yl] propanoate 162881918 Click to see CCC(=O)OC1C2CCC3(C1(CC2(C)O)C(C(C4(C(C3(C)O)C5C(C4(C)C)O5)O)OC(=O)C)O)O 498.60 unknown https://doi.org/10.1248/CPB.28.3124
[(1S,3S,4S,6R,8S,9S,10S,11R,14R,15R,17R)-3,4,10,15-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-17-yl] 2-hydroxypropanoate 137117256 Click to see CC(C(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)C5C(C4(C)C)O5)O)O)CC2(C)O)O 440.50 unknown https://doi.org/10.1254/JJP.36.205
5,5,10,15-Tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecane-2,3,4,10,15,17-hexol 162971969 Click to see CC1(C2C(O2)C3C1(C(C(C45CC(C(C4O)CCC5C3(C)O)(C)O)O)O)O)C 384.50 unknown https://doi.org/10.1248/CPB.28.3124
Asebotoxin III 115156 Click to see CC(C(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)C5C(C4(C)C)O5)O)O)CC2(C)O)O 440.50 unknown https://doi.org/10.1254/JJP.36.205
Pieristoxin J 101229269 Click to see CC(=O)OC1C(C23CC(C(C2O)CCC3(C(C4C1(C(C5C4O5)(C)C)O)(C)O)O)(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
(1S,3R,4R,6S,8R,9R,10R,13R,14R,16S)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,8]hexadecane-3,4,6,9,14,16-hexol 162932012 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2(C)O)(C)O)O)O)O)C 370.50 unknown https://doi.org/10.1248/YAKUSHI1947.79.8_1057
(2,4,6,9,14,16-Hexahydroxy-5,5,9,14-tetramethyl-3-tetracyclo[11.2.1.01,10.04,8]hexadecanyl) propanoate 12308649 Click to see CCC(=O)OC1C(C23CC(C(C2O)CCC3C(C4C1(C(C(C4)O)(C)C)O)(C)O)(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
(3,4,6,9,14-Pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl) 2-hydroxypropanoate 54493676 Click to see CC(C(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
[(1S,3R,4R,6S,8R,9R,10R,13R,14R,16S)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] acetate 162873377 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1002/RECL.18820011205
https://doi.org/10.1002/RECL.18820010904
[(1S,3R,4R,6S,8S,9R,10R,13R,14R,16R)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] (2R)-2-hydroxypropanoate 162975605 Click to see CC(C(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
[(1S,3R,4R,6S,8S,9R,10R,13R,14R)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] propanoate 135929163 Click to see CCC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 426.50 unknown https://doi.org/10.1254/JJP.36.205
Andromedol 3511 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2(C)O)(C)O)O)O)O)C 370.50 unknown https://doi.org/10.1248/YAKUSHI1947.79.8_1057
Asebotoxin I 168155 Click to see CCC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 426.50 unknown https://doi.org/10.1254/JJP.36.205
Asebotoxin IV 75124255 Click to see CCC(=O)OC1C(C23CC(C(C2O)CCC3C(C4C1(C(C(C4)O)(C)C)O)(C)O)(C)O)O 442.50 unknown https://doi.org/10.1248/CPB.28.3124
https://doi.org/10.1246/BCSJ.67.866
Rhodotoxin 231125 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1002/RECL.18820010904
https://doi.org/10.1002/RECL.18820011205
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
4-Methoxy-7-(7-methoxy-13-oxo-8,11-dioxatetracyclo[7.5.0.02,7.010,12]tetradec-1(14)-en-3-yl)-6-methylhepta-2,4,6-trienoic acid 74405763 Click to see CC(=CC1CCCC2(C1C3=CC(=O)C4C(C3O2)O4)OC)C=C(C=CC(=O)O)OC 402.40 unknown https://doi.org/10.1248/CPB.31.1567
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.31.1567
[(3S,6aR,8aR,12aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate 5321632 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.31.1567
[(4aS,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate 138114876 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.31.1567
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-octadecahydro-3(2H)-picenone 500344 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.31.1567
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.31.1567
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.31.1567
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.31.1567
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.31.1567
Taraxeryl acetate 5205968 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.31.1567
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(1R,3R,6S,8S,10R,13R,14R)-14-hydroxy-5,5,14-trimethyl-9-methylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.03,8]hexadecan-4-one 162980466 Click to see CC1(C(CC2C(C1=O)CC34CC(CCC3C2=C)C(C4)(C)O)OC5C(C(C(C(O5)CO)O)O)O)C 480.60 unknown https://doi.org/10.1016/S0031-9422(00)98570-4
14-Hydroxy-5,5,14-trimethyl-9-methylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.03,8]hexadecan-4-one 162980465 Click to see CC1(C(CC2C(C1=O)CC34CC(CCC3C2=C)C(C4)(C)O)OC5C(C(C(C(O5)CO)O)O)O)C 480.60 unknown https://doi.org/10.1016/S0031-9422(00)98570-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,10S,12aR,14bS)-10-acetyloxy-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 15917992 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1248/CPB.29.261
(2-Hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-yl) acetate 73821064 Click to see CC1CCC23C(CC4(C(C2C1(OC3=O)C)CCC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C)C)C)C)O 514.70 unknown https://doi.org/10.1248/CPB.29.261
(4,5,9,9,13,19,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl) acetate 73800256 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 496.70 unknown https://doi.org/10.1248/CPB.31.1567
[(1R,2R,4R,5R,8R,10S,13R,14R,17R,18S,19S,20S)-2-hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] acetate 162862836 Click to see CC1CCC23C(CC4(C(C2C1(OC3=O)C)CCC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C)C)C)C)O 514.70 unknown https://doi.org/10.1248/CPB.29.261
[(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 22294572 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C=O 482.70 unknown https://doi.org/10.1248/CPB.31.1567
10-Acetyloxy-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 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1248/CPB.29.261
3-Acetoxy-11-ursen-28,13-olide 21606662 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 496.70 unknown https://doi.org/10.1248/CPB.31.1567
3-O-Acetyloleanderolide 10929355 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(C45C3(CCC6(C4CC(CC6)(C)C)C(=O)O5)C)O)C)C 514.70 unknown https://doi.org/10.1248/CPB.31.1567
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1248/CPB.29.261
Acetic acid, 8a-hydroxymethyl-4,4,6a,6b,11,12,14b-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydropicen-3-yl ester 608726 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)CO 484.80 unknown https://doi.org/10.1248/CPB.31.1567
Acetylursolic acid 619164 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1248/CPB.29.261
beta-Ursolic acid 220774 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/CPB.29.261
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.29.261
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.29.261
Oleanderolide 3-acetate 85319558 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(C45C3(CCC6(C4CC(CC6)(C)C)C(=O)O5)C)O)C)C 514.70 unknown https://doi.org/10.1248/CPB.31.1567
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1248/CPB.29.261
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/CPB.29.261
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1248/CPB.29.261
Uvaol 3-acetate 101027370 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)CO 484.80 unknown https://doi.org/10.1248/CPB.31.1567
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 5490292 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.31.1567
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/CPB.29.261
24-Ethylcholest-5-en-3beta-ol 22012 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/CPB.29.261
3-Oxo-24-ethyl-cholest-5-ene 4358735 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.31.1567
Beta-Sitosterol 222284 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/CPB.29.261
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.31.1567
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,3R,4R,6S,8S,10S,13S,16S)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.01,10.04,8]hexadec-14-ene-3,4,6,16-tetrol 163086622 Click to see CC1=CC23CC(C4(C(CC(C4(C)C)O)C(=C)C2CCC1C3O)O)O 334.40 unknown https://doi.org/10.1248/CPB.33.4637
5,5,14-Trimethyl-9-methylidenetetracyclo[11.2.1.01,10.04,8]hexadec-14-ene-3,4,6,16-tetrol 15559564 Click to see CC1=CC23CC(C4(C(CC(C4(C)C)O)C(=C)C2CCC1C3O)O)O 334.40 unknown https://doi.org/10.1248/CPB.33.4637
CID 137092549 137092549 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)O)C 336.50 unknown https://doi.org/10.1248/CPB.33.4637
Grayanotox-10(20)-ene-3beta,5,6beta,16-tetrol 73817554 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)O)C 336.50 unknown https://doi.org/10.1248/CPB.33.4637
Grayanotoxa-10,15-diene-3,5,6,14-tetrol 198094 Click to see CC1=CC23CC(C4(C(CC(C4(C)C)O)C(=C)C2CCC1C3O)O)O 334.40 unknown https://doi.org/10.1248/CPB.33.4637
Grayanotoxin VII 101643282 Click to see CC1=CC23CC(C4(C(CC(C4(C)C)O)C(=C)C2CCC1C3O)O)O 334.40 unknown https://doi.org/10.1248/CPB.33.4637
Grayanotoxin XVIII 44559345 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)O)C 336.50 unknown https://doi.org/10.1248/CPB.33.4637
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,3R,4R,6S,8S,13R,14R)-3,4,14-trihydroxy-5,5,9,14-tetramethyl-6-tetracyclo[11.2.1.01,10.04,8]hexadec-9-enyl]oxy]oxane-3,4,5-triol 20056219 Click to see CC1=C2CCC3CC2(CC(C4(C1CC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)O)CC3(C)O 498.60 unknown https://doi.org/10.1248/CPB.33.4637
[5,6beta,16-Trihydroxygrayanotox-10(20)-en-3beta-yl]beta-D-glucopyranoside 45359849 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)C 498.60 unknown https://doi.org/10.1016/S0031-9422(00)98570-4
2-(Hydroxymethyl)-6-[(3,4,14-trihydroxy-5,5,9,14-tetramethyl-6-tetracyclo[11.2.1.01,10.04,8]hexadec-9-enyl)oxy]oxane-3,4,5-triol 73657312 Click to see CC1=C2CCC3CC2(CC(C4(C1CC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)O)CC3(C)O 498.60 unknown https://doi.org/10.1248/CPB.33.4637
Grayanoside B 101316949 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)C 498.60 unknown https://doi.org/10.1016/S0031-9422(00)98570-4
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Pierotin A 11192582 Click to see COC1=C(C(=C(C(=C1)O)C(=O)CCC2=CC=C(C=C2)O)O)CC3=C(C=C(C(=C3O)C(=O)CCC4=CC=C(C=C4)O)O)OC 588.60 unknown https://doi.org/10.1021/NP049698A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1007/978-0-387-77335-3_9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[3-hydroxy-2-[3-(4-hydroxyphenyl)propanoyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxan-3-yl] acetate 11431848 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=CC(=C2C(=O)CCC3=CC=C(C=C3)O)O)OC)CO)O)O 492.50 unknown https://doi.org/10.1021/NP049698A
[4,5-Dihydroxy-2-[3-hydroxy-2-[3-(4-hydroxyphenyl)propanoyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxan-3-yl] acetate 72958974 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=CC(=C2C(=O)CCC3=CC=C(C=C3)O)O)OC)CO)O)O 492.50 unknown https://doi.org/10.1021/NP049698A
1-[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)propan-1-one 4789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1021/NP049698A
3-(3,4-Dihydroxyphenyl)-1-[2-hydroxy-4-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 72807927 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC(=C(C=C3)O)O)O 466.40 unknown https://doi.org/10.1021/NP049698A
3-(4-hydroxyphenyl)-1-[4-methoxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]propan-1-one 11342511 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 612.60 unknown https://doi.org/10.1021/NP049698A
3-(4-Hydroxyphenyl)-1-[4-methoxy-3,5-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]propan-1-one 72808977 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 612.60 unknown https://doi.org/10.1021/NP049698A
3-Hydroxyasebotin 11340276 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC(=C(C=C3)O)O)O 466.40 unknown https://doi.org/10.1021/NP049698A
3,5-Dihydroxy-2-[3-hydroxy-2-[3-(4-hydroxyphenyl)propanoyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxan-4-one 72768085 Click to see COC1=CC(=C(C(=C1)OC2C(C(=O)C(C(O2)CO)O)O)C(=O)CCC3=CC=C(C=C3)O)O 448.40 unknown https://doi.org/10.1021/NP049698A
Asebogenin 2'-O-beta-D-ribohexo-3-ulopyranoside 11247865 Click to see COC1=CC(=C(C(=C1)OC2C(C(=O)C(C(O2)CO)O)O)C(=O)CCC3=CC=C(C=C3)O)O 448.40 unknown https://doi.org/10.1021/NP049698A
CID 11190157 11190157 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)O 450.40 unknown https://doi.org/10.1021/NP049698A
CID 12308643 12308643 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)O 450.40 unknown https://doi.org/10.1248/YAKUSHI1947.92.9_1173
https://doi.org/10.1021/NP049698A
Phlorizin 6072 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1021/NP049698A
https://doi.org/10.1248/YAKUSHI1947.92.9_1173
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Asebogenin 442255 Click to see COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.1021/NP049698A
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown https://doi.org/10.1021/NP049698A
Pierotin B 11338395 Click to see COC1=C2C3=CC(=C(C=C3OC2=C(C(=C1)O)C(=O)CCC4=CC=C(C=C4)O)O)O 394.40 unknown https://doi.org/10.1021/NP049698A

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