Pyrus pyrifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pyrus pyrifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pyrus pyrifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID6440402b7eebb293293397
Scientific name Pyrus pyrifolia
Authority (Burm.f.) Nakai
First published in Bot. Mag. (Tokyo) 40: 564 (1926)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ficus pyrifolia Burm.f. Fl. Indica : 226 (1768)
Pyrus arakiana Koidz. Acta Phytotax. Geobot. 3: 40 (1934)
Pyrus tobisimensis Koidz. Acta Phytotax. Geobot. 5: 48 (1936)
Pyrus togashiana Koidz. Acta Phytotax. Geobot. 5: 48 (1936)
Pyrus tungusiana Koidz. Acta Phytotax. Geobot. 5: 49 (1936)
Pyrus yohrohensis Koidz. Acta Phytotax. Geobot. 6: 214 (1937)
Pyrus asakeensis Koidz. Acta Phytotax. Geobot. 6: 215 (1937)
Pyrus nehiyamadonis Koidz. Acta Phytotax. Geobot. 8: 190 (1939)
Pyrus tajimaensis Koidz. Acta Phytotax. Geobot. 10: 59 (1941)
Pyrus saidaeana Koidz. Acta Phytotax. Geobot. 10: 60 (1941)
Pyrus incubacea Koidz. Bot. Mag. (Tokyo) 33: 124 (1919)
Pyrus cuneata Koidz. Bot. Mag. (Tokyo) 33: 125 (1919)
Pyrus lasiogyna Koidz. Bot. Mag. (Tokyo) 33: 125 (1919)
Pyrus sohayakiensis Koidz. Bot. Mag. (Tokyo) 38: 87 (1924)
Pyrus kiusiana Koidz. Bot. Mag. (Tokyo) 38: 88 (1924)
Pyrus tambana Koidz. Bot. Mag. (Tokyo) 38: 90 (1924)
Pyrus umemurana Koidz. Bot. Mag. (Tokyo) 39: 17 (1925)
Pyrus tsuchiyana Koidz. Bot. Mag. (Tokyo) 39: 27 (1925)
Pyrus autumnalis Koidz. Bot. Mag. (Tokyo) 43: 383 (1929)
Pyrus kleinhofiana Koidz. Bot. Mag. (Tokyo) 43: 384 (1929)
Pyrus uipongensis Uyeki & Uyeki J. Chosen Agric. Soc. 16: 5 (1921)
Pyrus pseudocalleryana Uyeki Bull. Agric. Coll. Suwon 1: 15 (1925)
Pyrus pseudouipongensis Uyeki Bull. Agric. Coll. Suwon 1: 17 (1925)
Pyrus babauttiagi Koidz. Fl. Austro-Higo. : 25 (1931)
Pyrus higoensis Koidz. Fl. Austro-Higo. : 26 (1931)
Pyrus kiushiana Koidz. Bot. Mag. (Tokyo) 38: 88 (1924)
Pyrus tobishimensis Koidz. Acta Phytotax. Geobot. 5: 48 (1936)
Pyrus serotina Rehder Proc. Amer. Acad. Arts 50: 231 (1915)
Pyrus uyematsuana Makino Bot. Mag. (Tokyo) 22: 68 (1908)

Common names Top

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Language Common/alternative name
English chinese pear
English apple pear
English asian pear
English japanese pear
English korean pear
English nashi pear
English sand pear
English taiwan pear
Spanish ficus pyrifolia
Spanish pera asiatica
Spanish pera asiática
Spanish pera coreana
Spanish pera de arena
Spanish pera japonesa
Spanish pera manzana
Spanish pera nashi
Spanish pera oriental
Spanish pyrus serotina
Arabic إجاص إجاصي الأوراق
Assamese নাচপতি
bho नाशपाती
Bengali নাশপাতি
Catalan naxi
Catalan pera nashi
Czech hrušeň asijská
Czech naš-li
Czech nashi
Czech naši
German apfelbirne
German asiatische birne
German chinesische birne
German japanische birne
German koreanische birne
German kumoi
German nashi-birne
German nashibirne
German nashi
Greek Αχλαδομηλιά
Estonian liiv-pirnipuu
Persian گلابی اسیایی
Persian گلابی آسیایی
Finnish hiekkapäärynä
Finnish japaninpäärynä
Finnish omenapäärynä
French nashi
frr nashi
Hebrew אגס אסייתי
Hindi नाशपाती
Hungarian japán körte
Italian nashi
Italian pera-mela
Italian peramela
Italian pero asiatico
Japanese なし
Japanese ナシ
Japanese
Japanese ヤマナシ
Korean 돌배나무
Korean 일본배
Korean 배나무
mai नास्पाती
Macedonian корејска круша
Macedonian наши
Macedonian кинеска круша
Malayalam പിയർ
Nepali नस्पाती
Nepali नास्पाती
Dutch appelpeer
Dutch aziatische peer
Dutch japanse appelpeer
Dutch japanse peer
Dutch nashi peer
Dutch nashi-peer
Dutch zandpeer
Dutch nashipeer
Polish grusza chińska
Polish grusza japońska
Polish nashi
Portuguese náxi
Portuguese pêra nashi
Portuguese pêra-nashi
Portuguese pera-nashi
Russian Груша грушелистная
Slovak Ázijská hruška
Slovak japonská hruška
Slovak hruška nashi
Swedish Äppelpäron
Swedish asienpäron
Swedish japanskt päron
Swedish kinesiskt päron
Swedish nashi
Swedish nashipäron
Swedish pyrus serotina
Swedish kinapäron
Swedish sandpäron
Thai สาลี่
Ukrainian Груша японська
Ukrainian Насі
Ukrainian Японська груша
Chinese
Chinese 梨花
Chinese 梨叶
Chinese 梨木灰
Chinese 梨木皮
Chinese 梨枝
Chinese 梨树根
Chinese 梨樹
Chinese 梨皮
Chinese 沙梨
Chinese 麻安梨
Chinese 日本梨
Chinese 水梨
Chinese 苹果梨
Chinese 黄金梨

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pyrus pyrifolia var. culta (Makino) Nakai Bot. Mag. (Tokyo) 40(no. 479): 564. 1926 [Nov 1926]

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
      • Inner Mongolia
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Tadzhikistan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Pakistan
    • Indo-China
      • Laos
      • Vietnam
  • Northern America
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • West Virginia
    • Southeastern U.S.A.
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001014308
UNII S034FKS13U
USDA Plants PYPY2
Tropicos 27801132
INPN 717440
KEW urn:lsid:ipni.org:names:731158-1
The Plant List rjp-6010
Open Tree Of Life 443418
NCBI Taxonomy 3767
Nature Serve 2.144147
IPNI 731158-1
iNaturalist 122783
GBIF 5362786
Freebase /m/02tq1j
EPPO PYUPY
EOL 631563
USDA GRIN 30569
Wikipedia Pyrus_pyrifolia
CMAUP NPO1786

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_016587475.1 PPY_r1.0 Contig Kazusa DNA Research Institute 2020-12-23 136.0x 480.55 Mb

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
Increased DNA methylation contributes to the early ripening of pear fruits during domestication and improvement Song B, Yu J, Li X, Li J, Fan J, Liu H, Wei W, Zhang L, Gu K, Liu D, Zhao K, Wu J Genome Biol 05-Apr-2024
PMCID:PMC10996114
doi:10.1186/s13059-024-03220-y
PMID:38581061
Identification and functional analysis of the LEAFY gene in longan flower induction Jue D, Li Z, Zhang W, Tang J, Xie T, Sang X, Guo Q BMC Genomics 25-Mar-2024
PMCID:PMC10962150
doi:10.1186/s12864-024-10229-x
PMID:38528464
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Salicylic Acid Spray Delays Sand Pear Fruit Senescence during Room Temperature Shelf Life by Regulating Antioxidant Capacity and Senescence-Related Genes Wang H, Li Y, Wassie M, Huo L, Shi H Plants (Basel) 15-Mar-2024
PMCID:PMC10975672
doi:10.3390/plants13060848
PMID:38592916
Transcriptome-Based Identification of Candidate Flowering-Associated Genes of Blueberry in a Plant Factory with Artificial Lighting (PFAL) under Short-Day-Length Conditions An H, Zhang J, Li S, Zhang X Int J Mol Sci 11-Mar-2024
PMCID:PMC10969908
doi:10.3390/ijms25063197
PMID:38542171
A self-compatible pear mutant derived from γ-irradiated pollen carries an 11-Mb duplication in chromosome 17 Nishio S, Shirasawa K, Nishimura R, Takeuchi Y, Imai A, Mase N, Takada N Front Plant Sci 05-Mar-2024
PMCID:PMC10948449
doi:10.3389/fpls.2024.1360185
PMID:38504898
Comprehensive Evolutionary Analysis of the SMXL Gene Family in Rosaceae: Further Insights into Its Origin, Expansion, Diversification, and Role in Regulating Pear Branching Liu C, Jiang X, Liu S, Liu Y, Li H, Wang Z, Kan J, Yang Q, Li X Int J Mol Sci 04-Mar-2024
PMCID:PMC10931622
doi:10.3390/ijms25052971
PMID:38474218
Protein/Lipid ratio of pollen biases the visitation of bumblebees (Bombus ignitus Smith) to male-fertile cultivars of the Japanese pear (Pyrus pyrifolia Nakai) Mori S, Mitsuhata M, Yokoi T PLoS One 26-Feb-2024
PMCID:PMC10896533
doi:10.1371/journal.pone.0297298
PMID:38408080
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Towards portable MRI in the plant sciences Blystone S, Nuixe M, Traoré AS, Cochard H, Picon-Cochard C, Pagés G Plant Methods 18-Feb-2024
PMCID:PMC10874549
doi:10.1186/s13007-024-01152-z
PMID:38369530
Retrospective survey of Dickeya fangzhongdai using a novel validated real-time PCR assay Alič Š, Bačnik K, Dreo T Front Microbiol 13-Feb-2024
PMCID:PMC10896844
doi:10.3389/fmicb.2023.1249955
PMID:38414710
Regulatory frameworks involved in the floral induction, formation and developmental programming of woody horticultural plants: a case study on blueberries Song GQ, Liu Z, Zhong GY Front Plant Sci 12-Feb-2024
PMCID:PMC10894941
doi:10.3389/fpls.2024.1336892
PMID:38410737
Identification of self-incompatibility alleles in Quince (Cydonia oblonga Mill.) Sadeghnejad S, Abdollahi H, Davoodi D, Tatari M, Khosroshahli M PLoS One 08-Feb-2024
PMCID:PMC10852308
doi:10.1371/journal.pone.0297595
PMID:38330081
Fungicide ingestion reduces net energy gain and microbiome diversity of the solitary mason bee Porras MF, Raygoza Garay JA, Brought M, López–Londoño T, Chautá A, Crone M, Rajotte EG, Phan N, Joshi NK, Peter K, Biddinger D Sci Rep 08-Feb-2024
PMCID:PMC10853529
doi:10.1038/s41598-024-53935-y
PMID:38332135

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Corynanthean-type alkaloids
16R-sitsirikine 5321352 Click to see COC(=O)C(CO)C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3 354.40 unknown https://doi.org/10.1021/JF2022868
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl benzoate 7165 Click to see CCOC(=O)C1=CC=CC=C1 150.17 unknown https://doi.org/10.1080/10412905.1992.9698151
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1080/10412905.1992.9698151
> Benzenoids / Benzene and substituted derivatives / Toluenes
Toluene 1140 Click to see CC1=CC=CC=C1 92.14 unknown https://doi.org/10.1080/10412905.1992.9698151
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1080/10412905.1992.9698151
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1080/10412905.1992.9698151
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1080/10412905.1992.9698151
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl butyrate 7762 Click to see CCCC(=O)OCC 116.16 unknown https://doi.org/10.1080/10412905.1992.9698151
Ethyl hexanoate 31265 Click to see CCCCCC(=O)OCC 144.21 unknown https://doi.org/10.1080/10412905.1992.9698151
Ethyl valerate 10882 Click to see CCCCC(=O)OCC 130.18 unknown https://doi.org/10.1080/10412905.1992.9698151
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(8S,11bS)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1,2,8,9-tetrahydronaphtho[2,1-f][1]benzofuran-6-one 11174780 Click to see CC1COC2=C(C3=C(C(=O)C=C4C3(CCC(=C4C)C)C)C(=C12)O)O 326.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698151
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) docosanoate 14486650 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 749.30 unknown https://doi.org/10.1271/BBB.65.1198
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) hexacosanoate 14486658 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 805.40 unknown https://doi.org/10.1271/BBB.65.1198
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) icosanoate 14486646 Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 721.20 unknown https://doi.org/10.1271/BBB.65.1198
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) octacosanoate 163037859 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 833.40 unknown https://doi.org/10.1271/BBB.65.1198
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) tetracosanoate 14486654 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 777.30 unknown https://doi.org/10.1271/BBB.65.1198
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] docosanoate 101048503 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 749.30 unknown https://doi.org/10.1271/BBB.65.1198
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] hexacosanoate 101104651 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 805.40 unknown https://doi.org/10.1271/BBB.65.1198
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] icosanoate 101104650 Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 721.20 unknown https://doi.org/10.1271/BBB.65.1198
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] octacosanoate 101104652 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 833.40 unknown https://doi.org/10.1271/BBB.65.1198
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] tetracosanoate 101104649 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 777.30 unknown https://doi.org/10.1271/BBB.65.1198
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 via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1271/BBB.65.1198
Friedelanol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1271/BBB.65.1198
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1271/BBB.65.1198
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/10.1271/BBB.65.1198
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/10.1271/BBB.65.1198
O-Acetyloleanolic aldehyde 14829106 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hexyl acetate 8908 Click to see CCCCCCOC(=O)C 144.21 unknown https://doi.org/10.1080/10412905.1992.9698151
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one 184824 Click to see C1CC(CCC1=O)(CCO)O 158.19 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Butyloctenal 25610 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown https://doi.org/10.1080/10412905.1992.9698151
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown https://doi.org/10.1080/10412905.1992.9698151
Non-2-enal 17166 Click to see CCCCCCC=CC=O 140.22 unknown https://doi.org/10.1080/10412905.1992.9698151
> Organoheterocyclic compounds / Benzofurans
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown via CMAUP database
Cleroindicin E 11744892 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
epi-Cleroindicin D 10749706 Click to see C1COC2C1(C(CC(=O)C2)O)O 172.18 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown https://doi.org/10.1080/10412905.1992.9698151
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Phaselic acid, (-)- 92299542 Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O 296.23 unknown https://doi.org/10.1021/JF2022868
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(3S)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-4-methoxy-4-oxobutanoic acid 163187702 Click to see COC(=O)C(CC(=O)O)OC(=O)C=CC1=CC=C(C=C1)O 294.26 unknown https://doi.org/10.1021/JF2022868
(3S)-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-4-methoxy-4-oxobutanoic acid 163187700 Click to see COC(=O)C(CC(=O)O)OC(=O)C=CC1=CC=C(C=C1)O 294.26 unknown https://doi.org/10.1021/JF2022868
(3S)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-4-methoxy-4-oxobutanoic acid 162892627 Click to see COC(=O)C(CC(=O)O)OC(=O)C=CC1=CC=C(C=C1)O 294.26 unknown https://doi.org/10.1021/JF2022868
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5318059 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown via CMAUP database
beta-D-Glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl 158227 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 492.40 unknown via CMAUP database
Scutellarin 185617 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
7-hydroxy-5-methoxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 101688473 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 476.40 unknown https://doi.org/10.1271/BBB.59.2244
7-Hydroxy-5-methoxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162884708 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 476.40 unknown https://doi.org/10.1271/BBB.59.2244
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101688472 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 476.40 unknown https://doi.org/10.1271/BBB.59.2244
2-(4-Hydroxy-3-methoxyphenyl)-5-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977771 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 476.40 unknown https://doi.org/10.1271/BBB.59.2244
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database

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