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Corylus heterophylla

Corylus heterophylla - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644035f880deb393437615
Scientific name Corylus heterophylla
Authority Fisch. ex Trautv.
First published in Pl. Imag. Descr. Fl. Russ. 1: 10 (1844)

Description Top

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Corylus heterophylla, also known as the Asian hazel, is a deciduous shrub or small tree found in eastern Asia. It can reach heights of up to 7 meters and has grey bark and rounded leaves with a serrated or lobed margin. The flowers are wind-pollinated and the fruit is a nut enclosed in a bract-like husk. This species is similar to the common hazel found in Europe and western Asia, but can be distinguished by its more lobed leaves. The nuts of this plant are edible and are commercially cultivated in China.

Synonyms Top

Scientific name Authority First published in
Corylus avellana var. davurica Ledeb. Fl. Ross. 3: 588. 1850
Corylus hasibani Siebold Kruidk. Naamlijst : 27 (1844)
Corylus heterophylla var. thunbergii Blume Mus. Bot. 1: 130. 1850
Corylus heterophylla var. yezoensis Koidz. Bot. Mag. (Tokyo) 27: 143. 1913
Corylus tetraphylla Ledeb. Denkschr. Bayer. Bot. Ges. Regensburg 3(2): 58 (1841)
Corylus yezoensis (Koidz.) Nakai Fl. Sylv. Kor. 2: 2. 1915 (1915)

Common names Top

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Language Common/alternative name
English siberian hazelnut
Azerbaijani müxtəlifyarpaq fındıq
Belarusian ляшчына разналістая
German mongolische hasel
Japanese ハシバミ
Korean 개암나무
Latvian dažādlapu lazda
lzh 榛
Russian Лещина разнолистная
Chinese 榛樹
Chinese 榛树
Chinese 榛*(榛子）
Chinese 棒子花
Chinese 榛子
Chinese 棒子
Chinese 榛
Chinese 川榛

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
Corylus heterophylla var. heterophylla Unknown
Corylus heterophylla var. sutchuenensis Franch. J. Bot. (Morot) 13: 199 (1899)

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
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Chita

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000925321
USDA Plants COHE12
Tropicos 3600390
KEW urn:lsid:ipni.org:names:295460-1
The Plant List kew-47893
PaleoBotany 103890
Open Tree Of Life 550611
Observations.org 127910
NCBI Taxonomy 80754
IUCN Red List 194468
IPNI 295460-1
iNaturalist 448040
GBIF 2876072
Freebase /m/03cnqg_
EPPO CYLHE
EOL 1147590
USDA GRIN 11650
Wikipedia Corylus_heterophylla

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_016403345.1 ASM1640334v1 Chromosome Chinese Academy of Forestry 2020-12-28 101.0x 353.58 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
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses Bejerman N, Dietzgen R, Debat H Viruses 10-Dec-2023
PMCID:PMC10747219
doi:10.3390/v15122402
PMID:38140643
Diaporthe Species on Palms: Molecular Re-Assessment and Species Boundaries Delimitation in the D. arecae Species Complex Pereira DS, Hilário S, Gonçalves MF, Phillips AJ Microorganisms 06-Nov-2023
PMCID:PMC10673533
doi:10.3390/microorganisms11112717
PMID:38004729
Differences of oribatid mite community and trophic structure between karst caves and surface different moss habitats Gong T, Yin X, Liu W, Chen H, Shi Z PLoS One 17-Aug-2023
PMCID:PMC10434907
doi:10.1371/journal.pone.0290144
PMID:37590253
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
Genome-wide identification and characterization of SRLK gene family reveal their roles in self-incompatibility of Erigeron breviscapus Xiang C, Tao H, Wang T, Meng H, Guan D, Li H, Wei X, Zhang W BMC Genomics 17-Jul-2023
PMCID:PMC10353254
doi:10.1186/s12864-023-09485-0
PMID:37460954
Effect of Climate and Competition on Radial Growth of Pinus sylvestris var. mongolica Forest in Hulunbuir Sandy Land of Inner Mongolia, China Wen S, Shi Z, Zhang X, Pan L, Kwon S, Li Y, Yang X, Li H Plants (Basel) 07-Jul-2023
PMCID:PMC10346728
doi:10.3390/plants12132584
PMID:37447145
The complete chloroplast genome sequence of Lithocarpus litseifolius (Hance) Chun 1837 (Fagaceae) and phylogenetic analysis Qiu X, Xiao S, Tian Y, Li Z Mitochondrial DNA B Resour 15-May-2023
PMCID:PMC10187088
doi:10.1080/23802359.2023.2210422
PMID:37200682
Population genomics reveals demographic history and selection signatures of hazelnut (Corylus) Yang Z, Ma W, Wang L, Yang X, Zhao T, Liang L, Wang G, Ma Q Hortic Res 10-Apr-2023
PMCID:PMC10208898
doi:10.1093/hr/uhad065
PMID:37249951
Low-Molecular-Mass Fragments of Collagen Improve Parameters Related to Mass and Inflammation of the Adipose Tissue in the Obese Rat Kalmukova O, Raksha N, Vovk T, Halenova T, Dzerzhynsky M, Mitrecic D, Savchuk O, Ostapchenko L Food Technol Biotechnol 01-Mar-2023
PMCID:PMC10187574
doi:10.17113/ftb.61.01.23.7926
PMID:37200797
Transcriptome sequencing and gene expression analysis revealed early ovule abortion of Paeonia ludlowii Chen TQ, Sun Y, Yuan T BMC Genomics 17-Feb-2023
PMCID:PMC9936667
doi:10.1186/s12864-023-09171-1
PMID:36803218
UPLC-MS/MS profiling, antioxidant and anti-inflammatory activities, and potential health benefits prediction of phenolic compounds in hazel leaf Zhao J, Wang X, Wang Y, Lv G, Lin H, Lin Z Front Nutr 01-Feb-2023
PMCID:PMC9929368
doi:10.3389/fnut.2023.1092071
PMID:36819681
Fungal diversities and community assembly processes show different biogeographical patterns in forest and grassland soil ecosystems Wang M, Wang C, Yu Z, Wang H, Wu C, Masoudi A, Liu J Front Microbiol 01-Feb-2023
PMCID:PMC9928764
doi:10.3389/fmicb.2023.1036905
PMID:36819045
Editorial: Recent advances in hazelnut (Corylus spp.) Cristofori V, Botta R, Rovira M, Molnar TJ, Mehlenbacher SA Front Plant Sci 04-Jan-2023
PMCID:PMC9847355
doi:10.3389/fpls.2022.1120595
PMID:36684751

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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 11972446 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.39.49
Quercetin 3-glucuronide 12004528 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.39.49
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.39.49
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.39.49
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.39.49
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R,12R,13R,15R)-3,4,5,12,21,22,23-heptahydroxy-8,18-dioxo-13-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 14481558 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.39.49
[(10R,11R,12R,13S,15R)-3,4,5,12,21,22,23-heptahydroxy-8,18-dioxo-13-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] (1S)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylate 163092259 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)OC4C(C(OC5C4OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC5)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O 908.60 unknown https://doi.org/10.1248/CPB.39.49
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.39.49
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 2-[[(10S,11R,12R,13S,15R)-3,4,5,11,12,22,23-heptahydroxy-8,18-dioxo-13-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate 16144491 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C85)O)O)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1571.10 unknown https://doi.org/10.1016/S0031-9422(97)01091-1
[(10S,11R)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzenecarboperoxoate 163007209 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OOC(=O)C8=CC(=C(C(=C8)O)O)O 952.60 unknown https://doi.org/10.1248/CPB.39.49
[10-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzenecarboperoxoate 163007208 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OOC(=O)C8=CC(=C(C(=C8)O)O)O 952.60 unknown https://doi.org/10.1248/CPB.39.49
1-O-Galloylpedunculagin 452242 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.39.49
1(beta)-O-Galloylpedunculagin 118701062 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.39.49
3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoic acid 16174833 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)O)O)O)O)O)O)O)O)O 1104.70 unknown https://doi.org/10.1248/CPB.39.49
Casuarictin 73644 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.39.49
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.39.49
CID 11766372 11766372 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1248/CPB.39.49
CID 16174834 16174834 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)O)O)O)O)O)O)O)O)O 1104.70 unknown https://doi.org/10.1248/CPB.39.49
CID 16174836 16174836 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.39.49
CID 16174839 16174839 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C1C(O9)COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1248/CPB.39.49
CID 16174842 16174842 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C8C(C(O7)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C26)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.39.49
CID 16174844 16174844 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC(C(OC(=O)C6=CC(=C(C(=C65)O)O)O)C7C8C(C9=C(C(=C(C(=C9C(=O)O8)C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.39.49
CID 16174846 16174846 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC(C(OC(=O)C7=CC(=C(C(=C76)O)O)O)C8C9C(C2=C(C(=C(C(=C2C(=O)O9)C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.39.49
Degalloylrugosin F 16174838 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C1C(O9)COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1248/CPB.39.49
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin A 471120 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin B 16174843 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC(C(OC(=O)C6=CC(=C(C(=C65)O)O)O)C7C8C(C9=C(C(=C(C(=C9C(=O)O8)C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin C 16174845 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC(C(OC(=O)C7=CC(=C(C(=C76)O)O)O)C8C9C(C2=C(C(=C(C(=C2C(=O)O9)C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin D 16174841 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C8C(C(O7)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C26)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin E 14824938 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)OC4C(C(OC5C4OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC5)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O 908.60 unknown https://doi.org/10.1248/CPB.39.49
Heterophylliin F 131751290 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C85)O)O)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1571.10 unknown https://doi.org/10.1016/S0031-9422(97)01091-1
Rugosin C 101590860 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC5=C(C6=C(C(=C(C=C6C(=O)O3)O)O)O)C(=C(C(=C5)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)O)O)O)O)O)O)O)O)O 1076.70 unknown https://doi.org/10.1248/CPB.39.49
Rugosin F 16174837 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.39.49
Tellimagrandin II 151590 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1248/CPB.39.49

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