Cercidiphyllum japonicum

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID64402d23a1675926808247
Scientific name	Cercidiphyllum japonicum
Authority	Siebold & Zucc. ex J.J.Hoffm. & J.H.Schult.bis
First published in	J. Asiat. , sér. 4, 20: 282 (1852)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Cercidiphyllum japonicum f. miquelianum	Inokuma	Bull. Tokyo Imp. Univ. Forests 25: 29 1937
Cercidiphyllum japonicum var. pendulum	Miyoshi ex Makino & Nemoto	Fl. Japan ed. 2: 307. 1931
Cercidiphyllum japonicum f. pendulum	(Miyoshi ex Makino & Nemoto) Ohwi	Fl. Jap. 510 1953
Cercidiphyllum japonicum var. sinense	Rehder & E.H.Wilson	Pl. Wilson. 1: 316. 1913
Cercidiphyllum magnificum f. pendulum	(Miyoshi ex Makino & Nemoto) Spongberg	J. Arnold Arbor. 60: 376 (1979)
Cercidiphyllum ovale	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 144 (1872)
Cercidiphyllum japonicum f. piramidale	V.V.Byalt & Firsov	Hortus Botanicus 11: 23 (2015)

Common names Top

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Filter by language:

Language	Common/alternative name
English	katsura
English	katsura tree
Belarusian	барвоўнік японскі
Czech	zmarličník japonský
Danish	almindelig hjertetræ
German	japanischer kuchenbaum
Greek	Κερκιδίφυλλο το ιαπωνικό
Greek	Κατσούρα
Esperanto	kacuro
Basque	karamelu-zuhaitza
Basque	katsura
Persian	ارغوانه ژاپنی
Finnish	katsura
Finnish	pikkulehtikatsura
Hungarian	kacurafa
Japanese	カツラ
Korean	계수나무
Lithuanian	japoninis puošmedis
Norwegian Bokmål	hjertetre
Dutch	koekjesboom
Dutch	katsuraboom
Polish	grujecznik japoński
Russian	Багрянник японский
Russian	Круглолистник
Serbian	Јапанска кацура
Swedish	katsura
Turkish	katsura ağacı
Chinese	毛叶连香树
Chinese	連香樹
Chinese	连香树
Chinese	连香树果
Chinese	银叶连香树

Subspecies (abbr. subsp./ssp.) Top

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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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea

Europe click to expand
- Middle Europe
  - Austria

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000834990
Cornell Woody Plants	51
Canadensys	31448
USDA Plants	CEJA2
UConn	101
KEW	urn:lsid:ipni.org:names:77084481-1
The Plant List	kew-37218
Plantarium	46271
Missouri Botanical Garden	279148
Open Tree Of Life	324758
Observations.org	189272
NCBI Taxonomy	13413
NBN Atlas	NBNSYS0500000382
Nature Serve	2.132745
IUCN Red List	32332
IPNI	77084481-1
iNaturalist	133356
IFPNI	E172064F-CCA4-491C-9B48-8B6117999BF8
GBIF	3152839
Freebase	/m/064r8g1
EPPO	CCPJA
EOL	488405
Elurikkus	639942
USDA GRIN	9935
Wikipedia	Cercidiphyllum_japonicum

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

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

Commodity risk assessment of Corylus avellana plants from the UK

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, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

12-Jan-2024

PMCID:	PMC10784871
doi:	10.2903/j.efsa.2024.8495
PMID:	38222930

High-quality assembly and methylome of a Tibetan wild tree peony genome (Paeonia ludlowii) reveal the evolution of giant genome architecture

Xiao PX, Li Y, Lu J, Zuo H, Pingcuo G, Ying H, Zhao F, Xu Q, Zeng X, Jiao WB

Hortic Res

10-Nov-2023

PMCID:	PMC10753165
doi:	10.1093/hr/uhad241
PMID:	38156287

Benefits of Urban Forest Healing Program on Depression and Anxiety Symptoms in Depressive Patients

Yeon PS, Kang SN, Lee NE, Kim IO, Min GM, Kim GY, Kim JG, Shin WS

Healthcare (Basel)

19-Oct-2023

PMCID:	PMC10606414
doi:	10.3390/healthcare11202766
PMID:	37893840

Recent Advances in the Application of Cucurbitacins as Anticancer Agents

Zieniuk B, Pawełkowicz M

Metabolites

14-Oct-2023

PMCID:	PMC10608718
doi:	10.3390/metabo13101081
PMID:	37887406

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

A chromosome-scale Rhubarb (Rheum tanguticum) genome assembly provides insights into the evolution of anthraquinone biosynthesis

Li Y, Wang Z, Zhu M, Niu Z, Li M, Zheng Z, Hu H, Lu Z, Zhang J, Wan D, Chen Q, Yang Y

Commun Biol

23-Aug-2023

PMCID:	PMC10447539
doi:	10.1038/s42003-023-05248-5
PMID:	37612424

Commodity risk assessment of Fagus sylvatica plants from the UK

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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

28-Jul-2023

PMCID:	PMC10375364
doi:	10.2903/j.efsa.2023.8118
PMID:	37522095

Commodity risk assessment of Acer pseudoplatanus plants from the UK

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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

06-Jul-2023

PMCID:	PMC10323731
doi:	10.2903/j.efsa.2023.8074
PMID:	37427019

Commodity risk assessment of Acer campestre plants from the UK

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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

06-Jul-2023

PMCID:	PMC10323733
doi:	10.2903/j.efsa.2023.8071
PMID:	37427018

Commodity risk assessment of Acer platanoides plants from the UK

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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

06-Jul-2023

PMCID:	PMC10323725
doi:	10.2903/j.efsa.2023.8073
PMID:	37427021

Commodity risk assessment of Acer palmatum plants from the UK

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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

06-Jul-2023

PMCID:	PMC10323724
doi:	10.2903/j.efsa.2023.8075
PMID:	37427020

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

Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review

Tshikhudo PP, Ntushelo K, Mudau FN

Microorganisms

10-Feb-2023

PMCID:	PMC9967847
doi:	10.3390/microorganisms11020453
PMID:	36838418

Differences in Male Mate Recognition between the Invasive Anoplophora glabripennis (Coleoptera: Cerambycidae) and Japanese Native A. malasiaca

Yasui H, Uechi N, Fujiwara-Tsujii N

Insects

09-Feb-2023

PMCID:	PMC9960942
doi:	10.3390/insects14020171
PMID:	36835739

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Cercidin	14830707	Click to see CC12C(C(=O)C=CO1)(OC3=C(C=C(C=C3O2)C(=O)OC)O)O	308.24	unknown	https://doi.org/10.1016/S0031-9422(00)95184-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1055/S-2002-35657
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4R,5R)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	92238311	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.37.50
[(2R,3R,4R,5R)-4,5-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	102157672	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.37.50
2',5-Digalloylhamamelofuranose	16211077	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.37.50
3-O-Galloylhamamelitannin	13270020	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.37.50
Hamamelitannin	253775	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.37.50
Hamamelofuranose 2'5'-digallate	44584241	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.37.50
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	https://doi.org/10.1007/S10600-019-02638-2
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	https://doi.org/10.1016/S0031-9422(00)83734-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see CC1=C(C(=O)C=CO1)O	126.11	unknown	https://doi.org/10.1016/S0031-9422(00)95184-7 https://doi.org/10.1016/S0031-9422(00)97400-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one	5153580	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1055/S-2002-35657
Dihydromyricetin	161557	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1055/S-2002-35657
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1055/S-2002-35657
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	662	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1055/S-2002-35657
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1055/S-2002-35657
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1055/S-2002-35657
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1055/S-2002-35657 https://doi.org/10.1007/S10600-019-02638-2
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1055/S-2002-35657
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1055/S-2002-35657
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose	374874	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)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1248/CPB.37.50
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.37.50
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.37.50
Pentagalloylglucose	65238	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)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1248/CPB.37.50
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,6a,10',11',12',15',16',17',31',32',36',37'-dodecahydroxy-2',5,7',20',28',41'-hexaoxospiro[3,3a-dihydro-2H-furo[3,2-b]furan-6,39'-3,6,21,24,27,38,42-heptaoxanonacyclo[35.2.2.133,36.01,35.04,23.05,26.08,13.014,19.029,34]dotetraconta-8,10,12,14,16,18,29,31,33-nonaene]-25'-yl) 3,4,5-trihydroxybenzoate	3459965	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1110.80	unknown	https://doi.org/10.1248/CPB.37.50
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate	138991573	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.37.50
(6,7,8,11,12,13,22,23-Octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl) 3,4,5-trihydroxybenzoate	5089683	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(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1248/CPB.37.50
[3,4,5,11,20,21,22-Heptahydroxy-8,17-dioxo-14-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate	14284543	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C6)O)O)O	786.60	unknown	https://doi.org/10.1248/CPB.37.50
[3,4,5,20,21,22-Hexahydroxy-8,17-dioxo-11,14-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate	14284541	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C7)O)O)O	938.70	unknown	https://doi.org/10.1248/CPB.37.50
CID 10533860	10533860	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C3C(C(C(O2)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)O3)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1248/CPB.37.50 https://doi.org/10.1248/CPB.49.486
CID 115063	115063	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.37.50
CID 338147	338147	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.37.50
Corilagin	73568	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(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1248/CPB.37.50
Geraniin	3001497	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1248/CPB.37.50
Mahtabin A	10557787	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C7)O)O)O	938.70	unknown	https://doi.org/10.1248/CPB.37.50
Pariin M	14284542	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C6)O)O)O	786.60	unknown	https://doi.org/10.1248/CPB.37.50
Xcxwmhrrisfuff-xngpzlstsa-	21636130	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1110.80	unknown	https://doi.org/10.1248/CPB.37.50

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Cercidiphyllum japonicum

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