Scientific name	Authority	First published in
Quercus aegilops	Scop.	Fl. Carniol. , ed. 2, 2: 241 (1772)
Quercus ambrozyana	Simonk.	Magyar Bot. Lapok 8: 355 (1909)
Quercus aspleniifolia	hort. ex A.DC.	Prodr. 16(2): 42 (1864)
Quercus austriaca	Willd.	Sp. Pl., ed. 4 , 4: 454 (1805)
Quercus cana	hort. ex Steud.	Nomencl. Bot. , ed. 2, 2: 426 (1841)
Quercus cerris subsp. austriaca	(Willd.) Nyman	Consp. Fl. Eur. 661. 1881 (1881)
Quercus cerris var. austriaca	(Willd.) Loudon	Arbor. Frutic. Brit. 3: 1848. 1838
Quercus cerris f. balatae	Boros ex Mátyás	Acta Bot. Acad. Sci. Hung. 16: 332 (1970 publ. 1971)
Quercus cerris f. basi-cuneata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 332 (1970 publ. 1971)
Quercus cerris var. bipinnatifida	Schur	Enum. Pl. Transsilv. 608. 1866
Quercus cerris var. bithynica	A.Camus	Chênes Texte 1: 600. 1938
Quercus cerris var. caramanica	Kotschy	Iter Cilic. 385 1866
Quercus cerris f. cyclloloba	Borbás	Oesterr. Bot. Wochenbl. 7: 22 1857
Quercus cerris var. haliphlaeos	(Lam.) Lam.	Fl. Franç. 3: 311. 1779
Quercus cerris f. laciniato-lyrata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 333 (1970 publ. 1971)
Quercus cerris f. lancifolia	Georgescu & Morariu	Analele Inst. Cercet. Exp. Forest. 9: 139 1943
Quercus cerris f. leviterlobata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 333 (1970 publ. 1971)
Quercus cerris var. longimucronata	Hausskn.	Unknown Publ.
Quercus cerris f. macrophylla	Georgescu & Morariu	Analele Inst. Cercet. Exp. Forest. 9: 138 1943
Quercus cerris var. pseudocerris	(Boiss.) Boiss.	Fl. Orient. 4: 1171. 1879
Quercus cerris f. roborilobata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 333 (1970 publ. 1971)
Quercus cerris var. sinuata	Schur	Oesterr. Bot. Wochenbl. 7: 22. 1857
Quercus cerris f. sinuato-lobata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 331 (1970 publ. 1971)
Quercus cerris var. tournefortii	(Willd.) K.Koch	Linnaea 22: 321. 1849
Quercus cerris subsp. tournefortii	(Willd.) O.Schwarz	Repert. Spec. Nov. Regni Veg. 33: 329. 1934 (1934)
Quercus cerris f. verae-csapodyae	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 331 (1970 publ. 1971)
Quercus crinita	Lam.	Encycl. 1: 718 (1785)
Quercus crispa	hort. ex Steud.	Nomencl. Bot. , ed. 2, 2: 426 (1841)
Quercus echinata	Salisb.	Prodr. Stirp. Chap. Allerton : 393 (1796)
Quercus frondosa	Mill.	Gard. Dict. ed. 7 n.° 3. 1759 (1759)
Quercus frondosa	Steud.	Nomencl. Bot. , ed. 2, 2: 426 (1841)
Quercus haliphlaeos	Lam.	Encycl. 1: 718 (1785)
Quercus heterophylla	Hort.Parment. ex A.DC.	Prodr. 16(2): 42 (1864)
Quercus lanuginosa	Lam.	Fl. Franç. 2: 209 (1779)
Quercus nicotrae	Lojac.	Fl. Sicul. 2(2): 375 (1907)
Quercus pseudocerris	Boiss.	Diagn. Pl. Orient. 12: 118 (1853)
Quercus ragnal	G.Lodd. ex Loudon	Arbor. Frutic. Brit. 3: 1849 (1838)
Quercus raynal	K.Koch	Dendrologie 2(2): 77 (1873)
Quercus recurvisquamosa	St.-Lag.	Cat. Fl. Bass. Rhone 674. 1882 (1882)
Quercus secondatii	Steud.	Nomencl. Bot. 1: 674 (1821)
Quercus thracica	Stef. & Nedjalkov	Izv. Bot. Inst. (Sofia) 5: 39 (1956)
Quercus tournefortii	Willd.	Sp. Pl., ed. 4 , 4: 453 (1805)
Quercus tukhtensis	Czeczott	Acta Soc. Bot. Poloniae 9: 44 (1932)
Quercus variegata	Lodd. ex Steud.	Nomencl. Bot. , ed. 2, 2: 428 (1841)
Cerris australis	Raf.	Alsogr. Amer. : 29 (1838)
Cerris austriaca	Raf.	Alsogr. Amer. : 29 (1838)
Cerris crinita	Raf.	Alsogr. Amer. : 29 (1838)
Cerris paliphleos	Raf.	Alsogr. Amer. : 29 (1838)
Quercus cerris var. pendula	Neill	Rem. Forest Scen. 1: 73. 1834
Quercus cerris f. pendula	(Neill) Asch. & Graebn.	Syn. Mitteleur. Fl. 4: 462 1911
Quercus cerris subsp. austriaca	(Willd.) O.Schwarz	Repert. Spec. Nov. Regni Veg. 33: 328 1934
Quercus cerris subsp. acuto-bipinnata	Mátyás	Acta Bot. Acad. Sci. Hung. 16: 332 (1970 publ. 1971)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	mossy-cup oak
English	european turkey oak
English	turkey oak
Spanish	roble de turquia
Spanish	roble de turquía
Afrikaans	turkse eik
Afrikaans	moseik
Arabic	سنديان أشعر
Arabic	بلوط تركي
Arabic	بلوط أشعر
Azerbaijani	avstriya palıdı
azb	ساچلی پالید
Bulgarian	Цер
Bulgarian	цер
Bosnian	hrast cer
Catalan	roure cerris
Czech	dub slovenský
Czech	dub cer
Welsh	derwen twrci
Danish	frynse-eg
German	zerreiche
German	zerr-eiche
Esperanto	muska kverko
Basque	turkiar haritz
Persian	بلوط ترک
Finnish	turkintammi
French	chêne lombard
French	chêne de turquie
French	chêne de bourgogne
French	chêne chevelu
French	doucier
French	chêne cerre
Hebrew	אלון טורקי
Hebrew	אלון תורכי
Hebrew	אלון שסוע
Croatian	hrast cer
Upper Sorbian	burgundski dub
Hungarian	csertölgy
Hungarian	cserfa
Icelandic	kögureik
Italian	cerro
Italian	cerri
Japanese	トルコオーク
Japanese	トルコカシ
Japanese	トルコナラ
Japanese	ターキー・オーク
Georgian	თურქული მუხა
Latvian	austrijas ozols
Macedonian	цер
Macedonian	даб цер
nap	cierr
Norwegian Bokmål	frynseeik
Dutch	moseik
Dutch	turkse eik
Polish	dąb burgundzki
Serbo-Croatian	cer
Serbo-Croatian	hrast cer
Slovak	dub cerový
Slovenian	cer
Albanian	qarri (dru)
Serbian	Цер
Swedish	turkisk ek
Turkish	saçlı meşe
Chinese	土耳其栎
Chinese	山羊栎
Chinese	土耳其櫟

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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 click to expand
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Turkey

Australasia click to expand
- New Zealand
  - New Zealand South

Europe click to expand
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France

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-0000290053
USDA Plants	QUCE
INPN	116670
Flora of Italy	267
KEW	urn:lsid:ipni.org:names:295941-1
The Plant List	kew-172055
Plantarium	31137
Missouri Botanical Garden	280767
PFAF	Quercus cerris
PaleoBotany	52584
Open Tree Of Life	520576
Observations.org	7283
NCBI Taxonomy	39468
NBN Atlas	NBNSYS0000003843
Nature Serve	2.784910
IUCN Red List	194074
IPNI	295941-1
iNaturalist	135408
IFPNI	FBC478B7-6910-4D6D-9E7B-B55111AF94E0
GBIF	2880580
Freebase	/m/01ylbk
EPPO	QUECE
EOL	1151719
Elurikkus	6676
Calflora (Californian flora)	12822
USDA GRIN	30655
Wikipedia	Quercus_cerris
CMAUP	NPO24675

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_963669245.1	dhQueCerr2.1	Chromosome	WELLCOME SANGER INSTITUTE	2023-12-09	36.0x	741.38 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

Importance of Habitat Context in Modelling Risk Maps for Two Established Invasive Alien Plant Species: The Case of Ailanthus altissima and Phytolacca americana in Slovenia (Europe)

de Groot M, Kozamernik E, Kermavnar J, Kolšek M, Marinšek A, Nève Repe A, Kutnar L

Plants (Basel)

19-Mar-2024

PMCID:	PMC10974566
doi:	10.3390/plants13060883
PMID:	38592890

The antioxidant and anticancer activity of Quercus coccifera plant leaves extracts

Jaber SA

Saudi J Biol Sci

10-Mar-2024

PMCID:	PMC10951596
doi:	10.1016/j.sjbs.2024.103979
PMID:	38510526

The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered

Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O

Stud Mycol

22-Feb-2024

PMCID:	PMC11003443
doi:	10.3114/sim.2024.107.03
PMID:	38600960

Rambellisea gigliensis and Rambellisea halocynthiae, gen. et spp. nov. (Lulworthiaceae) from the Marine Tunicate Halocynthia papillosa

Braconcini M, Gorrasi S, Fenice M, Barghini P, Pasqualetti M

J Fungi (Basel)

03-Feb-2024

PMCID:	PMC10890369
doi:	10.3390/jof10020127
PMID:	38392799

The Orophilous Shrubby Vegetation of the Juniperetalia hemisphaericae Order in Sicily: A Refuge Habitat for Many Endemic Vascular Species

Sciandrello S, Giusso del Galdo G

Plants (Basel)

31-Jan-2024

PMCID:	PMC10857485
doi:	10.3390/plants13030423
PMID:	38337957

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

Exploring the potential of Crotalaria juncea flower extracts as a source of antioxidants, antimicrobials, and cytoprotective agents for biomedical applications

Mahasawat P, Boukaew S, Prasertsan P

BioTechnologia (Pozn)

21-Dec-2023

PMCID:	PMC10777724
doi:	10.5114/bta.2023.132772
PMID:	38213478

Reconstructing the post-glacial spread of the sand fly Phlebotomus mascittii Grassi, 1908 (Diptera: Psychodidae) in Europe

Kniha E, Dvořák V, Koblmüller S, Prudhomme J, Ivović V, Hoxha I, Oerther S, Heitmann A, Lühken R, Bañuls AL, Sereno D, Michelutti A, Toniolo F, Alarcón-Elbal PM, Bravo-Barriga D, González MA, Lucientes J, Colella V, Otranto D, Bezerra-Santos MA, Kunz G, Obwaller AG, Depaquit J, Alić A, Kasap OE, Alten B, Omeragic J, Volf P, Walochnik J, Sebestyén V, Trájer AJ

Commun Biol

08-Dec-2023

PMCID:	PMC10709326
doi:	10.1038/s42003-023-05616-1
PMID:	38066195

Antibiofilm Effects of Oleuropein against Staphylococcus aureus: An In Vitro Study

Guo W, Xu Y, Yang Y, Xiang J, Chen J, Luo D, Xie Q

Foods

28-Nov-2023

PMCID:	PMC10706080
doi:	10.3390/foods12234301
PMID:	38231779

Turbidity reduction efficacies of seed kernels of Mango (Mangifera indica) genotypes in Uganda

Onyutha C, Auma N

Heliyon

21-Oct-2023

PMCID:	PMC10598518
doi:	10.1016/j.heliyon.2023.e21415
PMID:	37885706

Topographic depressions can provide climate and resource microrefugia for biodiversity

Frei K, Vojtkó A, Farkas T, Erdős L, Barta K, E-Vojtkó A, Tölgyesi C, Bátori Z

iScience

21-Oct-2023

PMCID:	PMC10656275
doi:	10.1016/j.isci.2023.108202
PMID:	38026156

Mutual Avoidance in the Spectacled Salamander and Centipede: A Discrepancy between Exploratory Field and Laboratory Data

Cerini F, Pardo C, Taurozzi D, Gambioli B, Vignoli L

Animals (Basel)

14-Oct-2023

PMCID:	PMC10603627
doi:	10.3390/ani13203214
PMID:	37893937

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

Mate‐guarding success depends on male investment in a butterfly

Gór Á, Lang Z, Pásztor K, Szigeti V, Vajna F, Kis J

Ecol Evol

17-Sep-2023

PMCID:	PMC10505759
doi:	10.1002/ece3.10533
PMID:	37727777

Platinum and Palladium Accumulation in Edible Mushroom Boletus aereus Bull. Growing in Unpolluted Soils of Sicily Region (Italy)

Alaimo MG, Varrica D

J Fungi (Basel)

09-Sep-2023

PMCID:	PMC10532657
doi:	10.3390/jof9090914
PMID:	37755022

Phytochemical Profile Top

Add a new one!

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 / Benzoic acid esters
Dimethyl anthranilate	6826	Click to see CNC1=CC=CC=C1C(=O)OC	165.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
1-Methyl-4-(prop-1-en-2-yl)benzene	62385	Click to see CC1=CC=C(C=C1)C(=C)C	132.20	unknown	via CMAUP database
alpha,3-Dimethylstyrene	70759	Click to see CC1=CC(=CC=C1)C(=C)C	132.20	unknown	via CMAUP database
o-Isopropenyltoluene	81886	Click to see CC1=CC=CC=C1C(=C)C	132.20	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine	854067	Click to see CNCC(C1=CC=C(C=C1)O)O	167.20	unknown	via CMAUP database
> Benzenoids / Phenols / 4-alkoxyphenols
4-(3-Methyl-2-butenoxy)phenol	11435274	Click to see CC(=CCOC1=CC=C(C=C1)O)C	178.23	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
6-Hexadecen-4-yne, (E)-	5367338	Click to see CCCCCCCCCC=CC#CCCC	220.39	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
12-Methyl-1,5,9,11-tridecatetraene	564371	Click to see CC(=CC=CCCC=CCCC=C)C	190.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic acid	10469	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	396.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate	8167	Click to see CCCCCCCCCCOC(=O)C	200.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Mollugogenol F	101281371	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC(C5C4(CCC5C(C)(C)O)C)O)C)C)C	460.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal	75427	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	via CMAUP database
(Z)-alpha-ocimene	5463455	Click to see CC(=C)CCC=C(C)C=C	136.23	unknown	via CMAUP database
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
D-Citronellol	101977	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-2-Carene	78249	Click to see CC1=CC2C(C2(C)C)CC1	136.23	unknown	via CMAUP database
(+)-trans-Sabinene hydrate	11228920	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	via CMAUP database
(1S,4beta)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2alpha,3alpha-diol	21626089	Click to see CC1(C2CCC1(C(C2O)O)C)C	170.25	unknown	via CMAUP database
alpha-THUJENE, (+/-)-	12444324	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
cis-Sabinene hydrate	11744854	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
(+)-Perillaldehyde	1548901	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	via CMAUP database
(5R)-5-isopropyl-2-methyl-2-cyclohexen-1-one	10888107	Click to see CC1=CCC(CC1=O)C(C)C	152.23	unknown	via CMAUP database
(R)-(+)-4-Isopropylcyclohex-1-ene-1-carboxaldehyde	12305140	Click to see CC(C)C1CCC(=CC1)C=O	152.23	unknown	via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enyl acetate	11333027	Click to see CC1=CCC(CC1)C(=C)COC(=O)C	194.27	unknown	via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, trans-	12618691	Click to see CC(=C)C1CCC(C=C1)(C)O	152.23	unknown	via CMAUP database
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R-trans)-	6951358	Click to see CC1=CCC(CC1OC(=O)C)C(=C)C	194.27	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Carvone, (-)-	439570	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
trans-1(7),8-p-Menthadien-2-ol	6428442	Click to see CC(=C)C1CCC(=C)C(C1)O	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(Z,Z)-alpha-Farnesene	5317320	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	via CMAUP database
alpha-Sinensal	5281534	Click to see CC(=CCC=C(C)C=C)CCC=C(C)C=O	218.33	unknown	via CMAUP database
trans,trans-Farnesol	445070	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Selinene	10856614	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene	6419725	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene	16061252	Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C	540.90	unknown	via CMAUP database
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
delta-Carotene	5281230	Click to see CC1=CCCC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)(C)C	536.90	unknown	via CMAUP database
Lycopene	446925	Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C	536.90	unknown	via CMAUP database
Phytofluene	6436722	Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C	542.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(3S,3'S,5R,5'R,6R,8'R)-5,5',6,8'-Tetrahydro-6,7-didehydro-5',8'-epoxy-beta,beta-carotene-3,3',5-triol	14034169	Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)O)(C)C	600.90	unknown	via CMAUP database
(3S,5R,6S)-beta-cryptoxanthin 5,6-epoxide	23256985	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C	568.90	unknown	via CMAUP database
(3S,5R,8R,3'R)-mutatoxanthin	21765300	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C	584.90	unknown	via CMAUP database
6-epi-Karpoxanthin	23258402	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	602.90	unknown	via CMAUP database
all-trans-Neoxanthin	5281247	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=C=C1C(CC(CC1(C)O)O)(C)C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C	600.90	unknown	via CMAUP database
beta-Cryptoxathin-5',6'-epoxide	21587177	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CCCC2(O3)C)(C)C)C)C	568.90	unknown	via CMAUP database
Cryptoxanthin	5281235	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	552.90	unknown	via CMAUP database
Rubixanthin	5281252	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C	552.90	unknown	via CMAUP database
Violaxanthin	448438	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C	600.90	unknown	via CMAUP database
Violaxanthin A	101341894	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C	600.90	unknown	via CMAUP database
Zeaxanthin	5280899	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
Zeinoxanthin	5281234	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3E,5E,7E,9E,11E,13E,15E,17E,19E)-20-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-5,9,14,18-tetramethylicosa-3,5,7,9,11,13,15,17,19-nonaen-2-one	101306769	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C)C)C	472.70	unknown	via CMAUP database
Apocarotenal	5478003	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C	416.60	unknown	via CMAUP database
beta-Citraurin	9845703	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C	432.60	unknown	via CMAUP database
beta-Citraurinene	90429320	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C)C)C	418.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	98050000	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(=O)OC7O)C)C)C	502.50	unknown	via CMAUP database
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	92966492	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
(2'R,5aR,7aR,8R,9S,11aR,11bR)-9-[(S)-furan-3-yl-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,5,7a,9,11b-pentamethyl-3,7-dioxospiro[6,10,11,11a-tetrahydro-5aH-benzo[g][2]benzoxepine-8,3'-oxirane]-2'-carboxylic acid	53363753	Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC(C34C(O4)C(=O)O)(C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O)C)C	634.70	unknown	via CMAUP database
Limonin	179651	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
Nomilin	72320	Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C	514.60	unknown	via CMAUP database
Obacunone	119041	Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C	454.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5,5'-Oxybis(5-methylene-2-furaldehyde)	12366272	Click to see C1=C(OC(=C1)C=O)COCC2=CC=C(O2)C=O	234.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(R)-alpha-Citronellal	72941638	Click to see CC(CCCC(=C)C)CC=O	154.25	unknown	via CMAUP database
Decanal	8175	Click to see CCCCCCCCCC=O	156.26	unknown	via CMAUP database
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
Octanal	454	Click to see CCCCCCCC=O	128.21	unknown	via CMAUP database
Undecanal	8186	Click to see CCCCCCCCCCC=O	170.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,4R,6S)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane	6857487	Click to see CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
Carvone oxide	11030188	Click to see CC(=C)C1CC2C(O2)(C(=O)C1)C	166.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-(4-Hydroxyphenyl)ethyl 3-(4-hydroxyphenyl)prop-2-enoate	86163337	Click to see C1=CC(=CC=C1CCOC(=O)C=CC2=CC=C(C=C2)O)O	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin	66548	Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C	258.27	unknown	via CMAUP database
Xanthyletin	65188	Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-4',5,6,7-tetramethoxyflavone	24752965	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)O	358.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4-acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	11262186	Click to see CC(=O)OC1C(C(OC(C1O)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O	636.60	unknown	https://doi.org/10.1002/JLAC.198819881010
[(2R,3S,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	162917949	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O	624.50	unknown	https://doi.org/10.1002/JLAC.198819881010
[4-Acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	72774322	Click to see CC(=O)OC1C(C(OC(C1O)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O	636.60	unknown	https://doi.org/10.1002/JLAC.198819881010
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	74977622	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O	624.50	unknown	https://doi.org/10.1002/JLAC.198819881010
isorhamnetin 3-O-(6"-O-p-coumaroyl)-glucoside	44429737	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O	624.50	unknown	https://doi.org/10.1002/JLAC.198819881010
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	102155802	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O	630.50	unknown	https://doi.org/10.1002/JLAC.198819881010
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14162289	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O	630.50	unknown	https://doi.org/10.1002/JLAC.198819881010
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperidin	10621	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	via CMAUP database
Naringin	442428	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O	580.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Takakin	44258588	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6-dimethoxyflavone	5481646	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=CC=C3)O	314.29	unknown	via CMAUP database
Eupatilin	5273755	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,4',6,7-Tetramethoxyflavone	14887080	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=CC(=C(C=C3O2)OC)OC)OC	342.30	unknown	via CMAUP database
3',4',5',5,7-Pentamethoxyflavone	493376	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC(=C(C(=C3)OC)OC)OC	372.40	unknown	via CMAUP database
5-Hydroxy-3',4',6,7-tetramethoxyflavone	152430	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC	358.30	unknown	via CMAUP database
8-Hydroxy-4',5,7-trimethoxyflavone	5318368	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)O	328.30	unknown	via CMAUP database
Apigenin trimethyl ether	79730	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC	312.30	unknown	via CMAUP database
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	via CMAUP database
Fastigenin	162464	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database
Salvigenin	161271	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	328.30	unknown	via CMAUP database
Sinensetin	145659	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,6,7,8-tetramethoxychromen-4-one	5318041	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC	374.30	unknown	via CMAUP database
2-(3,4-Dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one	44584772	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6,8-trimethoxy-4H-1-benzopyran-4-one	10452846	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
3,5,6,7,8,3',4'-Heptamethphoxyflavone	150893	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC	432.40	unknown	via CMAUP database
3'-Demethylnobiletin	183466	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O	388.40	unknown	via CMAUP database
4'-Hydroxy-3',5,6,7,8-pentamethoxyflavone	21593928	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O	388.40	unknown	via CMAUP database
4'-Hydroxy-5,6,7,8-tetramethoxyflavone	3010100	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC)OC	358.30	unknown	via CMAUP database
4',5-Dihydroxy-7,8-dimethoxyflavone	14585506	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC	314.29	unknown	via CMAUP database
5-Hydroxy-7,8,4'-trimethoxyflavone	14353376	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC	328.30	unknown	via CMAUP database
5-o-Desmethylnobiletin	358832	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC	388.40	unknown	via CMAUP database
6-Demethoxytangeretin	629964	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC	342.30	unknown	via CMAUP database
7-Hydroxy-4',5,6,8-tetramethoxyflavone	5318356	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)O)OC	358.30	unknown	via CMAUP database
8-Methoxycirsilineol	181092	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O	374.30	unknown	via CMAUP database
Acerosin	177696	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O	360.30	unknown	via CMAUP database
Gardenin B	96539	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	358.30	unknown	via CMAUP database
Gardenin D	3080750	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O	374.30	unknown	via CMAUP database
Isosinensetin	632135	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC	372.40	unknown	via CMAUP database
Linderoflavone B	97151	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC	386.40	unknown	via CMAUP database
Nobiletin	72344	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC	402.40	unknown	via CMAUP database
Sudachitin	12443122	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O	360.30	unknown	via CMAUP database
Tangeretin	68077	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4'-Hydroxy-3,6-dimethoxy-6'',6''-dimethylpyrano[2,3:7,8]flavone	44258693	Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)OC)C	380.40	unknown	via CMAUP database

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Quercus cerris

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