Prunus laurocerasus, also known as cherry laurel, is an evergreen species of cherry native to regions bordering the Black Sea in southwestern Asia and southeastern Europe. It is often used as an ornamental plant in gardens and parks, and has over 40 cultivars. However, it can also be an invasive species in some regions, out-competing and killing off native plants. The foliage is used in floristry and the fruits are edible but contain small amounts of hydrogen cyanide. The leaves and seeds are toxic if ingested. The wood of cherry laurel is creamy white and has a distinct almond smell, making it suitable for turning bowls. It is often confused with Prunus lusitanica, Portuguese laurel, which can be distinguished by its sharply toothed leaves and red petioles.

Synonyms Top

Scientific name	Authority	First published in
Laurocerasus officinalis	M.Roem.	Fam. Nat. Syn. Monogr. 3: 91 (1847)
Padus laurocerasus	(L.) Mill.	Gard. Dict. ed. 8 : Padus n.º 4 (1768)
Prunus grandifolia	Salisb.	Prodr. Stirp. Chap. Allerton : 356 (1796)
Laurocerasus ottinii	CarriŠre	Revue horticole; journal d'horticulture pratique ; 1866 159 1877
Laurocerasus vulgaris	CarriŠre	; 1863 90 1863
Laurocerasus otinii	CarriŠre	; 1873 240 1873
Cerasus laurocerasus	(L.) Dum.Cours.	Bot. Cult. 3: 390. 1802
Cerasus laurocerasus	(L.) Loisel.	Trait‚ des arbres et arbustes que l'on cultive en France ; 1800 6 1809
Lauro-cerasus officinalis	M.Roem.	Fam. Nat. Syn. Monogr. 3: 91 (1847)
Lauro-cerasus ottinii	Carrière	Rev. Hort. (Paris) 1873: 240 (1873)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	english laurel
English	common laurel
English	cherry laurel
English	cherry-laurel
Spanish	laurel-cerezo
Spanish	prunus grandifolia
Spanish	padus laurocerasus
Spanish	laurocerasus officinalis
Spanish	lauroceraso
Spanish	lauro-cerezo
Spanish	lauro-ceraso
Spanish	lauro cerezo
Spanish	lauro ceraso
Spanish	laurel romano
Spanish	laurel liso
Spanish	laurel cerezo
Spanish	cerasus laurocerasus
Spanish	laurela
ab	Ашымҳара
Arabic	كرز الغار
Arabic	غار الكرزي
Arabic	لوز الصين
Arabic	خوخ كرزي
Arabic	غار كرزي
Azerbaijani	laurocerasus officinalis
Bulgarian	лавровишня
Catalan	llorer-cirer
Catalan	laurocerasus officinalis
Catalan	llorer cirerer
Catalan	llorer reial
Czech	bobkovišeň lékařská
Welsh	coeden lawrgeirios
Danish	laurbær-kirsebær
Danish	laurbær kirsebær
Danish	laurbærkirsebær
German	zierlorbeer
German	lorbeer-kirsche
German	kirschlorbeer
German	pontische lorbeer-kirsche
German	lorbeerkirsche
Greek	λαουροκέρασο
Greek	Δαφνοκέρασος
Basque	gerezi-erramu
Basque	gerezi erramu
Persian	پرونوس لاروسراسوس
Finnish	laakerikirsikka
French	laurière
French	laurier cerise
French	laurier du caucase
French	laurier-palme
French	laurier palme
French	laurier-cerise
Irish	labhras silíní
Galician	loureiro real
Galician	lauroceraso
Croatian	lovorvišnja
Upper Sorbian	bobkowišeń
Hungarian	balkáni babérmeggy
Hungarian	közönséges babérmeggy
Hungarian	örökzöld babérmeggy
Armenian	դափնեկեռաս
io	cerizolauro
Italian	lauroceraso
Japanese	ベニバスモモ
Japanese	セイヨウバクチノキ
Georgian	წყავი
Macedonian	Ловор
Norwegian Bokmål	laurbærhegg
Dutch	gewone laurierkers
Dutch	laurierkers
Dutch	paplaurier
os	Лаврбал
Polish	laurocerasus officinalis
Polish	Śliwa wawrzynolistna
Polish	laurośliwa wschodnia
Polish	laurowiśnia wschodnia
Russian	Лавровишня
Serbo-Croatian	lovorvišnja
Slovak	vavrínovec lekársky
Serbian	Зеленичје
Serbian	Ловорвишња
Serbian	Зелениче
Swedish	lagerhägg
Turkish	taflan
Turkish	laurocerasus officinalis
Turkish	laz kirazı
Turkish	tanal
Turkish	tahnal
Turkish	karayemiş
Ukrainian	Лавровишня
xmf	წყი
Chinese	桂樱
Chinese	桂櫻

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Madeira
- Northern Africa
  - Libya

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Tadzhikistan
  - Uzbekistan
- Western Asia
  - Iran
  - Lebanon-Syria
  - Turkey

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Tasmania
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Ukraine
- Middle Europe
  - Germany
  - Netherlands
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southwestern U.S.A.
  - California
- Western Canada
  - British Columbia

Southern America click to expand
- Southern South America
  - Argentina South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001016516
UNII	516S28LU0T
Cornell Woody Plants	339
Canadensys	8866
USDA Plants	PRLA5
UConn	352
Tropicos	27801103
INPN	116089
Flora of Italy	2236
KEW	urn:lsid:ipni.org:names:324745-2
The Plant List	rjp-714
Missouri Botanical Garden	286448
Open Tree Of Life	156912
Observations.org	9200
NCBI Taxonomy	32242
NBN Atlas	NBNSYS0000003420
Nature Serve	2.144986
IUCN Red List	172277
IPNI	324745-2
iNaturalist	61432
GBIF	3021496
Freebase	/m/029dgc
EPPO	PRNLR
EOL	628559
Elurikkus	209998
Calflora (Californian flora)	8723
USDA GRIN	30027
Wikipedia	Prunus_laurocerasus
CMAUP	NPO24068

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

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

Identification and Biological Characteristics of Mortierella alpina Associated with Chinese Flowering Cherry (Cerasus serrulata) Leaf Blight in China

Shao D, Xu Y, Zhang C, Lai Z, Song L, Su J, Yang R, Jing X, Felix A, Abubakar YS, Lu G, Ye W

J Fungi (Basel)

05-Jan-2024

PMCID:	PMC10817311
doi:	10.3390/jof10010050
PMID:	38248959

DNA barcoding as new diagnostic tool to lethal plant poisoning in herbivorous mammals

Schweikle S, Häser A, Wetters S, Raisin M, Greiner M, Rigbers K, Fischer U, Pietsch K, Suntz M, Nick P

PLoS One

15-Nov-2023

PMCID:	PMC10650979
doi:	10.1371/journal.pone.0292275
PMID:	37967132

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

Holarctic Species in the Pluteus podospileus Clade: Description of Six New Species and Reassessment of Old Names

Ševčíková H, Malysheva EF, Antonín V, Borovička J, Dovana F, Ferisin G, Eyssartier G, Grootmyers D, Heilmann-Clausen J, Kalichman J, Kaygusuz O, Lebeuf R, Muñoz González G, Minnis AM, Russell SD, Saar I, Nielsen IB, Frøslev TG, Justo A

J Fungi (Basel)

31-Aug-2023

PMCID:	PMC10532425
doi:	10.3390/jof9090898
PMID:	37755006

Cuticular Waxes and Cutin in Terminalia catappa Leaves from the Equatorial São Tomé and Príncipe Islands

Pereira H, Simões R, Miranda I

Molecules

31-Aug-2023

PMCID:	PMC10489119
doi:	10.3390/molecules28176365
PMID:	37687194

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

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

Icerya purchasi Maskell (Hemiptera: Monophlebidae) Control Using Low Carbon Footprint Oligonucleotide Insecticides

Gal’chinsky NV, Yatskova EV, Novikov IA, Useinov RZ, Kouakou NJ, Kouame KF, Kra KD, Sharmagiy AK, Plugatar YV, Laikova KV, Oberemok VV

Int J Mol Sci

19-Jul-2023

PMCID:	PMC10380692
doi:	10.3390/ijms241411650
PMID:	37511407

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 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

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 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

Emerging Plant Intoxications in Domestic Animals: A European Perspective

Nagy AL, Ardelean S, Chapuis RJ, Bouillon J, Pivariu D, Dreanca AI, Caloni F

Toxins (Basel)

04-Jul-2023

PMCID:	PMC10467095
doi:	10.3390/toxins15070442
PMID:	37505711

Commodity risk assessment of Malus sylvestris plants from United Kingdom

Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, 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, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Kaczmarek A, Mosbach‐Schulz O, Yuen J

EFSA J

19-Jun-2023

PMCID:	PMC10277910
doi:	10.2903/j.efsa.2023.8076
PMID:	37342543

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 / Saturated hydrocarbons / Alkanes
Docosane	12405	Click to see CCCCCCCCCCCCCCCCCCCCCC	310.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Dotriacontane	11008	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	450.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Eicosane	8222	Click to see CCCCCCCCCCCCCCCCCCCC	282.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Heneicosane	12403	Click to see CCCCCCCCCCCCCCCCCCCCC	296.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Heptacosane	11636	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC	380.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Nonadecane	12401	Click to see CCCCCCCCCCCCCCCCCCC	268.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Octacosane	12408	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC	394.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Pentacosane	12406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCC	352.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Pentatriacontane	12413	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	492.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Tetratriacontane	26519	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	478.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Triacontane	12535	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	422.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Tritriacontane	12411	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	464.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
> 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
9-Octadecenoic acid	965	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Hexacosanoic acid	10469	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	396.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Octacosanoic acid	10470	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	424.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Triacontanoic acid	10471	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	452.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
> 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-Hentriacontanol	68345	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	452.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Heptacosanol	74822	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCO	396.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Hexacosanol	68171	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO	382.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Nonacosanol	243696	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	424.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Octacosanol	68406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO	410.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	via CMAUP database
1-Pentacosanol	92247	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCO	368.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Tetracosanol	10472	Click to see CCCCCCCCCCCCCCCCCCCCCCCCO	354.70	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Tetratriacontanol	185639	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	494.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Triacontanol	68972	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	438.80	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Tricosanol	18431	Click to see CCCCCCCCCCCCCCCCCCCCCCCO	340.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
1-Tritriacontanol	156150	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	480.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Docosanol	12620	Click to see CCCCCCCCCCCCCCCCCCCCCCO	326.60	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Dotriacontanol	96117	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	466.90	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid	3931	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1016/0031-9422(96)00241-5
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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3R,4S,5S,6R)-2-[2-[(2S,5R)-5-[(1S,3R,6S,8S,9S,11R,12S,14S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,14-dihydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-methyloxolan-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162849626	Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(CO9)(CO)O)O)C	947.10	unknown	https://doi.org/10.1016/S0031-9422(00)85371-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	12314479	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/BF00569611
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00569611
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00569611
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	https://doi.org/10.1016/S0031-9422(00)80522-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl alcohol xylopyranosyl-(1-6)-glucopyranoside	14730864	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	https://doi.org/10.1002/JLAC.1991199101124
Benzyl beta-primeveroside	131248	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	https://doi.org/10.1002/JLAC.1991199101124
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see C(C(C(C(C(=O)CO)O)O)O)O	180.16	unknown	https://doi.org/10.1006/JFCA.1997.0519
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	https://doi.org/10.1006/JFCA.1997.0519
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1006/JFCA.1997.0519
Benzoyl-beta-D-glucoside	12314096	Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(C(O2)CO)O)O)O	284.26	unknown	https://doi.org/10.1016/S0031-9422(00)85371-6
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1006/JFCA.1997.0519
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol	5780	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1006/JFCA.1997.0519
> 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 / Flavans / Catechins
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0031-9422(00)80522-1
> 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 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

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Prunus laurocerasus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top