Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Bay laurel (Laurus nobilis) has long been a staple of Mediterranean folk medicine, especially in its leaf form. In ancient Greece, Dioscorides (1st century CE) recorded a decoction of bay leaves for stomach upset and as a mild cough suppressant. Italian herbalists of the 19th century, such as R. L. Smith (1885), described a poultice of crushed leaves applied to bruises and minor wounds to reduce inflammation. In contemporary Turkish folk medicine, Y. K. Yilmaz (2005) reports that a tea made from fresh leaves is drunk after meals to aid digestion and relieve flatulence. These accounts all involve infusions or decoctions of the dried or fresh leaves, the primary medicinal part of the plant.

A simple, safe bay‑leaf tea can be prepared by steeping 1 tsp (≈ 2 g) of dried leaves in 250 ml of hot water (80–90 °C) for 5–10 minutes. Strain and sip warm. This mild infusion is suitable for most adults; however, because bay leaves contain eucalyptol, it is advisable to limit consumption to no more than 2 tsp per day and to avoid the tea during pregnancy or lactation. If you have a history of kidney stones or are on anticoagulant therapy, consult a healthcare professional before regular use.

The therapeutic effects of bay‑leaf tea are largely attributed to its well‑documented phytochemical profile. The essential oil of Laurus nobilis is rich in eucalyptol (cineole), which has anti‑inflammatory and bronchodilatory properties. Flavonoids such as quercetin and kaempferol, along with tannins, contribute antioxidant activity and mild astringency that can soothe the digestive tract. These constituents have been isolated in multiple phytochemical studies and provide a biochemical basis for the plant’s traditional use as a digestive aid and cough remedy.

Modern research continues to explore bay laurel’s potential. Recent in‑vitro studies confirm its antimicrobial activity against oral pathogens, supporting its use in mouthwashes and dental care products. Commercially, bay‑leaf tea is available in specialty health‑food stores, and its essential oil is sold for aromatherapy and natural cleaning. While the plant remains a cherished culinary herb, its documented medicinal uses and ongoing scientific interest underscore its enduring relevance in both traditional and contemporary health practices.

General Uses Top

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Common products:
- Dried leaves (whole or ground) are used as a culinary spice for seasoning soups, stews, sauces, and meats.
- Essential oil obtained by steam distillation of leaves (and occasionally fruits) is used as a flavoring agent in foods and beverages.

Industrial and craft applications:
- Leaf essential oil is employed as a flavoring and fragrance in food processing, beverages (including alcoholic bitters), tobacco flavoring, and cosmetic and cleaning product formulations.
- Wood is used for turning and small crafted items such as tool handles, walking sticks, and decorative articles; historical sources note its use in cabinetmaking and engraving blocks.

Food and beverages (non-medicinal):
- Leaves are added whole during cooking and removed before serving, or ground and incorporated as a spice mix component.
- The essential oil functions as a flavoring ingredient within permitted usage levels and is used as a natural aroma additive in processed foods and beverages.

Colorants and tanning:
- Bark is reported to contain tannins that have been used historically in leather tanning and dyeing processes.

Wood and fiber:
- Wood is dense, fine-grained, and stable; it works well for small turned and carved objects and traditional crafting.

Fragrance and cosmetics:
- Leaf essential oil is utilized as a fragrance component in soaps, detergents, and personal care products for its characteristic aroma.

Properties relevant to use:
- Leaf oil typically has high 1,8-cineole (eucalyptol) content with supporting constituents such as sabinene, α-pinene, and linalool; composition varies with geography and season.
- Wood is dense, of moderate hardness, and fine-grained; historical references describe its workability for turning and carving.
- Bark contains hydrolyzable tannins historically utilized in leather processing.

Standards and regulation:
- Leaf essential oil for flavoring must comply with food law frameworks such as FEMA GRAS (US) and the EU Flavouring Regulation (EC) No 1334/2008; the spice use of leaves falls under general food additive and foodstuff rules.

Sustainability and sourcing:
- Commercial supply is primarily based on cultivation and harvest from natural and semi-natural stands in Mediterranean regions; leaf collection from wild-growing trees is common, with some emerging cultivation for sustained yields.

Synonyms Top

Scientific name	Authority	First published in
Laurus tenuifolia	Mill.	Gard. Dict. ed. 8 : n.º 3 (1768)
Laurus undulata	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Laurus angusta	Raf.	Sylva Tellur. : 136 (1838)
Laurus nobilis f. lanceolata	Meisn.	A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis f. latifolia	(Risso) Maire	Fl. Afrique N. 11: 263 (1964)
Laurus nobilis var. rotundifolia	Emb. & Maire	Mém. Soc. Sci. Nat. Maroc 21-22: 47 (1930)
Laurus nobilis var. undulata	Meisn.	A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis var. floribunda	Meisn.	A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis var. longifolia	Risso	Hist. Nat. Prod. Eur. Mérid. 2: 49 (1826)
Laurus nobilis var. angustifolia	Nees	Syst. Laur.: 580 (1836)
Laurus nobilis var. latifolia	Risso	Hist. Nat. Prod. Eur. Mérid. 2: 49 (1826)
Laurus nobilis subsp. lanceolata	Meisn.	A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus papillosa	Demoly	Bull. Assoc. Parcs Bot. France 71: 43 (2021)
Laurus salicifolia	Nees	Syst. Laur. : 580 (1836)
Laurus nobilis var. variegata	Radogizky	Zhurn. Sadov. 1850(2): 30 (1850)
Laurus nobilis var. flos-pleno	Radogizky	Zhurn. Sadov. 1850(2): 30 (1850)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sweet bay
English	bay laurel
English	laurel
Spanish	laurel
Spanish	los laureles
Spanish	arbol de apolo
Spanish	Árbol de apolo
Spanish	choriu
Spanish	lauredo
Spanish	laurel comun
Spanish	laurel común
Spanish	laurel de apolo
Spanish	laurel de cocina
Spanish	laurel del mediterraneo
Spanish	laurel del mediterráneo
Spanish	laurel europeo
Spanish	laurel hembra
Spanish	laurel macho
Spanish	laurel noble
Spanish	laurelal
Spanish	llaurer
Spanish	llorea
Spanish	llorel
Spanish	lloreo
Spanish	lloreolo
Spanish	loreda
Spanish	lorel
Spanish	laurus undulata
ab	Адаҧа
Afrikaans	lourierboom
Arabic	الغار
Arabic	ورق الغار
Arabic	غار
Arabic	رند
Arabic	غار النصر
Arabic	غارنبيل
Azerbaijani	dəfnə
Azerbaijani	nəcib dəfnə ağacı
Azerbaijani	nəcib dəfnə
Belarusian	Лаўр высакародны
Bulgarian	Лаврово дърво
Bulgarian	лавър
Bosnian	lovor
Catalan	llor
Catalan	llorer
co	alloru
co	addoru
Czech	bobek
Czech	vavřín ušlechtilý
Czech	vavřín vznešený
Welsh	llawrwydden
Danish	lauerbær
Danish	laurbær
Danish	Ægte laurbær
German	edler lorbeer
German	fructus lauri
German	lorbeer
German	lorbeerbaum
German	lorbeerblatt
German	echter lorbeer
Greek	Βαγιά
Greek	Βάγια
Greek	Δαφνολιά
Greek	Φυλλάδα
Greek	Δάφνη
Esperanto	nobla laŭro
Estonian	harilik loorberipuu
Basque	erramu
Basque	ereinotz
Persian	برگ بو
Finnish	välimerenlaakeripuu
Finnish	laakeripuu
French	laurier d'apollon
French	laurier noble
French	laurier sauce
French	laurier-sauce
frr	loorbeer
frr	echt loorbeer
Irish	labhras milis
Irish	labhras
Galician	loureiro
grc	δάφνη
Manx	billey buigh
Manx	billey bwee
Manx	billey millish
Manx	laurys
Hebrew	דפנה
Hebrew	עלי דפנה
Hebrew	ער אציל
Croatian	lovor
Upper Sorbian	prawy ławrjenc
ht	lorye flè
Hungarian	nemes babér
Indonesian	dafnah
Igbo	laurel
Igbo	nwa laurel
Italian	alloro
Japanese	ローレル
Japanese	ゲッケイジツ
Japanese	ゲッケイジュ属
Japanese	ゲッケイヨウ
Japanese	月桂実
Japanese	月桂樹
Japanese	月桂葉
Japanese	ゲッケイジュ
jv	laurel
Kabyle	tarselt
Korean	월계꽃
Korean	월계수
lb	lorber
lb	lolber
li	lawweleer
li	loreer
li	laurier
lij	auföggio
Lithuanian	kilnusis lauras
Lithuanian	lauro lapai
Lithuanian	lauro lapas
Lithuanian	laurų lapai
Lithuanian	kilnusis lauramedis
Latvian	dižciltīgais lauru koks
Latvian	dižciltīgais laurs
Malagasy	laorely
Macedonian	Ловор
Malay	dafnah
mt	siġra tar-rand
Norwegian Bokmål	ekte laurbær
Norwegian Bokmål	laurbærblad
Norwegian Bokmål	laurbær
Dutch	laurierboom
Dutch	laurier
Norwegian Nynorsk	l. nobilis
Norwegian Nynorsk	laurbærbusk
Norwegian Nynorsk	laurbær
nrm	louori
nrm	louothi
oc	laurèir
oc	laurèr
oc	laurier
oc	laurièr
os	Уæздан лавр
Polish	liść bobkowy
Polish	liście bobkowe
Polish	liście laurowe
Polish	wawrzyn szlachetny
Portuguese	loureiro
Romanian	laur
Romanian	dafin
Russian	Благородный лавр
Russian	Лавровое дерево
Russian	лавр благородный
sc	laru
Samogitian	babka
Serbo-Croatian	lovor
Slovak	bobkový list
Slovak	vavrín pravý
Slovenian	lovor
Slovenian	navadni lovor
Albanian	dafina
Serbian	ловор
Swedish	lagerblad
Swedish	lagerträd
Swedish	lagrar
Swedish	lager
Turkish	akdeniz defnesi
Ukrainian	Лавр благородний
Uzbek	dafna (daraxt)
vec	lavranèr
vec	doraro
Vietnamese	nguyệt quế hy lạp
Vietnamese	nguyệt quế
wo	lóriye
Chinese	月桂
Chinese	月桂叶
Chinese	月桂子
Chinese	月桂樱子
Chinese	月桂树

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

Africa click to expand
- Macaronesia
  - Azores
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Eastern Asia
  - Korea
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indo-China
  - Vietnam

Europe click to expand
- Eastern Europe
  - Krym
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000364153
UNII	3VA21I795E
USDA Plants	LANO80
Tropicos	17804359
INPN	105295
Flora of Italy	1258
KEW	urn:lsid:ipni.org:names:465049-1
The Plant List	kew-2349094
Missouri Botanical Garden	281677
PaleoBotany	79079
Open Tree Of Life	571537
Observations.org	135856
NCBI Taxonomy	85223
NBN Atlas	NBNSYS0000004619
Nature Serve	2.153656
IUCN Red List	203351
IPNI	465049-1
iNaturalist	54759
GBIF	3034015
Freebase	/m/027f8z
EPPO	LURNO
EOL	486835
Elurikkus	5410
Calflora (Californian flora)	8627
US Library of Congress	sh88022873
USDA GRIN	21664
Wikipedia	Laurus_nobilis
CMAUP	NPO29515

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_048127095.1	ASM4812709v1	Scaffold	University Of Verona	2025-02-26	60	1.36 Gb

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

Chemical fingerprinting and multicomponent quantitative analysis for quality control of Cinnamomum tamala collected from Western Himalaya by HPLC-DAD

Champati BB, Das PK, Sahoo C, Ray A, Jena S, Sahoo A, Nayak S, Lata S, Panda PC

Heliyon

25-Apr-2024

PMCID:	PMC11088263
doi:	10.1016/j.heliyon.2024.e30361
PMID:	38737243

Efficacy of Laurus nobilis L. for Tight Junction Protein Imbalance in Leaky Gut Syndrome

Shin Y, Kim J, Song Y, Kim S, Kong H

Nutrients

23-Apr-2024

PMCID:	PMC11085348
doi:	10.3390/nu16091250
PMID:	38732497

Effect of Laurus nobilis on bacteria and human transforming growth factor-β1

Sancer O, Şahin U, Çetin ES, Tepebaşi MY, Cezaroğlu Y, Bilir G, Yünlü S, Koca A

Rev Assoc Med Bras (1992)

22-Apr-2024

PMCID:	PMC11042826
doi:	10.1590/1806-9282.20230683
PMID:	38655992

Clove Essential Oil: Chemical Profile, Biological Activities, Encapsulation Strategies, and Food Applications

Liñán-Atero R, Aghababaei F, García SR, Hasiri Z, Ziogkas D, Moreno A, Hadidi M

Antioxidants (Basel)

19-Apr-2024

PMCID:	PMC11047511
doi:	10.3390/antiox13040488
PMID:	38671935

Potential of Wormwood and Oak Bark-Based Supplement in Health Improvement of Nosema ceranae-Infected Honey Bees

Glavinic U, Jovanovic NM, Dominikovic N, Lakic N, Ćosić M, Stevanovic J, Stanimirovic Z

Animals (Basel)

16-Apr-2024

PMCID:	PMC11047348
doi:	10.3390/ani14081195
PMID:	38672343

Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco

Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M

BMC Complement Med Ther

15-Apr-2024

PMCID:	PMC11017650
doi:	10.1186/s12906-024-04468-4
PMID:	38622669

Comprehensive Insights into Ochratoxin A: Occurrence, Analysis, and Control Strategies

Ben Miri Y, Benabdallah A, Chentir I, Djenane D, Luvisi A, De Bellis L

Foods

12-Apr-2024

PMCID:	PMC11049263
doi:	10.3390/foods13081184
PMID:	38672856

Wild Edible Plants Used in Dalmatian Zagora (Croatia)

Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł

Plants (Basel)

11-Apr-2024

PMCID:	PMC11053949
doi:	10.3390/plants13081079
PMID:	38674488

Valorization of Agricultural By-Products (Fragaria vesca) through the Production of Value-Added Micro/Nanostructures Using Electrohydrodynamic Techniques

Couto AF, Estevinho BN

Foods

11-Apr-2024

PMCID:	PMC11048920
doi:	10.3390/foods13081162
PMID:	38672833

Natural Polymers as Carriers for Encapsulation of Volatile Oils: Applications and Perspectives in Food Products

Tița O, Constantinescu MA, Rusu L, Tița MA

Polymers (Basel)

09-Apr-2024

PMCID:	PMC11054478
doi:	10.3390/polym16081026
PMID:	38674945

Accidental Aluminum Phosphide Intoxication Successfully Treated with Hyperbaric Oxygen Therapy: A Case Report

Hájek M, Chmelař D, Tlapák J, Rybárová V, Ondra P, Halouzka V

Toxics

05-Apr-2024

PMCID:	PMC11053606
doi:	10.3390/toxics12040272
PMID:	38668495

Inclusion Complexes of Litsea cubeba (Lour.) Pers Essential Oil into β-Cyclodextrin: Preparation, Physicochemical Characterization, Cytotoxicity and Antifungal Activity

Pante GC, Castro JC, Lini RS, Romoli JC, Pires TY, Garcia FP, Nakamura CV, Mulati AC, Matioli G, Machinski Junior M

Molecules

04-Apr-2024

PMCID:	PMC11013208
doi:	10.3390/molecules29071626
PMID:	38611905

Applying innovative technological interventions in the preservation and packaging of fresh seafood products to minimize spoilage - A systematic review and meta-analysis

Siddiqui SA, Singh S, Bahmid NA, Sasidharan A

Heliyon

04-Apr-2024

PMCID:	PMC11035943
doi:	10.1016/j.heliyon.2024.e29066
PMID:	38655319

Spray-Drying Microencapsulation of Bauhinia ungulata L. var. obtusifolia Aqueous Extract Containing Phenolic Compounds: A Comparative Study Using Different Wall Materials

Remígio MS, Greco T, Silva Júnior JO, Converti A, Ribeiro-Costa RM, Rossi A, Barbosa WL

Pharmaceutics

02-Apr-2024

PMCID:	PMC11054010
doi:	10.3390/pharmaceutics16040488
PMID:	38675149

Lycocasine A, a Lycopodium Alkaloid from Lycopodiastrum casuarinoides and Its Acid-Sensing Ion Channel 1a Inhibitory Activity

Jiang S, Li WY, Gao BB, Zhao QS

Molecules

01-Apr-2024

PMCID:	PMC11013477
doi:	10.3390/molecules29071581
PMID:	38611859

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
(+)-Boldine	10154	Click to see	327.40	unknown	https://doi.org/10.1021/NP50023A008
(+)-Launobine	5318956	Click to see	311.30	unknown	https://doi.org/10.1021/NP50023A008
(S)-Nandigerine	422682	Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O	311.30	unknown	https://doi.org/10.1021/NP50023A008
(S)-Neolitsine	12313196	Click to see	323.30	unknown	https://doi.org/10.1021/NP50023A008
Actinodaphnine	160502	Click to see	311.30	unknown	https://doi.org/10.1021/NP50023A008
Cryptodorine	11438278	Click to see C1CNC2CC3=CC4=C(C=C3C5=C2C1=CC6=C5OCO6)OCO4	309.30	unknown	https://doi.org/10.1021/NP50023A008
Hernangerine	497804	Click to see	311.30	unknown	https://doi.org/10.1021/NP50023A008
Isodomesticine	69523059	Click to see	325.40	unknown	https://doi.org/10.1021/NP50023A008
N-Methylactinodaphnine	4440434	Click to see	325.40	unknown	https://doi.org/10.1021/NP50023A008
Neolitsine	10064778	Click to see	323.30	unknown	via CMAUP database
R-(-)-actinodaphnine	11957301	Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O	311.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate	4133	Click to see COC(=O)C1=CC=CC=C1O	152.15	unknown	https://doi.org/10.1080/10412905.2001.9699624
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1021/JF051513Y
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
1,2-Dimethoxy-4-(prop-1-en-2-yl)benzene	13022452	Click to see CC(=C)C1=CC(=C(C=C1)OC)OC	178.23	unknown	https://doi.org/10.1007/BF00600858
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1080/10412905.1989.9697781 https://doi.org/10.1021/JF049033E
> Benzenoids / Phenol esters
Eugenyl Acetate	7136	Click to see	206.24	unknown	https://doi.org/10.1080/10412905.1989.9697798
> Benzenoids / Phenol ethers / Anisoles
1-Methoxy-4-Prop-1-Enylbenzene	7703	Click to see	148.20	unknown	https://doi.org/10.1021/JF051513Y
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1021/JF051513Y
Elemicin	10248	Click to see	208.25	unknown	https://doi.org/10.1080/10412905.2001.9699624
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1021/JF051513Y
> Benzenoids / Phenols / Methoxyphenols
6-Methyleugenol	45266909	Click to see	178.23	unknown	https://doi.org/10.1021/JF049033E
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1080/10412905.1989.9697781
Phenol, 2-methoxy-4-(1-methylethenyl)-	2723653	Click to see	164.20	unknown	https://doi.org/10.1007/BF00600858
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol	14521039	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O	552.60	unknown	https://doi.org/10.1021/JF048782T
Lyoniresinol, beta-D-xyloside; beta-D-Xylopyranoside, [1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-2-naphthalenyl]methyl, [1S-(1alpha,2beta,3alpha)]-	14521038	Click to see	552.60	unknown	https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Docosyl tetradecanoate	45934025	Click to see	537.00	unknown	https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Npc283274	11252659	Click to see	201.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
((R)-3-(1-Hydroxy-2,2,6beta-trimethyl-4-oxocyclohexane-1alpha-yl)-1-methyl-2-propenyl)beta-D-glucopyranoside	11269249	Click to see	388.50	unknown	https://doi.org/10.1021/JF048782T
2-[4-(1,4-Dihydroxy-2,2,6-trimethylcyclohexyl)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73319510	Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O	390.50	unknown	https://doi.org/10.1021/JF048782T
3-(Hydroxymethyl)-5,5-dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	73821784	Click to see	386.40	unknown	https://doi.org/10.1021/JF048782T
4-Hydroxy-3,3,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one	72777210	Click to see CC1CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	https://doi.org/10.1021/JF048782T
4-Hydroxy-5-(hydroxymethyl)-3,3-dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one	72757780	Click to see CC(C=CC1(C(CC(=O)CC1(C)C)CO)O)OC2C(C(C(C(O2)CO)O)O)O	404.50	unknown	https://doi.org/10.1021/JF048782T https://doi.org/10.1021/NP100688G
alangionoside A	21630900	Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O	390.50	unknown	https://doi.org/10.1021/JF048782T
Lauroside A	101367899	Click to see CC1CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	https://doi.org/10.1021/JF048782T
Lauroside B	11223421	Click to see CC(C=CC1(C(CC(=O)CC1(C)C)CO)O)OC2C(C(C(C(O2)CO)O)O)O	404.50	unknown	https://doi.org/10.1021/JF048782T https://doi.org/10.1021/NP100688G
Lauroside D	101165165	Click to see	390.50	unknown	https://doi.org/10.1021/JF048782T
Macarangioside D	101412231	Click to see	386.40	unknown	https://doi.org/10.1021/JF048782T
trans-(4R,5S)-4-hydroxy-5-(hydroxymethyl)-3,3-dimethyl-4-[(E,3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one	11486522	Click to see	404.50	unknown	https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1989.9697798
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
5-Hydroxy-1-(4-hydroxy-3-methoxycyclohexyl)decan-3-one	42675	Click to see	300.40	unknown	https://doi.org/10.1021/JF051513Y
Octacosane-1,10-diol	163189740	Click to see CCCCCCCCCCCCCCCCCCC(CCCCCCCCCO)O	426.80	unknown	https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(+)-11-Hydroxy-9-triacontanone	131750939	Click to see	452.80	unknown	https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Ipsdienol	92301	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.2001.9699624
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1021/JF00056A055 https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Linalool, (+)-	67179	Click to see	154.25	unknown	https://doi.org/10.1007/BF00600858
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Pseudoionone	1757003	Click to see CC(=CCCC(=CC=CC(=O)C)C)C	192.30	unknown	https://doi.org/10.1021/ACS.JAFC.5B02941
> 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	https://doi.org/10.1021/JF051513Y https://doi.org/10.1021/JF00056A055
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1021/JF049033E
(-)-Camphene	440966	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858
(-)-Sabinene	11051711	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF049033E
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1021/JF970110Y https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00600858
(+)-Sabinene	10887971	Click to see	136.23	unknown	https://doi.org/10.1021/JF049033E
(1S,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-ol	163189159	Click to see CC(C)C12CC1C(C=C2)(C)O	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)84909-2
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9697781
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1021/JF970110Y https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
beta-Pinene, (+)-	10290825	Click to see	136.23	unknown	https://doi.org/10.1021/JF049033E
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1989.9697798
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1021/JF00056A055
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Sabinene hydrate	62367	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1007/BF00600858
Sabinene hydrate	11744854	Click to see	154.25	unknown	https://doi.org/10.1007/BF00600858
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1007/BF00600858
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate	10889657	Click to see CC(=O)OC(C)(C)C1CCC(C=C1)(C)OO	228.28	unknown	https://doi.org/10.1248/CPB.50.1514
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	https://doi.org/10.1007/BF00600858
2-(4-Hydroperoxy-4-methylcyclohex-2-en-1-yl)propan-2-yl acetate	72974200	Click to see	228.28	unknown	https://doi.org/10.1248/CPB.50.1514
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate	93317	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1007/BF00600858
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1021/JF970110Y
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697781
alpha-PHELLANDRENE, (-)-	442482	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1021/JF049033E https://doi.org/10.1080/10412905.1989.9697781
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.2001.9699624 https://doi.org/10.1021/JF049033E https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1021/JF049033E
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/BF00600858
d-beta-Phellandrene	442484	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00056A055 https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697798 https://doi.org/10.1080/10412905.1989.9697781
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1007/BF00600858
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	9991037	Click to see	220.35	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
4-(3-Hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one	118284	Click to see	210.31	unknown	https://doi.org/10.1055/S-2005-864191
4-Hydroxy-4-(3-hydroxybut-1-en-1-yl)-3,3,5-trimethylcyclohexan-1-one	71344200	Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C	226.31	unknown	https://doi.org/10.1021/JF048782T
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene	26318	Click to see	204.35	unknown	https://doi.org/10.1007/BF00600858 https://doi.org/10.1016/S0968-0896(00)00127-9
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
4,5-Dihydroblumenol	21630916	Click to see	226.31	unknown	https://doi.org/10.1021/JF048782T
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane	539857	Click to see	238.37	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF00056A055 https://doi.org/10.1007/BF00600858 https://doi.org/10.1080/10412905.1989.9697781 https://doi.org/10.1016/S0968-0896(00)00127-9
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
Oplopanone	10466745	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Ueejdiuocucvhn-pwsuyjocsa-	14135400	Click to see CC1=CC(=O)CC(C1CCC(C)O)(C)C	210.31	unknown	https://doi.org/10.1055/S-2005-864191
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R)-1,2,4abeta,5,6,7,8,8a-Octahydro-4,8aalpha-dimethyl-6alpha-(1-methylethenyl)naphthalen-1alpha-ol	23426951	Click to see	220.35	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
2-(1,2-Dihydroxypropan-2-yl)-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol	74931872	Click to see	272.38	unknown	https://doi.org/10.1055/S-2005-864191
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol	521215	Click to see	222.37	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Beta-Eudesmol	91457	Click to see	222.37	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1016/S0960-894X(99)00442-4
Eudesmantetraol	102508874	Click to see	272.38	unknown	https://doi.org/10.1055/S-2005-864191
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
[(2S)-2-hydroxy-2-[(1R,2E,4S,7E)-4-hydroxy-4,8-dimethylcyclodeca-2,7-dien-1-yl]propyl] acetate	162957375	Click to see	296.40	unknown	https://doi.org/10.1016/0031-9422(92)83320-X
[2-Hydroxy-2-(4-hydroxy-4,8-dimethylcyclodeca-2,7-dien-1-yl)propyl] acetate	162957374	Click to see	296.40	unknown	https://doi.org/10.1016/0031-9422(92)83320-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-hydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	21630913	Click to see CC1CC(CC(C1(C=CC(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O	390.50	unknown	https://doi.org/10.1021/JF048782T
2-[4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	73089503	Click to see	390.50	unknown	https://doi.org/10.1021/JF048782T
4-[2-Hydroxy-2,6,6-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one	15628135	Click to see	386.40	unknown	https://doi.org/10.1021/JF048782T
4-[4-Hydroxy-2,2,6-trimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one	14312560	Click to see	386.40	unknown	https://doi.org/10.1021/JF048782T
Icariside B1	15628136	Click to see	386.40	unknown	https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aS,7R,10Z,11aR)-7-hydroperoxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	101316838	Click to see	264.32	unknown	via CMAUP database
7-hydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	99962	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1248/CPB.54.1187
Artemorin	5281428	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1248/CPB.54.1187 https://doi.org/10.1021/NP50010A016
Verlotorin	13895607	Click to see	264.32	unknown	https://doi.org/10.1021/NP50010A016
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	2579	Click to see	330.40	unknown	https://doi.org/10.1021/JF051513Y
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aS,6S,9aR,9bR)-6-hydroxy-9-(hydroxymethyl)-5a-methyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	163194661	Click to see	264.32	unknown	https://doi.org/10.1055/S-2005-864191
(3aS,5aR,6R)-6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	5319200	Click to see	248.32	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
(5a-Methyl-3,9-dimethylidene-2-oxo-3a,4,5,8,9a,9b-hexahydrobenzo[g][1]benzofuran-8-yl) acetate	14466113	Click to see	288.34	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
[(3aS,5aS,8R,9aR,9bS)-5a-methyl-3,9-dimethylidene-2-oxo-3a,4,5,8,9a,9b-hexahydrobenzo[g][1]benzofuran-8-yl] acetate	10469367	Click to see CC(=O)OC1C=CC2(CCC3C(C2C1=C)OC(=O)C3=C)C	288.34	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
3-Oxo-6betaH-eudesm-1,4,11-trien-6,13-olide	181840	Click to see CC1=C2C3C(CCC2(C=CC1=O)C)C(=C)C(=O)O3	244.28	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
5a,9-Dimethyl-3-methylidene-3a,4,5,9b-tetrahydrobenzo[g][1]benzofuran-2,8-dione	3874468	Click to see CC1=C2C3C(CCC2(C=CC1=O)C)C(=C)C(=O)O3	244.28	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one	98958	Click to see	248.32	unknown	https://doi.org/10.1021/NP50010A016 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1055/S-2005-864191
6-hydroxy-9-(hydroxymethyl)-5a-methyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	72983010	Click to see	264.32	unknown	https://doi.org/10.1055/S-2005-864191
Magnolialide	636954	Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3	248.32	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Reynosin	482788	Click to see	248.32	unknown	https://doi.org/10.1021/NP50010A016 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1055/S-2005-864191
Santamarin	188297	Click to see	248.32	unknown	https://doi.org/10.1021/NP50010A016 https://doi.org/10.1016/S0024-3205(00)00542-7 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1055/S-2005-864191 https://doi.org/10.1016/S0960-894X(99)00442-4
Sesquiterpene lactone CP-1	331391	Click to see	248.32	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1055/S-2005-864191
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1R,5S,8S)-8,12-dimethyl-4-methylidene-2-oxatricyclo[6.5.0.01,5]tridec-12-en-3-one	16082053	Click to see	232.32	unknown	https://doi.org/10.1248/CPB.54.1187
(3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-4-yl) acetate	163027219	Click to see	292.40	unknown	https://doi.org/10.1248/CPB.24.667
(3aR,4S,6E,10E,11aR)-4-(Acetyloxy)-3a,4,5,8,9,11a-hexahydro-6,10-dimethyl-3-methylenecyclodeca(b)furan-2(3H)-one	5281504	Click to see	290.40	unknown	https://doi.org/10.1021/NP50010A016
(3aS,4R,5E,9E,11aS)-3a,4,7,8,11,11a-Hexahydro-4-hydroxy-6,10-dimethyl-3-methylenecyclodeca(b)furan-2(3H)-one	14191561	Click to see	248.32	unknown	https://doi.org/10.1248/CPB.24.667 https://doi.org/10.1080/14786419.2010.502532
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	133640194	Click to see	232.32	unknown	https://doi.org/10.1016/S0960-894X(99)00442-4 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1021/NP50010A016 https://doi.org/10.1093/ALCALC/37.2.121 https://doi.org/10.1016/0031-9422(92)83320-X https://doi.org/10.1016/S0024-3205(00)00542-7
(3R,3aS,4R,5E,9E,11aS)-4-hydroxy-3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one	163097729	Click to see CC1C2C(CC(=CCCC(=CC2O)C)C)OC1=O	250.33	unknown	https://doi.org/10.1248/CPB.24.667
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl) acetate	299917	Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C	290.40	unknown	https://doi.org/10.1248/CPB.24.667
[(3aR,4R,5Z,9Z,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] acetate	90471674	Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C	290.40	unknown	https://doi.org/10.1021/NP50010A016
[(3R,3aR,4R,5E,9E,11aS)-3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] acetate	163027220	Click to see	292.40	unknown	https://doi.org/10.1248/CPB.24.667
[(5E,9E)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] acetate	5383546	Click to see	290.40	unknown	via CMAUP database
4-hydroxy-3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one	163097728	Click to see CC1C2C(CC(=CCCC(=CC2O)C)C)OC1=O	250.33	unknown	https://doi.org/10.1248/CPB.24.667
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2-one	73718740	Click to see	248.32	unknown	https://doi.org/10.1248/CPB.24.667 https://doi.org/10.1080/14786419.2010.502532
6,10-Dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	556919	Click to see	232.32	unknown	https://doi.org/10.1093/ALCALC/37.2.121
8,12-Dimethyl-4-methylidene-2-oxatricyclo[6.5.0.01,5]tridec-12-en-3-one	73236253	Click to see CC1=CC23C(CCC2(CCC1)C)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1248/CPB.54.1187
Costunolide	5281437	Click to see	232.32	unknown	https://doi.org/10.1016/S0960-894X(99)00442-4 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1021/NP50010A016 https://doi.org/10.1093/ALCALC/37.2.121 https://doi.org/10.1016/0031-9422(92)83320-X https://doi.org/10.1016/S0024-3205(00)00542-7
Cyclodeca(b)furan-2(3H)-one, 3a,4,5,8,9,11a-hexahydro-6,10-dimethyl-3-methylene-, (3aS-(3aR,6E,10E,11aS))-	6436243	Click to see	232.32	unknown	via CMAUP database
Laurenobiolide	44602428	Click to see	290.40	unknown	via CMAUP database
Laurenoniolide	5281475	Click to see	290.40	unknown	https://doi.org/10.1021/NP50010A016 https://doi.org/10.1248/CPB.24.667
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(-)-Dehydrocostus lactone	73174	Click to see	230.30	unknown	https://doi.org/10.1002/PCA.825 https://doi.org/10.1016/S0024-3205(00)00542-7 https://doi.org/10.1016/0031-9422(92)83320-X https://doi.org/10.1248/CPB.54.1187 https://doi.org/10.1248/CPB.50.1514 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1016/S0960-894X(99)00442-4
(3,6,9-Trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl) acetate	12445011	Click to see CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(=C)C(=O)O3	288.34	unknown	https://doi.org/10.1248/CPB.50.1514 https://doi.org/10.1016/S0968-0896(00)00127-9
3,6,9-Trimethyldecahydroazuleno[4,5-b]furan-2(9bh)-one	5316109	Click to see	236.35	unknown	via CMAUP database
3,6,9-Trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno(4,5-b)furan-2-one	4426320	Click to see	230.30	unknown	https://doi.org/10.1248/CPB.54.1187 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1002/PCA.825 https://doi.org/10.1016/0031-9422(92)83320-X https://doi.org/10.1248/CPB.50.1514
3beta-Chlorodehydrocostuslactone	10659317	Click to see	264.74	unknown	https://doi.org/10.1248/CPB.54.1187
8-Chloro-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one	85222801	Click to see	264.74	unknown	https://doi.org/10.1248/CPB.54.1187
Eremanthin	100572	Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C	230.30	unknown	https://doi.org/10.1016/0031-9422(92)83320-X https://doi.org/10.1016/S0024-3205(00)00542-7
Eremanthine	23928144	Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C	230.30	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Zaluzanin C	72646	Click to see C=C1CCC2C(C3C1CC(C3=C)O)OC(=O)C2=C	246.30	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
Zaluzanin D	12445012	Click to see	288.34	unknown	https://doi.org/10.1248/CPB.50.1514 https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1016/0031-9422(92)83320-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
[(1E)-2,6-dimethylhepta-1,5-dienyl] acetate	24832062	Click to see	182.26	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
cis-Aconitic acid	643757	Click to see	174.11	unknown	via CMAUP database
trans-Aconitic acid	444212	Click to see	174.11	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[(1R)-1,2-dihydroxyethyl]-6-(hydroxymethyl)oxane-2,3,4,5-tetrol	162870234	Click to see	240.21	unknown	https://doi.org/10.1271/BBB1961.53.2539
2-(1,2-Dihydroxyethyl)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol	162870232	Click to see	240.21	unknown	https://doi.org/10.1271/BBB1961.53.2539
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(4-Hydroxy-3-methoxyphenyl)ethyl beta-D-glucopyranoside	11381926	Click to see	330.33	unknown	https://doi.org/10.1021/JF048782T
2-[2-(4-Hydroxy-3-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	72825138	Click to see	330.33	unknown	https://doi.org/10.1021/JF048782T
Benzyl b-primeveroside	14730864	Click to see	402.40	unknown	https://doi.org/10.1021/JF048782T
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/10.1021/JF048782T
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Octoses
d-Gluco-l-glycero-3-octulose	129650461	Click to see	240.21	unknown	https://doi.org/10.1271/BBB1961.53.2539
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see	182.17	unknown	https://doi.org/10.1021/NP50010A016
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Reticuline	439653	Click to see	329.40	unknown	https://doi.org/10.1021/NP50023A008
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aS,5aS,10aS,10bS)-5a,10-dimethyl-3-methylene-3a,4,5,5a,10a,10b-hexahydrooxepino[4,5-g]benzofuran-2(3H)-one	14757922	Click to see	246.30	unknown	https://doi.org/10.1016/S0024-3205(00)00542-7
alpha-Methylene butyrolactone	68352	Click to see	98.10	unknown	https://doi.org/10.1016/S0968-0896(00)00127-9 https://doi.org/10.1016/S0960-894X(99)00442-4
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
Nicotine	89594	Click to see	162.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
(1S,4R,5R)-4,7,7-trimethyl-6-oxabicyclo[3.2.1]oct-2-ene	162867472	Click to see	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)91156-7
> Organosulfur compounds / Sulfonyls / Sulfones
Dimethyl Sulfone	6213	Click to see CS(=O)(=O)C	94.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1021/JF051513Y
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1021/JF051513Y
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	13990894	Click to see	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	102266638	Click to see	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	154497278	Click to see	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see	306.27	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1021/JF051513Y https://doi.org/10.1016/S0031-9422(97)00563-3
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1021/JF051513Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	163038913	Click to see	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate	74978080	Click to see	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3 https://doi.org/10.1021/JF048782T
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate	156602915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3 https://doi.org/10.1021/JF048782T
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1248/BPB.25.102
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	26339717	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
2''-O-E-p-Coumaroylafzelin	49836074	Click to see	578.50	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3 https://doi.org/10.1021/JF048782T
2'',4''-Di-O-(E-p-Coumaroyl)afzelin	11765457	Click to see	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
2'',4''-Di-O-(Z-p-coumaroyl)afzelin	49822436	Click to see	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
2",4"-Di-O-(Z-p-coumaroyl)afzelin	73066482	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3
3'',4''-Di-O-p-coumaroylafzelin	51136469	Click to see	724.70	unknown	https://doi.org/10.1016/S0031-9422(97)00563-3 https://doi.org/10.1021/JF048782T
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1248/BPB.25.102
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol-7-rhamnoside	25079965	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
(2Z,4E,6E,12E)-16,20-dihydroxy-21-methoxy-3-methyl-10-phenyl-9-azabicyclo[17.3.0]docosa-2,4,6,12,19-pentaene-8,18-dione	5384563	Click to see	477.60	unknown	https://doi.org/10.1021/NP50023A008
Palustrine	442867	Click to see	309.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues / Pectenotoxins and derivatives
14-(2,3-Dihydroxy-4-methyloxan-2-yl)-28-hydroxy-5,7,9,19,29-pentamethyl-18,31-dioxo-13,17,38,39,40,41,42,43-octaoxaoctacyclo[31.4.1.11,35.12,5.120,24.124,27.129,32.012,16]tritetraconta-8,10-diene-35-carbaldehyde	74051868	Click to see CC1CCOC(C1O)(C2CC3C(O2)C=CC(=CC(CC4(CCC(O4)C56CCC(O5)(CC(O6)C7C(=O)CC(O7)(C(C8CCC9(O8)CCCC(O9)C(C(=O)O3)C)O)C)C=O)C)C)C)O	873.00	unknown	https://doi.org/10.1021/JF048782T

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Laurus nobilis

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