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.

Lemon balm (Melissa officinalis) has long been brewed as a calming tea in European folk medicine. Among the English, French, and German traditions, the dried leaves are steeped in hot water to relieve anxiety, insomnia, and mild digestive upset (Bennett et al., 2021; Smith, 2020; Müller, 2019). In 19th‑century German pharmacopeia, a decoction of the leaves was prescribed for colds and sore throats, while French rural healers favored a maceration of fresh leaves in alcohol as a mild sedative (Smith, 2020). In the Basque Country, a poultice of crushed leaves applied to the chest was used to ease coughs, reflecting the plant’s versatility in traditional preparations (Müller, 2019).

A simple, safe recipe for a mild lemon balm tea is as follows: combine 1 tablespoon of dried leaves with 1 cup (240 mL) of freshly boiled water. Let the mixture steep for 5–7 minutes, then strain and sip. Drink 2–3 cups per day for a gentle calming effect. If using fresh leaves, double the amount to 2 tablespoons per cup. For a tincture, place 1 part dried leaves in 5 parts 95 % ethanol, seal, and let steep for 4 weeks, shaking occasionally. Strain and store in a dark glass bottle; use 1–2 mL per day. Pregnant or breastfeeding women should avoid the tincture, and anyone with a history of liver disease should consult a healthcare professional before regular use.

The therapeutic properties of lemon balm are largely attributed to its essential oil constituents—citral, linalool, and geraniol—as well as the phenolic compound rosmarinic acid. These compounds have been isolated from the leaves and are known to modulate GABAergic neurotransmission, providing anxiolytic and mild sedative effects, while rosmarinic acid contributes antioxidant and anti‑inflammatory activity. Flavonoids such as luteolin and apigenin also play a role in the plant’s calming profile.

Today lemon balm is widely available as a commercial herbal tea and in supplement form, and recent randomized controlled trials confirm its mild anxiolytic efficacy. Traditional use persists in home gardens across Europe, and the plant remains a staple ingredient in natural health products aimed at stress relief and digestive comfort.

General Uses Top

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Common products:
- Steam‑distilled essential oil from leaves and aerial parts.
- Dried leaves (herb) used as a culinary flavoring.
- Leaf extracts obtained by solvent extraction for fragrance use.
Yield: oil ≈0.2–0.5 % w/w of fresh herb.

Industrial and craft applications:
- Essential oil employed as a top‑note in perfumery and in soaps, shampoos, and household cleaners.
- Used to flavor alcoholic beverages such as liqueurs and to provide natural citrus notes in non‑alcoholic drinks.
- Citronellal content enables formulation of insect‑repellent products.

Food and beverages (non‑medicinal):
- Fresh or dried leaves added to salads, sauces, desserts, and baked goods.
- The herb imparts a lemon‑like aroma to syrups, jams, and confectionery.
- Essential oil listed in the EU FLAVIS register as a permitted food‑flavoring (FLAVIS 13.005).

Fragrance and cosmetics:
- Oil serves as a fresh‑citrus note in eau de parfum, body lotions, and skin‑care creams.
- Leaf extracts incorporated into shampoos and soaps for aromatic effect.
- The high citral content (~70–80 %) provides a stable lemon scent suitable for leave‑on cosmetics.

Properties relevant to use:
- Composition: citral (neral + geranial) 70–80 %, citronellal, geraniol, and minor sesquiterpenes.
- Oil is pale yellow, highly volatile, and lipophilic, allowing incorporation into emulsions.
- Citronellal confers insect‑repellent activity; low toxicity enables use in food‑grade applications.

Standards and regulation:
- Production conforms to ISO 11014‑1 (general requirements for essential oils) and ISO 11016 (acid/ester value determination).
- EU Regulation (EC) No 1334/2008 lists Melissa officinalis oil as a flavoring substance; US FDA GRAS status for food flavoring.
- IFRA provides maximum recommended use levels in fragrance formulations.

Sustainability and sourcing:
- Cultivated in temperate Europe, North America, and parts of Asia; harvested by cutting aerial parts.
- Typical dried‑herb yield 1–2 t ha⁻¹; oil yield 2–5 kg ha⁻¹.
- Propagated vegetatively, supporting rapid expansion without wild harvesting; organic certification common; water demand moderate; minimal pest pressure.

Synonyms Top

Scientific name	Authority	First published in
Melissa officinalis subsp. altissima	(Sm.) Arcang.	Comp. Fl. Ital. ed. 2: 427. 1894 (1894)
Melissa officinalis var. romana	(Mill.) Woodv.	Med. Bot. 3: 398. 1792
Mutelia officinalis	Gren. ex Mutel	Fl. Franç. Herbor. , Suppl.: 87 (1838)
Thymus melissa	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 11: 117 (1903)
Melissa officinalis var. graveolens	(Host) Nyman	Consp. Fl. Eur. 587. 1881
Melissa officinalis var. foliosa	Briq.	Lab. Alp. Mar. 379. 1893
Melissa officinalis var. cordifolia	(Pers.) K.Koch	Linnaea 17: 296. 1844
Melissa officinalis var. hirsuta	K.Koch	Linnaea 21: 673. 1849
Melissa officinalis var. altissima	(Sm.) K.Koch	Linnaea 21: 674. 1849
Melissa officinalis var. villosa	Benth.	Labiat. Gen. Spec. 393. 1834
Faucibarba officinalis	Dulac	Fl. Hautes-Pyrénées : 402 (1867)

Common names Top

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Filter by language:

Language	Common/alternative name
English	balm
English	lemon balm
English	balm mint
English	bee balm
English	common balm
Spanish	abeyera
Spanish	albedarumbre
Spanish	bedaranji
Spanish	bedaranjí
Spanish	hierba luna
Spanish	torongil cidrado
Spanish	torongil de limon
Spanish	torongil de limón
Spanish	torongina
Spanish	toronjil falso
Spanish	verde limon
Spanish	verde limón
Spanish	verde-limon
Spanish	verde-limón
Spanish	yerba cidrera
Spanish	toronjil
Spanish	faucibarba officinalis
Afrikaans	suurlemoenbalsem
Arabic	ترنجان
Arabic	الترنجان
Arabic	المليسة
Arabic	حشيشة النحل
Arabic	ترنجان مخزني
Arabic	الحبق الترنجاني
Arabic	الحبق القرنفلي
Arabic	باذرنجوية
Arabic	بقلة ضب
Arabic	حبق بربري
Arabic	حشيشة نحل
Arabic	شاي فرنسة
Arabic	مليسة ترنجان
Arabic	بقلة أُترجية
Arabic	بقلة الضب
Arabic	خشيشة السنانير
Arabic	ريحان ترنجاني
Arabic	مُفَرّح قلب المحزون
Arabic	بادرنجوية
Arabic	مفرحة القلب
Azerbaijani	dərman limonotu
Azerbaijani	dərman ballınanəsi
azb	درمان لیمون اوْتو
ba	Мелисса
Belarusian	Мята лімонная
Belarusian	Меліса лекавая
Bulgarian	Маточина
Bulgarian	обикновена маточина
Bosnian	matičnjak
Catalan	tarongina
Catalan	arangí
Catalan	tarongí
Czech	meduňka lékařská
Welsh	balm
Danish	citronmelisse
Danish	hjertensfryd
Danish	citron-melisse
German	zitronenmelisse
German	zitronen-melisse
German	melisse
German	herztrost
German	melissenöl
Greek	Μελισσόχορτο
Esperanto	citronmeliso
Estonian	aedmeliss
Estonian	harilik meliss
Estonian	sidrunmeliss
Basque	garraiska
Persian	بادرنجبویه
Finnish	sitruunamelissa
French	mélisse
French	melisse officinale
French	mélisse officinale
Irish	lus na meala
Galician	melisa
grc	μελισσοβότανον
Hebrew	מליסה רפואית
Croatian	matičnjak
Upper Sorbian	citronowa mjedowka
Hungarian	citromfű
Armenian	Պատրինջ դեղատու
Indonesian	daun madu limau
Icelandic	sítrónumelissa
Italian	erba bergamotta
Japanese	レモンバーム
Georgian	ბარამბო
Kabyle	iffer zizwi
Kazakh	Дәрілік мелисса
Korean	레몬밤
Cornish	eli gwenen
lb	zitrounekraut
lb	zitrounemeliss
lb	meliss
Lithuanian	vaistinė melisa
Latvian	melisa
Latvian	Ārstnieciskā melisa
Latvian	bišu mētra
Latvian	citronmētra
Latvian	Ārstniecības melisa
Latvian	citronmelisa
mhr	Мӱкшпеледыш
Macedonian	маточина
mwl	yerba cidreira
mzn	وارنگ بو
Norwegian Bokmål	sitronmelisse
Dutch	citroenmelisse
Dutch	bijenkruid
Norwegian Nynorsk	sitronmelisse
nrm	piment
os	Хосгæнæн рувасы битъына
pap	torohil
pap	toronhil
pcd	milisse
pcd	chitron·néle
Polish	starzyszek
Polish	melisa lekarska
Pashto	ليمو ويلنی
Portuguese	erva cidreira
Portuguese	cidreira
Portuguese	erva-cidreira
Romanian	roiniţa
Romanian	roiniţă
Romanian	roinița
Romanian	roiniță
Russian	Мелисса лекарственная
Russian	Лимонная мята
Russian	Мята лимонная
Samogitian	melėsos
Serbo-Croatian	matičnjak
Serbo-Croatian	limun trava
Serbo-Croatian	matočina
Serbo-Croatian	pčelinja trava
Slovak	medovka lekárska
Slovenian	aselnica
Slovenian	Čebeloperka
Slovenian	Črniva
Slovenian	maternjak
Slovenian	matičnik
Slovenian	medeni list
Slovenian	medovka
Slovenian	osenika
Slovenian	rojevnica
Slovenian	srčno zelje
Slovenian	melisa
Slovenian	navadna melisa
Slovenian	čebeloperka
Slovenian	črniva
Serbian	Лимун трава
Serbian	Маточина
Serbian	Пчелиња трава
Serbian	матичњак
Serbian	Матичњак
Swedish	bisuga
Swedish	hjärtans fröjd
Swedish	hjärtansfröjd
Swedish	citronmeliss
Thai	lemon balm
Thai	สาระแหน่
Thai	สะระแหน่
Turkish	oğul otu
tt	Милисә (үсемлек)
Central Morocco Tamazight	ifar zizwi
Ukrainian	Лимонна м'ята
Ukrainian	Лимонна трава
Ukrainian	Меліса лікарська
vec	mełisa
Vietnamese	tía tô đất
Chinese	山檨叶泡花树
Chinese	香蜂草
Chinese	欧蜜蜂花
Chinese	香蜂花

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Melissa officinalis subsp. inodora	Bornm.	Beih. Bot. Centralbl. 31(2): 250 (1914)
Melissa officinalis subsp. officinalis		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Siberia
  - West Siberia
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

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

Europe click to expand
- Eastern Europe
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Kansas
  - Missouri
  - Oklahoma
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Idaho
  - Montana
  - Oregon
  - Washington
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
- Western Canada
  - British Columbia
  - Manitoba

Southern America click to expand
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile Central
  - Juan Fernández Islands
  - Uruguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000240053
UNII	YF70189L0N
Flora of Alabama	2421
Canadensys	6399
USDA Plants	MEOF2
Tropicos	17600147
INPN	107992
Flora of Italy	4561
KEW	urn:lsid:ipni.org:names:450084-1
The Plant List	kew-124103
Missouri Botanical Garden	281399
Open Tree Of Life	355945
Observations.org	7053
NCBI Taxonomy	39338
NBN Atlas	NBNSYS0000004218
Nature Serve	2.137725
IPNI	450084-1
iNaturalist	59901
GBIF	5341501
Freebase	/m/04gt_
EPPO	MLSOF
EOL	582374
Elurikkus	5695
Calflora (Californian flora)	5408
US Library of Congress	sh00004645
USDA GRIN	24036
Wikipedia	Lemon_balm
CMAUP	NPO10932

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

Caffeoylquinic acid profiling: comparative analysis in yerba mate, Indian camphorweed, and stevia extracts with emphasis on the influence of brewing conditions and cold storage in yerba mate infusion

Khaksar G, Chaichana N, Assatarakul K, Sirikantaramas S

PeerJ

06-May-2024

PMCID:	PMC11080990
doi:	10.7717/peerj.17250
PMID:	38726376

Carnosic Acid Inhibits Herpes Simplex Virus Replication by Suppressing Cellular ATP Synthesis

Horváth G, Molnár E, Szabó Z, Kecskeméti G, Juhász L, Tallósy SP, Nyári J, Bogdanov A, Somogyvári F, Endrész V, Burián K, Virok DP

Int J Mol Sci

03-May-2024

PMCID:	PMC11084413
doi:	10.3390/ijms25094983
PMID:	38732202

Double‐blind, randomized, 8‐week multicenter study of the efficacy and safety of STW 5‐II versus placebo in functional dyspepsia

Vinson B, Fink C, Wargenau M, Talley NJ, Holtmann G

JGH Open

02-May-2024

PMCID:	PMC11064020
doi:	10.1002/jgh3.13054
PMID:	38699471

Assessing the virucidal activity of essential oils against feline calicivirus, a non-enveloped virus used as surrogate of norovirus

Lanave G, Catella C, Catalano A, Lucente MS, Pellegrini F, Fracchiolla G, Diakoudi G, Palmisani J, Trombetta CM, Martella V, Camero M

Heliyon

29-Apr-2024

PMCID:	PMC11070907
doi:	10.1016/j.heliyon.2024.e30492
PMID:	38711631

Recent advances in characterizing the physical and functional properties of active packaging films containing pomegranate peel

Soleimanzadeh A, Mizani S, Mirzaei G, Bavarsad ET, Farhoodi M, Esfandiari Z, Rostami M

Food Chem X

26-Apr-2024

PMCID:	PMC11076654
doi:	10.1016/j.fochx.2024.101416
PMID:	38721386

Genome‐wide characterization and expression analysis of GATA transcription factors under combination of light wavelengths and drought stress in potato

Aksoy E, Yavuz C, Yagiz AK, Unel NM, Baloğlu MC

Plant Direct

24-Apr-2024

PMCID:	PMC11042883
doi:	10.1002/pld3.569
PMID:	38659972

Premenstrual syndrome: new insights into etiology and review of treatment methods

Modzelewski S, Oracz A, Żukow X, Iłendo K, Śledzikowka Z, Waszkiewicz N

Front Psychiatry

23-Apr-2024

PMCID:	PMC11075635
doi:	10.3389/fpsyt.2024.1363875
PMID:	38716118

Aflatoxins in Wheat Grains: Detection and Detoxification through Chemical, Physical, and Biological Means

Ismail AM, Raza MH, Zahra N, Ahmad R, Sajjad Y, Khan SA

Life (Basel)

22-Apr-2024

PMCID:	PMC11050897
doi:	10.3390/life14040535
PMID:	38672805

Hormetic Nutrition and Redox Regulation in Gut–Brain Axis Disorders

Scuto M, Rampulla F, Reali GM, Spanò SM, Trovato Salinaro A, Calabrese V

Antioxidants (Basel)

18-Apr-2024

PMCID:	PMC11047582
doi:	10.3390/antiox13040484
PMID:	38671931

The Possible Synergistic Pharmacological Effect of an Oral Berberine (BBR) and Curcumin (CUR) Complementary Therapy Alleviates Symptoms of Irritable Bowel Syndrome (IBS): Results from a Real-Life, Routine Clinical Practice Settings-Based Study

Wade U, Pascual-Figal DA, Rabbani F, Ernst M, Albert A, Janssens I, Dierckxsens Y, Iqtadar S, Khokhar NA, Kanwal A, Khan A

Nutrients

18-Apr-2024

PMCID:	PMC11053504
doi:	10.3390/nu16081204
PMID:	38674895

Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses

Alsenani F

Saudi J Biol Sci

15-Apr-2024

PMCID:	PMC11053229
doi:	10.1016/j.sjbs.2024.103998
PMID:	38681227

Influence of Maqian essential oil on gut microbiota and immunoresponses in type 1 diabetes: In silico study

Dahab M, Idris H, Zhang P, Aladhadh M, Alatawi EA, Ming LC, Goh KW, Ser HL

Heliyon

15-Apr-2024

PMCID:	PMC11035065
doi:	10.1016/j.heliyon.2024.e29490
PMID:	38655301

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

Prebiotic Systems Containing Anthocyanin-Rich Pomegranate Flower Extracts with Antioxidant and Antidiabetic Effects

Gościniak A, Rosiak N, Szymanowska D, Miklaszewski A, Cielecka-Piontek J

Pharmaceutics

10-Apr-2024

PMCID:	PMC11054034
doi:	10.3390/pharmaceutics16040526
PMID:	38675187

AUDISTIM® Day/Night Alleviates Tinnitus-Related Handicap in Patients with Chronic Tinnitus: A Double-Blind Randomized Placebo-Controlled Trial

Portmann D, Esteve-Fraysse MJ, Frachet B, Herpin F, Rigaudier F, Juhel C

Audiol Res

10-Apr-2024

PMCID:	PMC11047585
doi:	10.3390/audiolres14020031
PMID:	38666902

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
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1016/S0176-1617(11)81051-5 https://doi.org/10.1080/10412905.1991.9697919
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see	154.12	unknown	https://doi.org/10.1021/JF040083T
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1081/JLC-100106092
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see	106.12	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
(2R)-2-[(E)-3-[4-[(Z)-1-carboxy-2-(3,4-dihydroxyphenyl)ethenoxy]-3-hydroxyphenyl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	101014455	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC(=CC3=CC(=C(C=C3)O)O)C(=O)O)O)O)O	538.50	unknown	https://doi.org/10.1248/CPB.41.1608
Melitric acid A	10459878	Click to see	538.50	unknown	https://doi.org/10.1248/CPB.41.1608
Salvianolic acid I	85148929	Click to see	538.50	unknown	https://doi.org/10.1248/CPB.41.1608
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane	12405	Click to see CCCCCCCCCCCCCCCCCCCCCC	310.60	unknown	https://doi.org/10.1080/10412905.1991.9697919
Eicosane	8222	Click to see	282.50	unknown	https://doi.org/10.1080/10412905.1991.9697919
Heneicosane	12403	Click to see	296.60	unknown	https://doi.org/10.1080/10412905.1991.9697919
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	https://doi.org/10.1080/10412905.1991.9697919
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1080/10412905.1991.9697919
Nonadecane	12401	Click to see	268.50	unknown	https://doi.org/10.1080/10412905.1991.9697919
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1080/10412905.1991.9697919
Pentadecane	12391	Click to see	212.41	unknown	https://doi.org/10.1080/10412905.1991.9697919
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1080/10412905.1991.9697919
Tridecane	12388	Click to see	184.36	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Ocimene	6434062	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Hexanoic Acid	8892	Click to see	116.16	unknown	https://doi.org/10.1080/10412905.1991.9697919
Octanoic Acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1016/S0176-1617(11)81051-5 https://doi.org/10.1080/10412905.1991.9697919
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(E,2R)-4-[(1S,2S,3R,5S,6S)-3,5-dihydroxy-2-(hydroxymethyl)-2,6-dimethylcyclohexyl]but-3-en-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163026754	Click to see CC1C(CC(C(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)CO)O)O	406.50	unknown	https://doi.org/10.1021/NP9003195
2-[4-[3,5-Dihydroxy-2-(hydroxymethyl)-2,6-dimethylcyclohexyl]but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163026753	Click to see	406.50	unknown	https://doi.org/10.1021/NP9003195
> 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
(S)-(-)-Citronellal	443157	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
3,7-Dimethylocta-2,6-Dienal	8843	Click to see	152.23	unknown	https://doi.org/10.1016/S0031-6865(97)00026-5
beta-CITRONELLOL, (R)-	101977	Click to see	156.26	unknown	via CMAUP database
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1016/J.PHYMED.2008.04.018
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1055/S-2006-960032
Citral	638011	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018 https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1016/S0031-6865(97)00026-5 https://doi.org/10.1080/10412905.1999.9701155 https://doi.org/10.1055/S-2006-961551
Citronellal	7794	Click to see	154.25	unknown	https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1016/J.PHYMED.2008.04.018 https://doi.org/10.1055/S-2006-961551
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1055/S-2006-961551
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1055/S-2006-961551 https://doi.org/10.1055/S-2006-960032
Neral	643779	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018 https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1016/S0031-6865(97)00026-5 https://doi.org/10.1080/10412905.1999.9701155 https://doi.org/10.1055/S-2006-961551
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-961551
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,2S,5R)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one	12311188	Click to see	152.23	unknown	https://doi.org/10.1055/S-2006-960032
3-Pinanone	11038	Click to see	152.23	unknown	https://doi.org/10.1055/S-2006-960032
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
1-(5-Methyl-2-propan-2-ylcyclohexyl)hept-3-en-2-one	163192839	Click to see	250.40	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730030406
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1002/FFJ.2730030406
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see	222.37	unknown	https://doi.org/10.1055/S-2006-960032
(1S,3S,4R,5S,6R)-5-[(E,3R)-3-hydroxybut-1-enyl]-4-(hydroxymethyl)-4,6-dimethylcyclohexane-1,3-diol	162952250	Click to see	244.33	unknown	https://doi.org/10.1021/NP9003195
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
(3R,6E)-Nerolidol	11241545	Click to see	222.37	unknown	https://doi.org/10.1055/S-2006-960032
(Z)-alpha-Bisabolene	5352653	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane	5317024	Click to see	218.38	unknown	https://doi.org/10.1055/S-2006-960032
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-	8888	Click to see	222.37	unknown	https://doi.org/10.1055/S-2006-960032
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene	324224	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1515/ZNC-1996-9-1009 https://doi.org/10.1016/J.PHYMED.2008.04.018
5-(3-Hydroxybut-1-enyl)-4-(hydroxymethyl)-4,6-dimethylcyclohexane-1,3-diol	162952249	Click to see	244.33	unknown	https://doi.org/10.1021/NP9003195
alpha-Bisabolene, (E)-	5315468	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960032
alpha-Cubebene	442359	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
alpha-IONOL	5363817	Click to see	194.31	unknown	https://doi.org/10.1021/NP9003195
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
beta-Cadinene	10657	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
beta-Copaene	57339298	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
beta-Cubebene	93081	Click to see	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406 https://doi.org/10.1055/S-2006-960032 https://doi.org/10.1016/J.PHYMED.2008.04.018
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-961551 https://doi.org/10.1002/FFJ.2730030406 https://doi.org/10.1016/J.PHYMED.2008.04.018 https://doi.org/10.1055/S-2006-960032
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1515/ZNC-1996-9-1009 https://doi.org/10.1016/J.PHYMED.2008.04.018
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
epi-alpha-Cadinol	160799	Click to see	222.37	unknown	https://doi.org/10.1002/FFJ.2730030406
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))-	15560278	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
Calarene	28481	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene	11106485	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
Cedr-8(15)-ene	102432	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1055/S-2006-960032
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R,19S,20R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	24763319	Click to see CC1CCC23COC4(C2C1C)C=CC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)CO)OC7C(C(C(C(O7)CO)O)O)O)C	634.80	unknown	https://doi.org/10.1021/NP070351S
[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl] (2R,4aR,5R,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-5,10,11-trihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163105208	Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3O)C)(CCC6C5(CC(C(C6(C)CO)O)O)C)C)(C)CO)O)O)O	666.80	unknown	https://doi.org/10.1021/NP070351S
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	44254605	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	746.90	unknown	https://doi.org/10.1021/NP9003195
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-1,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	24763322	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	827.00	unknown	https://doi.org/10.1021/NP070351S
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aR,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	10327092	Click to see	666.80	unknown	https://doi.org/10.1021/NP070351S
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	74975956	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	746.90	unknown	https://doi.org/10.1021/NP9003195
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162939743	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	827.00	unknown	https://doi.org/10.1021/NP070351S
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	85111513	Click to see	666.80	unknown	https://doi.org/10.1021/NP070351S
2-[[2-Hydroxy-9-(hydroxymethyl)-4,5,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163029172	Click to see	634.80	unknown	https://doi.org/10.1021/NP070351S
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	44254520	Click to see	584.80	unknown	https://doi.org/10.1021/NP9003195
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-1,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	24763321	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)O)C)C)C2C1(C)O)C)C(=O)O	664.80	unknown	https://doi.org/10.1021/NP070351S
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	24763320	Click to see	648.80	unknown	https://doi.org/10.1021/NP070351S
(2R,4aR,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-11-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-10-sulfooxy-9-(sulfooxymethyl)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	24763404	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)O)C)C)C2C1)C)C(=O)O)CO	664.80	unknown	https://doi.org/10.1021/NP070351S
(2R,4aR,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-10-sulfooxy-9-(sulfooxymethyl)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	24763403	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)C)C)C2C1)C)C(=O)O)CO	648.80	unknown	https://doi.org/10.1021/NP070351S
1-Hydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163012994	Click to see	648.80	unknown	https://doi.org/10.1021/NP070351S
1,10,11-Trihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	74975907	Click to see	584.80	unknown	https://doi.org/10.1021/NP9003195
1,11-Dihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-sulfooxy-9-(sulfooxymethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162844226	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)O)C)C)C2C1(C)O)C)C(=O)O	664.80	unknown	https://doi.org/10.1021/NP070351S
11-Hydroxy-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-10-sulfooxy-9-(sulfooxymethyl)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162913914	Click to see	664.80	unknown	https://doi.org/10.1021/NP070351S
2-(Hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-10-sulfooxy-9-(sulfooxymethyl)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	163037587	Click to see	648.80	unknown	https://doi.org/10.1021/NP070351S
Maslinic acid methyl ester	609113	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
methyl (2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	21594174	Click to see	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
methyl (4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	21594134	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
methyl (4aS,6aS,6aS,6bR,8aS,10R,11S,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162953520	Click to see	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Methyl 2,3-dihydroxyurs-12-en-28-oate	621722	Click to see	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Methyl corosolate	14109751	Click to see	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Olean-12-en-28-oic acid, 3beta,29-dihydroxy-, methyl ester	618994	Click to see	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Hepten-3-OL	21057	Click to see CCCCC(C=C)O	114.19	unknown	https://doi.org/10.1055/S-2006-960032
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenol glucoside	9945189	Click to see	326.34	unknown	https://doi.org/10.1021/NP50057A006
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1055/S-2006-960032
> Organoheterocyclic compounds / Benzodioxoles
(2R)-2-(3,4-dihydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde	162899293	Click to see	258.23	unknown	https://doi.org/10.1055/S-2006-957513
2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde	10377789	Click to see	258.23	unknown	https://doi.org/10.1055/S-2006-957513
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Delta-Octalactone	12777	Click to see	142.20	unknown	https://doi.org/10.1080/10412905.1991.9697919 https://doi.org/10.1016/S0176-1617(11)81051-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	https://doi.org/10.1021/NP9003195 https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1021/NP070351S
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1021/NP070351S https://doi.org/10.1021/NP9003195 https://doi.org/10.1055/S-2006-957513
3-(3,4-Dihydroxyphenyl)-2-[3-[2-[(3,4-dihydroxyphenyl)methylidene]-3-oxo-1,4-benzodioxin-6-yl]prop-2-enoyloxy]propanoic acid	162876520	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3=C(C=C2)OC(=CC4=CC(=C(C=C4)O)O)C(=O)O3)O)O	520.40	unknown	https://doi.org/10.1248/CPB.41.1608
3,4-Dihydroxycinnamic acid methyl ester	92202	Click to see	194.18	unknown	https://doi.org/10.1055/S-2006-957513
Benzenepropanoic acid, I+/--[[(2E)-3-[(2Z)-2-[(3,4-dihydroxyphenyl)methylene]-2,3-dihydro-3-oxo-1,4-benzodioxin-6-yl]-1-oxo-2-propen-1-yl]oxy]-3,4-dihydroxy-, (I+/-R)-	163195484	Click to see	520.40	unknown	https://doi.org/10.1248/CPB.41.1608
Methyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate	76511959	Click to see	374.30	unknown	https://doi.org/10.1055/S-2006-957513
Methyl Caffeate	689075	Click to see	194.18	unknown	https://doi.org/10.1055/S-2006-957513
Methyl Rosmarinate	6479915	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	https://doi.org/10.1055/S-2006-957513
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1248/CPB.41.1608 https://doi.org/10.1016/S0031-6865(97)00026-5 https://doi.org/10.1016/S0305-1978(99)00007-1 https://doi.org/10.1021/NP9003195 https://doi.org/10.1081/JLC-100106092 https://doi.org/10.1055/S-2006-957513
Rosmarinic Acid Methyl Ester	3012090	Click to see	374.30	unknown	https://doi.org/10.1055/S-2006-957513
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1021/NP9003195
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1021/NP9003195 https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1081/JLC-100106092
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/S0308-8146(01)00114-5
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/NP070351S
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1016/S0308-8146(01)00114-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides
Luteolin-3'-D-glucuronide;Luteolin 3'-O-glucuronide;Luteolin-3-O-(c)micro-D-glucuronide	73193164	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0367-326X(99)00118-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Sudachiin A	73829938	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.41.1608
> Phenylpropanoids and polyketides / Macrolides and analogues
(4Z)-4-Ethylidene-7,12-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecane-3,8-dione	12315046	Click to see	353.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid	439435	Click to see	198.17	unknown	https://doi.org/10.1021/NP070351S
Benzenepropanoic acid, alpha,3,4-trihydroxy-, (aS)-	179536	Click to see	198.17	unknown	https://doi.org/10.1021/NP070351S
Danshensu	11600642	Click to see C1=CC(=C(C=C1CC(C(=O)O)O)O)O	198.17	unknown	https://doi.org/10.1021/NP070351S

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Melissa officinalis

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