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
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
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
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
mhr	Мӱкшпеледыш
Macedonian	маточина
mzn	وارنگ بو
Norwegian Bokmål	sitronmelisse
Dutch	citroenmelisse
Dutch	bijenkruid
Norwegian Nynorsk	sitronmelisse
nrm	piment
os	Хосгæнæн рувасы битъына
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
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
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

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - 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

Identification and variation analysis of the composition and content of essential oil and fragrance compounds in Phoebe zhennan wood at different tree ages

Yang H, Zhang S, Gu Y, Peng J, Huang X, Guo H, Chen L, Jiang Y, Liu M, Luo X, Xie J, Wan X

Front Plant Sci

26-Mar-2024

PMCID:	PMC11002133
doi:	10.3389/fpls.2024.1368894
PMID:	38595765

Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential

Asiminicesei DM, Fertu DI, Gavrilescu M

Plants (Basel)

21-Mar-2024

PMCID:	PMC10976221
doi:	10.3390/plants13060913
PMID:	38592933

Chemical profiling of bioactive compounds in the methanolic extract of wild leaf and callus of Vitex negundo using gas chromatography-mass spectrometry

Garg G, Bharadwaj A, Chaudhary S, Gupta V

World J Exp Med

20-Mar-2024

PMCID:	PMC10999060
doi:	10.5493/wjem.v14.i1.88064
PMID:	38590309

Chemical Composition and Bioactivity of Dill Seed (Anethum graveolens L.) Essential Oil from Plants Grown under Shading

Milenković L, Ilić ZS, Stanojević L, Danilović B, Šunić L, Kevrešan Ž, Stanojević J, Cvetković D

Plants (Basel)

19-Mar-2024

PMCID:	PMC10974297
doi:	10.3390/plants13060886
PMID:	38592874

Ultrasonic-assisted extraction to enhance the recovery of bioactive phenolic compounds from Commiphora gileadensis leaves

Bin Mokaizh AA, Nour AH, Kerboua K

Ultrason Sonochem

18-Mar-2024

PMCID:	PMC10979263
doi:	10.1016/j.ultsonch.2024.106852
PMID:	38518410

Cyanobacterial elicitor enhances the biomass of Mentha piperita L. and improves the production of high-value rosmarinic acid under in vitro culture of apical meristem

Shariatmadari Z, Zarezadeh S, Riahi H, Ghotbi-Ravandi AA, Seyed Hashtroudi M, Shahroudi E

BMC Plant Biol

15-Mar-2024

PMCID:	PMC10941488
doi:	10.1186/s12870-024-04876-1
PMID:	38486151

Corrigendum: Phytotherapy for attention deficit hyperactivity disorder (ADHD): a systematic review and meta-analysis

Dutta T, Anand U, Mitra SS, Ghorai M, Jha NK, Shaikh NK, Shekhawat MS, Pandey DK, Proćków J, Dey A

Front Pharmacol

14-Mar-2024

PMCID:	PMC10973837
doi:	10.3389/fphar.2024.1365806
PMID:	38549676

An in vitro analysis of an innovative standardized phospholipid carrier-based Melissa officinalis L. extract as a potential neuromodulator for emotional distress and related conditions

Kara M, Sahin S, Rabbani F, Oztas E, Hasbal-Celikok G, Kanımdan E, Kocyigit A, Kanwal A, Wade U, Yakunina A, Di Pierro F, Khan A

Front Mol Biosci

13-Mar-2024

PMCID:	PMC10965792
doi:	10.3389/fmolb.2024.1359177
PMID:	38545418

Improvement of Panax notoginseng saponin accumulation triggered by methyl jasmonate under arbuscular mycorrhizal fungi

Dai HY, Zhang XK, Bi Y, Chen D, Long XN, Wu Y, Cao GH, He S

Front Plant Sci

13-Mar-2024

PMCID:	PMC10965624
doi:	10.3389/fpls.2024.1360919
PMID:	38545393

Plant Essential Oils: Dual Action of Toxicity and Egg-Laying Inhibition on Tetranychus urticae (Acari: Tetranychidae), Unveiling Their Potential as Botanical Pesticides

Zhu Y, Wu T, Hu Q, He W, Zheng Y, Xie Y, Rao Q, Liu X

Plants (Basel)

08-Mar-2024

PMCID:	PMC10975855
doi:	10.3390/plants13060763
PMID:	38592755

Enhancing Therapeutic Efficacy of Donepezil, an Alzheimer’s Disease Drug, by Diplazium esculentum (Retz.) Sw. and Its Phytochemicals

Inthachat W, Chantong B, Pitchakarn P, Takoon C, Karinchai J, Suttisansanee U, Temviriyanukul P

Pharmaceuticals (Basel)

06-Mar-2024

PMCID:	PMC10975765
doi:	10.3390/ph17030341
PMID:	38543127

A review on traditional Chinese medicine natural products and acupuncture intervention for Alzheimer’s disease based on the neuroinflammatory

Chen Z, Wang X, Du S, Liu Q, Xu Z, Guo Y, Lin X

Chin Med

28-Feb-2024

PMCID:	PMC10900670
doi:	10.1186/s13020-024-00900-6
PMID:	38419106

The mechanistic role of natural antimicrobials in preventing Staphylococcus aureus invasion of MAC-T cells using an in vitro mastitis model

Balta I, McCleery D, David SR, Pet E, Stef D, Iancu T, Pet I, Stef L, Corcionivoschi N

Ir Vet J

27-Feb-2024

PMCID:	PMC10898119
doi:	10.1186/s13620-024-00265-0
PMID:	38414081

Exploring the Antibacterial Potential and Underlying Mechanisms of Prunella vulgaris L. on Methicillin-Resistant Staphylococcus aureus

Li Z, He Q, Xu F, Yin X, Guan Z, Song J, He Z, Yang X, Situ C

Foods

22-Feb-2024

PMCID:	PMC10931123
doi:	10.3390/foods13050660
PMID:	38472772

A Comprehensive Review of Various Therapeutic Strategies for the Management of Skin Cancer

Dachani SR, Kaleem M, Mujtaba MA, Mahajan N, Ali SA, Almutairy AF, Mahmood D, Anwer MK, Ali MD, Kumar S

ACS Omega

22-Feb-2024

PMCID:	PMC10918819
doi:	10.1021/acsomega.3c09780
PMID:	38463249

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 C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	https://doi.org/10.1021/JF040083T
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	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 C1=CC=C(C=C1)C=O	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
2-[3-[4-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethenoxy]-3-hydroxyphenyl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid	85148929	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 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
> 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 CCCCCCCCCCCCCCCCCCCC	282.50	unknown	https://doi.org/10.1080/10412905.1991.9697919
Heneicosane	12403	Click to see CCCCCCCCCCCCCCCCCCCCC	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 CCCCCCCCCCCCCCCCCCC	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 CCCCCCCCCCCCCCC	212.41	unknown	https://doi.org/10.1080/10412905.1991.9697919
Tetradecane	12389	Click to see CCCCCCCCCCCCCC	198.39	unknown	https://doi.org/10.1080/10412905.1991.9697919
Tridecane	12388	Click to see CCCCCCCCCCCCC	184.36	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Octatriene, dimethyl-	6434062	Click to see CC(C)C=CC=C(C)C=C	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
Caproic Acid	8892	Click to see CCCCCC(=O)O	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 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
> 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 CC(CCC=C(C)C)CC=O	154.25	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
3,7-Dimethyl-2,6-octadien-1-al	8843	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1016/S0031-6865(97)00026-5
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	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 CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960032
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	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 CC(CCC=C(C)C)CC=O	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
D-Citronellol	101977	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
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 CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1055/S-2006-961551 https://doi.org/10.1055/S-2006-960032
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	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
3-Pinanone	11038	Click to see CC1C2CC(C2(C)C)CC1=O	152.23	unknown	https://doi.org/10.1055/S-2006-960032
Bicyclo[3.1.1]Heptan-3-One, 2,6,6-Trimethyl-, [1S-(1a,2ss,5a)]-	12311188	Click to see CC1C2CC(C2(C)C)CC1=O	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 CCCC=CC(=O)CC1CC(CCC1C(C)C)C	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 CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730030406
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene	324224	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
(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 CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	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 CC1C(CC(C(C1C=CC(C)O)(C)CO)O)O	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 CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960032
(E)-alpha-bisabolene	5315468	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
(Z)-alpha-Bisabolene	5352653	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	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 CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	218.38	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
5-(3-Hydroxybut-1-enyl)-4-(hydroxymethyl)-4,6-dimethylcyclohexane-1,3-diol	162952249	Click to see CC1C(CC(C(C1C=CC(C)O)(C)CO)O)O	244.33	unknown	https://doi.org/10.1021/NP9003195
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 CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
alpha-Ionol	5363817	Click to see CC1=CCCC(C1C=CC(C)O)(C)C	194.31	unknown	https://doi.org/10.1021/NP9003195
beta-Bourbonene	62566	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1515/ZNC-1996-9-1009 https://doi.org/10.1016/J.PHYMED.2008.04.018
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 CC1CCC(C2C13C2C(=C)CC3)C(C)C	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 epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	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 CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYMED.2008.04.018
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730030406
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730030406
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960032
> 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	102432	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960032
beta-Cedrene	11106485	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	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 CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	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
[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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)CO	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 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
quadranoside III	10327092	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)CO	666.80	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)C)C)C2C1(C)O)C)C(=O)O	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COS(=O)(=O)O)OS(=O)(=O)O)C)C)C2C1(C)O)C)C(=O)O	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COS(=O)(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O	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 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
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 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
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 CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)OC)C)C)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 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 2,3-dihydroxyurs-12-en-28-oate	621722	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Methyl 3-epimaslinate	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 corosolate	14109751	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC	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 CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)OC)C)C)C	486.70	unknown	https://doi.org/10.1002/ARDP.19743070805
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1080/10412905.1991.9697919
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1080/10412905.1991.9697919
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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
> 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
Citrusin C	9945189	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	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 C1=CC2=C(C=C1C=O)OC(O2)C3=CC(=C(C=C3)O)O	258.23	unknown	https://doi.org/10.1055/S-2006-957513
2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde	10377789	Click to see C1=CC2=C(C=C1C=O)OC(O2)C3=CC(=C(C=C3)O)O	258.23	unknown	https://doi.org/10.1055/S-2006-957513
> Organoheterocyclic compounds / Lactones / Delta valerolactones
delta-Octalactone	12777	Click to see CCCC1CCCC(=O)O1	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 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/NP9003195 https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1021/NP070351S
3-(3,4-dihydroxyphenyl)-2-[(2E)-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
Benzenepropanoic acid, alpha-[[(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-, (alphaR)-	163195484	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
Caffeic acid methyl ester	689075	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1055/S-2006-957513
Methyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate	76511959	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
Methyl 3,4-dihydroxycinnamate	92202	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	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 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/10.1248/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 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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1055/S-2006-957513 https://doi.org/10.1021/NP9003195
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	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 C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	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 CC=C1CC(C(C(=O)OCC2C(CN3C2C(CC3)OC1=O)O)(C)O)C	353.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid	439435	Click to see C1=CC(=C(C=C1CC(C(=O)O)O)O)O	198.17	unknown	https://doi.org/10.1021/NP070351S
Benzenepropanoic acid, alpha,3,4-trihydroxy-, (aS)-	179536	Click to see C1=CC(=C(C=C1CC(C(=O)O)O)O)O	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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