Scientific name	Authority	First published in
Rosmarinus angustifolius	Mill.	Gard. Dict. ed. 8 : n.º 1 (1768)
Rosmarinus communis	Noronha	Verh. Batav. Genootsch. Kunsten 5(4): 25 (1790)
Rosmarinus flexuosus	Jord. & Fourr.	Brev. Pl. Nov. 1: 44 (1866)
Rosmarinus latifolius	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Rosmarinus laxiflorus	Noë	Exsicc. (Pl. Alger.) no. 443 1852
Rosmarinus officinalis subsp. palaui	(O.Bolòs & Molin.) Malag.	Las Subesp. y Variac. Geogr. : 23 (1973)
Rosmarinus officinalis var. palaui	O.Bolòs & Molin.	Collect. Bot. (Barcelona) 5: 757 (1959)
Rosmarinus prostratus	Mazziari	Ionios Antologia 2: 446 (1834)
Rosmarinus rigidus	Jord. & Fourr.	Brev. Pl. Nov. 1: 43 (1866)
Rosmarinus serotinus	Loscos	Trat. Pl. Aragon 1: 71. 1877
Rosmarinus tenuifolius	Jord. & Fourr.	Brev. Pl. Nov. 1: 43 (1866)
Salvia fasciculata	Fernald	Proc. Amer. Acad. Arts 40: 54. 1904
Rosmarinus officinalis var. prostratus	Pasq.	Cat. Ort. Bot. Napoli 91. 1867
Rosmarinus palaui	(O.Bolòs & Molin.) Rivas Mart. & M.J.Costa	Itin. Geobot. 15: 707 (2002)
Rosmarinus officinalis subsp. laxiflorus	(Noë) Nyman	Consp. Fl. Eur. 571 1881
Rosmarinus officinalis var. rigidus	(Jord. & Fourr.) Cariot & St.-Lag.	Étude Fl. ed. 8, 2: 657 1889
Rosmarinus officinalis var. angustissimus	Foucaud & E.Mandon	Bull. Soc. Bot. France 47: 95. 1900
Rosmarinus officinalis var. latifolius	(Mill.) DC.	Fl. Franç. éd. 3, 3: 506. 1805
Rosmarinus officinalis var. angustifolius	(Mill.) DC.	Fl. Franç. éd. 3, 3: 506. 1805
Rosmarinus officinalis var. nutans	Cout.	Bol. Soc. Brot. 23: 160. 1907
Rosmarinus laxiflorus	de Noé ex Lange	Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn (1863) 12.

Common names Top

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Filter by language:

Language	Common/alternative name
English	rosemary
English	anthos
English	salvia rosmarinus
Spanish	romero
Spanish	romero comun
Spanish	romero común
Spanish	romero coronario
Spanish	romero de huerta
Spanish	romero fino
Spanish	romeron
Spanish	romerón
Spanish	romiru
Spanish	rosmarino
Afrikaans	roosmaryn
Arabic	إكليل الجبل (نبات
Arabic	حصى البان
Arabic	روزماري
Arabic	اكليل الجبل
Arabic	إكليل الجبل
Arabic	إكليل الجبل (نبات)
ary	أزير
Azerbaijani	dərman rozmarini
azb	درمان روزمارینی
bcl	romero (tinanom)
Bulgarian	розмарин
Bulgarian	обикновен розмарин
Bengali	রোজমেরি
br	roumarin
Bosnian	ružmarin
Bosnian	ruzmarin
Catalan	romaní
Catalan	romer
Catalan	salvia rosmarinus
Czech	rozmarýn lékařský
Czech	rozmarýna lékařská
Czech	rozmarýna obecná
Czech	salvia rosmarinus
Czech	šalvěj rozmarýna
Welsh	rhosmari
Welsh	rhos mair
Welsh	rosmari
Danish	rosmarin
German	rosmarin
German	meertau
Greek	Δενδρολίβανο
Greek	Δεντρολίβανο
Greek	Λιβανωτίς
Greek	Ροσμαρίνον
Esperanto	oficina rosmareno
Estonian	harilik rosmariin
Basque	erromero
Persian	رزماری
Persian	اکلیل کوهی
Persian	رزماری (دارو)
Persian	رومارن
Finnish	rosmariini
Finnish	rohtorosmariini
French	romarin
French	salvia rosmarinus
frr	ruusmariin
Irish	marós
Galician	alecrín
Galician	romeiro
Galician	romeu
Hebrew	רוזמרין
Hebrew	רוזמרין רפואי
Hindi	गुलमेंहदी
Croatian	ružmarin
Croatian	ruzmarin
Upper Sorbian	Ćěłowe zelo
Upper Sorbian	rósmarja
Upper Sorbian	rosmarin
ht	womaren
Hungarian	rozmaring
Armenian	Հազրեվարդ բուժիչ
ia	rosmarino
Indonesian	rosemari
io	rosmarino
Icelandic	rósmarín
Italian	rosmarino
Japanese	ルテオリン
Japanese	オレアノール酸
Japanese	マンネンロウ
Japanese	ロズマリン酸
Japanese	ローズマリー
jv	rosméri
Georgian	როზმარინი
Kabyle	aklil
Kannada	ರೋಸ್ಮರಿ
Korean	로즈마리
Korean	로즈메리
Cornish	rosmari
lb	rosmarin
lb	rousemaräin
lb	romarin
lo	ຕົ້ນໂຣສ ເມຣີ
Lithuanian	kvapusis rozmarinas
Lithuanian	rozmarinas
Latvian	rozmarīns
Macedonian	Рузмарин
Malayalam	റോസ് മേരി
Malay	rosmari
mzn	ترم (سبزی)
Norwegian Bokmål	rosmarin
Dutch	rozemarijn
Dutch	e392
Norwegian Nynorsk	rosmarin
nrm	romathin
nrm	romathîn
oc	romanin
Polish	rozmaryn lekarski
Pashto	اکليل
Portuguese	alecrim
Quechua	rumiru
Quechua	rumpo
Quechua	sallika
Romanian	rozmarin
Russian	или Розмарин обыкновенный
Russian	Розмарин лекарственный
Russian	Розмарин обыкновенный
Kinyarwanda	romarin
sc	romasinu
sco	rosemary
Serbo-Croatian	ružmarin
Sinhala	රෝස්මෙරි
Slovak	rozmarín lekársky
Slovenian	navadni rožmarin
Slovenian	rozmarin
Albanian	rozmarina normalizon sheqerin në gjak
Albanian	rozmarina
Serbian	рузмарин
Serbian	Рузмарин
Swedish	rosmarin
Tamil	ரோஸ்மேரி
Tamil	ரோசுமேரி
tg	Руморан
Thai	rosemary
Thai	โรสแมรี
Turkish	kuşdili
Turkish	biberiye
Turkish	hasalban
Ukrainian	Розмарин
vec	rosmarin
Vietnamese	hương thảo
Walloon	rômarin
za	mizdezyangh
Chinese	迷迭香

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000298062
UNII	EA3289138M
USDA Plants	ROOF
Tropicos	17600561
INPN	118865
KEW	urn:lsid:ipni.org:names:455509-1
The Plant List	kew-179873
Missouri Botanical Garden	281457
Observations.org	7336
NBN Atlas	NBNSYS0000033609
Nature Serve	2.141396
IPNI	455509-1
iNaturalist	82921
GBIF	10902460
Freebase	/m/06cd7
EPPO	RMSOF
EOL	579379
Elurikkus	231149
Calflora (Californian flora)	8619
US Library of Congress	sh85115432
USDA GRIN	32207
Wikipedia	Rosemary
CMAUP	NPO26138
GBIF	2926634

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)!

Title

Authors

Publication

Released

IDs

Two Antioxidative Diterpenes from Rosemary (Rosmarinus officinalis L.) and a Revised Structure for Rosmanol†

Nobuji Nakatani, Reiko Inatani

Oxford University Press (OUP)

13-Apr-2016

doi:	10.1080/00021369.1984.10866436

A New Diterpene Lactone, Rosmadial, from Rosemary (Rosmarinus officinalisL.)

Nobuji Nakatani, Reiko Inatani

Oxford University Press (OUP)

13-Apr-2016

doi:	10.1080/00021369.1983.10865620

Structure of Rosmanol, A New Antioxidant from Rosemary (Rosmarinus officinalisL.)

Nobuji Nakatani, Reiko Inatani

Oxford University Press (OUP)

13-Apr-2016

doi:	10.1080/00021369.1981.10864897

Seasonal variations of rosmarinic and carnosic acids in rosemary extracts. Analysis of their in vitro antiradical activity

J.C. Luis, C.B. Johnson

Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria (INIA)

02-Jun-2014

doi:	10.5424/SJAR/2005031-130

The Essential Oil ofRosmarinus officinalisGrowing in Argentina

I. Mizrahi, M. A. Juarez, A. L. Bandoni

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1991.9697900

Essential Oil of Rosmarinus officinalis L. (Rosemary) from Rio de Janeiro, Brazil

Alexandre Porte, Ronoel Luiz de O. Godoy, Daíse Lopes, Midori Koketsu, Sueli Limp Gonçalves, Helena S. Torquilho

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.2000.9712163

Essential Oil of Rosemary(Rosmarinus officinalisL.) from Cuba

Jorge A. Pino, Mirna Estarrón, Victor Fuentes

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1998.9700854

Essential Oils of theRosmarinus eriocalyx-tomentosusComplex in Southeast Spain

M. C. Soriano Cano, J. A. Sotomayor Sánchez, P. Sánchez Gomez, M. C. Garcí Vallejo

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1993.9698216

Seasonal variations of phenolic compounds and biological properties in sage (Salvia officinalis L.).

Generalić I, Skroza D, Surjak J, Možina SS, Ljubenkov I, Katalinić A, Simat V, Katalinić V

Chem Biodivers

01-Feb-2012

doi:	10.1002/CBDV.201100219
PMID:	22344920

Two antioxidative diterpenes from rosemary (Rosmarinus officinalis L.) and a revised structure for rosmanol.

Nobuji NAKATANI, Reiko INATANI

Oxford University Press (OUP)

13-Jul-2011

doi:	10.1271/BBB1961.48.2081

Structure of a new antioxidative phenolic diterpene isolated from rosemary (Rosmarinus officinalis L.)

Reiko INATANI, Hidetsugu FUWA, Haruo SETO, Nobuji NAKATANI

Oxford University Press (OUP)

13-Jul-2011

doi:	10.1271/BBB1961.46.1661

Flavonoids and phenolic compounds from Rosmarinus officinalis.

Bai N, He K, Roller M, Lai CS, Shao X, Pan MH, Ho CT

J Agric Food Chem

12-May-2010

doi:	10.1021/JF100332W
PMID:	20397728

The corrected structure of rosmaridiphenol, a bioactive diterpene from Rosmarinus officinalis.

Pertino MW, Schmeda-Hirschmann G

Planta Med

01-Apr-2010

doi:	10.1055/S-0029-1240629
PMID:	19937552

New Antimicrobial Substances againstStreptomyces scabiesfrom Rosemary (Rosmarinus officinalisL.)

Makoto Takenaka, Toshiro Watanabe, Kazuo Sugahara, Yasuo Harada, Shigeo Yoshida, Fumio Sugawara

Informa UK Limited

14-Sep-2009

doi:	10.1271/BBB.61.1440

Production and use of natural antioxidants

U. Bracco, J. Löliger, J. ‐L. Viret

Wiley

04-May-2008

doi:	10.1007/BF02899449

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
> Alkaloids and derivatives
1-(1-Methylpyrrolidin-1-ium-2-yl)propan-2-one	25200410	Click to see CC(=O)CC1CCC[NH+]1C	142.22	unknown	via CMAUP database
> 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/10.1111/J.1745-4557.2006.00096.X
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1002/CBDV.201100219 https://doi.org/10.1007/S00216-007-1298-8
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1002/CBDV.201100219 https://doi.org/10.5424/SJAR/2005031-130 https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF010697N https://doi.org/10.1021/JF040083T https://doi.org/10.1007/S00216-007-1298-8
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1002/FFJ.2730090107
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
4-Methoxyphenethylamine	4657	Click to see COC1=CC=C(C=C1)CCN	151.21	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1080/10412905.1998.9700854
> Benzenoids / Tetralins
3-(7-hydroxy-1-methyl-6-propan-2-yl-2-prop-1-en-2-yl-3,4-dihydro-2H-naphthalen-1-yl)propanoic acid	85432094	Click to see CC(C)C1=C(C=C2C(=C1)CCC(C2(C)CCC(=O)O)C(=C)C)O	316.40	unknown	https://doi.org/10.1021/NP040154I
seco-Hinokiol	11197877	Click to see CC(C)C1=C(C=C2C(=C1)CCC(C2(C)CCC(=O)O)C(=C)C)O	316.40	unknown	https://doi.org/10.1021/NP040154I
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (6S,7S,16S)-6,7,16-tris(trimethylsilyloxy)heptadecanoate	162911043	Click to see CC(CCCCCCCCC(C(CCCCC(=O)OC)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	549.00	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
Methyl 6,7,16-tris(trimethylsilyloxy)heptadecanoate	162911042	Click to see CC(CCCCCCCCC(C(CCCCC(=O)OC)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	549.00	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(10R)-10,18-dihydroxyoctadecanoic acid	163034734	Click to see C(CCCCC(=O)O)CCCC(CCCCCCCCO)O	316.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
(6R,7S)-6,7,16-trihydroxyhexadecanoic acid	162873327	Click to see C(CCCCC(C(CCCCC(=O)O)O)O)CCCCO	304.42	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
(9R,10S,12R,13S)-9,10,12,13,18-pentahydroxyoctadecanoic acid	162989629	Click to see C(CCCC(C(CC(C(CCCCCO)O)O)O)O)CCCC(=O)O	364.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
(9R,10S)-9,10,17-trihydroxyheptadecanoic acid	162889316	Click to see C(CCCC(C(CCCCCCCO)O)O)CCCC(=O)O	318.40	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
(R)-10,16-Dihydroxyhexadecanoic acid	11781204	Click to see C(CCCCC(=O)O)CCCC(CCCCCCO)O	288.42	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
10-Hydroxystearic acid	9561835	Click to see CCCCCCCCC(CCCCCCCCC(=O)O)O	300.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
10-Hydroxystearic acid, (10S)-	91864452	Click to see CCCCCCCCC(CCCCCCCCC(=O)O)O	300.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
10,16-Dihydroxyhexadecanoic acid	441449	Click to see C(CCCCC(=O)O)CCCC(CCCCCCO)O	288.42	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
10,18-Dihydroxy-octadecanoic acid	85780051	Click to see C(CCCCC(=O)O)CCCC(CCCCCCCCO)O	316.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
12-Hydroxyoctadec-9-enoic acid	8839	Click to see CCCCCCC(CC=CCCCCCCCC(=O)O)O	298.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
16-Hydroxyhexadecanoic acid	10466	Click to see C(CCCCCCCC(=O)O)CCCCCCCO	272.42	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
6,7,16-Trihydroxyhexadecanoic acid	162873326	Click to see C(CCCCC(C(CCCCC(=O)O)O)O)CCCCO	304.42	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
9,10,12,13,18-Penta-hydroxystearic acid	85790104	Click to see C(CCCC(C(CC(C(CCCCCO)O)O)O)O)CCCC(=O)O	364.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
9,10,17-Trihydroxyheptadecanoic acid	85790101	Click to see C(CCCC(C(CCCCCCCO)O)O)CCCC(=O)O	318.40	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
Floionolic acid	12144794	Click to see C(CCCCO)CCCC(C(CCCCCCCC(=O)O)O)O	332.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
Phloionolic acid	5282938	Click to see C(CCCCO)CCCC(C(CCCCCCCC(=O)O)O)O	332.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
Ricinoleic acid	643684	Click to see CCCCCCC(CC=CCCCCCCCC(=O)O)O	298.50	unknown	https://doi.org/10.1016/S0031-9422(00)97374-6
> 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/10.1111/J.1365-2621.1985.TB10476.X
Heptanoic Acid	8094	Click to see CCCCCCC(=O)O	130.18	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Octanoic acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1-Octen-3-OL	18827	Click to see CCCCCC(C=C)O	128.21	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
2-Heptanol	10976	Click to see CCCCCC(C)O	116.20	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
3-Octanol	11527	Click to see CCCCCC(CC)O	130.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
3-Octen-1-OL	5364475	Click to see CCCCC=CCCO	128.21	unknown	https://doi.org/10.1080/10412905.1998.9700854
3-Octenol, cis-	28937	Click to see CCCCC=CCCO	128.21	unknown	https://doi.org/10.1080/10412905.1998.9700854
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,8R,9S,10S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yltetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	125181923	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3CC(=O)C24C3C(CCC4)(C)C)O)O)O	344.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(3R,8R)-14,15-dihydroxy-7,7-dimethyl-13-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),11,13-trien-4-one	162975815	Click to see CC(C)C1=C(C(=C2CC3C(CCC2=C1)C(CCC3=O)(C)C)O)O	316.40	unknown	https://doi.org/10.1055/S-0029-1240629
(4aR,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	36689575	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1055/S-2006-958094
[(4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]methanediol	162829555	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(O)O)OC)OC	362.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
[(4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]methanol	162851486	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)CO)OC)OC	346.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
12-O-Methylcarnosic acid	9974918	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC	346.50	unknown	https://doi.org/10.1021/JF0300745
5-Hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	74191744	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC	346.50	unknown	https://doi.org/10.1021/JF0300745
5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-3,4,4a,9,10,10a-hexahydro-2H-phenanthrene	162909921	Click to see CC(C)C1=C(C(=C2C3CCCC(C3CCC2=C1)(C)C)OC)OC	316.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydro-4bH-phenanthrene-3,4-diol	162820590	Click to see CC(C)C1=C(C(=C2C3CCCC(C3CCC2=C1)(C)C)O)O	288.40	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	270.50	unknown	via CMAUP database
Carnosic acid	65126	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1021/JF0002692 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1007/BF02899449 https://doi.org/10.5424/SJAR/2005031-130 https://doi.org/10.1007/S002990050763 https://doi.org/10.1055/S-2006-958094 https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF950374P https://doi.org/10.1248/BPB.26.1620 https://doi.org/10.1021/NP50098A031 https://doi.org/10.1007/BF02541065 https://doi.org/10.1021/NP040154I https://doi.org/10.1021/JF100332W https://doi.org/10.1007/BF01201582 https://doi.org/10.1021/JF970974J
Carnosic acid, Free acid	12302482	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1021/JF970974J
Carnosicacid	5024746	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O	332.40	unknown	https://doi.org/10.1021/JF970974J https://doi.org/10.1021/JF100332W https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF0002692 https://doi.org/10.1021/NP040154I https://doi.org/10.1248/BPB.26.1620 https://doi.org/10.1055/S-2006-958094
methyl (4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-4a-carboxylate	13966115	Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3C2(CCCC3(C)C)C(=O)OC)OC)OC	372.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
methyl (4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	59919881	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)OC)OC	374.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
methyl (4aS,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	162996818	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O	346.50	unknown	https://doi.org/10.1021/JF970974J
Methyl 11,12-bis(acetyloxy)abieta-9(11),8(14),12-trien-20-oate	11877519	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)OC(=O)C)OC(=O)C	430.50	unknown	https://doi.org/10.1021/JF0002692
Methyl 5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	10427743	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O	346.50	unknown	https://doi.org/10.1021/JF970974J https://doi.org/10.1021/JF0002692
Methyl Carnosate	11336941	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O	346.50	unknown	https://doi.org/10.1021/JF0002692
Rosmaridiphenol	9905016	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C(C2=O)CCCC3(C)C)O)O	316.40	unknown	https://doi.org/10.1007/BF02636212
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1-Hydroxy-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-11-yl) acetate	74051618	Click to see CC1=CCC2(CCC(C2CC(C(=CCC1)C)OC(=O)C)(C(C)C)O)C	348.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
Miltirone	160142	Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(CCC3)(C)C)C(=O)C1=O	282.40	unknown	https://doi.org/10.1007/BF02541500
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	https://doi.org/10.1080/10412905.1998.9700854
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1993.9698216
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.2000.9712163 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
> 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/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1998.9700854
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1998.9700854
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Verbenone	92874	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	via CMAUP database
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid	20327362	Click to see CC1(C2CCC1(C(C2)CC(=O)O)C)C	196.29	unknown	https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one	6973628	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1021/JF980437E
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1300/J044V06N03_03
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol	88298	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	unknown	via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1300/J044V06N03_03 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1993.9698216
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.2000.9712163 https://doi.org/10.1300/J044V06N03_03 https://doi.org/10.1002/FFJ.2730100209 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1021/JF980437E
alpha-Thujone	12304613	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1300/J044V06N03_03 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
beta-Thujene	520384	Click to see CC1C=CC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1300/J044V06N03_03
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1300/J044V06N03_03
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1300/J044V06N03_03 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1021/JF980437E
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1300/J044V06N03_03 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1021/JF980437E https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1080/10412905.2000.9712163 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1998.9700854
L-Born-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1080/10412905.1998.9700854
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730090107
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1021/JF980437E https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Hydroxypiperitone	79023	Click to see CC1=C(C(=O)C(CC1)C(C)C)O	168.23	unknown	via CMAUP database
3-(4-Propan-2-ylcyclohexa-1,3-dien-1-yl)propanoic acid	163192527	Click to see CC(C)C1=CC=C(CC1)CCC(=O)O	194.27	unknown	https://doi.org/10.1002/FFJ.2730090107
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1016/S0021-9673(00)00231-4 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
alpha,alpha-Dimethyl-4-methylenecyclohexanemethanol	81722	Click to see CC(C)(C1CCC(=C)CC1)O	154.25	unknown	via CMAUP database
beta-Terpineol	8748	Click to see CC(=C)C1CCC(CC1)(C)O	154.25	unknown	via CMAUP database
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730090107
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1021/JF980437E
Piperitenone	381152	Click to see CC1=CC(=O)C(=C(C)C)CC1	150.22	unknown	https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107
Piperitone	6987	Click to see CC1=CC(=O)C(CC1)C(C)C	152.23	unknown	https://doi.org/10.1080/10412905.1998.9700854
Pulegone	442495	Click to see CC1CCC(=C(C)C)C(=O)C1	152.23	unknown	https://doi.org/10.1080/10412905.1998.9700854
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1016/S0021-9673(00)00231-4
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(2R)-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)chroman-6-ol	8989	Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O	416.70	unknown	https://doi.org/10.1007/BF01201582
Alpha-Tocopherol	14985	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	https://doi.org/10.1007/BF01201582
beta-Tocopherol	6857447	Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O	416.70	unknown	https://doi.org/10.1007/BF01201582
Covi-ox	6560141	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	https://doi.org/10.1007/BF01201582
delta-Tocopherol	92094	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O	402.70	unknown	https://doi.org/10.1007/BF01201582
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1993.9698216
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene	134687947	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730090107
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1993.9698216
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1016/S0021-9673(00)00231-4 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730090107
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X https://doi.org/10.1002/FFJ.2730090107 https://doi.org/10.1080/10412905.1998.9700854 https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Zingiberene	92776	Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
beta-Gurjunene	6450812	Click to see CC1CCC2C(C2(C)C)C3C1CCC3=C	204.35	unknown	https://doi.org/10.1002/FFJ.2730090107
> 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/10.1080/10412905.1991.9697900 https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (6bR,12aR)-5,10-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	6325375	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	634.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,6R,7R)-9-[(Z)-2-methoxycarbonyl-3-methylbut-1-enyl]-5,5-dimethyl-8,11-dioxo-12-oxatricyclo[5.3.2.01,6]dodec-9-ene-10-carboxylic acid	133562190	Click to see CC(C)C(=CC1=C(C23CCCC(C2C(C1=O)OC3=O)(C)C)C(=O)O)C(=O)OC	390.40	unknown	https://doi.org/10.1271/BBB.61.1440
2H-1,4a-(Epoxymethano)naphthalene-4-carboxylic acid, 1,5,6,7,8,8a-hexahydro-3-[(1Z)-2-(methoxycarbonyl)-3-methyl-1-butenyl]-8,8-dimethyl-2,9-dioxo-, (1R,4aS,8aR)-rel-(+)-	102586055	Click to see CC(C)C(=CC1=C(C23CCCC(C2C(C1=O)OC3=O)(C)C)C(=O)O)C(=O)OC	390.40	unknown	https://doi.org/10.1271/BBB.61.1440
9-(2-Methoxycarbonyl-3-methylbut-1-enyl)-5,5-dimethyl-8,11-dioxo-12-oxatricyclo[5.3.2.01,6]dodec-9-ene-10-carboxylic acid	156602862	Click to see CC(C)C(=CC1=C(C23CCCC(C2C(C1=O)OC3=O)(C)C)C(=O)O)C(=O)OC	390.40	unknown	https://doi.org/10.1271/BBB.61.1440
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	26202935	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1055/S-2006-958094
(1R,8R,9S,10S)-9-ethoxy-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	15801060	Click to see CCOC1C2C3=CC(=C(C(=C3C4(C1C(CCC4)(C)C)C(=O)O2)O)O)C(C)C	374.50	unknown	https://doi.org/10.1021/JF0002692
(1R,8S,10R)-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	51377211	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1055/S-2006-958094
(1R,8S,10S)-8-ethoxy-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	14314750	Click to see CCOC1C2C3C(CCCC3(C4=C(C(=C(C=C14)C(C)C)O)O)C(=O)O2)(C)C	374.50	unknown	https://doi.org/10.1055/S-2006-962754
(1R,8S,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	26202937	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1055/S-2006-958094
(1R,8S,9S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	455261	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1007/BF01201582 https://doi.org/10.1055/S-2006-962754 https://doi.org/10.1016/0021-9673(94)80582-2 https://doi.org/10.1080/00021369.1983.10865620 https://doi.org/10.1271/BBB.61.1440 https://doi.org/10.1021/NP50098A031 https://doi.org/10.1021/JF0002692 https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041 https://doi.org/10.1055/S-2006-958094
(1R,8S)-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	6324890	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
(1R,8S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	14379075	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)OC)OC	358.50	unknown	https://doi.org/10.1016/S0040-4020(01)88671-3
(1R,9S,10S)-3,4-dihydroxy-8-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	137706557	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O	360.40	unknown	https://doi.org/10.1271/BBB.61.1440
(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 CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1021/JF970974J https://doi.org/10.1021/JF100332W https://doi.org/10.1021/JF0300745 https://doi.org/10.1271/BBB1961.46.1661 https://doi.org/10.5424/SJAR/2005031-130 https://doi.org/10.1021/JF0002692 https://doi.org/10.1080/00021369.1981.10864897 https://doi.org/10.1248/BPB.26.1620 https://doi.org/10.1055/S-2006-958094
(1S,8R,10R)-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	29010901	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1021/JF970974J
11,12-Dihydroxy-7,14-dimethoxy-8,11,13-abietatrien-20,6-olide	76401227	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C34CCCC(C3C(C2OC)OC4=O)(C)C)OC	390.50	unknown	https://doi.org/10.1271/BBB.61.1440
11,12,14-Trihydroxy-7-methoxy-8,11,13-abietatrien-20,6-olide	131751217	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C34CCCC(C3C(C2OC)OC4=O)(C)C)O	376.40	unknown	https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6-dihydroxy-8,9-dimethoxy-1,1-dimethyl-7-(1-methylethyl)-, [4aR-(4aalpha,9beta,10alpha,10abeta)]-	95224642	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C34CCCC(C3C(C2OC)OC4=O)(C)C)OC	390.50	unknown	https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6,8-trihydroxy-9-methoxy-1,1-dimethyl-7-(1-methylethyl)-, [4aR-(4aalpha,9beta,10alpha,10abeta)]-	102586056	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C34CCCC(C3C(C2OC)OC4=O)(C)C)O	376.40	unknown	https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 9-amino-1,3,4,9,10,10a-hexahydro-5,6-dihydroxy-1,1-dimethyl-7-(1-methylethyl)-, (4aR-(4aalpha,9alpha,10alpha,10abeta))-	5320998	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)N)O)O	345.40	unknown	via CMAUP database
3,4,8-Trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	9884612	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1271/BBB1961.46.1661 https://doi.org/10.1271/BBB.61.1440 https://doi.org/10.1021/JF0002692 https://doi.org/10.1080/00021369.1981.10864897 https://doi.org/10.1080/00021369.1984.10866436 https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041 https://doi.org/10.1055/S-2006-958094
3,4,9-Trihydroxy-11,11-dimethyl-5-(propan-2-yl)-16-oxatetracyclo[6.6.2.0^{1,10}.0^{2,7}]hexadeca-2(7),3,5-trien-15-one	11996616	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1080/00021369.1984.10866436 https://doi.org/10.1021/JF0002692
7-Methylrosmanol	9950773	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O	360.40	unknown	https://doi.org/10.1271/BBB.61.1440 https://doi.org/10.1021/JF0002692
7-O-Methylrosmanol	23243692	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O	360.40	unknown	https://doi.org/10.1021/NP50054A030 https://doi.org/10.1271/BBB.61.1440
7beta-Methoxyrosmanol	46883406	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O	360.40	unknown	https://doi.org/10.1021/JF0002692
8-Methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2(7),5-diene-3,4,15-trione	75225295	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2OC)OC4=O)(C)C	358.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
9-Ethoxy-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	163038552	Click to see CCOC1C2C3=CC(=C(C(=C3C4(C1C(CCC4)(C)C)C(=O)O2)O)O)C(C)C	374.50	unknown	https://doi.org/10.1021/JF0002692
Carnosol	442009	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1055/S-2006-962754 https://doi.org/10.1021/JF0002692 https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1007/BF02899449 https://doi.org/10.1080/00021369.1981.10864897 https://doi.org/10.1007/BF02541016 https://doi.org/10.1055/S-2006-958094 https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF950374P https://doi.org/10.1021/JF9603893 https://doi.org/10.1248/BPB.26.1620 https://doi.org/10.1021/NP50098A031 https://doi.org/10.1007/BF02541065 https://doi.org/10.1080/00021369.1983.10865620 https://doi.org/10.1016/S0040-4020(01)88671-3 https://doi.org/10.1271/BBB1961.46.1661 https://doi.org/10.1021/JF100332W https://doi.org/10.1007/BF01201582 https://doi.org/10.1016/0021-9673(94)80582-2
Epiisorosmanol	13820510	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1021/JF0002692
Epirosmanol	23243694	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1080/00021369.1984.10866436 https://doi.org/10.1007/BF01201582 https://doi.org/10.1080/00021369.1981.10864897 https://doi.org/10.1021/JF0002692 https://doi.org/10.1271/BBB1961.48.2081 https://doi.org/10.1016/0021-9673(94)80582-2 https://doi.org/10.1055/S-2006-958094 https://doi.org/10.1271/BBB1961.46.1661
Isorosmanol	13820511	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1080/00021369.1984.10866436 https://doi.org/10.1271/BBB1961.48.2081
Rosmanol	13966122	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	https://doi.org/10.1007/BF01201582 https://doi.org/10.1055/S-2006-962754 https://doi.org/10.1016/0021-9673(94)80582-2 https://doi.org/10.1080/00021369.1983.10865620 https://doi.org/10.1271/BBB.61.1440 https://doi.org/10.1021/NP50098A031 https://doi.org/10.1021/JF0002692 https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041 https://doi.org/10.1055/S-2006-958094
Rosmaquinone A	101763939	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2OC)OC4=O)(C)C	358.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
rosmaquinone B	46883407	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2OC)OC4=O)(C)C	358.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,8R,9S,11aR,11bR,13aR,13bS)-9-hydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	158620014	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol	51340201	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
(4aR,6aR,6bS,8aS,11S,12R,12aR,14aR,14bR)-11-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one	101763940	Click to see CC1C2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)C	440.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(6aR,6bS,8aR,11R,12S,12aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one	5318252	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C	424.70	unknown	https://doi.org/10.1055/S-2006-959670
10-Hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	11568718	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C	454.70	unknown	https://doi.org/10.1021/JF062610+
23-Hydroxybetulinic acid	21672692	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
3-epi-alpha-Amyrin	12358389	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
3-Hydroxyolean-12-en-28-oic acid	619166	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	https://doi.org/10.1021/JF062610+
3-O-Acetyloleanolic acid	151202	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1055/S-2006-959670
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
alpha-Amyrenone	12306155	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C	424.70	unknown	https://doi.org/10.1055/S-2006-959670
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1055/S-2006-959670
Anemosapogenin	5318667	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Augustic acid	15560128	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1055/S-2006-959670
beta-Amyrine	15942855	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
beta-Amyrone	12306160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	https://doi.org/10.1055/S-2006-959670
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/JF062610+
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041 https://doi.org/10.1021/NP50054A030
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1248/BPB.25.1485 https://doi.org/10.1055/S-2006-962754 https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
CID 15560533	15560533	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C	454.70	unknown	https://doi.org/10.1021/JF062610+
Lup-20(29)-ene-3beta,28-diol	221023	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
methyl (1R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	102401402	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)OC)C)C)(C)C)O)C	468.70	unknown	https://doi.org/10.1021/JF062610+
Methyl 10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162851026	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)OC)C)C)(C)C)O)C	468.70	unknown	https://doi.org/10.1021/JF062610+
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	https://doi.org/10.1055/S-2006-959670 https://doi.org/10.1248/BPB.25.1485 https://doi.org/10.1021/JF062610+
Rofficerone	131752699	Click to see CC1C2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)C	440.70	unknown	https://doi.org/10.1055/S-2006-959670 https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Urs-12-en-3beta-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/BF02541065 https://doi.org/10.1007/BF02541016 https://doi.org/10.1055/S-2006-959670 https://doi.org/10.1248/BPB.25.1485 https://doi.org/10.1021/JF062610+
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1055/S-2006-959670
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol	5991	Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O	296.40	unknown	https://doi.org/10.1080/10412905.1993.9698216 https://doi.org/10.1002/FFJ.2730090107
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Labriformidin	441861	Click to see CC1CC(=O)C2(C(O1)OC3CC4CC5C6(O5)C(C4(CC3O2)C)C(C(=O)C7(C6(CCC7C8=CC(=O)OC8)O)C)O)O	560.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol	6276	Click to see CCCCCO	88.15	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-Pentanol	22386	Click to see CCCC(C)O	88.15	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-(1-hydroxyethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	5318226	Click to see CC(C1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4-hydroxybenzoate	14132341	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)CO)O)O)O)O	300.26	unknown	https://doi.org/10.1021/JF100332W
1-(4-Hydroxybenzoyl)glucose	14132342	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)CO)O)O)O)O	300.26	unknown	https://doi.org/10.1021/JF100332W
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Valeraldehyde	8063	Click to see CCCCC=O	86.13	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal	8130	Click to see CCCCCCC=O	114.19	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial	72996596	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1080/00021369.1983.10865620
Rosmadial	15801061	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1080/00021369.1983.10865620
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Gentiacaulein	5281634	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)OC)O	288.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridopyrimidines
Lycocernuine, 14,15-didehydro-	596405	Click to see CC1=CC2C(CCC3N2C(C1)CC4N3C(=O)CCC4)O	276.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
(6aR,10R,10aR)-4-hydroxy-9,9-dimethyl-6-oxo-3-propan-2-yl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromene-1,10-dicarbaldehyde	162963774	Click to see CC(C)C1=C(C2=C(C3C(CCC(C3C=O)(C)C)C(=O)O2)C(=C1)C=O)O	344.40	unknown	https://doi.org/10.1021/JF0002692
4-hydroxy-9,9-dimethyl-6-oxo-3-propan-2-yl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromene-1,10-dicarbaldehyde	162963773	Click to see CC(C)C1=C(C2=C(C3C(CCC(C3C=O)(C)C)C(=O)O2)C(=C1)C=O)O	344.40	unknown	https://doi.org/10.1021/JF0002692
> 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/JF0300745 https://doi.org/10.1021/JF100332W
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/JF100332W https://doi.org/10.1021/JF0300745
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/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.1021/JF950374P https://doi.org/10.1016/J.CHROMA.2007.01.090 https://doi.org/10.5424/SJAR/2005031-130
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	72983454	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1021/JF100332W
1-O-feruloyl-beta-D-glucose	13962928	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1021/JF100332W
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1002/CBDV.201100219
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1016/J.CHROMA.2007.01.090
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1002/CBDV.201100219 https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF010697N https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B https://doi.org/10.5424/SJAR/2005031-130
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF040083T https://doi.org/10.1007/S00216-007-1298-8
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1002/CBDV.201100219 https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1002/CBDV.201100219
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1002/CBDV.201100219
> 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/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.5424/SJAR/2005031-130
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/10.1016/S0031-9422(00)90434-5 https://doi.org/10.1021/JF100332W https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF010697N
Scutellarein	5281697	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O	286.24	unknown	https://doi.org/10.1021/JF0002692
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
(8R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-8,9,9-trimethyl-8H-furo[2,3-h]chromen-4-one	162955921	Click to see CC1C(C2=C(O1)C=C(C3=C2OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)(C)C	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
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/10.1021/JF100332W
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF040083T https://doi.org/10.1002/CBDV.201100219
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides
(2S,3S,4R,5R,6S)-3-acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-4,5-dihydroxyoxane-2-carboxylic acid	10097618	Click to see CC(=O)OC1C(C(C(OC1C(=O)O)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O	504.40	unknown	https://doi.org/10.1016/S0031-9422(00)90434-5
(2S,3S,4S,5R,6S)-4-acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,5-dihydroxyoxane-2-carboxylic acid	10368818	Click to see CC(=O)OC1C(C(OC(C1O)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)C(=O)O)O	504.40	unknown	https://doi.org/10.1021/JF100332W https://doi.org/10.1016/S0031-9422(00)90434-5
3-Acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-4,5-dihydroxyoxane-2-carboxylic acid	74977669	Click to see CC(=O)OC1C(C(C(OC1C(=O)O)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O	504.40	unknown	https://doi.org/10.1016/S0031-9422(00)90434-5
4-Acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,5-dihydroxyoxane-2-carboxylic acid	74977668	Click to see CC(=O)OC1C(C(OC(C1O)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)C(=O)O)O	504.40	unknown	https://doi.org/10.1021/JF100332W https://doi.org/10.1016/S0031-9422(00)90434-5
Luteolin 3'-o-glucuronide	10253785	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/10.1021/JF100332W https://doi.org/10.1021/JF040078P https://doi.org/10.1016/S0031-9422(00)90434-5
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/10.1021/JF100332W https://doi.org/10.1021/JF040078P https://doi.org/10.1016/S0031-9422(00)90434-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1111/J.1745-4557.2006.00096.X https://doi.org/10.1021/JF010697N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	129010007	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1016/S0031-9422(00)90434-5
2-(3,4-Dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12314010	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	478.40	unknown	https://doi.org/10.1021/JF100332W
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	3564542	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	596.50	unknown	https://doi.org/10.1021/JF040078P
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)-	3594	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1016/S0031-9422(00)90434-5 https://doi.org/10.1021/JF040078P
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	53384378	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	via CMAUP database
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	5353588	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1021/JF040078P
5-Hydroxy-2-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13940617	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/JF040078P
5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	101260296	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF040078P
5,8-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	74977912	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF040078P
Diosmin	5281613	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1021/JF040078P
Eriocitrin	83489	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	596.50	unknown	https://doi.org/10.1021/JF040078P
Hesperidin	10621	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1021/JF040078P https://doi.org/10.1016/S0031-9422(00)90434-5
Homoplantaginin	5318083	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/JF040078P https://doi.org/10.1055/S-2007-969135
Naringin	442428	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O	580.50	unknown	https://doi.org/10.5424/SJAR/2005031-130 https://doi.org/10.1021/JF010697N
Nepitrin	120742	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	478.40	unknown	https://doi.org/10.1021/JF100332W https://doi.org/10.1016/S0031-9422(00)84935-3 https://doi.org/10.1055/S-2007-969135
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin	5317284	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1055/S-2007-969135 https://doi.org/10.1016/S0031-9422(00)84935-3
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1021/JF010697N https://doi.org/10.5424/SJAR/2005031-130
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether	5281601	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O	298.29	unknown	via CMAUP database
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	https://doi.org/10.1021/NP50054A030 https://doi.org/10.5424/SJAR/2005031-130 https://doi.org/10.1021/JF0002692
Genkwanin	5281617	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1021/JF0300745 https://doi.org/10.1021/JF0002692 https://doi.org/10.1055/S-2006-962754 https://doi.org/10.1021/JF040078P https://doi.org/10.1021/JF100332W
Ladanein	3084066	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O	314.29	unknown	https://doi.org/10.1021/JF100332W
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
6-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2,2-dimethyl-8-phenyl-8,9-dihydropyrano[2,3-f]chromen-10-one	5318656	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C3C(=C4C(=C2O)C=CC(O4)(C)C)C(=O)CC(O3)C5=CC=CC=C5)O	516.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(2S,3R,4S,5S,6R)-2-[[3-(6-hydroxy-4,5-dimethoxycyclohex-2-en-1-yl)-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972371	Click to see COC1C=CC(C(C1OC)O)C2CC3=C(C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC2	468.50	unknown	via CMAUP database
> 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
(2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-1-(3,4-dihydroxyphenyl)-3-oxoprop-1-en-2-yl]oxypropanoic acid	15801059	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=CC2=CC(=C(C=C2)O)O)C=O)O)O	360.30	unknown	https://doi.org/10.1021/JF0002692
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid	49770232	Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O	364.30	unknown	via CMAUP database
3-(3,4-Dihydroxyphenyl)-2-[1-(3,4-dihydroxyphenyl)-3-oxoprop-1-en-2-yl]oxypropanoic acid	162851105	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=CC2=CC(=C(C=C2)O)O)C=O)O)O	360.30	unknown	https://doi.org/10.1021/JF0002692
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	via CMAUP database

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Rosmarinus officinalis

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