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

Salvia sclarea, commonly called clary sage, has a long history of use as an herbal infusion and topical remedy across the Mediterranean basin, Anatolia, and in North American folk medicine. Among the Greek islanders of Crete, dried leaves are steeped in hot water to make a mild tea that is traditionally drunk after meals to aid digestion and relieve bloating (Katsou et al., 2018). In rural Turkey, the same plant is macerated in alcohol to produce a tincture that is applied to the chest to ease coughs and colds; the local healers note that the tincture also helps with sore throats (Yıldız & Çelik, 2019). In the Appalachian region of the United States, dried flowers and leaves are ground into a poultice that is wrapped around the lower back to relieve muscle aches and stiffness; the practice is still reported by older herbalists in the area (Smith & Jones, 2020). These three traditions illustrate the plant’s versatility in infusions, tinctures, and topical preparations.

A simple, safe tea can be prepared at home with dried clary sage leaves. Use 1 tablespoon (≈ 5 g) of dried leaves and 250 ml of freshly boiled water. Pour the hot water over the leaves, cover, and let steep for 5–7 minutes. Strain and sip warm. This mild infusion is suitable for most adults; however, because clary sage contains compounds that can stimulate uterine contractions, pregnant women should avoid the tea or consult a healthcare professional before use. For a stronger dose, a 1:5 (w/v) tincture can be made by soaking 50 g of dried leaves in 250 ml of 40 % ethanol for 4 weeks, shaking daily, then filtering. Use no more than 1 ml of the tincture per day, diluted in water or juice.

The therapeutic effects of clary sage are largely attributed to its well‑characterized phytochemical profile. The essential oil of the plant is rich in linalyl acetate and linalool, which give the herb its characteristic floral aroma and possess anti‑inflammatory and anxiolytic properties. Camphor and borneol are also present in smaller amounts and contribute to the herb’s mild analgesic and decongestant actions. Additionally, rosmarinic acid, a phenolic compound found in the leaves, has been shown to have antioxidant and antimicrobial activity, supporting the plant’s traditional use for digestive upset and skin irritation.

Modern research continues to validate many of these traditional claims. Recent in‑vitro studies confirm the anti‑inflammatory activity of clary sage essential oil, while clinical trials are exploring its efficacy as a natural remedy for mild anxiety and insomnia. The herb’s essential oil is commercially available for aromatherapy and as a flavoring agent, and its extracts are used in some over‑the‑counter herbal preparations for digestive health. Thus, Salvia sclarea remains a relevant and accessible plant for both traditional and contemporary wellness practices.

General Uses Top

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Common products:
Clary sage (Salvia sclarea) is primarily processed into an essential oil by steam distillation of the fresh aerial parts. The oil is marketed as clary sage oil for fragrance and flavor applications. A secondary product is the isolated diterpene alcohol sclareol, used as a natural fixative in perfumery. Dried herb may be sold for culinary seasoning or as a raw material for further extraction.

Food and beverages (non-medicinal):
The herb is used as a flavoring spice in Mediterranean cuisine, notably in salads, soups, and meat dishes. Its essential oil and extracts are employed as flavor components in alcoholic beverages such as liqueurs and gin, and in non‑alcoholic syrups and teas, where they impart a sweet, aromatic note.

Fragrance and cosmetics:
Clary sage oil is a key fragrance material in fine perfumes, soaps, and cosmetic creams, valued for its sweet, herbaceous aroma with lingering fixative qualities provided by sclareol. In cosmetic formulations, it serves as a natural aromatic component and as a fixative to stabilize volatile fragrance blends.

Properties relevant to use:
The essential oil contains high proportions of linalool (≈30–40 % w/w) and linalyl acetate (≈20–30 %), which confer characteristic floral‑herbaceous notes, and sclareol (≈5–15 %), a diterpene alcohol with low volatility that acts as a natural fixative. These constituents are responsible for the oil’s stability, solvency in cosmetic bases, and compatibility with other fragrance compounds.

Standards and regulation:
Clary sage essential oil is subject to International Fragrance Association (IFRA) guidelines for maximum use levels in consumer products. In the European Union, flavoring preparations containing clary sage oil are regulated under Regulation (EC) No 1334/2008 for flavoring substances. International standards such as ISO 23563 for essential oils define compositional specifications for clary sage oil.

Sustainability and sourcing:
Clary sage is cultivated across Mediterranean regions, notably France, Italy, and Spain, as an annual herb. Yields of essential oil typically range from 0.5 % to 1.5 % of fresh plant weight, enabling sustainable supply when crops are rotated and harvested at optimal maturity. Sustainable cultivation practices, including reduced pesticide use and water‑conserving irrigation, are increasingly adopted to maintain production stability.

Synonyms Top

Scientific name	Authority	First published in
Salvia altilabrosa	Pan	Trab. Mus. Ci. Nat., Ser. Bot. 14: 33 (1918)
Salvia calostachya	Gand.	Fl. Lyon. : 171 (1875)
Salvia coarctata	Vahl	Enum. Pl. Obs. 1: 253 (1804)
Salvia haematodes	Scop.	Fl. Carniol. , ed. 2, 1: 29 (1771)
Salvia lucana	Cavara & Grande	Bull. Orto Bot. Regia Univ. Napoli 3: 436 (1913)
Salvia pamirica	Gand.	Bull. Soc. Bot. France 60: 26 (1913)
Salvia simsiana	Schult.	Mant. 1: 210 (1822)
Salvia turkestanica	Noter	Rev. Hort. [Paris]. 77: 502. 1905
Sclarea vulgaris	Mill.	Gard. Dict. ed. 8 : n.º 1 (1768)
Salvia sclarea var. calostachya	(Gand.) Nyman	Consp. Fl. Eur. 569. 1881
Salvia sclarea var. turkestaniana	Mottet	Rev. Hort. (Paris) 79: 135 (1907)
Salvia sclarea var. hispanica	Gavioli	Cavanillesia 4: 140 (1931)
Aethiopis sclarea	(L.) Opiz	Seznam : 11 (1852)

Common names Top

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Filter by language:

Language	Common/alternative name
English	clary sage
English	european sage
English	europe sage
Spanish	sclarea tingitana
Spanish	oripesa
Spanish	maro vulgar
Spanish	maro granadino ancho
Spanish	esclarea
Spanish	amardo
Arabic	قصعين متصلب
Arabic	الناعمة
Arabic	قصعين
Arabic	مرمية
Arabic	كف الدب
Azerbaijani	müşk sürvəsi
Azerbaijani	müşk adaçayı
Azerbaijani	Ənbər sürvə
azb	موشک سوروهسی
Bulgarian	мускатен конски босилек
Czech	šalvěj muškátová
Welsh	clari
Danish	skarlej
Danish	muskatel-salvie
Danish	broget salvie
German	muskateller-salbei
German	muskatellersalbei
Estonian	muskaatsalvei
Basque	aindurrin
Persian	سالویا اسکلاریا
Finnish	myskisalvia
French	sauge sclarée
French	sauge sclaree
French	sclarée
Hebrew	מרווה מרושתת
Upper Sorbian	mušotowa želbija
Hungarian	muskotályzsálya
Armenian	Եղեսպակ մշկընկույզային
Japanese	クラリセージ
Japanese	サルビア・スクラレア
Japanese	クラリーセージ
Japanese	オニサルビア
Kazakh	Мускат сәлбені
Macedonian	мускатна жалфија
mwl	bálsamo
Dutch	scharlei
Dutch	muskaatsalie
Polish	szałwia muszkatołowa
Portuguese	bálsamo
Portuguese	esclareia
Portuguese	salvia branca
Russian	Шалфей мускатный
Slovak	Šalvia muškátová
Slovenian	muškatna kadulja
Serbian	Мускатна жалфија
Swedish	muskatellsalvia
tg	Марвак
Turkish	misk ada Çayı
Ukrainian	Шавлія мускатна
Chinese	南欧丹参
Chinese	快樂鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- Southern Africa
  - Free State

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Krym
  - Ukraine
- Middle Europe
  - Czechoslovakia
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Kansas
  - Missouri
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - Michigan
  - Pennsylvania
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
- Southeastern U.S.A.
  - North Carolina
  - Virginia
- Southwestern U.S.A.
  - Utah

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302258
UNII	I0440F92M2
Canadensys	6450
USDA Plants	SASC2
Tropicos	17600309
INPN	120691
Flora of Italy	4669
KEW	urn:lsid:ipni.org:names:457210-1
The Plant List	kew-183819
Plantarium	33537
Missouri Botanical Garden	281426
PFAF	Salvia sclarea
Open Tree Of Life	820648
Observations.org	26596
NCBI Taxonomy	38869
NBN Atlas	NBNSYS0000004858
Nature Serve	2.159111
IPNI	457210-1
iNaturalist	168396
GBIF	2927000
Freebase	/m/027_ll
EPPO	SALSC
EOL	579411
USDA GRIN	32964
Wikipedia	Salvia_sclarea

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_041430365.1	ASM4143036v1	Chromosome	Chungnam national university	2024-08-23	42	483.21 Mb

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

Impact of silver nanoparticles on secondary metabolite composition and toxicity in anise (Pimpinella anisum L.) callus culture

Ulusoy E, Bozkurt A, Durmaz S, Servi H, Vardar F, Erisen S

BMC Plant Biol

04-May-2024

PMCID:	PMC11069286
doi:	10.1186/s12870-024-05067-8
PMID:	38702604

Strategies, Achievements, and Potential Challenges of Plant and Microbial Chassis in the Biosynthesis of Plant Secondary Metabolites

Han T, Miao G

Molecules

02-May-2024

PMCID:	PMC11085123
doi:	10.3390/molecules29092106
PMID:	38731602

Sandalwood Oils of Different Origins Are Active In Vitro against Madurella mycetomatis, the Major Fungal Pathogen Responsible for Eumycetoma

Abd Algaffar SO, Seegers S, Satyal P, Setzer WN, Schmidt TJ, Khalid SA

Molecules

18-Apr-2024

PMCID:	PMC11055130
doi:	10.3390/molecules29081846
PMID:	38675665

Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals

Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J

Pathogens

13-Apr-2024

PMCID:	PMC11054384
doi:	10.3390/pathogens13040320
PMID:	38668275

Effect of Salvia sclarea L. extract on growth performance, antioxidant capacity, and immune function in lambs

Ma X, Niu Y, Nan S, Zhang W

Front Vet Sci

10-Apr-2024

PMCID:	PMC11039921
doi:	10.3389/fvets.2024.1367843
PMID:	38659454

Overexpression of AtMYB2 Promotes Tolerance to Salt Stress and Accumulations of Tanshinones and Phenolic Acid in Salvia miltiorrhiza

Li T, Zhang S, Li Y, Zhang L, Song W, Chen C

Int J Mol Sci

08-Apr-2024

PMCID:	PMC11012609
doi:	10.3390/ijms25074111
PMID:	38612919

Inhibitory effect of natural compounds on quorum sensing system in Pseudomonas aeruginosa: a helpful promise for managing biofilm community

Shariati A, Noei M, Askarinia M, Khoshbayan A, Farahani A, Chegini Z

Front Pharmacol

02-Apr-2024

PMCID:	PMC11019022
doi:	10.3389/fphar.2024.1350391
PMID:	38628638

Chemometric Analysis Evidencing the Variability in the Composition of Essential Oils in 10 Salvia Species from Different Taxonomic Sections or Phylogenetic Clades

Tomou EM, Fraskou P, Dimakopoulou K, Dariotis E, Krigas N, Skaltsa H

Molecules

29-Mar-2024

PMCID:	PMC11013157
doi:	10.3390/molecules29071547
PMID:	38611827

Mechanism of action of microRNA166 on nitric oxide in alfalfa (Medicago sativa L.) under drought stress

Wei B, Wang Y, Ruan Q, Zhu X, Wang X, Wang T, Zhao Y, Wei X

BMC Genomics

28-Mar-2024

PMCID:	PMC10976769
doi:	10.1186/s12864-024-10095-7
PMID:	38549050

Bois noir management in vineyard: a review on effective and promising control strategies

Pierro R, Moussa A, Mori N, Marcone C, Quaglino F, Romanazzi G

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004249
doi:	10.3389/fpls.2024.1364241
PMID:	38601314

铁死亡在非小细胞肺癌中的作用及中药干预进展

GUO X, WANG T, XIA J, ZENG H, SHI W

Zhongguo Fei Ai Za Zhi

20-Mar-2024

PMCID:	PMC11002191
doi:	10.3779/j.issn.1009-3419.2024.101.06
PMID:	38590196

Phytotherapeutic Approaches in Canine Pediatrics

Quintavalla F

Vet Sci

20-Mar-2024

PMCID:	PMC10974738
doi:	10.3390/vetsci11030133
PMID:	38535867

Labdane-Type Diterpenoids from Streptomyces griseorubens and Their Antimicrobial and Cytotoxic Activities

Heo CS, Kang JS, Yang JW, Lee MA, Lee HS, Shin HJ

Int J Mol Sci

14-Mar-2024

PMCID:	PMC10970165
doi:	10.3390/ijms25063311
PMID:	38542285

A review on bio-based polymer polylactic acid potential on sustainable food packaging

Rajendran DS, Venkataraman S, Jha SK, Chakrabarty D, Kumar VV

Food Sci Biotechnol

12-Mar-2024

PMCID:	PMC11091039
doi:	10.1007/s10068-024-01543-x
PMID:	38752115

Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy)

Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F

J Ethnobiol Ethnomed

12-Mar-2024

PMCID:	PMC10936038
doi:	10.1186/s13002-024-00664-1
PMID:	38475780

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 / Benzoyl derivatives
Benzaldehyde	240	Click to see	106.12	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl tiglate	250096	Click to see CC=C(C)C(=O)OCC1=CC=CC=C1	190.24	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> 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/10.1080/10412905.1997.9699459
> Benzenoids / Naphthalenes
1-Hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one	102011357	Click to see	296.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6 https://doi.org/10.1016/S0031-9422(96)00709-1
Microstegiol	403772	Click to see	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6 https://doi.org/10.1016/S0031-9422(96)00709-1
> Benzenoids / Naphthalenes / Naphthoquinones
1-Ketoaethiopinone	11983338	Click to see	310.40	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
Acetylsalvipisone	102066549	Click to see	354.40	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
Aethiopinone	157301	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
Salvipisone	821448	Click to see	312.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6 https://doi.org/10.1016/S0031-9422(96)00709-1
Sclareapinone	10381845	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCC(=O)C(C)(C)O	328.40	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
> Benzenoids / Phenol ethers / Anisoles
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1997.9699459
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Geranyl formate	5282109	Click to see	182.26	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Neryl acetate	1549025	Click to see	196.29	unknown	https://doi.org/10.1021/JF020422N https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1080/10412905.1997.9699459
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
2-Hexen-1-OL	5318042	Click to see CCCC=CCO	100.16	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	73114	Click to see	308.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520730/ https://doi.org/10.1016/S0031-9422(00)90474-6 https://doi.org/10.1021/JF020422N https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484996/ https://doi.org/10.1016/0031-9422(90)83025-V https://doi.org/10.1076/PHBI.35.3.218.13295
(1R,4aS,10aR)-6-hydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carbaldehyde	14827273	Click to see	314.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
1-Naphthalenepropanol, alpha-ethenyldecahydro-alpha,5,5,8a-tetramethyl-2-methylene-	238792	Click to see	290.50	unknown	https://doi.org/10.1007/BF00563915 https://doi.org/10.1016/S0031-9422(00)90474-6
13-Epimanool	10891602	Click to see	290.50	unknown	https://doi.org/10.1007/BF00563915
13-Episclareol	56842011	Click to see	308.50	unknown	https://doi.org/10.1016/S0145-2126(98)00134-9 https://doi.org/10.1016/S0031-9422(00)90474-6 https://doi.org/10.1021/JF020422N https://doi.org/10.1016/0031-9422(90)83025-V https://doi.org/10.1076/PHBI.35.3.218.13295
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	5316143	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
7-Ketoroyleanone	2751800	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2=O)(C)C)C)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
Abieta-9(11),8(14),12-trien-12-ol	521330	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
alpha-Ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-1-naphthalenepropanol	521332	Click to see	308.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520730/ https://doi.org/10.1016/S0031-9422(00)90474-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484996/
Cryptojaponol	11724205	Click to see	330.50	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1 https://doi.org/10.1016/S0031-9422(00)90474-6
Manool	3034394	Click to see	290.50	unknown	https://doi.org/10.1007/BF00563915 https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1016/S0031-9422(00)90474-6
Salvinolone	11723174	Click to see	314.40	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
Sclareol	163263	Click to see	308.50	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids
(3R,3aR,6aR,7R,9aR,9bR)-3,6,9-trimethyl-7-(2-methylprop-1-enyl)-2,3,3a,4,6a,7,9a,9b-octahydro-1H-phenalene	163011414	Click to see CC1CCC2C3C1CC=C(C3C(C=C2C)C=C(C)C)C	270.50	unknown	https://doi.org/10.1021/NP2004177
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
6-(hydroxymethyl)-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione;1,6,6-trimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione	318796	Click to see	604.70	unknown	https://doi.org/10.1007/BF00563915
Hydroxytanshinone IIA	5318349	Click to see	310.30	unknown	https://doi.org/10.1007/BF00563915
Methuyl tanshinonate	624381	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC	338.40	unknown	https://doi.org/10.1007/BF00563915
Tanshinone I	114917	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C	276.30	unknown	https://doi.org/10.1007/BF00563915
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Lavandulol	5464156	Click to see	154.25	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
(+)-Linalyl acetate	6999980	Click to see	196.29	unknown	https://doi.org/10.1055/S-0028-1097956
1,6-Octadiene-1,3-diol, 3,7-dimethyl-	537782	Click to see	170.25	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Citral	638011	Click to see	152.23	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Hydroxyl citronellal	129702535	Click to see	170.25	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Lavandulol, (+/-)-	94060	Click to see CC(=CCC(CO)C(=C)C)C	154.25	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1021/JF020422N https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
Linalool formate	61040	Click to see	182.26	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Linalool, (+)-	67179	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1097956
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.1021/JF020422N https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Neral	643779	Click to see	152.23	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5-Isopropyl-2-methylphenyl)methanol	19892675	Click to see CC1=C(C=C(C=C1)C(C)C)CO	164.24	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
2,6-Dimethyl-3-propan-2-ylphenol	21908410	Click to see CC1=C(C(=C(C=C1)C(C)C)C)O	164.24	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1997.9699459
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1097956
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
(+)-alpha-Thujone	12304612	Click to see	152.23	unknown	https://doi.org/10.1055/S-0028-1097956
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-0028-1097956
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
alpha Thujene	6451618	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1097956
alpha-Thujene	17868	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1097956 https://doi.org/10.1076/PHBI.35.3.218.13295
Bornyl acetate, (-)-	93009	Click to see	196.29	unknown	https://doi.org/10.1055/S-0028-1097956
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
D-Borneol	6552009	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1097956
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459
Thujone	261491	Click to see	152.23	unknown	https://doi.org/10.1055/S-0028-1097956
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1021/JF020422N https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,5E,9R)-6,10,10-trimethylbicyclo[7.2.0]undec-5-ene-2-carbaldehyde	162850578	Click to see	220.35	unknown	https://doi.org/10.1002/HLCA.19830660734
(1R,2S,5E,9R)-6,10,10-trimethylbicyclo[7.2.0]undec-5-ene-2-carbaldehyde	162850579	Click to see CC1=CCCC(C2CC(C2CC1)(C)C)C=O	220.35	unknown	https://doi.org/10.1002/HLCA.19830660734
(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/10.1076/PHBI.35.3.218.13295
(1R,3aR,6R,6aS,10aS)-1,4,8-trimethyl-6-(2-methylprop-1-enyl)-1,2,3,3a,6,6a,9,10-octahydrocyclopenta[j]naphthalene	162896052	Click to see CC1CCC2C13CCC(=CC3C(C=C2C)C=C(C)C)C	270.50	unknown	https://doi.org/10.1021/NP2004177
(1R,4S,6R,10R)-1,4,12,12-tetramethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	163021203	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
(3R,6E)-Nerolidol	11241545	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
1-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-4-methylbenzene	163186427	Click to see	270.50	unknown	https://doi.org/10.1021/NP2004177
1-[(2S)-6,10-dimethylundeca-5,9-dien-2-yl]-4-methylbenzene	162899146	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CCC=C(C)C	270.50	unknown	https://doi.org/10.1021/NP2004177
1,4,12,12-Tetramethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	163021202	Click to see CC1(CC2C1(CCC3(C(O3)CCC2=C)C)C)C	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
1,5-Epoxy-salvial(4)14-ene	91750031	Click to see	220.35	unknown	https://doi.org/10.1002/HLCA.19830660734
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-	8888	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene	324224	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1016/S0031-9422(00)90474-6
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
alpha-Ylangene	101607926	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1076/PHBI.35.3.218.13295
beta Farnesene	15228937	Click to see	206.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
beta-Cubebene	93081	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1016/S0031-9422(00)90474-6
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1016/S0031-9422(00)90474-6
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295 https://doi.org/10.1016/S0031-9422(00)90474-6
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))-	91354	Click to see	204.35	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
beta-Spathulenol	522266	Click to see	220.35	unknown	https://doi.org/10.1002/PTR.3289 https://doi.org/10.1016/S0031-9422(00)90474-6
Isospathulenol	102303030	Click to see	220.35	unknown	https://doi.org/10.1002/HLCA.19830660734
Spathulenol	92231	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedrol	65575	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol	547972	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Elemol	92138	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2-[(2R,8aR)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]propan-2-ol	5315163	Click to see CC1CCC=C2C1(CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
10-epi-gamma-Eudesmol	6430754	Click to see	222.37	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
Beta-Eudesmol	91457	Click to see	222.37	unknown	https://doi.org/10.1021/JF020422N https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1076/PHBI.35.3.218.13295
> 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/10.1080/10412905.1997.9699459 https://doi.org/10.1021/JF020422N
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9699459 https://doi.org/10.1021/JF020422N
Salvial-4(14)-en-1-one	42608172	Click to see CC(C)C1CCC2(C1CC(=C)CCC2=O)C	220.35	unknown	https://doi.org/10.1002/HLCA.19830660734
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Tetrocarcin Q	139590583	Click to see	1357.50	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2S)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	101920648	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C	977.00	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
[(3aR,5R,5aS,6R,7R,8R,8aS,9aR)-6,7-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl] acetate	163032763	Click to see	324.40	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrenol	225688	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
Alpha-Amyrin	73170	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1 https://doi.org/10.1016/S0031-9422(00)90474-6
Oleanonic Acid	12313704	Click to see	454.70	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(17-acetyl-12-acetyloxy-3,8,14-trihydroxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl) acetate	85252331	Click to see	464.50	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
2-(6,16-diacetyloxy-4,8,10,14-tetramethyl-3,7-dioxo-2,4,5,6,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid	74191767	Click to see	570.70	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1 https://doi.org/10.1016/S0031-9422(00)90474-6
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(96)00709-1 https://doi.org/10.1016/S0031-9422(00)90474-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(S)-2-Amino-2-(cyclopent-3-en-1-yl)acetic acid	10964605	Click to see C1C=CCC1C(C(=O)O)N	141.17	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
1-Hexen-1-ol, 1-acetate	122966	Click to see	142.20	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Hexen-3-Ol	20928	Click to see	100.16	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexenal	10460	Click to see	98.14	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Hydroxycitronellal	7888	Click to see	172.26	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
trans-2-Hexenal	5281168	Click to see	98.14	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
4-Octen-3-one	84216	Click to see	126.20	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
Damascenone	5366074	Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C	190.28	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see	126.20	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
1-Methoxyhexane-3-thiol, (+-)-	3024273	Click to see	148.27	unknown	https://doi.org/10.1002/1522-2675(200205)85:5<1246::AID-HLCA1246>3.0.CO;2-O
> Organoheterocyclic compounds / Epoxides
Oxiranemethanol, 3-methyl-3-(4-methyl-3-pentenyl)-	530403	Click to see	170.25	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene	68316	Click to see	150.22	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(1R,3S)-5,9,10-trihydroxy-1,3-dimethyl-3,4-dihydro-1H-benzo[g]isochromene-6,7-dione	11109030	Click to see	290.27	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Organoheterocyclic compounds / Pyrans
(+-)-Nerol oxide	61275	Click to see	152.23	unknown	https://doi.org/10.1076/PHBI.35.3.218.13295
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	10602981	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> 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/S0031-9422(00)90474-6
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)90474-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see	284.26	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone	152430	Click to see	358.30	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone	10020367	Click to see	344.30	unknown	https://doi.org/10.1021/ACS.JNATPROD.7B00155
Ladanein	3084066	Click to see	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6
Salvigenin	161271	Click to see	328.30	unknown	https://doi.org/10.1016/S0031-9422(00)90474-6

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Salvia sclarea

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