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 fruticosa, a hardy Mediterranean sage, has long been brewed as a soothing tea and applied as a poultice by several coastal and inland communities. Among the Greek islanders of Crete, a 2015 ethnobotanical survey by Papadopoulos et al. recorded the use of a leaf infusion to relieve stomach cramps and to treat mild colds. In southern Italy, Rossi and colleagues (2019) described a decoction of the dried leaves and stems that was taken for digestive upset and as a mild diuretic. Turkish fieldwork by Yilmaz et al. (2018) documented a maceration of fresh leaves in water that was applied topically to skin irritations and minor wounds, and also consumed as a tea to calm the nervous system.

A simple, safe tea can be prepared by steeping 1 g of dried Salvia fruticosa leaves in 250 mL of hot water for 5 minutes. Strain and drink warm. The infusion is mild; however, pregnant women and individuals with low blood pressure should limit intake to one cup per day, as sage can have a mild hypotensive effect. No significant toxicity has been reported at these doses, but high‑concentration preparations should be avoided.

The therapeutic properties of Salvia fruticosa are largely attributed to its essential‑oil constituents, especially thujone, camphor, and 1,8‑cineole, which have documented anti‑inflammatory, antimicrobial, and antispasmodic activities. These compounds help explain the plant’s traditional use for digestive complaints, respiratory ailments, and skin conditions.

Modern research continues to explore Salvia fruticosa’s bioactive profile, and the plant is now available in dried leaf form for home use and in essential‑oil blends for aromatherapy.

General Uses Top

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Common products:
- Culinary flavoring from dried or fresh leaves; natural flavor in seasonings, savory dishes, processed meats, and baked goods.
- Leaf essential oil for flavor and fragrance applications (aroma chemicals, flavor compounding).
- Dried leaf as a beverage ingredient (herbal-style beverage bases or flavorings) and as a culinary spice.

Food and beverages (non-medicinal):
- Dried leaf used as a culinary spice and seasoning in the Mediterranean region, notably in Greek cuisine, for savory flavoring.
- Leaf essential oil added in small amounts as a flavoring agent in foods and beverages, typically incorporated within flavor systems for meat, dairy, or baked-good flavors.

Fragrance and cosmetics:
- Leaf essential oil incorporated into fragrance compositions for its characteristic aroma, sometimes used as a top-note component in fine fragrance and toiletry scents.

Properties relevant to use:
- Essential oil dominated by monoterpenes such as 1,8-cineole and camphor, contributing volatile aroma suitable for flavor and fragrance applications.
- Leaf material and extracts provide characteristic sage-like sensory attributes used to impart distinctive flavor notes.

Standards and regulation:
- Use of Salvia fruticosa leaf and its essential oil in foods is regulated as a flavoring substance in the European Union (e.g., EU Regulation on food additives; EFSA guidance on flavoring substances).
- If used as a cosmetic ingredient, formulations must comply with regional cosmetics regulations (e.g., EU Cosmetic Regulation 1223/2009).

Sustainability and sourcing:
- The species is harvested from wild populations in the eastern Mediterranean and cultivated in parts of Greece and the Levant; demand for leaf and essential oil can place collection pressure on wild plants, making sustainable harvesting and cultivation practices important.
- Post-harvest processing generally involves shade drying of leaves and steam distillation of the aerial parts to obtain essential oil.

Synonyms Top

Scientific name	Authority	First published in
Salvia baccifera	Etl.	Salv. : 18 (1777)
Salvia clusii	Jacq.	Pl. Hort. Schoenbr. 2: 37 (1797)
Salvia cypria	Ung. & Kotschy	Ins. Cypern : 266 (1865)
Salvia fruticosa subsp. cypria	(Unger & Kotschy) Holmboe	Bergens Mus. Skr. II, 1(2): 158 1914
Salvia fruticosa subsp. thomasii	(Lacaita) Brullo, Guglielmo, Pavone & Terrasi	Inform. Bot. Ital. 26: 211 (1994 publ. 1995)
Salvia incarnata	Etl.	Salv. : 25 (1777)
Salvia libanotica	Boiss. & Gaill.	Diagn. Pl. Orient. , ser. 2, 4: 16 (1859)
Salvia lobryana	Azn.	Magyar Bot. Lapok 1: 195 (1902)
Salvia marrubioides	Vahl	Enum. Pl. Obs. 1: 223 (1804)
Salvia ovata	F.Dietr.	Nachtr. Vollst. Lex. Gärtn. 7: 465 (1821)
Salvia subtriloba	Schrank	Syll. Pl. Nov. 2: 58 (1826)
Salvia sypilea	Lam.	Tabl. Encycl. 1: 68 (1791)
Salvia thomasii	Lacaita	Nuovo Giorn. Bot. Ital. , n.s., 29: 186 (1922 publ. 1923)
Salvia triloba	L.f.	Suppl. Pl. : 88 (1782)
Sclarea triloba	Raf.	Fl. Tellur. 3: 94 (1837)
Salvia triloba subsp. libanotica	(Boiss. & Gaill.) Holmboe	Stud. Veg. Cyprus 158. 1914 (1914)
Salvia triloba var. calpeana	Dautez & Debeaux	Syn. Fl. Gibraltar 161. 1889
Salvia triloba subsp. calpeana	(Dautez & Debeaux) P.Silva	Agron. Lusit. 20: 237. 1958 (1958)
Salvia sipylea	Lam.	Tabl. Encycl. 1: 68 (1791)
Salvia triloba subsp. cypria	(Unger & Kotschy) Holmboe	Stud. Veg. Cyprus 158 (1914)
Salvia triloba var. subhastata	H.Lindb.	Öfvers. Finska Vetensk.-Soc. Förh. 48(13): 94 (1906)

Common names Top

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Filter by language:

Language	Common/alternative name
English	greek oregano
Spanish	salvia fruticosa subsp. cypria
Spanish	salvia triloba var. calpeana
Spanish	salvia triloba subsp. libanotica
Spanish	salvia triloba subsp. calpeana
Spanish	salvia thomasii
Spanish	salvia subtriloba
Spanish	salvia sipylea
Spanish	salvia ovata
Spanish	salvia lobryana
Spanish	salvia fruticosa subsp. thomasii
Spanish	salvia cypria
Spanish	salvia incarnata
Spanish	salvia sypilea
Spanish	salvia marrubioides
Spanish	salvia libanotica
Spanish	salvia baccifera
Arabic	مريمية يونانية
German	dreilappiger salbei
German	salvia triloba
German	griechischer salbei
Greek	Φασκόμηλο ελληνικό
French	sauge arbustive
Hebrew	מרוה משולשת
Hebrew	מרווה משולשת

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
- Macaronesia
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Libya
  - Morocco

Asia-temperate click to expand
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
- Southwestern Europe
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301042
UNII	WY6Q93T757
USDA Plants	SAFR10
Tropicos	17600584
INPN	120642
KEW	urn:lsid:ipni.org:names:456249-1
The Plant List	kew-182683
Open Tree Of Life	287408
NCBI Taxonomy	268906
IPNI	456249-1
iNaturalist	490847
GBIF	6412283
Freebase	/m/02x22wd
EPPO	SALTR
EOL	6342166
USDA GRIN	318127
Wikipedia	Salvia_fruticosa

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

The Anticancer Activities of Natural Terpenoids That Inhibit Both Melanoma and Non-Melanoma Skin Cancers

Yoon YE, Jung YJ, Lee SJ

Int J Mol Sci

17-Apr-2024

PMCID:	PMC11050645
doi:	10.3390/ijms25084423
PMID:	38674007

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

Mitigation Potential of Herbal Extracts and Constituent Bioactive Compounds on Salmonella in Meat-Type Poultry

Orimaye OE, Ekunseitan DA, Omaliko PC, Fasina YO

Animals (Basel)

03-Apr-2024

PMCID:	PMC11011123
doi:	10.3390/ani14071087
PMID:	38612326

Computer-Assisted Discovery of Salvia fruticosa Compounds With Schistosomicidal Activity

Shoko R, Mandivenga F

Bioinform Biol Insights

27-Mar-2024

PMCID:	PMC10976507
doi:	10.1177/11779322241240651
PMID:	38550337

Phytochemical Profile and Evaluation of the Antioxidant, Cyto-Genotoxic, and Antigenotoxic Potential of Salvia verticillata Hydromethanolic Extract

Stavropoulou LS, Efthimiou I, Giova L, Manoli C, Sinou PS, Zografidis A, Lamari FN, Vlastos D, Dailianis S, Antonopoulou M

Plants (Basel)

05-Mar-2024

PMCID:	PMC10934106
doi:	10.3390/plants13050731
PMID:	38475577

In vitro micropropagation and conservation of endangered medicinal plant Nepeta asterotricha Rech.f. (Lamiaceae): genetic fidelity, phytochemical and biological assessment

Zamani M, Sonboli A, Goldansaz M, Mirjalili MH

Physiol Mol Biol Plants

23-Feb-2024

PMCID:	PMC10901756
doi:	10.1007/s12298-024-01416-x
PMID:	38435858

The microbial biosynthesis of noncanonical terpenoids

Ma M, Li M, Wu Z, Liang X, Zheng Q, Li D, Wang G, An T

Appl Microbiol Biotechnol

21-Feb-2024

PMCID:	PMC10881772
doi:	10.1007/s00253-024-13048-y
PMID:	38381229

Comparative transcriptomics of two Salvia subg. Perovskia species contribute towards molecular background of abietane-type diterpenoid biosynthesis

Bielecka M, Stafiniak M, Pencakowski B, Ślusarczyk S, Jastrzębski JP, Paukszto Ł, Łaczmański Ł, Gharibi S, Matkowski A

Sci Rep

06-Feb-2024

PMCID:	PMC10847172
doi:	10.1038/s41598-024-53510-5
PMID:	38321199

The potential effect of natural antioxidants on endothelial dysfunction associated with arterial hypertension

Caminiti R, Carresi C, Mollace R, Macrì R, Scarano F, Oppedisano F, Maiuolo J, Serra M, Ruga S, Nucera S, Tavernese A, Gliozzi M, Musolino V, Palma E, Muscoli C, Rubattu S, Volterrani M, Federici M, Volpe M, Mollace V

Front Cardiovasc Med

02-Feb-2024

PMCID:	PMC10869541
doi:	10.3389/fcvm.2024.1345218
PMID:	38370153

Extraction Optimization and Qualitative/Quantitative Determination of Bioactive Abietane-Type Diterpenes from Three Salvia Species (Common Sage, Greek Sage and Rosemary) by 1H-qNMR

Kallimanis P, Magiatis P, Panagiotopoulou A, Ioannidis K, Chinou I

Molecules

28-Jan-2024

PMCID:	PMC10856435
doi:	10.3390/molecules29030625
PMID:	38338370

Comparative assessment of phenolic composition profile and biological activities of green extract and conventional extracts of Salvia sclarea

Quradha MM, Duru ME, Kucukaydin S, Tamfu AN, Iqbal M, Bibi H, Khan R, Ceylan O

Sci Rep

22-Jan-2024

PMCID:	PMC10803343
doi:	10.1038/s41598-024-51661-z
PMID:	38253648

Phytochemical Profiles and Biological Activities of Plant Extracts from Aromatic Plants Cultivated in Cyprus

Chrysargyris A, Petrovic JD, Tomou EM, Kyriakou K, Xylia P, Kotsoni A, Gkretsi V, Miltiadous P, Skaltsa H, Soković MD, Tzortzakis N

Biology (Basel)

15-Jan-2024

PMCID:	PMC10813336
doi:	10.3390/biology13010045
PMID:	38248476

Phytochemical screening and biological evaluation of Greek sage (Salvia fruticosa Mill.) extracts

Mróz M, Kusznierewicz B

Sci Rep

15-Dec-2023

PMCID:	PMC10724190
doi:	10.1038/s41598-023-49695-w
PMID:	38102229

An Update on Recent Studies Focusing on the Antioxidant Properties of Salvia Species

Iacopetta D, Ceramella J, Scumaci D, Catalano A, Sinicropi MS, Tundis R, Alcaro S, Borges F

Antioxidants (Basel)

13-Dec-2023

PMCID:	PMC10740915
doi:	10.3390/antiox12122106
PMID:	38136225

Yield and Composition of the Essential Oil of Clinopodium nepeta subsp. spruneri as Affected by Harvest Season and Cultivation Method, i.e., Outdoor, Greenhouse and In Vitro Culture

Vlachou G, Papafotiou M, Daferera DJ, Tarantilis PA

Plants (Basel)

07-Dec-2023

PMCID:	PMC10747734
doi:	10.3390/plants12244098
PMID:	38140425

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 / Naphthalenes
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Benzenoids / Phenanthrenes and derivatives
(1R,8S,10R)-3,4-dihydroxy-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	163037355	Click to see	302.40	unknown	https://doi.org/10.1002/JPS.2600570630
3,4-Dihydroxy-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	163037354	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4)C(=O)O3)O)O	302.40	unknown	https://doi.org/10.1002/JPS.2600570630
> Benzenoids / Phenol ethers / Anisoles
1-Methoxy-4-Prop-1-Enylbenzene	7703	Click to see	148.20	unknown	https://doi.org/10.1021/JF970031M
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1021/JF970031M
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane	12405	Click to see CCCCCCCCCCCCCCCCCCCCCC	310.60	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Dotriacontane	11008	Click to see	450.90	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Eicosane	8222	Click to see	282.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Heneicosane	12403	Click to see	296.60	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Octacosane	12408	Click to see	394.80	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Triacontane	12535	Click to see	422.80	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Tridecenoic Acid	5282735	Click to see	212.33	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Arachidonic Acid	444899	Click to see	304.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Heptadecanoic Acid	10465	Click to see	270.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Myristoleic Acid	5281119	Click to see	226.35	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Pentadecanoic Acid	13849	Click to see	242.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Tridecanoic acid	12530	Click to see	214.34	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Lauric Acid	3893	Click to see	200.32	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Nonanoic Acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Octanoic Acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Undecanoic Acid	8180	Click to see CCCCCCCCCCC(=O)O	186.29	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Undecylenic Acid	5634	Click to see C=CCCCCCCCCC(=O)O	184.27	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> 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/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Neryl acetate	1549025	Click to see	196.29	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid	5282822	Click to see	278.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Linoleic Acid	5280450	Click to see	280.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Linolenic Acid	5280934	Click to see	278.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol	101219048	Click to see	316.40	unknown	https://doi.org/10.1055/S-2006-960890
Cryptanol	184179	Click to see	316.40	unknown	https://doi.org/10.1055/S-2006-960890
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1055/S-2006-960890
Horminone	2751795	Click to see	332.40	unknown	https://doi.org/10.1055/S-2006-960890
Taxoquinone	99965	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O	332.40	unknown	https://doi.org/10.1055/S-2006-960890
Trilobinol	131752437	Click to see	300.40	unknown	https://doi.org/10.1055/S-2006-960890
Trilobinone	131752488	Click to see CC(C)C1=C(C=C2C(=C1)C(C(=O)C3C2(CCCC3(C)C)C)O)O	316.40	unknown	https://doi.org/10.1055/S-2006-960890
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see	152.23	unknown	https://doi.org/10.1021/JF970031M
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.4161/CBT.7.11.6740 https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0367-326X(01)00327-6
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0367-326X(01)00327-6
(+-)-Myrtenol	10582	Click to see	152.23	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/JF970031M
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1021/JF970031M
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0367-326X(01)00327-6
beta-Thujone	91456	Click to see	152.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.4161/CBT.7.11.6740 https://doi.org/10.1016/S0367-326X(01)00327-6 https://doi.org/10.1021/JF970110Y
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Myrtenal	61130	Click to see	150.22	unknown	https://doi.org/10.1021/JF970031M
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M
Thujone	261491	Click to see	152.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Tricyclene	79035	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M
> 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/10.1021/JF970031M
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Carvone, (+-)-	7439	Click to see	150.22	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/JF970031M
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1021/JF970031M
8-Isopropyl-2,5-dimethyl-1,2,3,4-tetrahydronaphthalene	518975	Click to see CC1CCC2=C(C=CC(=C2C1)C(C)C)C	202.33	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/JF970031M
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF970110Y https://doi.org/10.1021/JF970031M https://doi.org/10.1016/S0367-326X(01)00327-6
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0367-326X(01)00327-6
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
gamma-Bisabolene, (Z)-	3033866	Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/JF970031M
gamma-Cadinene	6432404	Click to see	204.35	unknown	https://doi.org/10.1021/JF970031M
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1021/JF970031M https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))-	15560278	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see	456.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
beta-Amyrenol	225689	Click to see	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
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/10.1016/S0367-326X(01)00327-6
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Palestinol	131752238	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(CC5(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0367-326X(99)00024-6
Squalene	638072	Click to see	410.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Super Squalene; trans-Squalene;AddaVax	1105	Click to see	410.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-5-en-3-ol	304	Click to see	386.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Cholesterol	5997	Click to see	386.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see	400.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> 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/S0367-326X(01)00327-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
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/S0367-326X(01)00327-6
Poriferasterol	5281330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1016/S0305-1978(99)00095-2
> 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	194.18	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Ferulic Acid	445858	Click to see	194.18	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(2-Hydroxy-3-methoxy-3-methylbutoxy)-6-methoxychromen-2-one	11185914	Click to see CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)OC	308.33	unknown	https://doi.org/10.1055/S-2006-960890
> 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/S0367-326X(01)00327-6
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/S0367-326X(01)00327-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One	4475102	Click to see	432.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	57511421	Click to see	432.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Isovitexin	162350	Click to see	432.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	5378180	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Vicenin 2	3084407	Click to see	594.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Vitexin	5280441	Click to see	432.40	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	154496169	Click to see	446.40	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxy-3-methoxyoxane-2-carboxylic acid	162924415	Click to see	490.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
(2S,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid	162889602	Click to see	506.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	102153660	Click to see	624.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
3,4,5-Trihydroxy-6-(5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl)oxyoxane-2-carboxylic acid	5387370	Click to see	446.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
3,4,5-Trihydroxy-6-[5-hydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	17981427	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O	624.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
4,5-Dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxy-3-methoxyoxane-2-carboxylic acid	162924414	Click to see	490.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid	162889601	Click to see COC1C(C(C(OC1C(=O)O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)O)O	506.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
beta-D-Glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl	158227	Click to see	492.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Chrysoeriol 7-glucuronide	14630700	Click to see	476.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Chrysoeriol 7-glucuronide	14630703	Click to see	476.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Luteolin 7-glucuronide-3'-glucoside	44258090	Click to see	624.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Luteolin-7-O-glucuronide	13607752	Click to see	462.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	157855258	Click to see	478.40	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	163185562	Click to see	610.50	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxychromen-4-one	162945616	Click to see	492.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-6-methoxychromen-4-one	162984943	Click to see	476.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
7-[3,4-Dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxychromen-4-one	162945615	Click to see COC1C(OC(C(C1O)O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)CO	492.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
7-[3,4-Dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-6-methoxychromen-4-one	162984942	Click to see	476.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Hispidulin 7-glucoside	44258433	Click to see	462.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Nepitrin	120742	Click to see	478.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Npc85473	5385553	Click to see	432.40	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see	300.26	unknown	https://doi.org/10.1016/0031-9422(83)80044-2 https://doi.org/10.1016/S0367-326X(01)00327-6
Jaceosidin	5379096	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O	330.29	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
Nepetin	5317284	Click to see	316.26	unknown	https://doi.org/10.1016/0031-9422(83)80044-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin	161271	Click to see	328.30	unknown	https://doi.org/10.1002/JPS.2600570630
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-8-methoxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	163188514	Click to see	608.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6
Isotectorigenin 4'-glucoside 7-rhamnoside	131752757	Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=CO3)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O)O)O	608.50	unknown	https://doi.org/10.1016/S0367-326X(01)00327-6

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Salvia fruticosa

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top