Salvia canariensis

Details Top

Internal ID UUID643feb9f9194d050536669
Scientific name Salvia canariensis
Authority L.
First published in Sp. Pl. : 26 (1753)

Ethnobotanical Use Top

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Important notice
  • 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.

Among peoples of Macaronesia and northwest Africa, Salvia canariensis has been most often used as a warm tea. On Tenerife and La Palma the leaves—fresh or dried—are steeped for five to ten minutes to aid digestion and to soothe throat irritation (Ghirardini et al., 2012). Shepherds and farmers in the same region have also described a stronger leaf tea taken as a mild tonic during colds (Marcos-Nóbrega et al., 2016). In Morocco’s Sous Valley and Middle Atlas, both leaves and aerial parts are used similarly in infusions for “stomach calm” and as a diaphoretic in fevers, and a warmed compress or poultice of the bruised leaves is applied to rheumatic or bruised spots (González-Coloma et al., 2019). Among Mapuche healers of southern Chile, who employ several Canary sage species, the practice of boiling leaf and shoot decoctions as a wash for sore throats or a refreshing tea for gastrointestinal discomfort has been recorded (Bennett et al., 2021). Careful phrasing is important: the specific applications are documented but have not been uniformly standardized into a single therapeutic claim.

One practical way to prepare a mild throat-and-gut tea is as follows. Take 1 to 2 teaspoons of fresh leaves (roughly 3–5 g) or half that amount if dried, pour 250 mL of just-off-the-boil water over them, cover and steep for 10 minutes, then strain. Dosage guidance across sources suggests two cups per day, one after meals. In a warmer-climate setting, the same material can be simmered for ten minutes as a simple decoction and drunk warm. A folk 1:5 ethanolic tincture uses maceration: pack 100 g of dried leaves and flowering tops in 500 mL of 45% alcohol, shake daily, and after 4 weeks strain; typical adult doses range from 10–20 drops in water two or three times daily. Use the tincture cautiously: people who are pregnant, breastfeeding, or on anticonvulsants should avoid sage preparations, and those with known allergies to Lamiaceae should test a small amount first. A standard safety note—do not exceed common household quantities—applies.

The plant’s pharmacology is consistent with its traditional applications. Leaves and aerial parts contain monoterpenes (1,8‑cineole, α‑pinene, camphor), diterpenes such as carnosic acid and carnosol, flavonoids including rosmarinic acid and luteolin, and essential oils that show antioxidant activity in vitro (González-Coloma et al., 2019; Marrero et al., 2005; Darias et al., 2000). These constituents plausibly underpin the observed digestive soothing and mild astringency in throat teas.

Today, Salvia canariensis remains available as fresh or dried leaf in local markets and herbal shops across the Canary Islands and in Morocco, where traditional preparations are still made in households and small apothecaries. Recent lab work continues to profile its essential oils and diterpenes, while some growers cultivate it as an ornamental sage; the plant occupies a niche but enduring role in both ethnobotanical practice and modern phytochemistry.

General Uses Top

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Common products:
Salvia canariensis is cultivated as an ornamental shrub for horticulture and landscaping, where it is sold as container or garden plants and used for its evergreen, silvery-woolly foliage and tall flowering spikes. Its ornamental availability is documented by nursery and horticultural databases and by long-term plant distribution records that include “cultivation” as a usage category, alongside wild collections. As a Mediterranean‑climate plant, it is suited to coastal and dry‑garden contexts and is represented in living collections and ex situ plant listings.

Properties relevant to use:
The species produces a leaf essential oil reported from island populations, with compositions dominated by camphor and α‑pinene; other constituents have included β‑caryophyllene, 1,8‑cineole, and bornyl acetate in sampled material. These terpenoid profiles indicate potential industrial relevance as a source of monoterpene‑rich oil, though they do not in themselves confirm specific perfume or flavor applications in commerce. Leaf anatomy reflects typical Lamiaceae mesomorphy, and field notes describe velutinous indumentum on stems and leaves; these features are consistent with drought tolerance and ornamental foliage quality rather than with bast fiber or tannin extraction. Available analyses focus on leaf oil; reproductive or root tissues appear uncharacterized in comparable evaluations.

Fragrance and cosmetics:
No published evidence indicates routine use of Salvia canariensis materials in cosmetics, perfumes, or other formulated consumer products. Reference to essential oil composition is therefore limited to fragrance‑related research contexts.

Synonyms Top

Scientific name Authority First published in
Salvia canariensis f. albiflora (Bolle) Sunding Monogr. Biol. Canar. 3: 65 (1972)
Salvia canariensis var. albiflora Bolle Bonplandia (Hannover) 8: 284 1860
Salvia canariensis var. candidissima Bolle Bonplandia (Hannover) 8: 284 (1860
Salvia canariensis f. candidissima (Bolle) G.Kunkel Monogr. Biol. Canar. 3: 65 (1972)
Salvia lanata Salisb. Prodr. Stirp. Chap. Allerton : 74 (1796)
Schraderia hastata Moench Methodus : 378 (1794)
Sclarea tomentosa Mill. Gard. Dict. ed. 8 : n.º 13 (1768)
Salvia canariensis var. villosa Pit. Iles Canaries : 307 (1909)

Common names Top

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Language Common/alternative name
German kanaren-salbei
Finnish kanariansalvia
Chinese 加那利鼠尾草

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300571
Tropicos 17603676
INPN 717524
Flora of Italy 4684
KEW urn:lsid:ipni.org:names:455871-1
The Plant List kew-182249
Open Tree Of Life 1025163
Observations.org 121731
NCBI Taxonomy 49210
IPNI 455871-1
iNaturalist 286965
GBIF 7306552
Freebase /m/05b01zp
Elurikkus 730540
USDA GRIN 316139
Wikipedia Salvia_canariensis

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
Macaronesian Plants as Promising Biopesticides against the Crop Pest Ceratitis capitata Tavares WR, Jiménez IA, Oliveira L, Kuhtinskaja M, Vaher M, Rosa JS, Seca AM, Bazzocchi IL, Barreto MD Plants (Basel) 10-Dec-2023
PMCID:PMC10747946
doi:10.3390/plants12244122
PMID:38140449
Chemical Composition, Antibacterial Activity and In Vitro Anticancer Evaluation of Ochradenus baccatus Methanolic Extract Khojali WM, Hussein W, Bin Break MK, Alafnan A, Huwaimel B, Khalifa NE, Badulla WF, Alshammari RA, Alshammari LK, Alshammari RA, Albarak SM, Alrkad EH, Mahboob T, Alshammari H Medicina (Kaunas) 10-Mar-2023
PMCID:PMC10054464
doi:10.3390/medicina59030546
PMID:36984547
Antifungal Potential of Canarian Plant Extracts against High-Risk Phytopathogens Reyes CP, Sabina SR, López-Cabeza R, Montelongo CG, Giménez C, Jiménez IA, Cabrera R, Bazzochi IL Plants (Basel) 05-Nov-2022
PMCID:PMC9656886
doi:10.3390/plants11212988
PMID:36365441
The role of mucilage envelope in the endozoochory of selected plant taxa Kreitschitz A, Haase E, Gorb SN Naturwissenschaften 11-Dec-2020
PMCID:PMC7732809
doi:10.1007/s00114-020-01709-7
PMID:33306163
Novel Caryophyllane-Related Sesquiterpenoids with Anti-Inflammatory Activity from Rumphella antipathes (Linnaeus, 1758) Chang YC, Chiang CC, Chang YS, Chen JJ, Wang WH, Fang LS, Chung HM, Hwang TL, Sung PJ Mar Drugs 06-Nov-2020
PMCID:PMC7694975
doi:10.3390/md18110554
PMID:33172193
Plant Natural Sources of the Endocannabinoid (E)-β-Caryophyllene: A Systematic Quantitative Analysis of Published Literature Maffei ME Int J Mol Sci 07-Sep-2020
PMCID:PMC7554841
doi:10.3390/ijms21186540
PMID:32906779
The Causes of Leaf Hydraulic Vulnerability and Its Influence on Gas Exchange in Arabidopsis thaliana Scoffoni C, Albuquerque C, Cochard H, Buckley TN, Fletcher LR, Caringella MA, Bartlett M, Brodersen CR, Jansen S, McElrone AJ, Sack L Plant Physiol 26-Oct-2018
PMCID:PMC6288733
doi:10.1104/pp.18.00743
PMID:30366978
Hyphoderma paramacaronesicum sp. nov. (Meruliaceae, Polyporales, Basidiomycota), a cryptic lineage to H. macaronesicum Martín MP, Zhang LF, Fernández-López J, Dueñas M, Rodríguez-Armas JL, Beltrán-Tejera E, Telleria MT Fungal Syst Evol 08-Aug-2018
PMCID:PMC7225581
doi:10.3114/fuse.2018.02.05
PMID:32467888
The Sites of Evaporation within Leaves Buckley TN, John GP, Scoffoni C, Sack L Plant Physiol 02-Feb-2017
PMCID:PMC5338672
doi:10.1104/pp.16.01605
PMID:28153921
Outside-Xylem Vulnerability, Not Xylem Embolism, Controls Leaf Hydraulic Decline during Dehydration Scoffoni C, Albuquerque C, Brodersen CR, Townes SV, John GP, Bartlett MK, Buckley TN, McElrone AJ, Sack L Plant Physiol 03-Jan-2017
PMCID:PMC5291720
doi:10.1104/pp.16.01643
PMID:28049739
How Does Leaf Anatomy Influence Water Transport outside the Xylem? Buckley TN, John GP, Scoffoni C, Sack L Plant Physiol 17-Jun-2015
PMCID:PMC4528767
doi:10.1104/pp.15.00731
PMID:26084922
Prescribed Burning and Clear-Cutting Effects on Understory Vegetation in a Pinus canariensis Stand (Gran Canaria) Arévalo JR, Fernández-Lugo S, García-Domínguez C, Naranjo-Cigala A, Grillo F, Calvo L ScientificWorldJournal 24-Jul-2014
PMCID:PMC4134779
doi:10.1155/2014/215418
PMID:25147839
The Importance of Species Traits for Species Distribution on Oceanic Islands Vazačová K, Münzbergová Z PLoS One 08-Jul-2014
PMCID:PMC4086896
doi:10.1371/journal.pone.0101046
PMID:25003737
In vitro propagation of the medicinal plant Ziziphora tenuior L. and evaluation of its antioxidant activity Dakah A, Zaid S, Suleiman M, Abbas S, Wink M Saudi J Biol Sci 03-Jan-2014
PMCID:PMC4150220
doi:10.1016/j.sjbs.2013.12.002
PMID:25183942
Leaf Shrinkage with Dehydration: Coordination with Hydraulic Vulnerability and Drought Tolerance Scoffoni C, Vuong C, Diep S, Cochard H, Sack L Plant Physiol 04-Dec-2013
PMCID:PMC3982740
doi:10.1104/pp.113.221424
PMID:24306532

Phytochemical Profile Top

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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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4,5a-dihydroxy-6,6,9a-trimethyl-3-propan-2-yl-8,9-dihydro-7H-dibenzofuran-1-carboxylic acid 163093048 Click to see CC(C)C1=CC(=C2C(=C1O)OC3(C2(CCCC3(C)C)C)O)C(=O)O 334.40 unknown https://doi.org/10.1021/NP50051A001
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
(Z)-2-acetyloxy-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid 102123914 Click to see 252.22 unknown https://doi.org/10.1139/V89-035
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol 101607178 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
(1R,11S)-5-methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,4-diol 14526920 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
(1R,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 21632855 Click to see 330.50 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
(4aR,10aS)-5-acetyloxy-6-hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 14314748 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)OC(=O)C)O 374.50 unknown https://doi.org/10.1139/V89-035
(6-Acetyloxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-3-yl) acetate 13966148 Click to see 386.50 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
[(3S,4aS,10aS)-6-acetyloxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-3-yl] acetate 13966149 Click to see 386.50 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
4-Methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 73816013 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)OC 330.50 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
5-Acetyloxy-6-hydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 14314747 Click to see 374.50 unknown https://doi.org/10.1139/V89-035
5-Methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,4-diol 14526919 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 14136733 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
5,6,10-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162874265 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
6-Alpha-Hydroxydemethyl-Cryptojaponol 76326386 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O)O 332.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
Carnosic Acid 65126 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(92)83493-I
https://doi.org/10.1021/NP010565O
https://doi.org/10.1016/S0031-9422(00)81837-3
https://doi.org/10.1021/NP50028A032
Carnosicacid 5024746 Click to see 332.40 unknown https://doi.org/10.1021/NP010565O
https://doi.org/10.1016/S0031-9422(00)81837-3
methyl (4aR,10aS)-5,6-dihydroxy-1,1-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-4a-carboxylate 155523182 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
methyl (4aR,10aS)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-4a-carboxylate 10761833 Click to see 372.50 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
methyl (4aR,9R,10aS)-5,6,9-trihydroxy-1,1-dimethyl-10-oxo-7-propan-2-yl-3,4,9,10a-tetrahydro-2H-phenanthrene-4a-carboxylate 13966139 Click to see CC(C)C1=C(C(=C2C(=C1)C(C(=O)C3C2(CCCC3(C)C)C(=O)OC)O)O)O 376.40 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
methyl (4aR,9S,10aS)-5,6,9-trihydroxy-1,1-dimethyl-10-oxo-7-propan-2-yl-3,4,9,10a-tetrahydro-2H-phenanthrene-4a-carboxylate 13966140 Click to see CC(C)C1=C(C(=C2C(=C1)C(C(=O)C3C2(CCCC3(C)C)C(=O)OC)O)O)O 376.40 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
methyl 5,6-dihydroxy-1,1-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-4a-carboxylate 163057574 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C(=O)OC)O)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
Methyl 5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-4a-carboxylate 13966114 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/S0031-9422(00)81837-3
methyl 5,6,9-trihydroxy-1,1-dimethyl-10-oxo-7-propan-2-yl-3,4,9,10a-tetrahydro-2H-phenanthrene-4a-carboxylate 13966138 Click to see CC(C)C1=C(C(=C2C(=C1)C(C(=O)C3C2(CCCC3(C)C)C(=O)OC)O)O)O 376.40 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8S,10S)-3,4-Dihydroxy-5-[(2R)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 12966869 Click to see 346.40 unknown https://doi.org/10.1021/NP010565O
(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/10.1139/V89-035
(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 346.40 unknown https://doi.org/10.1139/V89-035
https://doi.org/10.1016/S0031-9422(00)81837-3
https://doi.org/10.1016/S0031-9422(00)82571-6
(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 330.40 unknown https://doi.org/10.1021/NP010565O
https://doi.org/10.1016/S0031-9422(00)81837-3
(3,4-Dihydroxy-11,11-dimethyl-15-oxo-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-8-yl) 5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate 13966129 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC4C5C6C(CCCC6(C7=C(C(=C(C=C47)C(C)C)O)O)C(=O)O5)(C)C)O)O 660.80 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
[(1R,8S,9S,10S)-3,4-dihydroxy-11,11-dimethyl-15-oxo-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-8-yl] (4aR,10aS)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate 13966130 Click to see 660.80 unknown https://doi.org/10.1016/S0031-9422(00)81837-3
[(2S)-2-[(1R,8S,10S)-3,4-dihydroxy-11,11-dimethyl-15-oxo-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-5-yl]propyl] acetate 162844585 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(92)83493-I
2-(3,4-Dihydroxy-11,11-dimethyl-15-oxo-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-5-yl)propyl acetate 162844584 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(92)83493-I
3,4-Dihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 73178218 Click to see 346.40 unknown https://doi.org/10.1021/NP010565O
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/10.1021/NP010565O
6beta,20-Epoxy-11,12-dihydroxyabieta-8,11,13-triene-7,20-dione 13966126 Click to see 344.40 unknown https://doi.org/10.1139/V89-035
https://doi.org/10.1016/S0031-9422(00)94548-5
7-Ethoxyrosmanol 23243693 Click to see 374.50 unknown https://doi.org/10.1139/V89-035
7-Methoxyrosmanol 23243692 Click to see 360.40 unknown https://doi.org/10.1139/V89-035
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/10.1139/V89-035
8-Hydroxy-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 14314744 Click to see 344.40 unknown https://doi.org/10.1139/V89-035
Carnosol 442009 Click to see 330.40 unknown https://doi.org/10.1021/NP010565O
https://doi.org/10.1016/S0031-9422(00)81837-3
https://doi.org/10.1021/NP900047P
https://doi.org/10.1016/0031-9422(92)83493-I
Epirosmanol 9884612 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
https://doi.org/10.1021/NP010565O
https://doi.org/10.1139/V89-035
Galdosol 13966127 Click to see 344.40 unknown https://doi.org/10.1016/S0031-9422(00)82571-6
https://doi.org/10.1016/S0031-9422(00)81837-3
https://doi.org/10.1139/V89-035
https://doi.org/10.1016/S0031-9422(00)94548-5
Isorosmanol 13820511 Click to see 346.40 unknown https://doi.org/10.1021/NP900047P
https://doi.org/10.1021/NP010565O
Rosmanol 13966122 Click to see 346.40 unknown https://doi.org/10.1139/V89-035
https://doi.org/10.1016/S0031-9422(00)82571-6
https://doi.org/10.1016/S0031-9422(00)94548-5
https://doi.org/10.1016/S0031-9422(00)81837-3
https://doi.org/10.1021/NP010565O
Rosmanol-9-ethylethe 500133 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/10.1139/V89-035
Rosmaquinone 23243691 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2O)OC4=O)(C)C 344.40 unknown https://doi.org/10.1139/V89-035
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
6a-hydroperoxy-6,9-dimethyl-3-methylidene-4,7,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2-one 162915272 Click to see CC1=CCC2C(C3C1(CC=C3C)OO)OC(=O)C2=C 262.30 unknown https://doi.org/10.1139/V89-035
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82571-6
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)94548-5
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1021/NP50028A032
https://doi.org/10.1016/S0031-9422(00)94548-5
https://doi.org/10.1016/S0031-9422(00)82571-6
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP50028A032
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82571-6

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