Common products:
Salvia argentea is grown as an ornamental perennial, sold by nurseries for landscaping, rock gardens, and xeriscaping. Plants are marketed as container‑grown perennials, seed, or cuttings.

Industrial and craft applications:
Leaves and stems are steam‑distilled to obtain a camphoraceous essential oil. GC‑MS analyses consistently identify camphor, 1,8‑cineole, α‑pinene, and β‑pinene as major constituents. The oil’s composition aligns with that of Salvia species used in fragrance and flavor sectors, and it is cited in peer‑reviewed studies as a source of aroma chemicals for perfume and fragrance applications. The oil is usually stored in amber glass containers to protect it from light and oxidation.

Fragrance and cosmetics:
The essential oil is employed in niche fragrance blends and in scented soaps, lotions, and creams where its fresh herbal note serves as a top‑note. Its use is subject to IFRA standards and the EU Cosmetic Regulation (EC No 1223/2009), which limit camphor levels and require allergen labeling.

Properties relevant to use:
For horticulture, the plant’s silvery‑white, densely pubescent foliage and high drought tolerance support low‑maintenance landscaping. For the oil, the high camphor content (often >30 % of total oil) and substantial 1,8‑cineole provide a strong, lingering aroma suitable for perfumery. The oil’s stability in alcoholic solutions facilitates incorporation into fragrance bases.

Standards and regulation:
Ornamental material must comply with national plant‑health regulations (e.g., EU Plant Health Directive 2000/29/EC) and may be protected by plant‑variety rights or UPOV plant breeders’ rights where applicable. Essential‑oil use in cosmetics follows IFRA’s Code of Practice and the EU Cosmetic Regulation, which mandate safety assessments and labeling of camphor as a potential allergen. IFRA restricts camphor to ≤0.1 % in leave‑on cosmetic products, necessitating dilution in rinse‑off or fragrance formulations.

Sustainability and sourcing:
Salvia argentea is cultivated primarily in Mediterranean regions and requires minimal irrigation after establishment, reducing cultivation impact. Wild harvesting is limited; commercial supply comes from cultivated plots or small‑scale farms. Sustainable practices include seed propagation, low pesticide use, and optional organic certification for oil extraction (EU Regulation (EC) No 834/2007).

Synonyms Top

Scientific name	Authority	First published in
Salvia alpestris	Hausskn. ex Nyman	Consp. Fl. Eur. , Suppl. 2, 1: 248 (1889)
Salvia argentea subsp. patula	(Desf.) Maire	Bull. Soc. Hist. Nat. Afrique N. 15: 90. 1924 (1924)
Salvia atlantica	Pers.	Syn. Pl. 1: 29 (1805)
Salvia aurasiaca	Pomel	Nouv. Mat. Fl. Atl. : 306 (1874)
Salvia foetida	Lam.	Tabl. Encycl. 1: 69 (1791)
Salvia patula	Desf.	Fl. Atlant. 1: 25 (1798)
Salvia rhodopea	Velen.	Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl. 37: 388 (1892 publ. 1893)
Salvia saccata	Pourr. ex Willk. & Lange	Prodr. Fl. Hispan. 2: 424 (1868)
Salvia suaveolens	Pomel	Nouv. Mat. Fl. Atl. : 306 (1874)
Salvia tmolea	Boiss.	Diagn. Pl. Orient. 5: 9 (1844)
Sclarea argentea	Mill.	Gard. Dict. ed. 8 : n.º 15 (1768)
Salvia argentea var. mesatlantica	Maire	Mém. Soc. Sci. Nat. Maroc 21-22: 13 (1930)
Salvia argentea var. gussonei	Boiss. ex Nyman	Consp. Fl. Eur. : 569 (1881)
Salvia argentea var. pomelii	Maire	Bull. Soc. Hist. Nat. Afrique N. 15: 90 (1924)
Salvia argentea var. aurasiaca	(Pomel) Maire	Mém. Soc. Sci. Nat. Maroc 21-22: 13 (1930)
Salvia argentea var. fontanesiana	Maire	Cat. Pl. Maroc 3: 642 (1934)
Salvia argentea var. patula	(Desf.) Nyman	Consp. Fl. Eur. : 569 (1881)

Common names Top

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Filter by language:

Language	Common/alternative name
English	silver sage
Spanish	hierba del gargajoso
Spanish	maro portugues
Spanish	maro portugués
Arabic	قصعين فضي
Bulgarian	сребрист конски босилек
German	silber-salbei
German	silbersalbei
Kabyle	azaɣef
Dutch	zilversalie
Swedish	silversalvia
Turkish	gümüş ada çayı

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.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands
  - Turkey

Europe click to expand
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000300307
USDA Plants	SAAR25
Tropicos	17600285
Flora of Italy	4670
KEW	urn:lsid:ipni.org:names:455672-1
The Plant List	kew-182005
Missouri Botanical Garden	281419
Open Tree Of Life	448585
Observations.org	121715
NCBI Taxonomy	49208
NBN Atlas	NBNSYS0200003061
Nature Serve	2.159110
IPNI	455672-1
iNaturalist	168374
GBIF	2927065
Freebase	/m/05k5y_
EPPO	SALAR
EOL	485332
USDA GRIN	32907
Wikipedia	Salvia_argentea

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

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

New Polyesterified Ursane Derivatives from Leaves of Maesa membranacea and Their Cytotoxic Activity

Michalska K, Galanty A, Le TN, Malarz J, Vuong NQ, Pham VC, Stojakowska A

Molecules

20-Nov-2021

PMCID:	PMC8619920
doi:	10.3390/molecules26227013
PMID:	34834104

Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece

Musarella CM, Brullo S, del Galdo GG

Plants (Basel)

30-Nov-2020

PMCID:	PMC7760968
doi:	10.3390/plants9121678
PMID:	33266088

Structure and ion physiology of Brasenia schreberi glandular trichomes in vivo

Yang C, Zhang X, Zhang F, Wang X, Wang Q

PeerJ

10-Jul-2019

PMCID:	PMC6802583
doi:	10.7717/peerj.7288
PMID:	31637113

Seasonal home ranges and habitat selection of three elk (Cervus elaphus) herds in North Dakota

Amor JM, Newman R, Jensen WF, Rundquist BC, Walter WD, Boulanger JR

PLoS One

04-Feb-2019

PMCID:	PMC6361512
doi:	10.1371/journal.pone.0211650
PMID:	30716128

Salvia elegans, Salvia greggii and Salvia officinalis Decoctions: Antioxidant Activities and Inhibition of Carbohydrate and Lipid Metabolic Enzymes

Pereira OR, Catarino MD, Afonso AF, Silva AM, Cardoso SM

Molecules

01-Dec-2018

PMCID:	PMC6321363
doi:	10.3390/molecules23123169
PMID:	30513773

Changes in Photosynthetic Pigments, Total Phenolic Content, and Antioxidant Activity of Salvia coccinea Buc’hoz Ex Etl. Induced by Exogenous Salicylic Acid and Soil Salinity

Grzeszczuk M, Salachna P, Meller E

Molecules

29-May-2018

PMCID:	PMC6099562
doi:	10.3390/molecules23061296
PMID:	29843455

Ethnobotanical Survey, Preliminary Physico-Chemical and Phytochemical Screening of Salvia argentea (L.) Used by Herbalists of the Saïda Province in Algeria

Benabdesslem Y, Hachem K, Kahloula K, Slimani M

Plants (Basel)

05-Dec-2017

PMCID:	PMC5750635
doi:	10.3390/plants6040059
PMID:	29206161

Chemical composition of volatile and fixed oils from of Salvia argentea L. (Lamiaceae) growing wild in Sicily.

Riccobono L, Maggio A, Rosselli S, Ilardi V, Senatore F, Bruno M

Nat Prod Res

01-Jan-2016

doi:	10.1080/14786419.2015.1030742
PMID:	25880372

Triterpenoids from Salvia argentea var. aurasiaca (Pomel) Batt. & Trab. and their chemotaxonomic significance.

Lakhal H, Kabouche A, Alabdul Magid A, Voutquenne-Nazabadioko L, Harakat D, Kabouche Z

Phytochemistry

01-Jun-2014

doi:	10.1016/J.PHYTOCHEM.2014.03.009
PMID:	24697905

Glandular Trichomes and Essential Oil of Thymus quinquecostatus

Jia P, Liu H, Gao T, Xin H

ScientificWorldJournal

23-Oct-2013

PMCID:	PMC3821910
doi:	10.1155/2013/387952
PMID:	24250266

Biological activities of Wiedemannia multifida (Linnaeus) Bentham and Wiedemannnia orientalis Fisch. & Mey.

Albayrak S, Aksoy A

Asian Pac J Trop Biomed

01-Mar-2013

PMCID:	PMC3631749
doi:	10.1016/S2221-1691(13)60049-0
PMID:	23620837

Diterpenoids from Salvia glutinosa, S. austriaca, S. tomentosa and S. verticillata roots

Gábor Nagy, Gábor Günther, Imre Máthé, Gerald Blunden, Ming-he Yang, Trevor A. Crabb

Elsevier BV

26-Jul-2002

doi:	10.1016/S0031-9422(99)00343-X

Ursane and oleanane triterpenoids from Salvia argentea

Maurizio Bruno, Giuseppe Savona, Juan A. Hueso-Rodríguez, Conrad Pascual, Benjamín Rodríguez

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)81441-7

20-Nor-abietane and rearranged abietane diterpenoids from the root of Salvia argentea

Antonio Michavila, María C. De La Torre, Benjamín Rodríguez

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)81178-4

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 / Naphthoquinones
1-Ketoaethiopinone	11983338	Click to see	310.40	unknown	https://doi.org/10.1016/0031-9422(91)83665-8 https://doi.org/10.1016/S0031-9422(00)81178-4 https://doi.org/10.1016/S0031-9422(99)00343-X
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/10.1016/0031-9422(91)83665-8 https://doi.org/10.1016/S0031-9422(99)00343-X https://doi.org/10.1016/S0031-9422(00)81178-4
Salvipisone	821448	Click to see	312.40	unknown	https://doi.org/10.1016/0031-9422(91)83665-8 https://doi.org/10.1016/S0031-9422(00)81178-4
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12,15-Octadecatrienoic acid, methyl ester, (9Z,12Z,15Z)-	9316	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC	292.50	unknown	https://doi.org/10.1080/14786419.2015.1030742
Methyl Linolenate	5319706	Click to see	292.50	unknown	https://doi.org/10.1080/14786419.2015.1030742
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bR,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol	12309872	Click to see	286.50	unknown	https://doi.org/10.1016/S0031-9422(00)81178-4
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(99)00343-X https://doi.org/10.1016/S0031-9422(00)81178-4
Arucadiol	11011966	Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C2C(=O)CCC3(C)C)O)O	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)81178-4
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/0031-9422(91)83665-8 https://doi.org/10.1016/S0031-9422(00)81178-4 https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(5R)-5-hydroxy-8,8-dimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthrene-3,4-dione	163045617	Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(CCC3O)(C)C)C(=O)C1=O	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)81178-4
5-hydroxy-8,8-dimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthrene-3,4-dione	163045616	Click to see	298.40	unknown	https://doi.org/10.1016/S0031-9422(00)81178-4
> 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(99)00343-X https://doi.org/10.1016/S0031-9422(00)81178-4
> 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(99)00343-X
> 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)81441-7
(1,2,11,14-Tetrahydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	162923021	Click to see	532.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
(1,2,14-Trihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	75048982	Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)O)O	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
(1R,3S,6aR,6bS,7S,8aR,11R,12S,12aR,14R,14bS)-14-methoxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,7-triol	163185928	Click to see CC1CCC2(CC(C3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)OC)C2C1C)C)O)C	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1R,3S,6aR,6bS,7S,8aR,11R,12S,12aR,14R,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,7,14-tetrol	163195283	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1R,3S,6aR,6bS,7S,8aS,11R,12S,12aS,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,7-triol	163191183	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1R,3S,6aR,6bS,8aR,11R,12S,12aR,14R,14bS)-14-methoxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3-diol	163193028	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1R,3S,6aR,6bS,8aS,11R,12S,12aS,14R,14bS)-8a-(hydroxymethyl)-14-methoxy-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3-diol	163190557	Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)OC)C2C1C)C)CO	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1R,6S,6aR,6bR,7S,8aS,11R,12S,12aS,14bS)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,6,7-triol	163188802	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1S,2R,4aS,6S,6aS,6bR,10S,12R,12aR,14bS)-6,10,12-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carbaldehyde	163194756	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1S,2R,4aS,6S,6aS,6bR,10S,12R,12aS,13R,14bS)-6,10,12-trihydroxy-13-methoxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carbaldehyde	163191405	Click to see CC1CCC2(CC(C3(C(=CC(C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)OC)C2C1C)C)O)C=O	502.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1S,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-1,3,14-triol	163188741	Click to see	458.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(1S,4S,5R,10S,12R,13S,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-ene-10,12-diol	163194905	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
(2,11,14-Trihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	163002896	Click to see	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
(2,14-Dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	162957445	Click to see	500.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
(2,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) acetate	163070396	Click to see	500.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
(3S,6S,6aR,6bR,7S,8aS,12aS,14bS)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,6,7-triol	163189241	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.009
[(1S,2R,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-1,2,14-trihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate	22212738	Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(C(C(C(C5(C)C)OC(=O)C)O)O)C)C)O)C2C1C)C)C	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
[(1S,2R,3R,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-1,2,14-trihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	44575565	Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CCC3(C2C(C=C4C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C)O)O	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
[(1S,2R,3R,4aS,6aR,6bS,8aS,11S,12R,12aR,14R,14aS,14bS)-1,2,11,14-tetrahydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	162923022	Click to see	532.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
[(2R,3R,4aR,6aR,6bS,8aR,12aR,14R,14aR,14bS)-2,14-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	162957446	Click to see	500.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
[(2R,3R,4aS,6aR,6bS,8aR,11R,12S,12aR,14R,14aS,14bS)-2,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate	163070398	Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)O)C2C1C)C)C	500.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
[(2R,3R,4aS,6aR,6bS,8aS,11S,12R,12aR,14R,14aS,14bS)-2,11,14-trihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	163002897	Click to see	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
1,2,11-Trihydroxyurs-12-en-3-yl acetate	537138	Click to see	516.80	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)81441-7
> 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(99)00343-X

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Salvia argentea

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