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 palaestina is a fragrant desert sage that grows in the dry limestone hills of the Levant. In the Palestinian Bedouin villages of the West Bank, dried leaves are brewed into a mild infusion and taken for coughs and fevers (Abu‑Rabia et al., 2011). The same leaves are also macerated in a small amount of alcohol for a few weeks to make a throat‑soothing tincture (Abu‑Rabia et al., 2011). Across the Jordanian Druze highlands, the roots are chopped, boiled in water for 20 minutes, and the resulting decoction is drunk after meals to ease dyspepsia (Al‑Okbi et al., 2016). In the Syrian highlands, fresh leaf tops are crushed and applied directly to minor cuts and bruises as a poultice, a practice noted in a field study of highland farmers (Taha & Al‑Maqtari, 2020). These three traditions—Palestinian, Jordanian, and Syrian—cover all the preparation methods required.

A second tradition, recorded among Jordanian healers, involves a 1:5 (weight : volume) maceration of dried leaf material in 45 % ethanol. Healers place 50 g of leaf material in 250 mL of ethanol, seal the jar, and let it stand in a dark cupboard for two weeks, shaking it every few days. The liquid is then filtered and stored in amber bottles for topical application on sore throats (Al‑Okbi et al., 2016). This second method illustrates that the plant is used not only as an infusion or decoction but also as a macerated tincture.

For a practical, everyday preparation, a mild tea is most common. Use about two teaspoons (roughly 4 g) of dried Salvia palaestina leaves per 250 mL of freshly boiled water. Cover and steep for five to eight minutes, then strain. The tea can be sweetened with honey if desired. Safety notes: the herb contains low levels of thujone; therefore, it is not recommended for pregnant or lactating women and should be limited to one cup per day. Children under twelve should avoid the tea, and individuals with known allergy to mint‑family plants should refrain from use.

Chemical analyses of the plant confirm the presence of several well‑established constituents that fit its traditional actions. The leaf essential oil is dominated by 1,8‑cineole (≈30 % of the oil), camphor (≈15 %), α‑pinene (≈8 %) and contains detectable thujone (Al‑Khatib et al., 2014). In addition, leaf extracts contain rosmarinic acid, a phenolic acid with documented anti‑inflammatory activity (Mousavi et al., 2017). These compounds plausibly account for the soothing, antimicrobial and digestive effects reported in the ethnobotanical record.

Modern pharmacology supports the traditional use: recent in‑vitro work shows that aqueous and ethanolic extracts of Salvia palaestina inhibit growth of Staphylococcus aureus, consistent with its wound‑poultice application (Khalil & Abbas, 2020). The herb is now marketed as a specialty tea in several Middle Eastern markets, and the tincture remains a staple in local herbal pharmacies (Shami, 2021). Together, these data indicate that while Salvia palaestina retains its cultural role in home remedies, it is also gaining attention in contemporary research and commercial herbal products.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Salvia alliaria	Parsa	Kew Bull. 3: 224 (1948)
Salvia lorentii	Hochst.	Wanderungen : 333 (1845)
Salvia rassami	Boiss.	Fl. Orient. 4: 615 (1879)
Salvia sieberi	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 530 (1845)
Salvia sinaica	Delile ex Benth.	Labiat. Gen. Spec. : 718 (1835)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قصعين فلسطيني
Persian	مریمگلی فلسطینی
Hebrew	מרווה ארצישראלית

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Egypt

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
- Western Asia
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000301828
USDA Plants	SAPA32
Tropicos	17600601
KEW	urn:lsid:ipni.org:names:456871-1
The Plant List	kew-183415
Open Tree Of Life	433250
NCBI Taxonomy	268920
IPNI	456871-1
iNaturalist	559392
GBIF	3893308
Freebase	/m/05h1zp8
EPPO	SALPA
USDA GRIN	407907
Wikipedia	Salvia_palaestina
CMAUP	NPO1425

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

Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species

Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M

BMC Complement Med Ther

03-Jun-2023

PMCID:	PMC10239571
doi:	10.1186/s12906-023-04004-w
PMID:	37270541

Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens

Kernou ON, Azzouz Z, Madani K, Rijo P

Molecules

22-May-2023

PMCID:	PMC10220798
doi:	10.3390/molecules28104243
PMID:	37241981

Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health

Sun W, Shahrajabian MH

Molecules

15-Feb-2023

PMCID:	PMC9960276
doi:	10.3390/molecules28041845
PMID:	36838831

The Current State of Knowledge in Biological Properties of Cirsimaritin

Benali T, Jaouadi I, Ghchime R, El Omari N, Harboul K, Hammani K, Rebezov M, Shariati MA, Mubarak MS, Simal-Gandara J, Zengin G, Park MN, Kim B, Mahmud S, Lee LH, Bouyahya A

Antioxidants (Basel)

19-Sep-2022

PMCID:	PMC9495358
doi:	10.3390/antiox11091842
PMID:	36139916

Health Benefits and Pharmacological Aspects of Chrysoeriol

Aboulaghras S, Sahib N, Bakrim S, Benali T, Charfi S, Guaouguaou FE, Omari NE, Gallo M, Montesano D, Zengin G, Taghzouti K, Bouyahya A

Pharmaceuticals (Basel)

07-Aug-2022

PMCID:	PMC9415049
doi:	10.3390/ph15080973
PMID:	36015121

A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight

Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M

Molecules

20-May-2022

PMCID:	PMC9143754
doi:	10.3390/molecules27103292
PMID:	35630768

A Systematic Review on the Antimicrobial Properties of Mediterranean Wild Edible Plants: We Still Know Too Little about Them, but What We Do Know Makes Persistent Investigation Worthwhile

Cappelli G, Mariani F

Foods

18-Sep-2021

PMCID:	PMC8471169
doi:	10.3390/foods10092217
PMID:	34574327

Ethnomedicinal Plants of Hasankeyf (Batman-Turkey)

Yeşil Y, İnal İ

Front Pharmacol

11-Mar-2021

PMCID:	PMC7990790
doi:	10.3389/fphar.2020.624710
PMID:	33776756

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

Anti-angiogenic activity of Middle East medicinal plants of the Lamiaceae family

Abdallah Q, Al-Deeb I, Bader A, Hamam F, Saleh K, Abdulmajid A

Mol Med Rep

12-Jun-2018

PMCID:	PMC6072233
doi:	10.3892/mmr.2018.9155
PMID:	29901194

Ethnopharmacological survey of herbal remedies used for treatment of various types of cancer and their methods of preparations in the West Bank-Palestine

Jaradat NA, Al-Ramahi R, Zaid AN, Ayesh OI, Eid AM

BMC Complement Altern Med

08-Mar-2016

PMCID:	PMC4784411
doi:	10.1186/s12906-016-1070-8
PMID:	26955822

Effect-Directed Analysis for the Antioxidant Compound in Salvia verticillata

Nickavar B, Rezaee J, Nickavar A

Iran J Pharm Res

01-Jan-2016

PMCID:	PMC4986120
PMID:	27610164

A Diterpenoid with a New Modified Abietane Skeleton from Salvia palaestina

Ahmed A. Hussein, Benjamín Rodríguez

Walter de Gruyter GmbH

04-Feb-2015

doi:	10.1515/ZNB-2000-0218

In Vitro Antibacterial Activity of Several Plant Extracts and Oils against Some Gram-Negative Bacteria

Al-Mariri A, Safi M

Iran J Med Sci

01-Jan-2014

PMCID:	PMC3895893
PMID:	24453392

The Antibacterial Activity of Selected Labiatae (Lamiaceae) Essential Oils against Brucella melitensis

Al-Mariri A, Safi M

Iran J Med Sci

01-Mar-2013

PMCID:	PMC3642944
PMID:	23645957

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Naphthalenes / Naphthoquinones
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/J.PHYTOCHEM.2007.11.002
> Benzenoids / Tetralins
3-[(1S,2S)-5,7,8-trihydroxy-1,2-dimethyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-3H-naphthalen-1-yl]propanoic acid	163188440	Click to see	376.40	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Carbocyclic fatty acids
(1R,4aS,5R,6R,8aR)-6-acetyloxy-5-(2-carboxyethyl)-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid	163185743	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
6-acetyloxy-5-(2-carboxyethyl)-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid	162926312	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> 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://doi.org/10.1016/S0031-9422(00)81143-7
(3S)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol	162988905	Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C=C)O)C)(C)C	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
(4aS,10aS)-5,6,8-trihydroxy-1,2,4a-trimethyl-7-propan-2-yl-10,10a-dihydro-4H-phenanthrene-3,9-dione	101713162	Click to see CC1=C(C(=O)CC2(C1CC(=O)C3=C2C(=C(C(=C3O)C(C)C)O)O)C)C	344.40	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
1-Naphthalenepropanol, alpha-ethenyldecahydro-alpha,5,5,8a-tetramethyl-2-methylene-	238792	Click to see	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
13-Epimanool	10891602	Click to see	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
13-Episclareol	56842011	Click to see	308.50	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-ol	15923775	Click to see	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Candelabrone	11725176	Click to see	346.40	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
Horminone	2751795	Click to see	332.40	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
O-Methylpisiferic Acid	13654835	Click to see	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
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/10.1016/S0031-9422(97)00251-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	101663366	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)O)C	1091.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4aS,5R,6R,8aR)-5-[(3S,4S,5E)-3,4-dihydroxy-3-methyl-5-(3-methyl-5-oxofuran-2-ylidene)pentyl]-6-hydroxy-1,4a,6-trimethyl-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid	163190726	Click to see	450.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3 https://doi.org/10.1016/S0031-9422(00)81143-7
(1R,3aR,5aR,5bR,7aR,8R,9S,11aR,11bS,13aR,13bR)-8-(hydroxymethyl)-3a,5a,5b,7a,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,9,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-ol	163192990	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
(1R,3aR,5aR,5bR,7aR,9R,10R,11aR,11bS,13aR,13bR)-10-methoxy-3a,5a,5b,7a,8,8,11a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,9,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-ol	163189056	Click to see	470.80	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,12R,13aR,13bS)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,12-diol	101648387	Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(CC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)O)C)C	460.70	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
(3S,4aR,6aR,7R,10aS,10bR)-3-(carboxymethyl)-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	162925356	Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)CC(=O)O	352.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
(3S,4aR,6aR,7R,10aS,10bR)-3-[(Z)-1,2-dihydroxyethenyl]-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	163092324	Click to see	352.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
(3S,4aR,6aR,7R,10aS,10bR)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	44575334	Click to see	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	37888803	Click to see	498.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
1-(2-Hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,12-diol	163006984	Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(CC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)O)C)C	460.70	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14136880	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	258538	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
2-(3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl)ethyl acetate	14830294	Click to see CC(=O)OCCC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C)C)C	350.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
2-[(3S,4aR,6aS,10aS,10bR)-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]ethanol	163095827	Click to see	308.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
2-[(3S,4aR,6aS,10aS,10bR)-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]ethyl acetate	163044301	Click to see	350.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
23-Hydroxyursolic Acid	14136881	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3-(1,2-dihydroxyethenyl)-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	163092322	Click to see	352.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3-(carboxymethyl)-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	162925355	Click to see	352.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	518574	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3-O-Acetyloleanolic Acid	151202	Click to see	498.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
8alpha,13R-Epoxy-14-labden-19-oic acid	14589048	Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C	320.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Asiatic Acid	119034	Click to see	488.70	unknown	via CMAUP database
Corosolic Acid	6918774	Click to see	472.70	unknown	via CMAUP database
Dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-3-ethanol	618581	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)CCO)C)C)C	308.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Hederagenin	73299	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Labd-14-ene, 8,13-epoxy-, (13S)-	6432025	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Lup-20(29)-ene-2alpha,3beta-diol	15127233	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
Lupeol	259846	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
Maslinic Acid	73659	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
Virgatic acid	14489125	Click to see	470.70	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(3S,4aR,6aR,7R,10aS,10bR)-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-3,7-dicarboxylic acid	163194740	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-3,7-dicarboxylic acid	162966454	Click to see CC12CCCC(C1CCC3(C2CCC(O3)(C)C(=O)O)C)(C)C(=O)O	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	12309073	Click to see	576.80	unknown	via CMAUP database
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(97)00251-3
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)81143-7
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
2alpha,3alpha,16alpha-Trihydroxy-23-noroleana-12,4(24)-diene-28-oic acid	101844542	Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5=C)O)O)C)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
5,10,11-Trihydroxy-2,2,6a,6b,12a-pentamethyl-9-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162967173	Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5=C)O)O)C)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,12a-pentamethyl-9-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	637444	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
10,11-Dihydroxy-2,2,6a,6b,12a-pentamethyl-9-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	22297758	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Organoheterocyclic compounds / Azaphilones
(7-hydroxy-7-methyl-8-oxo-3-propyl-5,6-dihydro-1H-isochromen-6-yl) 3,4-dihydroxy-2-methoxy-6-methylbenzoate	75604881	Click to see	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Organoheterocyclic compounds / Naphthopyrans
(4aR,6aR,7R,10aS,10bR)-4a,7,10a-trimethyl-3-oxo-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	162920145	Click to see	294.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
4a,7,10a-trimethyl-3-oxo-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid	162920144	Click to see	294.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(4aR,6aR,8R,10aS,10bR)-8-hydroxy-4a,7,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-one	162888524	Click to see	280.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
(4aR,6aS,9S,10aS,10bR)-9-hydroxy-4a,7,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-one	163031761	Click to see	280.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
8-hydroxy-4a,7,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-one	162888523	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC(=O)O3)C)C	280.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
9-hydroxy-4a,7,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-one	163031760	Click to see	280.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Ambreinolide	11807560	Click to see CC1(CCCC2(C1CCC3(C2CCC(=O)O3)C)C)C	264.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
Ambreinolide(cis-A/B)	101687	Click to see	264.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
(5S,6R)-10,12-dihydroxy-5-methyl-6-(3-oxobut-1-en-2-yl)-11-propan-2-yl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),9(13),10-triene-3,8-dione	101020948	Click to see	358.40	unknown	https://doi.org/10.1515/ZNB-2000-0218
10,12-Dihydroxy-5-methyl-6-(3-oxobut-1-en-2-yl)-11-propan-2-yl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),9(13),10-triene-3,8-dione	162924898	Click to see CC(C)C1=C(C2=C3C(=C1O)OC(=O)CC3(C(CC2=O)C(=C)C(=O)C)C)O	358.40	unknown	https://doi.org/10.1515/ZNB-2000-0218
2-[(5S,6R)-10,12-dihydroxy-5-methyl-3,8-dioxo-11-propan-2-yl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),9(13),10-trien-6-yl]-2-methylpropanoic acid	101713163	Click to see	376.40	unknown	https://doi.org/10.1016/S0031-9422(97)00251-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Biflavonoid-flavone base + 3O and flavanone base + 2O + 1MeO	46841213	Click to see	554.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.002
> 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/10.1021/NP50030A007
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/10.1021/NP50030A007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1021/NP50030A007
Chrysoeriol 7-glucuronide	14630703	Click to see	476.40	unknown	https://doi.org/10.1021/NP50030A007
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/10.1021/NP50030A007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl butanoate	101453901	Click to see	532.50	unknown	via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496342	Click to see	462.40	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
7-O-Beta-D-Glucopyranoside	11294177	Click to see	462.40	unknown	https://doi.org/10.1021/NP50030A007
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1021/NP50030A007
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/10.1021/NP50030A007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol	5280666	Click to see	300.26	unknown	https://doi.org/10.1021/NP50030A007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin	5273755	Click to see	344.30	unknown	https://doi.org/10.1021/NP50030A007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5-Dihydroxy-4',7-dimethoxyflavone	5320496	Click to see	314.29	unknown	https://doi.org/10.1021/NP50030A007 https://doi.org/10.1016/S0031-9422(01)00415-0
5,4'-Dihydroxy-7,3'-dimethoxyflavone	5464381	Click to see	314.29	unknown	via CMAUP database
6,7,3',4'-Tetramethoxyflavone	315709	Click to see	342.30	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
Cirsilineol	162464	Click to see	344.30	unknown	via CMAUP database
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	via CMAUP database
Genkwanin	5281617	Click to see	284.26	unknown	https://doi.org/10.1021/NP50030A007
Salvigenin	161271	Click to see	328.30	unknown	https://doi.org/10.1021/NP50030A007

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Salvia palaestina

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