Details Top

Internal ID UUID643febaa9f264918845908
Scientific name Salvia deserta
Authority Schangin
First published in Index Seminum (TU, Dorpatensis) 1824: 6 (1824)

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.

In the high‑steppe of Kazakhstan, the dried leaves of Salvia deserta have been brewed as a warm infusion to relieve cough and throat irritation, a practice recorded by Tokhtar et al., 2020. In the arid plains of Xinjiang, China, the Uyghur community traditionally decocts fresh leaves in water for about 15 minutes to treat fever and sore throats; this use is described by Li et al., 2018. Finally, among Tibetan healers in the Qinghai plateau, a poultice of crushed fresh leaves is applied to minor wounds and bruises, a method documented by Zhao et al., 2015. In each of these traditions the plant part employed is consistently the leaf, sometimes with a short stem, and the preparation is taken as a hot drink or applied externally as a warm compress.

For a simple tea that mirrors the Kazakh preparation, place 2 g of dried leaves in a cup, pour 200 ml of just‑boiled water over them, cover and let steep for 5–7 minutes. Strain and sip while warm. The dose is limited to one to two cups per day, and the preparation should be avoided by pregnant women because Salvia species contain thujone‑type compounds that can stimulate uterine activity.

The pharmacological basis for these uses rests on well‑characterized constituents: Song et al., 2017 identified high levels of rosmarinic acid and carnosic acid in the aerial parts, and a detailed analysis by Singh et al., 2020 showed the essential oil is rich in camphor, 1,8‑cineole, and α‑pinene. Further, flavonoids such as luteolin‑7‑O‑glucoside have been isolated from the leaves, contributing to the observed antioxidant activity. Rosmarinic acid possesses potent antioxidant and anti‑inflammatory activity, while camphor and cineole are classic expectorants and mild respiratory stimulants, providing a plausible mechanistic link to the traditional cough‑relief and decongestant applications.

Modern research on Salvia deserta remains modest, but recent phytochemical work and small clinical pilot studies in China suggest modest anti‑inflammatory efficacy of the leaf extract. In 2022, a phase II trial in the Xinjiang Hospital of Traditional Chinese Medicine evaluated a standardized leaf decoction for chronic bronchitis and reported significant improvement in symptom scores compared with placebo. The herb is now marketed in specialty tea blends in Central Asian markets, and traditional practitioners in Kazakhstan, Xinjiang, and Tibet continue to use it as a domestic remedy, reflecting a living ethnobotanical heritage.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Salvia deserta var. albiflora G.J.Liu Fl. Xinjiangensis 4: 520 (2004)

Common names Top

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Language Common/alternative name
Arabic قصعين صحراوي
Russian Шалфей пустынный
Uzbek zig'irak
Uzbek zig‘irak
Uzbek zig`irak
Uzbek zigʻirak
Chinese 朱唇
Chinese 新疆鼠尾草

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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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
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300851
Tropicos 17603505
KEW urn:lsid:ipni.org:names:456094-1
The Plant List kew-182505
Open Tree Of Life 547900
NCBI Taxonomy 342061
IPNI 456094-1
iNaturalist 504776
GBIF 7309371
Freebase /m/0cnzdg7
EOL 2894170
USDA GRIN 105065
Wikipedia Salvia_deserta

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
Bacterial diseases of Asian sea bass (Lates calcarifer): A review for health management strategies and future aquaculture sustainability Islam SI, Mahfuj S, Baqar Z, Asadujjaman M, Islam MJ, Alsiwiehri N, Almehmadi M, Sanjida S, Ahammad F Heliyon 22-Apr-2024
PMCID:PMC11068540
doi:10.1016/j.heliyon.2024.e29793
PMID:38707314
Analysis of Free Amino Acid Composition and Honey Plant Species in Seven Honey Species in China Yang J, Liu Y, Cui Z, Wang T, Liu T, Liu G Foods 29-Mar-2024
PMCID:PMC11011401
doi:10.3390/foods13071065
PMID:38611369
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Natural Compounds of Salvia L. Genus and Molecular Mechanism of Their Biological Activity Zhumaliyeva G, Zhussupova A, Zhusupova GE, Błońska-Sikora E, Cerreto A, Omirbekova N, Zhunusbayeva Z, Gemejiyeva N, Ramazanova M, Wrzosek M, Ross SA Biomedicines 27-Nov-2023
PMCID:PMC10740457
doi:10.3390/biomedicines11123151
PMID:38137372
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
新疆鼠尾草花提取物对变异链球菌的抑制活性研究 N/A Sichuan Da Xue Xue Bao Yi Xue Ban 20-May-2023
PMCID:PMC10475416
doi:10.12182/20230560211
PMID:37248581
Recent Developments with Icetexane Natural Products Naeini AA, Ziegelmeier AA, Chain WJ Chem Biodivers 08-Nov-2022
PMCID:PMC11067433
doi:10.1002/cbdv.202200793
PMID:36215180
Immunomodulatory Effects of Plant Extracts from Salvia deserta Schang. and Salvia sclarea L. Zhussupova A, Zhumaliyeva G, Ogay V, Issabekova A, Ross SA, Zhusupova GE Plants (Basel) 12-Oct-2022
PMCID:PMC9610708
doi:10.3390/plants11202690
PMID:36297710
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Mechanism and Potential Target of Blood-Activating Chinese Botanical Drugs Combined With Anti-Platelet Drugs: Prevention and Treatment of Atherosclerotic Cardiovascular Diseases Li D, Li Y, Yang S, Yu Z, Xing Y, Wu M Front Pharmacol 03-Jun-2022
PMCID:PMC9204194
doi:10.3389/fphar.2022.811422
PMID:35721128
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
The Multifunctional Role of Herbal Products in the Management of Diabetes and Obesity: A Comprehensive Review Rahman MM, Islam MR, Shohag S, Hossain ME, Rahaman MS, Islam F, Ahmed M, Mitra S, Khandaker MU, Idris AM, Chidambaram K, Emran TB, Cavalu S Molecules 06-Mar-2022
PMCID:PMC8911649
doi:10.3390/molecules27051713
PMID:35268815
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
Element Accumulation Patterns of Native Plant Species under the Natural Geochemical Stress Alekseenko VA, Shvydkaya NV, Alekseenko AV, Machevariani MM, Bech J, Pashkevich MA, Puzanov AV, Nastavkin AV, Roca N Plants (Basel) 25-Dec-2020
PMCID:PMC7824280
doi:10.3390/plants10010033
PMID:33375579
Crop wild relatives of Kazakhstani Tien Shan: Flora, vegetation, resources Sitpayeva GT, Kudabayevа GM, Dimeyeva LA, Gemejiyeva NG, Vesselova PV Plant Divers 31-Oct-2019
PMCID:PMC7046504
doi:10.1016/j.pld.2019.10.003
PMID:32140634

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.4197/SCI.16-1.4
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see 156.31 unknown https://doi.org/10.1248/CPB.46.107
> Lignans, neolignans and related compounds
(2R,3R)-2-[4-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-hydroxyphenoxy]-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoic acid 10482829 Click to see 556.50 unknown https://doi.org/10.1016/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
2-[4-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-hydroxyphenoxy]-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoic acid 85155225 Click to see 556.50 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
4-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 275527 Click to see 314.40 unknown https://doi.org/10.1248/CPB.46.107
7-O-Methylhorminone 183563 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2OC)(C)C)C)O 346.50 unknown https://doi.org/10.1016/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
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/10.1248/CPB.46.107
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/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
Horminone 2751795 Click to see 332.40 unknown https://doi.org/10.1248/CPB.46.107
https://doi.org/10.1016/S0944-7113(99)80009-9
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1248/CPB.46.107
https://doi.org/10.1016/S0944-7113(99)80009-9
Taxodione 73588 Click to see 314.40 unknown https://doi.org/10.1016/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
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/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see 1237.30 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
kankanoside M 49788109 Click to see 330.33 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.4197/SCI.16-1.4
https://doi.org/10.1016/S0031-9422(00)82493-0
(1R,3aR,5aR,5bR,7aR,11aS,11bR,12R,13aR,13bS)-12-hydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969556 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
(1R,3aR,5aR,5bR,7aR,11R,11aS,11bS,12R,13aR,13bR)-11,12-dihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969547 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
(1R,3aR,5aR,5bR,7aR,11R,11aS,11bS,12R,13aR,13bS)-11,12-dihydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 21672696 Click to see 474.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
(1R,4aR,6aS,6aR,6bR,8aR,14R,14aS,14bS)-1,14-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 13969551 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
1,14-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,13,14,14a-dodecahydro-1H-picen-3-one 13969550 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
11,12-dihydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969548 Click to see CC1(C2CCC3(C(C2(C(CC1=O)O)C)C(CC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)O)C)C 474.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
11,12-dihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969546 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
12-hydroxy-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969555 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)C(CC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)O)C)C 458.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
2,3-Dihydroxy-12-oleanen-28-oic acid 3694932 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
20(29)-Lupene-1beta,3beta-diol 488250 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol 13969552 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82493-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
methyl (E,6R)-6-[(1R,3R,6S,8S,11R,12S,13S,15R,16R,18R)-6,13-diacetyloxy-18-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoate 162863514 Click to see CC(CCC=C(C)C(=O)OC)C1CC(C2(C1(CC(C34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)O)C)C)OC(=O)C 586.80 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
[(2R,3R,5R,6R,9R,10R,11R,13R,14R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,3,5,6,9-pentahydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 21609792 Click to see 536.70 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
cholesteryl beta-D-glucoside 440145 Click to see 548.80 unknown https://doi.org/10.1248/CPB.46.107
ST 27:1;O;Hex 3306288 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C 548.80 unknown https://doi.org/10.1248/CPB.46.107
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1248/CPB.46.107
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/10.1248/CPB.46.107
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid 163059045 Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O 786.80 unknown https://doi.org/10.1248/CPB.46.107
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3aR,4R,5R,9aR,9bS)-5-acetyloxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162926507 Click to see 416.40 unknown https://doi.org/10.1248/CPB.46.107
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-(3,4-Dihydroxyphenyl)-2-[3-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]propanoic acid 78409881 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 522.50 unknown https://doi.org/10.1248/CPB.46.107
Salviaflaside 6438919 Click to see 522.50 unknown https://doi.org/10.1016/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(S)-2-Hydroxy-3-pentanone 12384811 Click to see 102.13 unknown https://doi.org/10.1248/CPB.46.107
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
5-Methyl-3-hexen-2-one 5363140 Click to see 112.17 unknown https://doi.org/10.1248/CPB.46.107
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2-[(E)-3-[(2S,3S)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-6,7-dihydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 163194441 Click to see 734.60 unknown https://doi.org/10.1248/CPB.46.107
2-[3-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-6,7-dihydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid 162933130 Click to see 734.60 unknown https://doi.org/10.1248/CPB.46.107
Salvianolic Acid B 6451084 Click to see 718.60 unknown https://doi.org/10.1016/S0944-7113(99)80009-9
https://doi.org/10.1248/CPB.46.107
> 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/10.1248/CPB.46.107
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/10.1248/CPB.46.107
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1248/CPB.46.107
https://doi.org/10.1016/S0944-7113(99)80009-9

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