Salvia virgata
Details Top
| Internal ID | UUID643fec01ee574210974453 |
| Scientific name | Salvia virgata |
| Authority | Jacq. |
| First published in | Hort. Bot. Vindob. 1: 14 (1770) |
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 communities in the Kopet Dag foothills and the Voronezh steppe of Central Asia and western Asia, Salvia virgata is gathered as a simple remedy for colds, coughs, and low fevers. Healers and housewives dry the herb and use the aerial parts in infusions; among Iranian Turkmen in Khorasan, dried aerial material is steeped to treat respiratory complaints, and the same preparation is employed for fever reduction by neighbors across the northern Iranian steppe (Jassbi et al., 2016). In some mixed-steppe and foothill villages, the herb is also poulticed onto superficial cuts or insect bites to calm irritation, and in the eastern Balkans the dried aerial parts are added to a “yayla tea” blend for mild expectorant and soothing effects (Babulka et al., 2008). Collectors prize young, leafy stems collected just before or at early flowering to maximize the fresh scent and preserve camphor-rich essential oil.
A practical mild tea can be made by infusing 1–2 teaspoons (about 1–2 g) of the dried aerial parts of Salvia virgata in 250 mL of just-off-the-boil water for 10–15 minutes, covered, then straining. As the herb is naturally camphor-rich, most users find 1–2 cups per day sufficient and keep the brew mild; pregnant women and people with epilepsy are advised to avoid camphor-containing teas because salvinorin-like diterpenoids have not been thoroughly screened and potential interactions are unknown (Houghton et al., 2014; P. M. Coates et al., eds., 2000). For folk or commercial low‑dose tinctures, a typical weight-to-solvent ratio of 1:5 by dry weight in 45% ethanol can be macerated for 4–6 weeks in the dark with daily shaking; the finished tincture is pressed, filtered, and most people dose by the drop, keeping intake modest.
The medicinal odor and flavor of the herb come from an essential oil dominated by camphor, which can account for 20–50% of the oil in some populations, with 1,8‑cineole (eucalyptol) as a regular companion (Jassbi et al., 2016; Karamenderes et al., 2007). Flavonoids and phenolic acids, especially rosmarinic acid, are well documented in the aerial parts (Teimouri et al., 2019). Both rosmarinic acid and camphor are consistent with the herb’s traditional soothing, cough‑calming, and antiseptic profiles.
Modern relevance: Recent work continues to verify essential-oil composition and antioxidant activity of Salvia virgata, and simple home teas remain common where the plant is locally available (Babulka et al., 2008; Jassbi et al., 2016; Teimouri et al., 2019).
General Uses Top
Suggest a correction!Common products:
Salvia virgata is cultivated as an ornamental herbaceous perennial for garden borders, rock gardens, and low‑maintenance landscaping. The species appears in horticultural databases (e.g., RHS Plant Finder) and is sold by commercial nurseries for its violet‑blue flower spikes and silvery foliage.
Fragrance and cosmetics:
The aerial parts yield an essential oil that has been chemically characterized in peer‑reviewed studies. The oil contains high levels of monoterpenes such as 1,8‑cineole, camphor, and α‑pinene, which are compounds commonly exploited in perfumery and cosmetics for their aromatic and functional properties. Ongoing research has highlighted the oil’s potential as a natural fragrance component (e.g., studies in the Journal of Essential Oil Research, 2016).
Properties relevant to use:
- Ornamental: compact habit, long flowering period (late spring to early summer), tolerance to drought and poor soils, and attractive foliage color.
- Essential oil: density ≈0.90 g cm⁻³ at 20 °C, refractive index ≈1.470, and major constituent composition (percentages of 1,8‑cineole, camphor, etc.) as reported in the cited essential‑oil analyses.
Sustainability and sourcing:
Salvia virgata is propagated by seed or vegetative cuttings and is cultivated under standard horticultural practices without reported wild‑harvest pressure. The plant’s ability to thrive on marginal soils makes it a low‑input ornamental species suitable for sustainable landscaping.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Salvia affinis | Spreng. ex Steud. | Nomencl. Bot. 1: 724 (1821) |
| Salvia amplexicaulis | hort. ex Benth. | Labiat. Gen. Spec. : 236 (1833) |
| Salvia barrelieri | hort. ex Benth. | Labiat. Gen. Spec. : 235 (1833) |
| Salvia bauhini | hort. ex Benth. | Labiat. Gen. Spec. : 235 (1833) |
| Salvia caduca | Vahl ex Hornem. | Hort. Bot. Hafn. 1: 30 (1813) |
| Salvia campestris | M.Bieb. | Fl. Taur.-Caucas. 1: 20 (1808) |
| Salvia caucasica | Schrank | Syll. Pl. Nov. 2: 58 (1826) |
| Salvia extersa | Klokov | Fl. RSS Ukr. 9: 654 (1960) |
| Salvia garganica | Ten. | Index Seminum (NAP, Neapolitano) 1829: 17 (1829) |
| Salvia gigantea | Desf. | Tabl. École Bot. , ed. 2: 68 (1815) |
| Salvia grandidentata | Ten. | Index Seminum (NAP, Neapolitano) 1833: 15 (1833) |
| Salvia hypanica | Andrz. | Enum. Pl. : 3 (1821) |
| Salvia mollis | J.Jacq. | Ecl. Pl. Rar. : 56 (1813) |
| Salvia nudicaulis | K.Koch | Linnaea 19: 24 (1846) |
| Salvia oblonga | K.Koch | Linnaea 19: 24 (1846) |
| Salvia praecox | Loisel. | Not. Fl. France : 6 (1810) |
| Salvia quercifolia | hort. ex Benth. | Labiat. Gen. Spec. : 235 (1833) |
| Salvia rubra | Spreng. | Syst. Veg. 4(2): 17 (1827) |
| Salvia sibthorpii | Sm. | Fl. Graec. Prodr. 1: 15 (1806) |
| Salvia similata | Hausskn. | Mitth. Thüring. Bot. Vereins , n.f., 11: 36 (1897) |
| Salvia utilis | Braun ex Engl. | Abh. Königl. Akad. Wiss. Berlin 1891: 367 (1892) |
| Sclarea sibthorpii | (Sm.) Soják | Cas. Nár. Mus., Odd. Prír. 152: 22 (1983) |
| Sclarea virgata | (Jacq.) Soják | Cas. Nár. Mus., Odd. Prír. 152: 22 (1983) |
| Salvia virgata var. garganica | (Ten.) Nyman | Consp. Fl. Eur. 570. 1881 |
| Salvia virgata var. campestris | (M.Bieb.) Nyman | Consp. Fl. Eur. 570. 1881 |
| Salvia virgata f. campestris | (M.Bieb.) E.Peter | Repert. Spec. Nov. Regni Veg. 39: 184 1936 |
| Euriples rugosa | Raf. | Fl. Tellur. 3: 94 (1837) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | wand sage |
| Bulgarian | прътовиден конски босилек |
| Persian | مریمگلی هرز |
| Polish | szałwia rózgowata |
| Russian | Шалфей прутьевидный |
Germination/Propagation Top
Suggest a correction or add new data!| Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment. |
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000302613 |
| USDA Plants | SAVI18 |
| INPN | 717529 |
| Flora of Italy | 4679 |
| The Plant List | kew-184143 |
| Open Tree Of Life | 4724791 |
| Observations.org | 150012 |
| NCBI Taxonomy | 1298553 |
| NBN Atlas | NBNSYS0200003065 |
| Nature Serve | 2.860110 |
| IPNI | 457510-1 |
| iNaturalist | 78974 |
| GBIF | 2927041 |
| Freebase | /m/0j64n5k |
| EPPO | SALVG |
| EOL | 480285 |
| Calflora (Californian flora) | 8623 |
| USDA GRIN | 70597 |
| Wikipedia | Salvia_virgata |
| CMAUP | NPO4164 |
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)!
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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 |
|---|---|---|---|---|---|
| > 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-2006-962043 |
| 7-Acetylhorminone | 2751796 | Click to see | 374.50 | unknown | https://doi.org/10.1055/S-2006-962043 |
| Cryptanol | 184179 | Click to see | 316.40 | unknown | https://doi.org/10.1055/S-2006-962043 |
| 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-2006-962043 |
| Horminone | 2751795 | Click to see | 332.40 | unknown | https://doi.org/10.1055/S-2006-962043 |
| 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-2006-962043 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate | 24864449 | Click to see | 298.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (6-hydroxy-4-methoxy-1-benzofuran-7-yl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 24864268 | Click to see | 430.50 | unknown | via CMAUP database |
| [(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 101855692 | Click to see | 540.70 | unknown | via CMAUP database |
| [(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone | 101855694 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 | 540.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| 4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one | 440244 | Click to see | 224.30 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| Caryophyllene | 5281515 | Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C | 204.35 | unknown | https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S |
| Corchoionol C | 137705650 | Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C | 224.30 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids | |||||
| (1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol | 97032059 | Click to see | 220.35 | unknown | https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids | |||||
| Germacrene B | 5281519 | Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C | 204.35 | unknown | https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S |
| Germacrene D | 5317570 | Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C | 204.35 | unknown | https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Ursolic Acid | 64945 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| 10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-12-oxo-3,4,5,6,6a,7,8,8a,10,11,13,14b-dodecahydro-1H-picene-4a-carboxylic acid | 14489124 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C | 470.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89010-X |
| 10,11-Dihydroxy-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 | 5320146 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C | 488.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| 2,3-Dihydroxy-12-oleanen-28-oic acid | 3694932 | Click to see | 472.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| 2alpha,3alpha,23-Trihydroxyolean-12-en-28-oic acid | 11504083 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C | 488.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| 3-Hydroxyolean-12-en-28-oic acid | 619166 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| 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/10.1016/0031-9422(90)85143-4 |
| Corosolic Acid | 6918774 | Click to see | 472.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| epi-Maslinic acid | 25564831 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C | 472.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- | 220774 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(90)85143-4 |
| Virgatic acid | 14489125 | Click to see | 470.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89010-X |
| > Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans | |||||
| Panduratin E | 24864269 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 | 472.60 | unknown | via CMAUP database |
| > 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-2006-962043 |
| > Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids | |||||
| (-)-Nicolaioidesin B | 637029 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O | 406.50 | unknown | via CMAUP database |
| (1'R,2'S,6'R)-2-Hydroxyisopanduratin A | 23656472 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O | 392.50 | unknown | via CMAUP database |
| (2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 44444916 | Click to see | 420.50 | unknown | via CMAUP database |
| (2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 25023021 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 | 406.50 | unknown | via CMAUP database |
| 4-hydroxypanduratin A | 636530 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 | 392.50 | unknown | via CMAUP database |
| Isopanduratin A | 10069916 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 | 406.50 | unknown | via CMAUP database |
| Isopanduratin A1 | 44444913 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O | 406.50 | unknown | via CMAUP database |
| Panduratin A | 6483648 | Click to see | 406.50 | unknown | via CMAUP database |
| Panduratin C | 6483647 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O | 422.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones | |||||
| (2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one | 44444915 | Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C | 392.50 | unknown | via CMAUP database |
| (2S)-6-Geranylpinostrobin | 44444914 | Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| (2R)-8-geranylpinostrobin | 23656470 | Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones | |||||
| Pinocembrin | 68071 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 | 256.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids | |||||
| 5-O-Methylnaringenin | 182315 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O | 286.28 | unknown | via CMAUP database |
| Alpinetin | 154279 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O | 270.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| (-)-Pinostrobin | 73201 | Click to see | 270.28 | unknown | via CMAUP database |
| (2R)-5,7-Dimethoxyflavanone | 689012 | Click to see | 284.31 | unknown | via CMAUP database |
| (2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one | 689011 | Click to see | 284.31 | unknown | via CMAUP database |
| 3,5,7,4'-Tetramethoxyflavone | 631095 | Click to see | 342.30 | unknown | via CMAUP database |
| 5-Hydroxy-3,7-dimethoxyflavone | 5748697 | Click to see | 298.29 | unknown | via CMAUP database |
| 5-Hydroxy-7,4'-dimethoxyflavone | 5281601 | Click to see | 298.29 | unknown | via CMAUP database |
| 5,7-Dimethoxyflavone | 88881 | Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 | 282.29 | unknown | via CMAUP database |
| 5,7,3',4'-Tetramethoxyflavone | 631170 | Click to see | 342.30 | unknown | via CMAUP database |
| Apigenin trimethyl ether | 79730 | Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC | 312.30 | unknown | via CMAUP database |
| Galangin 3,5,7-trimethyl ether | 117900 | Click to see | 312.30 | unknown | via CMAUP database |
| Gonzalitosin I | 5272653 | Click to see | 328.30 | unknown | https://doi.org/10.1016/S0031-9422(01)00415-0 |
| Kaempferol 3,7,4'-trimethyl ether | 5468749 | Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC | 328.30 | unknown | via CMAUP database |
| Pentamethylquercetin | 97332 | Click to see | 372.40 | unknown | via CMAUP database |
| Pinostrobin | 6950539 | Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O | 270.28 | unknown | via CMAUP database |
| Retusin | 5352005 | Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC | 358.30 | unknown | via CMAUP database |
| Sakuranetin | 73571 | Click to see | 286.28 | unknown | via CMAUP database |
| Tectochrysin | 5281954 | Click to see | 268.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Kavalactones | |||||
| 7,8-Dihydro-5,6-dehydrokawain | 160673 | Click to see | 230.26 | unknown | via CMAUP database |
| Demethoxyyangonin | 5273621 | Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 | 228.24 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones | |||||
| 4,2',4'-Trihydroxy-6'-methoxydihydrochalcone | 42607705 | Click to see | 288.29 | unknown | via CMAUP database |
| Phloretin | 4788 | Click to see | 274.27 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones | |||||
| (E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one | 101306880 | Click to see | 390.50 | unknown | via CMAUP database |
| 3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one | 460718 | Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O | 256.25 | unknown | via CMAUP database |
| Cardamonin | 641785 | Click to see | 270.28 | unknown | via CMAUP database |
| Flavokawain C | 6293081 | Click to see | 300.30 | unknown | via CMAUP database |
| Helichrysetin | 6253344 | Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O | 286.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones | |||||
| (E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one | 23656471 | Click to see | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Stilbenes | |||||
| Geranyl-2,4-dihydroxy-6-phenethylbenzoate | 23656469 | Click to see | 394.50 | unknown | via CMAUP database |
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