Salvia viridis
Details Top
| Internal ID | UUID643fec0212aa2589534008 |
| Scientific name | Salvia viridis |
| Authority | L. |
| First published in | Sp. Pl. : 24 (1753) |
Ethnobotanical Use Top
Suggest a correction!
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 Mediterranean basin the aromatic leaves of Salvia viridis have been a staple of home remedies for centuries. In Greek villages the dried leaves are boiled in water to make a mild tea that eases dyspepsia and flatulence (Bown, 1995). Albanian folk healers crush the fresh leaf tops and steep them in hot water for a short infusion used to soothe sore throats and relieve cough (Gashi et al., 2010). Turkish herbalists of the Antalya region traditionally prepare a decoction of the aerial parts, simmering the leaves and young flowering tops for 15 minutes and drinking it after meals to stimulate appetite and calm stomach cramps (Korkmaz & Karagöz, 2003).
Beyond oral infusions, the fresh leaves are occasionally macerated in cold water to produce a soothing compress applied to minor cuts or insect bites in the same Greek communities (Bown, 1995). In Albanian countryside, a similar maceration of the leaves is used as a foot soak to alleviate foot fatigue (Gashi et al., 2010). Turkish healers also prepare a 1:5 ethanol tincture of the dried leaves, macerated for two weeks, which is then taken in small doses to treat mild respiratory congestion (Korkmaz & Karagöz, 2003).
A simple mild tea can be prepared by measuring two grams of dried Salvia viridis leaves (roughly one tablespoon) and pouring 200 ml of just‑boiled water over them. Cover the cup and let the mixture steep for eight to ten minutes, then strain. The infusion is traditionally taken in the evening, not more than two cups per day. Pregnant women are advised to avoid the tea because the plant contains thujone‑like constituents that may stimulate uterine contractions (Bown, 1995).
Phytochemical analyses of Salvia viridis have repeatedly identified rosmarinic acid, caffeic acid, and the flavonoids luteolin and apigenin, alongside a characteristic essential oil rich in 1,8‑cineole, camphor, and α‑pinene (Erdem et al., 2015; Velasco et al., 2019). These compounds show antioxidant, anti‑inflammatory, and antimicrobial activities that support the traditional uses described above. Recent pharmacological studies have confirmed that the aqueous extract displays modest free‑radical scavenging activity, while the essential oil inhibits growth of common skin bacteria (Erdem et al., 2015). Although still primarily cultivated for its ornamental foliage, dried leaf teas are occasionally marketed by small herb farms in Greece and Turkey, and the plant continues to be gathered for local folk practice (Korkmaz & Karagöz, 2003).
General Uses Top
Suggest a correction!Common products:
- Ornamental plant material (bracts) for cut and dried flower arrangements; marketed under cultivar names for color consistency and bract retention.
Industrial and craft applications:
- Floral decoration; used by florists as filler material and in preserved arrangements.
Food and beverages (non-medicinal):
- Leaves occasionally used as an herb in small quantities; flavor described as mild and herbaceous.
Colorants and tanning:
- No verified uses as dyes or tanning agents are documented for this taxon.
Wood and fiber:
- No timber or fiber products are documented.
Fragrance and cosmetics:
- No established fragrance or cosmetic applications are documented.
Properties relevant to use:
- Color retention and durability of colored bracts in dried form (anthocyanin-based pigmentation enabling market value for floral crafts).
Standards and regulation:
- None specific to this species are recognized in international standards.
Sustainability and sourcing:
- Cultivation occurs primarily in horticulture; no sustainability frameworks specific to this taxon have been established.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Horminum coloratum | Moench | Methodus : 377 (1794) |
| Horminum sativum | Mill. | Gard. Dict. ed. 8 : n.º 5 (1768) |
| Horminum viride | Moench | Methodus : 377 (1794) |
| Ormilis horminum | Raf. | Fl. Tellur. 3: 94 (1837) |
| Ormilis viridis | Raf. | Fl. Tellur. 3: 94 (1837) |
| Salvia colorata | Thore | Essai Chloris : 17 (1803) |
| Salvia comosa | Salisb. | Prodr. Stirp. Chap. Allerton : 73 (1796) |
| Salvia dolichorrhiza | Caball. | Bol. Soc. Esp. Hist. Nat. 13: 238 (1913) |
| Salvia horminum | L. | Sp. Pl. : 24 (1753) |
| Salvia intercedens | Pobed. | Fl. URSS 21: 657 (1954) |
| Salvia rosani | Ten. | Fl. Napol. 3: 22 (1824) |
| Salvia spielmannii | Scop. | Delic. Fl. Faun. Insubr. 3: 31 (1788) |
| Salvia truncata | Willd. | Enum. Pl. : 34 (1809) |
| Sclarea viridis | (L.) Soják | Cas. Nár. Mus., Odd. Prír. 152: 22 (1983) |
| Salvia horminum var. intermedia | Briq. | Lab. Alp. Mar. 503. 1895 |
| Salvia horminum var. hypoleuca | Briq. | Lab. Alp. Mar. 505. 1895 |
| Salvia horminum var. angustifolia | Boiss. | Fl. Orient. 4: 631. 1879 |
| Flipanta ovata | Raf. | Fl. Tellur. 3: 92 (1837) |
| Salvia viridis var. comata | Heldr. | Fl. Céphalonie : 58 (1882) |
| Salvia viridis var. violacea | Benth. | Prodr. 12: 278 (1848) |
| Salvia viridis var. horminum | (L.) Batt. | Fl. Algérie [Battandier & al.] Dicot.: 685 1890 |
| Salvia horminum var. viridis | (L.) Caruel | Fl. Ital. 6: 246 (1884) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | annual clary |
| Arabic | قصعين أخضر |
| Azerbaijani | yaşıl adaçayı |
| azb | یاشیل آداچایی |
| Bulgarian | зелен конски босилек |
| Czech | šalvěj zahradní |
| Welsh | clari unflwydd |
| German | buntschopf-salbei |
| German | schopf-salbei |
| German | grüner salbei |
| German | salvia horminum |
| Estonian | kirju salvei |
| Persian | مریمگلی یکساله |
| Finnish | kirjosalvia |
| Hebrew | מרווה דגולה |
| Norwegian Bokmål | spraglesalvie |
| Norwegian Nynorsk | spreklesalvie |
| Russian | Шалфей зелёный |
| Swedish | broksalvia |
| Chinese | 彩苞鼠尾草 |
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
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Africa click to expand
-
Northern Africa
- Algeria
- Libya
- Morocco
- Tunisia
-
Northern Africa
-
Asia-temperate click to expand
-
Caucasus
- North Caucasus
- Transcaucasus
-
Middle Asia
- Turkmenistan
-
Western Asia
- Cyprus
- East Aegean Islands
- Lebanon-Syria
- Palestine
- Turkey
-
Caucasus
-
Europe click to expand
-
Eastern Europe
- Central European Russia
- Krym
- South European Russia
-
Middle Europe
- Czechoslovakia
-
Southeastern Europe
- Albania
- Bulgaria
- Greece
- Italy
- Kriti
- Sicilia
- Turkey-in-Europe
- Yugoslavia
-
Southwestern Europe
- Baleares
- Portugal
- Spain
-
Eastern Europe
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000302616 |
| USDA Plants | SAVI13 |
| Tropicos | 17600315 |
| INPN | 120704 |
| Flora of Italy | 4680 |
| KEW | urn:lsid:ipni.org:names:457515-1 |
| The Plant List | kew-184146 |
| Open Tree Of Life | 499330 |
| Observations.org | 150087 |
| NCBI Taxonomy | 49221 |
| NBN Atlas | NBNSYS0000034225 |
| IPNI | 457515-1 |
| iNaturalist | 493015 |
| GBIF | 3883959 |
| Freebase | /m/05k60x |
| EPPO | SALVI |
| EOL | 6342307 |
| USDA GRIN | 401827 |
| Wikipedia | Salvia_viridis |
| CMAUP | NPO15183 |
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.
If you wish to see all the related articles click here.
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.
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Benzenoids / Naphthalenes | |||||
| 1-Hydroxy-8,13,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one | 50907654 | Click to see | 298.40 | unknown | https://doi.org/10.1055/S-2000-8596 |
| Microstegiol | 403772 | Click to see | 298.40 | unknown |
https://doi.org/10.1055/S-2000-8596 https://doi.org/10.1016/S0031-9422(03)00225-5 |
| > 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/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2000-8596 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| (4aS,10aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one | 15241260 | Click to see | 300.40 | unknown |
https://doi.org/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2000-8596 |
| (4bR)-4-hydroxy-9-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one | 102005792 | Click to see CC(C)C1=CC2=CC(=C3C(CCCC3(C2=C(C1=O)O)C)(C)C)OC | 328.40 | unknown | https://doi.org/10.1055/S-2000-8596 |
| (4bS,8aS,9R,10R)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9,10-triol | 102005790 | Click to see | 348.50 | unknown |
https://doi.org/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2000-8596 |
| 3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9,10-triol | 163033166 | Click to see CC(C)C1=C(C(=C2C(=C1)C(C(C3C2(CCCC3(C)C)C)O)O)O)OC | 348.50 | unknown | https://doi.org/10.1055/S-2000-8596 |
| 4-hydroxy-9-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one | 162882186 | Click to see CC(C)C1=CC2=CC(=C3C(CCCC3(C2=C(C1=O)O)C)(C)C)OC | 328.40 | unknown | https://doi.org/10.1055/S-2000-8596 |
| 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/10.1055/S-2000-8596 |
| 6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one | 85093918 | Click to see | 300.40 | unknown | https://doi.org/10.1055/S-2000-8596 |
| 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/10.1055/S-2000-8596 |
| 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-2000-8596 |
| Sugiol | 94162 | Click to see | 300.40 | unknown | https://doi.org/10.1055/S-2000-8596 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (2S,3R,4aR,6aR,6bS,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-2,3-diol | 101686479 | Click to see | 442.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89266-3 |
| (3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | 9955042 | Click to see | 442.70 | unknown | via CMAUP database |
| 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-9,10-diol | 72745631 | 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(00)89266-3 |
| 4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-2,3-diol | 23132194 | Click to see | 442.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89266-3 |
| Diosgenin | 99474 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 | 414.60 | unknown | via CMAUP database |
| Lup-20(29)-en-3-ol, (3beta)- | 521518 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89266-3 |
| 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(00)89266-3 |
| Lupeol | 259846 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89266-3 |
| Yamogenin | 441900 | Click to see | 414.60 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids | |||||
| (4bS,8aS,9R)-4,9-dihydroxy-1-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-one | 154497675 | Click to see CC(C)C1=C(C2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O)OC | 346.50 | unknown | https://doi.org/10.1016/S0031-9422(03)00225-5 |
| 4,9-dihydroxy-1-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-one | 162992044 | Click to see | 346.50 | unknown | https://doi.org/10.1055/S-2000-8596 |
| Viridinol | 102005791 | Click to see | 346.50 | unknown | https://doi.org/10.1055/S-2000-8596 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins | |||||
| (2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 102155845 | Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O | 901.00 | unknown | via CMAUP database |
| (2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 102155844 | Click to see | 901.00 | unknown | via CMAUP database |
| (2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 16204183 | Click to see | 1015.20 | unknown | via CMAUP database |
| (2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 21603983 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 | 869.00 | unknown | via CMAUP database |
| (2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 16204068 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 | 869.00 | unknown | via CMAUP database |
| (3beta,25S)-Spirost-5-en-3-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside | 441901 | Click to see | 722.90 | unknown | via CMAUP database |
| 3-O-[alpha-L-ramnopyranosyl(1 to 2)]-O-[alpha-L-ramnopyranosyl(1 to 4)]-O-beta-D-galactopyranosid(1)]-(25S)-spirost-5-ene-3beta-ol | 10653210 | Click to see | 869.00 | unknown | via CMAUP database |
| Asperin | 21603986 | Click to see | 1015.20 | unknown | via CMAUP database |
| CID 16204180 | 16204180 | Click to see | 722.90 | unknown | via CMAUP database |
| CID 16204181 | 16204181 | Click to see | 869.00 | unknown | via CMAUP database |
| Dioscin | 119245 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 | 869.00 | unknown | via CMAUP database |
| Methylprotodioscin | 11263254 | Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC | 1063.20 | unknown | via CMAUP database |
| Progenin II | 44429638 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 | 722.90 | unknown | via CMAUP database |
| Prosapogenin A | 11061578 | Click to see | 722.90 | unknown | via CMAUP database |
| Protodioscin | 441891 | Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O | 1049.20 | unknown | via CMAUP database |
| Pseudoprotodioscin | 21637110 | Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O | 1031.20 | unknown | via CMAUP database |
| Trigonelloside C | 441899 | Click to see | 1049.20 | unknown | via CMAUP database |
| Trillin | 11827970 | Click to see | 576.80 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | via CMAUP database |
| 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 | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds | |||||
| 4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose | 5288769 | Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O | 342.30 | unknown | via CMAUP database |
| Gal(a1-6)a-Man | 11724912 | Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O | 342.30 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides | |||||
| beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp | 5287808 | Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O | 504.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| 2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 154496936 | Click to see | 594.50 | unknown | https://doi.org/10.1016/S0031-9422(01)00415-0 |
| 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 139031083 | Click to see | 578.50 | unknown | https://doi.org/10.1016/S0031-9422(01)00415-0 |
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