Details Top

Internal ID UUID6440452a4e074753305273
Scientific name Astragalus dissectus
Authority B.Fedtsch. & N.A.Ivanova
First published in Trudy Tadzhiksk. Bazy2: 148 (1936)

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.

Inula helenium has a long history as a warming, respiratory herb. Among the Khatri community of Punjab, Pakistan, dried root was regularly made into tea for coughs and asthma (Ahmed et al., 2006). In the Western Himalaya, decoctions of the root were used for chronic bronchitis and bronchial catarrh (Ahmed & Ahmad, 2020), while in parts of Iran and parts of Central Europe the same infusion was taken for colds and as a digestive tonic (Gurbuz & Heinrich, 2004; M. Heinrich et al., 2004). It was also taken as a general strength and convalescence tonic (Sperber, 2003). To prepare a mild root tea, simmer about 6–12 g of dried, sliced root in 250–500 ml of water for 15–30 minutes, cool, and sip 1/2–1 cup several times daily during an acute cold or cough. Do not use in pregnancy; children and long-term use require supervision. A 1:5 ethanol tincture is made by macerating 100 g sliced, dried root in 500 ml of 40–50% ethanol for 2–3 weeks, shaking weekly, then straining and pressing. Typical adult dose is 1–2 ml 2–3 times daily for respiratory relief.

Key constituents reported for this species help explain its traditional actions. Isoalantolactone is a prominent sesquiterpene lactone, accompanied by alantolactone and related helenalin-type compounds, flavonoids such as quercetin and rutin, and polyacetylenes including falcarindiol (Gurbuz & Heinrich, 2004; Gertsch, 2011; H.-M. Ernst et al., 2018). These molecules account for the plant’s bitter, warming character and its expectorant and carminative effects.

Modern relevance is visible both in research and in the marketplace. Recent studies show the sesquiterpene lactones possess notable anti-inflammatory activity against NF-κB and TNF-α, while polyacetylenes demonstrate anti-bacterial and neuroprotective potential (Ravipati et al., 2012; Bohm et al., 2015; Jiang et al., 2020; Liang et al., 2022). Derivatives are under investigation as anti-tumor and anti-diabetic leads (Gao et al., 2011; Sun et al., 2015). Commercially, elecampane root continues to be sold in pharmacies and herbal shops throughout Europe and Asia as a tea, tincture, syrup, and lozenge, and rural communities still prepare the home decoction during winter for cough and congestion.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Astracantha hilariae (Boriss.) Czerep. Vasc. Pl. Russia & Adj. States: 230 (1995)
Astracantha dissecta (B.Fedtsch. & N.A.Ivanova) Podl
Astracantha tenuispina (Boriss.) Czerep. Vasc. Pl. Russia & Adj. States: 230 (1995)
Astragalus munitus Boriss. V.L.Komarov (ed.), Fl. URSS12: 350 (1946)
Astragalus tenuispina Boriss.
Astragalus chionocalyx (Nevski) Boriss. V.L.Komarov (ed.), Fl. URSS12: 347 (1946)
Astragalus devius (Boriss.) Boriss. V.L.Komarov (ed.), Fl. URSS12: 349 (1946)
Tragacantha kuhitangi Nevski Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast.4: 258 (1937)
Tragacantha chionocalyx Nevski Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast.4: 258 (1937)
Astracantha chionocalyx (Nevski) Czerep. Vasc. Pl. Russia & Adj. States: 229 (1995)
Tragacantha proxima Boriss. Fl. Tadzhiksk. S.S.R.5: 681 (1937)
Tragacantha hilariae Boriss. Fl. Tadzhiksk. S.S.R.5: 683 (1937)
Tragacantha tenuispina Boriss. Fl. Tadzhiksk. S.S.R.5: 683 (1937)
Astracantha devia (Boriss.) Czerep. Vasc. Pl. Russia & Adj. States: 229 (1995)
Astragalus hilariae (Boriss.) Širj. Repert. Spec. Nov. Regni Veg.47: 256 (1939)
Astragalus kuhitangi (Nevski) Širj. Repert. Spec. Nov. Regni Veg.47: 256 (1939)
Tragacantha devia Boriss. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R.10: 62 (1947)
Tragacantha dissecta (B.Fedtsch. & N.A.Ivanova) Boriss. Fl. Uzbekistan.3: 676 (1955)
Astracantha dissecta (B.Fedtsch. & N.A.Ivanova) Podlech Mitt. Bot. Staatssamml. München19: 9 (1983)
Astracantha kuhitangi (Nevski) Podlech Mitt. Bot. Staatssamml. München19: 13 (1983)
Astragalus proximus (Boriss.) Boriss. Fl. URSS 12: 348 (1946)

Common names Top

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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
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001055690
Tropicos 13038840
KEW urn:lsid:ipni.org:names:477168-1
The Plant List tro-13038840
Open Tree Of Life 3929514
IPNI 477168-1
GBIF 5352830
CMAUP NPO6938

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)!
Title Authors Publication Released IDs
Triterpene glucosides of Astragalus and their genins. LXXIV. Cyclotrisectoside, the first trisdesmoside of cyclocephalogenin I. A. Sukhina, R. P. Mamedova, M. A. Agzamova, M. I. Isaev Springer Science and Business Media LLC 19-Aug-2007
doi:10.1007/S10600-007-0068-3
Cyclosieversigenin 3-O-β-D-glucopyranoside fromAstragalus kuhitangi R. Karimov, R. U. Umarova, Z. Saatov, M. G. Levkovich, N. D. Abdullaev Springer Science and Business Media LLC 15-Mar-2006
doi:10.1007/BF02336091
Triterpene glycosides ofAstragalus and their genins LX. Cyclodissectoside — A new dixyloside of cyclocephalogenin I. A. Sukhina, M. A. Agzamova, M. I. Isaev Springer Science and Business Media LLC 25-Jan-2006
doi:10.1007/BF02282514
Triterpene glycosides ofAstragalus and their genins. LI. isoprenoids ofAstragalus dissectus, a.ephemerotorum, andA. kulabensis I. A. Sukhina, M. I. Isaev Springer Science and Business Media LLC 15-Feb-2005
doi:10.1007/BF01164901
Triterpene glycosides of Astragalus and their genins. XXIX. Cycloartanes of Astragalus kuhitangi M. A. Agzamova, M. I. Isaev, I. I. Mal'tsev, M. B. Gorovits, N. K. Abubakirov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00598208

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
> Benzenoids / Indanes / Indanones
(2S,3s)-2,3-dihydro-3-hydroxy-6-(2-hydroxyethyl)-5-hydroxymethyl-2,7-dimethyl-1h-inden-1-one 21670042 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)CO)CCO)C)O 250.29 unknown via CMAUP database
(2S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one 169739 Click to see 234.29 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
15-Hydroxydehydroabietic Acid 14487943 Click to see 316.40 unknown via CMAUP database
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown via CMAUP database
Imbricatolic Acid 70688370 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CCO 322.50 unknown via CMAUP database
Junicedric acid 38347252 Click to see 336.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4R,5R,6S)-6-[(3S)-5-[(1S,2R,4S,4aR,8aR)-4-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 10509989 Click to see 907.00 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 24882166 Click to see 614.80 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 16109823 Click to see CC1CC(C2(C(C1(C)CCC(=CCO)C)CCC=C2C)C)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)CO)O)O)O)O)O 614.80 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(3S)-3-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-methylpent-4-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 10724564 Click to see CC1CC(C2(C(C1(C)CCC(C)(C=C)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)C)O)O)O)O)O)CCC=C2C)C)OC5C(C(C(C(O5)C)OC6C(C(C(C(O6)COC(=O)C)O)O)O)O)O 949.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,4S)-4-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163185654 Click to see 785.00 unknown https://doi.org/10.1007/BF00598208
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(3S,6R)-6-[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-7,7,12,16-tetramethyl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2,2,6-trimethyloxan-3-yl]oxyoxane-3,4,5-triol 162916022 Click to see 947.10 unknown https://doi.org/10.1007/S10600-007-0068-3
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,5S)-5-hydroxy-2,6,6-trimethyloxan-2-yl]-7,7,12,16-tetramethyl-9-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 162851484 Click to see 754.90 unknown https://doi.org/10.1007/BF02282514
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6,14-dihydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 101683491 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(CO7)O)O)O)O)C 622.80 unknown https://doi.org/10.1007/BF02282514
2-(Hydroxymethyl)-6-[6-[14-hydroxy-7,7,12,16-tetramethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(3,4,5-trihydroxyoxan-2-yl)oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2,2,6-trimethyloxan-3-yl]oxyoxane-3,4,5-triol 76012006 Click to see 947.10 unknown https://doi.org/10.1007/S10600-007-0068-3
2-[[14-Hydroxy-15-(5-hydroxy-2,6,6-trimethyloxan-2-yl)-7,7,12,16-tetramethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 162851483 Click to see CC1(C(CCC(O1)(C)C2C(CC3(C2(CCC45C3CC(C6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)O)O)C 754.90 unknown https://doi.org/10.1007/BF02282514
2-[[14-Hydroxy-15-[4-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162989487 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CC(CO6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C 785.00 unknown https://doi.org/10.1007/BF00598208
2-[[6,14-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14241107 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)O)C 652.90 unknown https://doi.org/10.1007/BF02282514
https://doi.org/10.1007/BF02336091
2-[[6,14-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 85111280 Click to see 622.80 unknown https://doi.org/10.1007/BF02282514
Astramembrangenin 3664530 Click to see 490.70 unknown https://doi.org/10.1007/BF02336091
Brachyoside B 14241109 Click to see 652.90 unknown https://doi.org/10.1007/BF02336091
https://doi.org/10.1007/BF02282514
Cycloastragenol 13943286 Click to see 490.70 unknown https://doi.org/10.1007/BF02336091
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,4S)-4-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 162982254 Click to see 490.70 unknown https://doi.org/10.1007/BF00598208
15-[4-(2-Hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 162982253 Click to see 490.70 unknown https://doi.org/10.1007/BF00598208
Lycoclavanol 91895419 Click to see 458.70 unknown https://doi.org/10.1007/BF01164901
https://doi.org/10.1007/BF02336091
https://doi.org/10.1007/BF00598208
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,5S)-5-hydroxy-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101794561 Click to see 949.10 unknown https://doi.org/10.1007/BF00598208
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-14-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 100989392 Click to see 787.00 unknown https://doi.org/10.1007/BF00598208
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 102069296 Click to see 754.90 unknown https://doi.org/10.1007/BF02282514
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 14241104 Click to see 622.80 unknown https://doi.org/10.1007/BF02336091
2-[[14-Hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 500122 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C 785.00 unknown https://doi.org/10.1007/BF02336091
https://doi.org/10.1007/BF02282514
2-[[14-Hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 3665113 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C 754.90 unknown https://doi.org/10.1007/BF02282514
2-[[14-Hydroxy-15-[5-hydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75985736 Click to see 949.10 unknown https://doi.org/10.1007/BF00598208
2-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 4979431 Click to see CC(CCC(C(C)(C)O)O)C1C(CC2(C1(CCC34C2CC(C5C3(C4)CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O 787.00 unknown https://doi.org/10.1007/S10600-007-0068-3
https://doi.org/10.1007/BF02282514
2-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-9-hydroxy-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-14-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 4297917 Click to see 787.00 unknown https://doi.org/10.1007/BF00598208
2-[[9,14-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 3826638 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)OC7C(C(C(CO7)O)O)O)C 622.80 unknown https://doi.org/10.1007/BF02336091
Astragaloside IV 13943297 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C 785.00 unknown https://doi.org/10.1007/BF02336091
https://doi.org/10.1007/BF02282514
Astragaloside VII 14241100 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(CO9)O)O)O)C 947.10 unknown https://doi.org/10.1007/BF02336091
https://doi.org/10.1007/S10600-007-0068-3
astragaloside VII 3752972 Click to see 947.10 unknown https://doi.org/10.1007/S10600-007-0068-3
https://doi.org/10.1007/BF02336091
Cyclocanthoside E 21633193 Click to see 787.00 unknown https://doi.org/10.1007/BF02282514
https://doi.org/10.1007/S10600-007-0068-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/BF02282514
(3S,8R,9R,10R,13R,14R,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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 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/10.1007/BF02282514
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/10.1007/BF02282514
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(2,4-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 102392053 Click to see 316.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
Isotachioside 15098566 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Nonacosan-10-one 441490 Click to see 422.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-4-benzopyrone 442396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-chroman-4-one 49770782 Click to see 314.30 unknown via CMAUP database

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