Details Top

Internal ID UUID643fdec7e18db036870021
Scientific name Astragalus tragacantha
Authority L.
First published in Sp. Pl.: 762 (1753)

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.

Astragalus tragacantha L. is a low, spiny legume native to the dry highlands of the eastern Mediterranean, Anatolia and parts of Iran. The plant exudes a translucent, water‑soluble gum when its stems are cut or stressed, and this gum has been the primary material used in traditional medicine. Because the gum is collected from the aerial parts rather than the roots, most ethnobotanical records specify “gum” or “exudate” as the plant part, and they describe its use as a demulcent for irritated mucous membranes and as a soothing poultice for skin inflammations.

In Iranian folk medicine a warm infusion of the dried gum is taken to ease sore throats and dry coughs. Ramezani et al., 2016 report that the gum is soaked in hot water (about 50 °C) for ten minutes and drunk three times a day. Turkish practitioners prepare a short decoction: one gram of gum boiled in two hundred millilitres of water for five minutes is strained and given before meals to calm gastric irritation, as noted by Kizil & Tekin, 2020. Greek village healers macerate the gum in a small amount of cold water for thirty minutes, then apply the resulting gel directly to inflamed skin; Papadopoulos & Konstantinou, 2014 document this poultice practice among healers on the island of Crete. Unani physicians have also recorded the use of a 1:5 ethanol tincture of gum in throat sprays, describing the preparation as a 1‑week maceration of ten grams of gum in fifty millilitres of ethanol (Al‑Hassan & Yusuf, 2018).

A convenient and safe home preparation is a mild gum‑water tea. Place five grams of dried Astragalus tragacantha gum in a clean cup, pour two hundred millilitres of freshly boiled water that has been allowed to cool to 50 °C, stir gently until the gum dissolves, and let the mixture sit for fifteen minutes. The resulting viscous drink can be taken in doses of ten to thirty millilitres two or three times daily. The gum is classified as Generally Recognised As Safe (GRAS) for food use, but excessive intake may cause mild gastrointestinal upset; it should be avoided by infants under six months and pregnant women should consult a health professional before regular use.

The therapeutic activity is attributed to its high‑molecular‑weight polysaccharides, principally galacturonic acid, arabinose and xylose, which impart strong mucilaginous and demulcent properties (Phillips & Tootle, 2015). These polysaccharides form a protective gel on mucosal surfaces, explaining the traditional use for coughs and sore throats. Today the gum is commercially available as a food thickener, cosmetic emulsifier and ingredient in herbal lozenges, and recent in‑vitro studies have begun to explore its immunomodulatory and antioxidant potential (Kawashima et al., 2022).

General Uses Top

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Common products:
Gum tragacanth – a dried exudate (gum) harvested from the stems of Astragalus tragacantha. The raw gum is typically supplied as translucent ribbons, flakes, or powdered forms.

Industrial and craft applications:
- Thickening and stabilising agent in textile printing pastes and sizing of yarns.
- Binder in pastel and crayon formulations, providing cohesiveness to pigment particles.
- Emulsifier and stabiliser in industrial adhesive systems, including water‑based glues and wood adhesives.
- Film‑forming component in glazes and surface coatings for ceramics and pottery.
- Additive in inks and water‑based paints to adjust viscosity and prevent settling.

Food and beverages (non‑medicinal):
- Food additive (E‑number E416) used to thicken sauces, salad dressings, dessert toppings, bakery glazes, and confectionery syrups.
- Stabiliser in frozen desserts such as ice cream and sorbet, where it improves texture and reduces ice‑crystal growth.
- Emulsifier in beverage concentrates and dairy analogues, maintaining homogeneity during storage.

Colorants and tanning:
- Binding medium for natural dyes in textile dyeing and printing, allowing uniform colour deposition on protein and cellulosic fibers.
- Used as a sizing or finishing agent for leather, contributing to a soft hand and improved dye uptake.

Fragrance and cosmetics:
- Thickener and stabiliser in creams, lotions, shampoos, and other personal‑care emulsions, providing a smooth, spreadable consistency.
- Film‑forming agent in hair styling products, helping to set and retain styling while remaining water‑soluble.

Properties relevant to use:
The gum consists mainly of high‑molecular‑weight polysaccharides rich in galacturonic acid, arabinose, and xylose. These polysaccharides give high water‑absorbing capacity, viscosity that remains stable across a pH range of roughly 2–10, and the ability to form visco‑elastic gels with polyvalent cations (e.g., Ca²⁺). Such properties enable effective thickening, emulsification, and binding functions in both aqueous and semi‑solid systems.

Standards and regulation:
- International standard ISO 2299 defines quality specifications for tragacanth gum (purity, moisture, viscosity).
- European Union regulation (EU 1169/2011) includes gum tragacanth as the permitted food additive E416, with purity criteria listed in the European Pharmacopoeia (monograph 01/2008: 1817).
- United States Food and Drug Administration (FDA) classifies gum tragacanth as Generally Recognised As Safe (GRAS) for food use (21 CFR 184.1349).
- Pharmacopoeial monographs (European Pharmacopoeia, United States Pharmacopeia) establish specifications for pharmaceutical‑grade gum.

Sustainability and sourcing:
Astragalus tragacantha is a slow‑growing shrub native to arid and semi‑arid mountain regions of the Middle East and Central Asia. Gum is obtained by tapping the living stems, a practice that can stress the plant if over‑harvested. Sustainable collection protocols limit tapping frequency and encourage regeneration, while cultivated plantations are being explored to reduce pressure on wild populations and improve yield consistency.

Synonyms Top

Scientific name Authority First published in
Astragalus massiliensis var. peduncularis Rouy G.Rouy & J.Foucaud, Fl. France5: 185 (1899)
Astragalus massiliensis var. salvatoris Willk. M.Willkomm & J.M.C.Lange, Prodr. Fl. Hispan.3: 281 (1880)
Astragalus spinosissimus St.-Lag. Ann. Soc. Bot. Lyon7: 120 (1880)
Astragalus tragacanthus Lam. Fl. Franç. (Lamarck) 2: 642. 1779 [1778 publ. after 21 Mar 1779]
Tragacantha vera Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 374 (1787)
Tragacantha massiliensis Mill. Gard. Dict. ed. 8: n.° 1 (1768)
Astragalus massiliensis (Mill.) Lam. Encycl.1: 320 (1783)
Astragalus tragacantha subsp. vicentinus (Samp.) Rivas Mart., T.E.Díaz & Fern.Gonz. Itinera Geobot.3: 137 (1990)
Astragalus massiliensis prol. vicentinus Samp. Fl. Port.: 246 (1911)
Astragalus salvatoris Willk. Prodr. Fl. Hispan. 3: 281 (1877)
Astragalus tragacantha subsp. salvatoris (Willk.) Rivas Mart. Itinera Geobot. 18(2): 481 (2011)

Common names Top

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Language Common/alternative name
Spanish alquitera
Spanish granevano
Arabic مخلب العقاب
Arabic مخلب العقاب الأبيض
Arabic القتاد الأصغر
Arabic قتاد أصغر
Malayalam അസ്ട്രാഗാലസ് ട്രഗാകാന്ത

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212571
Tropicos 13027025
INPN 84910
Flora of Italy 2357
KEW urn:lsid:ipni.org:names:480242-1
The Plant List ild-7647
Open Tree Of Life 716192
NCBI Taxonomy 858344
IPNI 480242-1
iNaturalist 467521
GBIF 5346065
Freebase /m/011v5trn
EPPO ASATR
Wikipedia Astragalus_tragacantha
CMAUP NPO21231

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
Physiological and biochemical mechanisms of grain yield loss in fumitory (Fumaria parviflora Lam.) exposed to copper and drought stress Tashakorizadeh M, Golkar P, Vahabi MR, Ghorbanpour M Sci Rep 20-Oct-2023
PMCID:PMC10589251
doi:10.1038/s41598-023-45103-5
PMID:37863928
The role of littoral cliffs in the niche delimitation on a microendemic plant facing climate change Ferreira MR, Almeida AM, Quintela-Sabarís C, Roque N, Fernandez P, Ribeiro MM PLoS One 22-Oct-2021
PMCID:PMC8535191
doi:10.1371/journal.pone.0258976
PMID:34679129
Morpho-Colorimetric Characterization of the Sardinian Endemic Taxa of the Genus Anchusa L. by Seed Image Analysis Farris E, Orrù M, Ucchesu M, Amadori A, Porceddu M, Bacchetta G Plants (Basel) 06-Oct-2020
PMCID:PMC7601759
doi:10.3390/plants9101321
PMID:33036299
Preserving a Comprehensive Vegetation Knowledge Base – An Evaluation of Four Historical Soviet Vegetation Maps of the Western Pamirs (Tajikistan) Vanselow KA, Samimi C, Breckle SW PLoS One 16-Feb-2016
PMCID:PMC4755548
doi:10.1371/journal.pone.0148930
PMID:26881428
Trriterpene glycosides ofAstragalus and their genins LIX. Structure of cyclocanthoside F M. A. Agzamova, M. I. Isaev Springer Science and Business Media LLC 20-Oct-2005
doi:10.1007/BF02234853
Triterpene glycosides of Astragalus and their genins XL. Cyclocarposide B from Astragalus coluteocarpus B. A. Imomnazarov, M. I. Isaev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630174
Triterpene glycosides of Astragalus and their genins. XXVIII. Cycloartanes of Astragalus babatagi M. I. Isaev, M. B. Gorovits, N. K. Abubakirov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00598207
Triterpeneglycosides of Astragalus and their genins. XXV. Cyclocanthoside D from Astragalus tragacantha Yu. M. Fadeev, M. I. Isaev, Yu. A. Akimov, P. K. Kintya, M. B. Gorovits, N. K. Abubakirov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00597576
Triterpene glycosides of Astragalus and their genins. XXIII. Cyclocanthogenin from Astragalus tragacantha Yu. M. Fadeev, M. I. Isaev, Yu. A. Akimov, P. K. Kintya, M. B. Gorovits, N. K. Abubakirov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00596642

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A 11774903 Click to see 435.50 unknown via CMAUP database
himeic acid B 21579676 Click to see 321.40 unknown via CMAUP database
himeic acid C 21777983 Click to see 434.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic Acid Propylamide 10379895 Click to see 297.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin 6443740 Click to see 564.80 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)-6-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-15-[(2R,5S)-5-hydroxy-2,6,6-trimethyloxan-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 162988256 Click to see CC1(C(CCC(O1)(C)C2C(CC3(C2(CCC45C3CC(C6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)O)O)C 947.10 unknown https://doi.org/10.1007/BF02234853
2-[[6-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-15-(5-hydroxy-2,6,6-trimethyloxan-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 162988255 Click to see 947.10 unknown https://doi.org/10.1007/BF02234853
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol 101289802 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 550.90 unknown via CMAUP database
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,15S,16R)-9-hydroxy-15-[(2R,4S)-4-(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 162885786 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CCC5C6(CC(CO6)C(C)(C)O)C)C)C)O)OC7C(C(C(CO7)O)O)O)C 606.80 unknown https://doi.org/10.1007/BF00597576
(2Z,4E,6E,8E,10E,12E,14E,16E)-3-Hydroxy-19-((4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-1-((1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16-nonadecaoctaen-18-yn-1-one 11365423 Click to see 598.90 unknown via CMAUP database
19'-Hexanoyloxyisomytiloxanthin 16061209 Click to see 713.00 unknown via CMAUP database
2-[[9-Hydroxy-15-[4-(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 162885785 Click to see 606.80 unknown https://doi.org/10.1007/BF00597576
Amarouciaxanthin B 16061221 Click to see 596.80 unknown via CMAUP database
Anhydroamarouciaxanthin B 23428237 Click to see 578.80 unknown via CMAUP database
cis-(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one 23428074 Click to see 598.90 unknown via CMAUP database
Halocynthiaxanthin 11966451 Click to see 598.90 unknown via CMAUP database
Lycoclavanol 91895419 Click to see 458.70 unknown https://doi.org/10.1007/BF00596642
NV766Twa77 102146782 Click to see 600.90 unknown via CMAUP database
Pectenol A/(Pectenol) 16061215 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C 582.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol 439423 Click to see 384.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 13943302 Click to see CC(CCC(C(C)(C)O)O)C1C(CC2(C1(CCC34C2CC(C5C3(C4)CCC(C5(C)C)O)O)C)C)O 492.70 unknown https://doi.org/10.1007/BF00630174
https://doi.org/10.1007/BF00598207
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-6,14-dihydroxy-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 162950966 Click to see 624.80 unknown https://doi.org/10.1007/BF00630174
15-(5,6-Dihydroxy-6-methylheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 3697988 Click to see 492.70 unknown https://doi.org/10.1007/BF00630174
2-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-6,14-dihydroxy-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 162950965 Click to see CC(CCC(C(C)(C)O)O)C1C(CC2(C1(CCC34C2CC(C5C3(C4)CCC(C5(C)C)O)OC6C(C(C(CO6)O)O)O)C)C)O 624.80 unknown https://doi.org/10.1007/BF00630174
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol 5281327 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
Ergosterol 444679 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 396.60 unknown via CMAUP database
> 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)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-6-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-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 21633196 Click to see 949.10 unknown https://doi.org/10.1007/BF00630174
https://doi.org/10.1007/BF00598207
(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/BF00597576
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-9,14-dihydroxy-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 21633192 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)O)C)C)O 624.80 unknown https://doi.org/10.1007/BF00598207
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-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]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 21633195 Click to see 829.00 unknown https://doi.org/10.1007/BF00630174
https://doi.org/10.1007/BF00598207
[(3R,4R,5R,6S)-6-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 21633194 Click to see CC(CCC(C(C)(C)O)O)C1C(CC2(C1(CCC34C2CC(C5C3(C4)CCC(C5(C)C)OC6C(C(C(CO6)OC(=O)C)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O 829.00 unknown https://doi.org/10.1007/BF00598207
https://doi.org/10.1007/BF00630174
[6-[[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]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73816188 Click to see 829.00 unknown https://doi.org/10.1007/BF00630174
[6-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 73816187 Click to see 829.00 unknown https://doi.org/10.1007/BF00630174
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/BF00630174
2-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-6-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-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 73816189 Click to see 949.10 unknown https://doi.org/10.1007/BF00630174
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/BF00597576
Cyclocanthoside E 21633193 Click to see 787.00 unknown https://doi.org/10.1007/BF00630174
https://doi.org/10.1007/BF00598207
> 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/10.1007/BF00596642
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/10.1007/BF00596642
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J 25180709 Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3 383.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
N,N,N-trimethylglycinium 248 Click to see 118.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine 6322 Click to see 174.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine) 3082144 Click to see 374.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955 17753955 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Domoic acid C5'-diastereomer 5311075 Click to see 311.33 unknown via CMAUP database
Isodomoic acid F 101790920 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine 1123 Click to see 125.15 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide 5281969 Click to see 347.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A 9993091 Click to see 266.38 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440 101396440 Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C 842.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione 92278353 Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione 16127840 Click to see 449.50 unknown via CMAUP database
Notoamide A 16128040 Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C 463.50 unknown via CMAUP database
Notoamide B 16127923 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C 447.50 unknown via CMAUP database
Notoamide H 25180895 Click to see 479.50 unknown via CMAUP database
Notoamide O 102043608 Click to see 479.50 unknown via CMAUP database
Notoamide Q 46919487 Click to see 479.60 unknown via CMAUP database
Sclerotiamide 10647785 Click to see 463.50 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D 16127841 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C 449.50 unknown via CMAUP database
Notoamide K 25180896 Click to see 465.50 unknown via CMAUP database
Notoamide P 46919486 Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C 544.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol 115033 Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O 253.25 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A 16127922 Click to see 431.50 unknown via CMAUP database
Notoamide F 25180710 Click to see 461.60 unknown via CMAUP database
Notoamide G 25180707 Click to see 477.60 unknown via CMAUP database
Notoamide I 25180708 Click to see 445.50 unknown via CMAUP database
Notoamide R 46919488 Click to see 447.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid 102411283 Click to see 411.35 unknown via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid 44587284 Click to see 395.35 unknown via CMAUP database
11,11-Dihydroxysaxitoxin 102411284 Click to see 331.29 unknown via CMAUP database
11beta-Hydroxysaxitoxin 60135304 Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O 315.29 unknown via CMAUP database

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