Details Top

Internal ID UUID643fd95ae071f760158595
Scientific name Astragalus gummifer
Authority Labill.
First published in J. Phys. (Halle)1: 46 (1790)

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.

This thorny milkvetch produces the gum tragacanth that has been collected for centuries across Iran and the Near East. In the Unani tradition of Iran, the gum is used as a demulcent in syrups and throat remedies, and as a soothing infusion for coughs and gastric upset, often taken with honey (Ghraibeghi, 1993). Turkish herbal texts record the gum being mucilaginous infusions or light decoctions for coughs, and occasionally as a lozenge or poultice to calm irritated mucosa or facilitate wound healing (Baytop, 1999). Ethnobotanical surveys in southern France also note historic use of tragacanth gum in mild demulcent teas and throat preparations for local children (Comar and Bonmarin, 1908).

A simple recipe for a demulcent tea is to stir 1–2 teaspoons of finely powdered gum tragacanth into a cup of just-boiled water, stir until a thick, cloudy mixture forms, then let it cool to lukewarm and drink in small sips. It is generally very mild, but only a small amount is needed; excessive doses can cause loose stools. People with peanut or legume allergy should avoid it, and pregnant or nursing individuals should check with a clinician before use. For a 1:5 ethanol tincture, macerate 50 g of gum tragacanth in 250 mL of 45–50% ethanol for 4–6 weeks in a cool, dark place, shaking every few days. Typical drops are 10–20 in water as needed; do not exceed the doses listed in your herbal reference.

Gum tragacanth is rich in neutral polysaccharides, especially tragacanthin (a galacturonic acid‑based pectic polysaccharide) and bassorin, which swell to form viscous, demulcent gels. The gum also contains some minor terpenoids and triterpenes associated with tragacanthic acid that likely contribute to its soothing action.

Modern relevance: Tragacanth gum remains widely available as a food and cosmetic ingredient today, and recent analytical studies continue to investigate its polysaccharide structure and bioactivity.

General Uses Top

Suggest a correction!

Common products:
Exudate from stems is harvested as tragacanth gum (also called gum tragacanth). Trade forms include ribbon gum (flakes) and powder. It is listed as a food additive (E413) for its thickening and stabilizing functions.

Food and beverages (non-medicinal):
Used as a stabilizer, thickener, emulsifier, and texture-modifier in foods such as icings, fillings, frozen desserts, confectionery, baked goods, and beverages. Typical roles include viscosity control, moisture retention, and preventing sugar crystallization in syrups and icing. In brewing and beverages, it reduces haze and aids clarity without contributing significant flavor.

Industrial and craft applications:
In printing inks and artist’s colors, tragacanth improves flow and color density. Paper industries use it as a surface size, coating binder, and calender sizing to enhance smoothness and printability. In adhesives and coatings, it acts as a binder for ceramics, plaster, paints, and wood finishes. Used in dusting textiles and yarn as a sizing agent and as a film-former in cosmetic and pharmaceutical formulations. Also applied to stop lamination in glued wood products and as an anti-dusting agent in powdered products.

Colorants and tanning:
The gum is not a colorant or tannin; it does not provide dyestuffs or tanning agents.

Wood and fiber:
Wood is not a significant commercial product; the resource is used for gum exudation. Fiber uses are minor and derived from the gum rather than bast or bast fiber.

Fragrance and cosmetics:
In cosmetics and toiletries, tragacanth stabilizes emulsions and suspensions, thickens aqueous systems, and provides film-forming properties in creams, lotions, gels, and toothpastes. It also serves as an emulsifying base for lipsticks and a fixative/setting agent in hair preparations.

Properties relevant to use:
An anionic galacturonan-based polysaccharide with high molecular weight, soluble in cold water and forming viscous, stable solutions. In hot water it partially hydrolyzes; neutral to slightly acidic pH preserves stability. Solutions exhibit shear-thinning behavior and good freeze–thaw stability. The exudate contains two fractions: a water-soluble portion (tragacanthin) and a water-swellable fraction (bassorin), contributing to thickening and emulsification.

Standards and regulation:
Recognized as a food additive (E413) with specifications and purity criteria defined in national and international compendia for food ingredients. Compliance with national food additive listings and cosmetics ingredient regulations applies in major markets.

Sustainability and sourcing:
Gum is harvested from wild, spiny shrubs in arid and semi-arid regions of its native range. Collection generally involves tapping or injury to branches to induce exudation, followed by drying and grading. Sustained harvest depends on maintaining wild populations and avoiding over-tapping, as shrubs regenerate slowly and are sensitive to disturbance.

Synonyms Top

Scientific name Authority First published in
Astragalus rayatensis Eig Syst. Stud. Astragalus Near East: 75 (1955)
Tragacantha gummifera (Labill.) Kuntze Revis. Gen. Pl.2: 945 (1891)
Tragacantha tournefortii (Boiss.) Kuntze Revis. Gen. Pl.2: 948 (1891)
Tragacantha eriantha (Willd.) Kuntze Revis. Gen. Pl.2: 944 (1891)
Astragalus adpressus Ehrenb. ex Walp. Ann. Bot. Syst.4: 502 (1858)
Astragalus erianthus Willd. Sp. Pl., ed. 4, 3: 1332 (1802)
Astragalus noemiae Eig Syst. Stud. Astragalus Near East: 74 (1955)
Astragalus tournefortii Boiss. Diagn. Pl. Orient.9: 92 (1849)
Astragalus gummifer subsp. tournefortii (Boiss.) Ponert Feddes Repert.83: 622 (1972 publ. 1973)
Astracantha adanica (Ivan.) Greuter Willdenowia15: 425 (1986)
Astragalus adanicus Ivan. Zametki Sist. Geogr. Rast.35: 71 (1978)
Astracantha gummifera (Labill.) Podlech Mitt. Bot. Staatssamml. München19: 12 (1983)
Astracantha rayatensis (Eig) Podlech Mitt. Bot. Staatssamml. München19: 19 (1983)
Astracantha tournefortii (Boiss.) Podlech Mitt. Bot. Staatssamml. München19: 21 (1983)
Astragalus gummifer f. macrophyllus Širj. Repert. Spec. Nov. Regni Veg.47: 207 (1939)
Astragalus gummifer var. villosus Širj. Repert. Spec. Nov. Regni Veg.47: 207 (1939)
Astragalus noemiae var. brantii Eig Syst. Stud. Astragalus Near East: 75 (1955)
Astragalus gummifera Labill.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English gum tragacanth milkvetch
Arabic قتاد صمغي
Arabic قتاد
Arabic كثيراء بيضاء
ceb astracantha gummifera
Persian گون پنبهای
Persian گون سفید
Persian گون کتیرا
Polish traganek gumodajny
Swedish astracantha gummifera
Vietnamese astracantha gummifera
war astracantha gummifera

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185138
UNII 9QXI33LU43
USDA Plants ASGU
Tropicos 13026007
KEW urn:lsid:ipni.org:names:477705-1
Open Tree Of Life 886333
NCBI Taxonomy 339493
IPNI 477705-1
GBIF 5352898
Freebase /m/010hq93w
EPPO ASAGU
USDA GRIN 5794
Wikipedia Astragalus_gummifer
CMAUP NPO28912
PFAF Astragalus gummifer

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
Agar-tragacanth/silk fibroin hydrogel containing Zn-based MOF as a novel nanobiocomposite with biological activity Lalebeigi F, Kashtiaray A, Aghamirza Moghim Aliabadi H, Moghadaskhou F, Pajoum Z, Nokandeh SM, Mahdavi M, Eivazzadeh-Keihan R, Maleki A Sci Rep 07-May-2024
PMCID:PMC11076289
doi:10.1038/s41598-024-61329-3
PMID:38714808
Preliminary Assessment of Polysaccharide-Based Emulgels Containing Delta-Aminolevulinic Acid for Oral Lichen planus Treatment Szymańska E, Potaś J, Maciejczyk M, Sulewska ME, Pietruska M, Zalewska A, Pietruska A, Winnicka K Pharmaceuticals (Basel) 30-Oct-2023
PMCID:PMC10674658
doi:10.3390/ph16111534
PMID:38004400
Evaluation of Oromucosal Natural Gum-Based Emulgels as Novel Strategy for Photodynamic Therapy of Oral Premalignant Lesions Szymańska E, Potaś J, Baranowski M, Czarnomysy R, Sulewska ME, Basa A, Pietruska M, Bielawski K, Winnicka K Pharmaceutics 23-Oct-2023
PMCID:PMC10610218
doi:10.3390/pharmaceutics15102512
PMID:37896272
Mapping of traditional healthcare providers and their healing approaches in a tribal community of district Sirohi, Rajasthan Dwivedi R, Goyal P, Yadav SS, Dwivedi P, Singh P, Singh K J Family Med Prim Care 30-Jun-2023
PMCID:PMC10451593
doi:10.4103/jfmpc.jfmpc_1610_22
PMID:37636156
Synergistic Effects of Tragacanth and Anti-ethylene Treatments on Postharvest Quality Maintenance of Mango (Mangifera indica L.) Khedr EH, Al-Khayri JM Plants (Basel) 05-May-2023
PMCID:PMC10180912
doi:10.3390/plants12091887
PMID:37176945
Natural Gum-Based Functional Bioactive Films and Coatings: A Review Nehra A, Biswas D, Siracusa V, Roy S Int J Mol Sci 28-Dec-2022
PMCID:PMC9820387
doi:10.3390/ijms24010485
PMID:36613928
General Nutritional Profile of Bee Products and Their Potential Antiviral Properties against Mammalian Viruses Asma ST, Bobiş O, Bonta V, Acaroz U, Shah SR, Istanbullugil FR, Arslan-Acaroz D Nutrients 30-Aug-2022
PMCID:PMC9460612
doi:10.3390/nu14173579
PMID:36079835
Identification of Potent Bioassay Guided Terpenoid and Glycoside Root Fractions of Astragalus candolleanus against Clinically Significant Bacterial Strains Nagarajan K, Ghai R, Varshney G, Grover P, Genovese C, D'Angeli F, Goel R, Prasad T, Kalaivani M, Teotia AK Int J Microbiol 28-Apr-2022
PMCID:PMC9072053
doi:10.1155/2022/4584799
PMID:35528313
Assessing the Ameliorative Effect of Selenium Cinnamomum verum, Origanum majorana, and Origanum vulgare Nanoparticles in Diabetic Zebrafish (Danio rerio) Pérez Gutiérrez RM, Soto Contreras JG, Martínez Jerónimo FF, de la Luz Corea Téllez M, Borja-Urby R Plants (Basel) 28-Mar-2022
PMCID:PMC9002390
doi:10.3390/plants11070893
PMID:35406873
Comparative Study of Polysaccharide-Based Hydrogels: Rheological and Texture Properties and Ibuprofen Release Mikušová V, Ferková J, Žigrayová D, Krchňák D, Mikuš P Gels 07-Mar-2022
PMCID:PMC8951473
doi:10.3390/gels8030168
PMID:35323281
Influence of Storage Conditions on the Stability of Gum Arabic and Tragacanth Ramos P, Broncel M Molecules 23-Feb-2022
PMCID:PMC8911758
doi:10.3390/molecules27051510
PMID:35268614
Bioactive-Based Cosmeceuticals: An Update on Emerging Trends Goyal A, Sharma A, Kaur J, Kumari S, Garg M, Sindhu RK, Rahman MH, Akhtar MF, Tagde P, Najda A, Banach-Albińska B, Masternak K, Alanazi IS, Mohamed HR, El-kott AF, Shah M, Germoush MO, Al-malky HS, Abukhuwayjah SH, Altyar AE, Bungau SG, Abdel-Daim MM Molecules 27-Jan-2022
PMCID:PMC8837976
doi:10.3390/molecules27030828
PMID:35164093
Flame retardant high-power Li-S flexible batteries enabled by bio-macromolecular binder integrating conformal fractions Senthil C, Kim SS, Jung HY Nat Commun 10-Jan-2022
PMCID:PMC8748741
doi:10.1038/s41467-021-27777-5
PMID:35013313
A Novel Superabsorbent Polymer from Crosslinked Carboxymethyl Tragacanth Gum with Glutaraldehyde: Synthesis, Characterization, and Swelling Properties Bachra Y, Grouli A, Damiri F, Talbi M, Berrada M Int J Biomater 20-Nov-2021
PMCID:PMC8627358
doi:10.1155/2021/5008833
PMID:34845410
The Role of Diet and Medicinal Herbs for Management of Sjögren’s Syndrome in Traditional Persian Medicine Minaei B, SaffarShahroodi A, Dadmehr M, Nimrouzi M Iran J Public Health 01-Nov-2021
PMCID:PMC8826329
doi:10.18502/ijph.v50i11.7599
PMID:35223618

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.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
N-(2,5-Dihydroxyphenyl)pyridinium(1+) 411955 Click to see 188.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin, (-)- 382073 Click to see 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 11386564 Click to see 504.50 unknown via CMAUP database
I(2)-D-Glucopyranoside, (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenyl 6-O-D-apio-I(2)-D-furanosyl 11408873 Click to see 474.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(18|A)-Oleanolic acid 7048528 Click to see 456.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see 488.70 unknown via CMAUP database
24-Hydroxyursolic Acid 44568920 Click to see 472.70 unknown via CMAUP database
Beta-Sitosteryl Acetate 5354503 Click to see 456.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
CID 3003153 3003153 Click to see 470.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see 426.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Punicanolic acid 25132490 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C(=O)O)C)C)(C)C)O)C 474.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
Estrone 5870 Click to see 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 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
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 11166301 Click to see 430.40 unknown via CMAUP database
Icariside D1 13893575 Click to see 416.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
3-O-Methylpentopyranosyl-(1->6)-3-O-methylhexopyranosyl-(1->4)-2,6-anhydro-1-deoxyheptitol 24847856 Click to see 500.50 unknown https://doi.org/10.1016/S0008-6215(02)00023-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see 182.17 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
1-[(2S)-1-methylpiperidin-2-yl]propan-2-one 820378 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
N-Methylpelletierine 1548928 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
Pelletierine 3034881 Click to see 141.21 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
Pseudopelletierine 6602484 Click to see 153.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
6-[(E)-prop-1-enyl]-2,3,4,5-tetrahydropyridine 15937508 Click to see CC=CC1=NCCCC1 123.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Tricetin 5281701 Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Delphinidin 3,5-diglucoside 10100906 Click to see 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 101675298 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 418.30 unknown via CMAUP database
Apigenin 4'-O-beta-D-glucopyranoside 5491384 Click to see 432.40 unknown via CMAUP database
Luteolin 3'-glucoside 12309350 Click to see 448.40 unknown via CMAUP database
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see 292.20 unknown via CMAUP database
7,8,9-Trihydroxy-1,2-dihydrocyclopenta[c]isochromene-3,5-dione 10131135 Click to see 248.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3-Tri-O-galloyl-beta-D-glucose 5322038 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO)O 636.50 unknown via CMAUP database
1,2,4-tri-O-galloyl-beta-glucopyranose 88204715 Click to see 636.50 unknown via CMAUP database
1,2,4,6-Tetra-O-galloyl-beta-D-glucose 11297287 Click to see 788.60 unknown via CMAUP database
1,2,6-Tri-O-Galloyl-Beta-D-Glucose 440308 Click to see 636.50 unknown via CMAUP database
1,3,4-tri-O-galloyl-beta-glucopyranose 16066749 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,4,6-Tri-O-Galloyl-Beta-D-Glucose 10077822 Click to see 636.50 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown via CMAUP database
(10R,11R)-10-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,11,17,18,19,22,23,34,35-undecahydroxy-9,13,25,32-tetraoxaheptacyclo[25.8.0.02,7.015,20.021,30.024,29.028,33]pentatriaconta-1(35),2,4,6,15,17,19,21,23,27,29,33-dodecaene-8,14,26,31-tetrone 44567110 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C4C5=C3C(=O)OC6=C(C(=C(C7=C(C(=C(C=C7C(=O)O1)O)O)O)C(=C56)C(=O)O4)O)O)O)O)O)O)O)C8C9C(C1=C(C(=C(C(=C1C(=O)O9)C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 Click to see 936.60 unknown via CMAUP database
[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate 14411426 Click to see 786.60 unknown via CMAUP database
13-Hydroxy-12-methoxy-3,5,10,17-tetraoxapentacyclo[9.6.2.02,6.08,18.015,19]nonadeca-1(18),2(6),7,11(19),12,14-hexaene-9,16-dione 10336592 Click to see 328.23 unknown via CMAUP database
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown via CMAUP database
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown via CMAUP database
3,3a(2),4a(2)-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
3,4,8,9,10-Pentahydroxybenzo[c]chromen-6-one 18504424 Click to see C1=CC(=C(C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O 276.20 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see 330.24 unknown via CMAUP database
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown via CMAUP database
6-[[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-2-methyl-6-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-7,13,14-trihydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 11968423 Click to see 894.60 unknown via CMAUP database
8-O-[(1R,19R,21R,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 1-O-methyl (1R,3aR,8bR)-5,6-dihydroxy-3a-(2-methoxy-2-oxoethyl)-3-oxo-1,8b-dihydrofuro[3,4-b][1]benzofuran-1,8-dicarboxylate 71475292 Click to see 998.70 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
beta-Punicalagin 16148440 Click to see 1084.70 unknown via CMAUP database
CID 5464368 5464368 Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O 782.50 unknown via CMAUP database
Corilagin 73568 Click to see 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Eschweilenol C 10026656 Click to see 448.30 unknown via CMAUP database
Flavogallonic acid 14503023 Click to see 470.30 unknown via CMAUP database
Gallagic acid 14754405 Click to see 638.40 unknown via CMAUP database
Gallagyldilactone 5281711 Click to see 602.40 unknown via CMAUP database
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Punigluconin 21637585 Click to see 802.60 unknown via CMAUP database
Strictinin 73330 Click to see 634.50 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.