Details Top

Internal ID UUID643fdd9dd5798833072498
Scientific name Astragalus microcephalus
Authority Willd.
First published in Sp. Pl., ed. 4, 3: 1332 (1802)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Gum tragacanth (a hydrocolloid exudate from stems and branches) is the principal commercial product obtained from Astragalus microcephalus.

Industrial and craft applications:
The gum is used in printing and textile printing pastes, where it acts as a thickener and rheology control agent; in paper and board coatings as a stabilizer for pigment dispersions; in ceramic glazes to modify viscosity and prevent flocculation; as an emulsifier in microencapsulation of flavors and aromas; as an adhesive and film-former in specialty papers, adhesive labels, and laminates; and as a release aid in molding and casting.

Food and beverages (non-medicinal):
Edible tragacanth gum (classified as a dietary fiber) functions as a thickener, stabilizer, and emulsifier in dairy products (e.g., ice cream, yogurts), bakery fillings and icings, confectionery glazes, processed meats and fish products, and beverages (including syrups and plant-based beverages). It is used in bakery improvers to control dough rheology, in ice cream and frozen desserts to improve body and melt behavior, and in fruit preparations to maintain integrity during thermal processing.

Colorants and tanning:
The gum’s hydroxyacid-rich hydrocolloid matrix and high carbohydrate content make it useful as a dispersant and stabilizer for natural and synthetic dyes and pigments, and as a carrier for mordant solutions in dyeing.

Wood and fiber:
The gum is employed as a sizing agent and wet-end additive in paper manufacturing and as a sizing/stiffening agent for textiles and cordage, where it forms cohesive films on fibers.

Fragrance and cosmetics:
Tragacanth gum serves as a stabilizer and film-former in lotions, creams, emulsions, mascaras, lipsticks, and hair styling products, as well as a suspending agent in dentifrices and a viscosity control agent in toothpaste bases.

Properties relevant to use:
The gum comprises tragacanthin (water‑soluble fraction) and bassorin (water‑swelling fraction), with a high proportion of uronic acids and galacturonic acid. Solutions exhibit pseudoplastic flow, high viscosity at low concentrations, and good shear‑thinning recovery; they are stable over a broad pH range and compatible with most hydrocolloids, proteins, and solvents. The two‑fraction structure imparts both solubility and swelling behavior, enabling both thickening and film‑formation functions. Its polysaccharide profile confers resistance to oxidative and enzymatic degradation under typical product conditions, supporting long‑term stability of emulsions and suspensions.

Standards and regulation:
Gum tragacanth is monographed in major pharmacopoeias (e.g., Ph. Eur., USP‑NF), and traded specifications are aligned with ISO/ASTM practices for food‑grade hydrocolloids (e.g., ISO 2291 for sampling and ISO 9001 quality management in the gum trade). Food applications follow national additive and labeling rules; cosmetic uses comply with cosmetic regulatory frameworks.

Sustainability and sourcing:
Astragalus microcephalus occurs in steppe and mountain habitats in Turkey and northern Iran. Commercial gum is obtained by tapping mature individuals; guidelines for sustainable tapping emphasize moderate incision frequency, seasonal timing, and regeneration monitoring to maintain stands and biodiversity.

Synonyms Top

Scientific name Authority First published in
Astracantha erinacea (Fisch.) Podlech
Astracantha microcephala (Willd.) Podlech Mitt. Bot. Staatssamml. München19: 15 (1983)
Tragacantha microcephala Kuntze Revis. Gen. Pl.2: 946 (1891)
Astracantha gudrathi (Al.Fed., Fed. & Rzazade) Podlech Mitt. Bot. Staatssamml. München 19: 12 (1983)
Astracantha carthlica (Al.Fed., Fed. & Rzazade) Podle

Common names Top

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Language Common/alternative name
Azerbaijani xırdabaş gəvən
Azerbaijani xırdabaşlıqlı gəvən
Armenian Գազ մանրագլխիկ

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Astragalus microcephalus subsp. microcephalus Unknown
Astragalus microcephalus subsp. pycnocladus (Boiss. & Hausskn.) Širj. Repert. Spec. Nov. Regni Veg.47: 205 (1939)

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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000207511
Tropicos 13026393
KEW urn:lsid:ipni.org:names:478648-1
Open Tree Of Life 6096393
NCBI Taxonomy 1960787
IPNI 478648-1
GBIF 5352983
USDA GRIN 5827
Wikipedia Astragalus_microcephalus
PFAF Astragalus microcephalus

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
Neuroprotective metabolites via fungal biotransformation of a novel sapogenin, cyclocephagenol Küçüksolak M, Üner G, Ballar Kırmızıbayrak P, Bedir E Sci Rep 02-Nov-2022
PMCID:PMC9630500
doi:10.1038/s41598-022-22799-5
PMID:36323752
An Ethnobotanical study of medicinal plants in Taşköprü (Kastamonu–Turkey) Senkardes I, Dogan A, Emre G Front Pharmacol 20-Oct-2022
PMCID:PMC9630845
doi:10.3389/fphar.2022.984065
PMID:36339567
In Silico, In Vitro, and In Vivo Wound Healing Activity of Astragalus microcephalus Willd. Akbari F, Azadbakht M, Bagheri A, Vahedi L Adv Pharmacol Pharm Sci 04-Oct-2022
PMCID:PMC9553362
doi:10.1155/2022/2156629
PMID:36238201
A descriptive study of commercial herbal dietary supplements used for dyslipidemia—Sales data and suspected adverse reactions Allkanjari O, Menniti‐Ippolito F, Ippoliti I, Di Giacomo S, Piccioni T, Vitalone A Phytother Res 07-May-2022
PMCID:PMC9321615
doi:10.1002/ptr.7473
PMID:35524700
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
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
Classification of Plant Ecological Units in Heterogeneous Semi-Steppe Rangelands: Performance Assessment of Four Classification Algorithms Aghababaei M, Ebrahimi A, Naghipour AA, Asadi E, Verrelst J Remote Sens (Basel) 29-Aug-2021
PMCID:PMC7613391
doi:10.3390/rs13173433
PMID:36082038
Monofloral Honeys as a Potential Source of Natural Antioxidants, Minerals and Medicine Mărgăoan R, Topal E, Balkanska R, Yücel B, Oravecz T, Cornea-Cipcigan M, Vodnar DC Antioxidants (Basel) 25-Jun-2021
PMCID:PMC8300703
doi:10.3390/antiox10071023
PMID:34202118
Plant-Based Gums and Mucilages Applications in Pharmacology and Nanomedicine: A Review Amiri MS, Mohammadzadeh V, Yazdi ME, Barani M, Rahdar A, Kyzas GZ Molecules 22-Mar-2021
PMCID:PMC8004199
doi:10.3390/molecules26061770
PMID:33809917
Gum Tragacanth (GT): A Versatile Biocompatible Material beyond Borders Taghavizadeh Yazdi ME, Nazarnezhad S, Mousavi SH, Sadegh Amiri M, Darroudi M, Baino F, Kargozar S Molecules 10-Mar-2021
PMCID:PMC8000171
doi:10.3390/molecules26061510
PMID:33802011
Polyphenol Profile and Biological Activity Comparisons of Different Parts of Astragalus macrocephalus subsp. finitimus from Turkey Sarikurkcu C, Zengin G Biology (Basel) 17-Aug-2020
PMCID:PMC7464095
doi:10.3390/biology9080231
PMID:32824439
Bumble bee parasite strains vary in resistance to phytochemicals Palmer-Young EC, Sadd BM, Stevenson PC, Irwin RE, Adler LS Sci Rep 24-Nov-2016
PMCID:PMC5121629
doi:10.1038/srep37087
PMID:27883009
Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases Ozkan G, Kamiloglu S, Ozdal T, Boyacioglu D, Capanoglu E Molecules 25-Feb-2016
PMCID:PMC6273156
doi:10.3390/molecules21030257
PMID:26927038
Flavonoids from the Genus Astragalus: Phytochemistry and Biological Activity Bratkov VM, Shkondrov AM, Zdraveva PK, Krasteva IN Pharmacogn Rev 01-Jan-2016
PMCID:PMC4791984
doi:10.4103/0973-7847.176550
PMID:27041870
Ethnobotanical survey of plants used in Afyonkarahisar-Turkey Arı S, Temel M, Kargıoğlu M, Konuk M J Ethnobiol Ethnomed 23-Dec-2015
PMCID:PMC4690277
doi:10.1186/s13002-015-0067-6
PMID:26701098

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / 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-[(2S,5S)-5-hydroxy-2,6,6-trimethyloxan-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 101942833 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(C(O8)CO)O)O)O)C)C)O)O)C 785.00 unknown https://doi.org/10.1021/NP9704011
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,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]-6-(hydroxymethyl)oxane-3,4,5-triol 100927164 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/10.1021/NP9801763
Cycloastragenol 13943286 Click to see 490.70 unknown https://doi.org/10.1021/NP9801763
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5R,6R)-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-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 124930706 Click to see 785.00 unknown https://doi.org/10.1021/NP9704011
[(2R,3R,4S,5S)-3-acetyloxy-5-hydroxy-2-[[(1S,3R,6R,8S,9R,11S,12R,14S,15S,16R)-14-hydroxy-15-[(2R,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-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]oxan-4-yl] acetate 154496212 Click to see 869.00 unknown https://doi.org/10.1021/NP9801763
[(2S,3R,4S,5R)-3-acetyloxy-5-hydroxy-2-[[14-hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-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]oxan-4-yl] acetate 11968893 Click to see 869.00 unknown https://doi.org/10.1055/S-2006-957677
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270750/
https://doi.org/10.1021/NP9801763
[(3R,4R,5R,6S)-4,5-dihydroxy-6-[[(1S,3R,6S,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-[(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]oxan-3-yl] acetate 100927166 Click to see 827.00 unknown https://doi.org/10.1021/NP9801763
[3-Acetyloxy-5-hydroxy-2-[[14-hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-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]oxan-4-yl] acetate 3715266 Click to see 869.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270750/
[4,5-dihydroxy-2-[[(1S,3R,6S,11S,14S,16R)-14-hydroxy-15-[(5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-oxapentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-yl]oxy]oxan-3-yl] acetate 369514 Click to see 829.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270750/
https://doi.org/10.1021/NP9801763
[4,5-Dihydroxy-2-[[14-hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-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]oxan-3-yl] acetate 4872994 Click to see 827.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270750/
2-[[(1S,3R,8R,11R,12S,15S,16R)-14-hydroxy-15-[(2R)-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 137706357 Click to see 785.00 unknown https://doi.org/10.1021/NP9704011
Astragaloside II 13996693 Click to see 827.00 unknown https://doi.org/10.1021/NP9801763
Cyclocanthoside E 21633193 Click to see 787.00 unknown https://doi.org/10.1021/NP9704011
https://doi.org/10.1021/NP9801763
> Phenylpropanoids and polyketides / Aurone flavonoids
6,3',4'-Trihydroxyaurone 67111 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1007/S10600-011-9800-0
https://doi.org/10.1007/S10600-009-9314-1
Sulfuretin 5281295 Click to see 270.24 unknown https://doi.org/10.1007/S10600-011-9800-0
https://doi.org/10.1007/S10600-009-9314-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4',7-Dihydroxyflavanone 1889 Click to see 256.25 unknown https://doi.org/10.1007/S10600-011-9800-0
Liquiritigenin 114829 Click to see 256.25 unknown https://doi.org/10.1007/S10600-011-9800-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-Hydroxyflavone 5281894 Click to see 238.24 unknown https://doi.org/10.1007/S10600-011-9800-0
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1007/S10600-011-9800-0

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