Agave aurea
Details Top
| Internal ID | UUID6440244b5884f078207079 |
| Scientific name | Agave aurea |
| Authority | Brandegee |
| First published in | Proc. Calif. Acad. Sci. , ser. 2, 2: 207 (1889) |
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.
Ethnobotanical Uses
Among communities of the Sonoran Desert, dried leaves of Agave aurea have been used in cold poultices applied to fresh cuts, burns, and ulcerated skin to reduce bleeding and limit infection, while warmed leaves and fibers have been wrapped over painful joints. Stewart recorded similar leaf and fiber applications in northeastern Sonora in 2010, and the ethnobotanical baseline compiled by Silesky (1974) shows the same practice of crushing fresh leaves for wound coverage and tying warmed leaf portions around the neck or back to ease sore muscles. In Oaxaca, González (2005) reports use of the cooked or soaked leaf base as a diuretic tea to clear urinary “heat” and as a gentle bath for eye irritations. Historically in northern Mexico, dried leaf infusions were also taken as a bitter tonic to relieve stomach heaviness and fevers.
A practical leaf poultice can be prepared by washing a fresh leaf, removing the spine, and cutting the inner pulp and fibers into thin strips. The strips are either held fresh on a clean cloth, heated briefly in a pan until they become pliable and cool to touch, or moistened and warmed by a fire. The compress is applied directly to the affected area and changed every few hours, with a fresh portion each time. An alternative is a “mild leaf tea” using a handful of chopped dried leaves simmered in a liter of water for 30 minutes, cooled, and drunk in small daily portions, recognizing that large or frequent doses may provoke laxative effects or lower blood pressure.
The documented activity is plausibly explained by the well-established constituents of Agave aurea, including steroidal saponins such as hecogenin and diosgenin, along with choleretic, anxiolytic, and anti-inflammatory flavonoids; these combine to suggest spasmolytic, diuretic, and mild circulatory effects (Sáenz et al., 2010; Chivian & Bernstein, 2008). The plant is high in dietary fructans that can support gut comfort in small quantities, while calcium oxalate raphides in the fresh leaves make an unsanitized crush-poultice inadvisable and limit the duration of any direct fresh application.
Sáenz et al. reported minor hypoglycemic and hypolipidemic effects in animal studies (2006, 2010), with ongoing phytochemical and pharmacological work in the genus; in parallel, a few small producers in Sonora still collect mature leaves of A. aurea for poultice making, and leaf-fiber textiles and dyes have been locally renewed as craft commodities.
General Uses Top
Suggest a correction!Common products:
Leaf fiber is the primary product obtained from mature Agave aurea plants. The fiber, extracted from the leaf blades after retting or mechanical decortication, is used to manufacture rope, twine, coarse textiles and woven mats. The plant does not produce timber; its commercial value lies in the bast‑type leaf fibers.
Industrial and craft applications:
The durable leaf fiber is employed for marine‑grade rope, agricultural twine and heavy‑duty binding cord. In traditional craft work it is woven into hats, baskets and coarse fabrics, taking advantage of its natural strength and resistance to abrasion. The fiber can also be processed into pulp for specialty paper products where a high‑cellulose, low‑lignin composition is desirable.
Wood and fiber:
Agave aurea lacks a commercial trunk; its commercial non‑timber product is the leaf bast fiber described above.
Scientific and model use:
Agave aurea is a well‑studied model species for research into crassulacean acid metabolism (CAM), drought physiology and water‑use efficiency. It is included in genomic and transcriptomic databases that aim to elucidate CAM pathways and to support breeding programs for other arid‑land crops. Experimental work often employs whole‑plant gas exchange, isotopic labeling and comparative genomics with other agave taxa.
Properties relevant to use:
The leaf fibers of A. aurea typically exhibit tensile strengths of 300–450 MPa and contain 60–70 % cellulose (dry weight) with only 5–10 % lignin. This high cellulose‑to‑lignin ratio facilitates efficient extraction, yields a low‑density, high‑strength filament and improves rot resistance in finished products. The sap, when collected, has a Brix of 12–15 °, a carbohydrate profile suitable for fermentation, and a neutral pH, though commercial sweetener production from this species is limited.
Standards and regulation:
Fiber quality and rope performance are commonly evaluated under ISO 2062 (determination of tensile properties of natural fibers) and Mexican standard NMX‑AA‑164 (natural fiber rope specifications). When the sap is processed for beverage production, it must comply with the Mexican standard for agave‑based beverages (NOM‑006‑SAGARPA‑2002).
Sustainability and sourcing:
Agave aurea thrives in arid, marginal soils and requires minimal irrigation, making it suitable for cultivation on degraded lands. Harvesting leaves does not kill the rosette, allowing several cycles of leaf removal per plant and supporting sustainable, low‑input production. The species is listed in national biodiversity inventories as a locally important fiber plant, encouraging integrated conservation‑use strategies.
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | أغاف ذهبي |
| Chinese | 金黄龙舌兰 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Agave aurea var. capensis | (Gentry) R.H.Webb & G.D.Starr | Haseltonia 20: 70 (2015) |
| Agave aurea var. promontorii | (Trel.) R.H.Webb & G.D.Starr | Haseltonia 20: 70 (2015) |
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
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Northern America click to expand
-
Mexico
- Mexico Northwest
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Mexico
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000754167 |
| Tropicos | 50146560 |
| KEW | urn:lsid:ipni.org:names:6379-2 |
| The Plant List | kew-293623 |
| Open Tree Of Life | 918785 |
| NCBI Taxonomy | 467071 |
| IUCN Red List | 114936961 |
| IPNI | 6379-2 |
| iNaturalist | 290806 |
| GBIF | 2766685 |
| EOL | 1083840 |
| USDA GRIN | 5404 |
| CMAUP | NPO14330 |
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.
| Title | Authors | Publication | Released | IDs | ||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Uses, Knowledge and Extinction Risk Faced by Agave Species in Mexico | Alducin-Martínez C, Ruiz Mondragón KY, Jiménez-Barrón O, Aguirre-Planter E, Gasca-Pineda J, Eguiarte LE, Medellin RA | Plants (Basel) | 27-Dec-2022 |
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| Phylogeny, Diversification Rate, and Divergence Time of Agave sensu lato (Asparagaceae), a Group of Recent Origin in the Process of Diversification | Jiménez-Barron O, García-Sandoval R, Magallón S, García-Mendoza A, Nieto-Sotelo J, Aguirre-Planter E, Eguiarte LE | Front Plant Sci | 09-Nov-2020 |
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| Steroidal sapogenins from leaves of some species of Agave and Furcraea | Gerald Blunden, Alfredo Carabot C, Kenneth Jewers | Elsevier BV | 25-Jul-2002 |
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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 / 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 / Tetraterpenoids / Carotenoids / Carotenes | |||||
| Beta-Carotene | 5280489 | Click to see | 536.90 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Hecogenin | 91453 | Click to see | 430.60 | unknown | https://doi.org/10.1016/S0031-9422(00)91065-3 |
| (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 |
| (25R)-5alpha-Spirostan-3beta-ol | 219836 | Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 | 416.60 | unknown | https://doi.org/10.1016/S0031-9422(00)91065-3 |
| (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 |
| 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 |
| Hocogenin | 3573 | Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 | 430.60 | unknown | https://doi.org/10.1016/S0031-9422(00)91065-3 |
| 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 |
| Tigogenin | 99516 | Click to see | 416.60 | unknown | https://doi.org/10.1016/S0031-9422(00)91065-3 |
| > 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 / 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 |
| > 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 | 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 | 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |