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

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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.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic أغاف ذهبي
Chinese 金黄龙舌兰

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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)

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

Links to other databases Top

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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.
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
PMCID:PMC9824392
doi:10.3390/plants12010124
PMID:36616253
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
PMCID:PMC7680843
doi:10.3389/fpls.2020.536135
PMID:33240289
Steroidal sapogenins from leaves of some species of Agave and Furcraea Gerald Blunden, Alfredo Carabot C, Kenneth Jewers Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)91065-3

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

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