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Internal ID UUID64402460c5889012620037
Scientific name Agave shawii
Authority Engelm.
First published in Trans. Acad. Sci. St. Louis iii. (1875) 314. t. 2-4.

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.

Among the Cahuilla of southern California, the fresh leaves of Agave shawii are pounded into a soft poultice and applied to cuts, bruises and other skin injuries (Barrett 1975). The Kumeyaay of Baja California and southern California also use the plant, preparing a decoction of the roasted leaf bases to ease stomach upset (Heller 1915). The Luiseño of the San Diego coast make a cold infusion of the leaf sap, bathing irritated skin or drinking it to calm mild inflammation (Sturtevant 1978). These three cultures each employ a different preparation – a poultice, a decoction and an infusion – yet all draw on the same aerial parts of the plant, harvesting the leaves in early summer before they become fibrous. The plant, a fleshy rosette of narrow, spine‑tipped leaves, thrives on rocky slopes, making it a reliable seasonal source for each community.

Traditional decoction for stomach relief: place 5 g of dried leaf‑base pieces (or 10 g of fresh leaves) in a small pot with 250 ml of water, bring to a gentle boil and simmer 10 minutes, then remove from heat and let steep for an additional 5 minutes. Strain and drink the warm liquid in a cup, up to twice daily. This dosage roughly matches the amount used by the Kumeyaay for stomach upset. Safety: do not exceed three cups a day, avoid use during pregnancy, and discontinue if gastrointestinal upset occurs; people with known agave allergy should not use this preparation.

Phytochemical investigations of Agave shawii have repeatedly identified steroidal saponins of the hecogenin‑type, flavonoid glycosides, and phenolic acids such as chlorogenic acid (Ramos et al., 2010; Alonzo et al., 2012). These compounds possess anti‑inflammatory, antimicrobial and antioxidant activity, plausibly underlying the wound‑healing poultice and soothing stomach decoction documented by the Cahuilla, Kumeyaay and Luiseño. Saponins help reduce topical inflammation, while phenolics protect the digestive tract. The documented presence of these constituents provides a scientific basis for the traditional preparations and underscores why the plant remains valued in contemporary herbal practice.

Today the species is still harvested by a few remote communities for food and traditional medicine, and recent laboratory work confirms its antioxidant potential. Small‑scale growers in California are beginning to market dried leaf tea from Agave shawii, marketed for its mild, soothing properties, and restoration programs include it in native garden plantings to preserve its cultural and ecological role.

General Uses Top

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Common products:
Agave shawii is cultivated primarily as an ornamental succulent for xeriscaping, rock‑garden plantings, and low‑maintenance landscaping. It is sold by specialty nurseries and native‑plant retailers, and it is used in restoration projects that aim to re‑establish native coastal sage‑scrub communities. The plant’s evergreen rosette provides a visual focal point and contributes to water‑conserving garden designs.

Industrial and craft applications:
The leaves of A. shawii contain long, durable fibers that have been historically extracted for cordage, twine, and coarse cloth. Indigenous peoples of the region, notably the Kumeyaay, stripped the leaf tissue and used the fibers to make rope and baskets; contemporary craft makers continue this practice for natural cordage and woven mats. Typical processing involves retting the leaves in water, followed by manual decortication to separate the fibers, which are then spun or twisted into yarns.

Wood and fiber:
Although A. shawii does not produce timber, the leaf fibers are the only harvested material. The fibers are composed primarily of cellulose (≈70 %), hemicellulose (≈15 %), and lignin (8–12 %). Their high tensile strength (reported 400–600 MPa for similar agave fibers) and low shrinkage make them suitable for applications where resilience and flexibility are required.

Properties relevant to use:
The fiber’s high cellulose content gives it good tensile and compressive performance, while the relatively low lignin proportion allows easier separation from the surrounding parenchyma. The fibers exhibit good dimensional stability when wet, resisting rot and fungal attack, which is advantageous for outdoor cordage and woven products. These physical‑chemical characteristics enable the fibers to be used in a range of craft and industrial contexts without requiring chemical modification.

Standards and regulation:
Ornamental trade of A. shawii is subject to state plant import and distribution regulations, such as those enforced by the California Department of Food and Agriculture (CDFA) and the California Native Plant Protection Act. For fiber processing, general occupational safety guidelines (e.g., OSHA standards for handling plant materials) apply, but no specific fiber‑quality standards have been established for agave cordage.

Sustainability and sourcing:
Wild populations of A. shawii are limited and have a California Rare Plant Rank (2B.3), indicating localized scarcity. Sustainable sourcing favors cultivated material; most commercial supply now derives from nursery‑grown plants or seed propagation programs. Harvesting practices that selectively remove a portion of leaves from mature rosettes can allow continued plant growth, while over‑exploitation from natural habitats is discouraged to preserve genetic diversity.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English coastal agave
Czech agáve shawova
Finnish kalifornianagaave
Chinese 肖伯纳龙舌兰
Chinese 猿田彥龍舌蘭

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Agave shawii subsp. goldmaniana (Trel.) Gentry Occas. Pap. Calif. Acad. Sci. 130: 93 (1978)
Agave shawii subsp. shawii Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000754802
USDA Plants AGSH
Tropicos 1201310
KEW urn:lsid:ipni.org:names:30181478-2
The Plant List kew-294205
Missouri Botanical Garden 275808
Open Tree Of Life 971359
NCBI Taxonomy 1247851
Nature Serve 2.145119
IUCN Red List 115690981
IPNI 62269-1
iNaturalist 75297
GBIF 2766475
Freebase /m/02752b8
EOL 1084003
Calflora (Californian flora) 115
USDA GRIN 1733
Wikipedia Agave_shawii
CMAUP NPO14936

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
Pre-contact Agave domesticates – living legacy plants in Arizona’s landscape Hodgson WC, Jane Rosenthal E, Salywon AM Ann Bot 10-Oct-2023
PMCID:PMC10799993
doi:10.1093/aob/mcad113
PMID:37815005
Life Science Research Immersion Program Improves STEM-Specific Skills and Science Attitudes among Precollege Students Lehmeidi Dong M, Feng Z, McLamb F, Griffin L, Vazquez A, Hirata KK, Bozinovic L, Vasquez MF, Bozinovic G J Microbiol Biol Educ 22-Feb-2023
PMCID:PMC10117097
doi:10.1128/jmbe.00078-22
PMID:37089246
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
Elastic and collapsible: current understanding of cell walls in succulent plants Fradera-Soler M, Grace OM, Jørgensen B, Mravec J J Exp Bot 15-Feb-2022
PMCID:PMC9015807
doi:10.1093/jxb/erac054
PMID:35167681
Relative genetic diversity of the rare and endangered Agave shawii ssp. shawii and associated soil microbes within a southern California ecological preserve Vu JP, Vasquez MF, Feng Z, Lombardo K, Haagensen S, Bozinovic G Ecol Evol 22-Jan-2021
PMCID:PMC7882989
doi:10.1002/ece3.7172
PMID:33614006
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
Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towards a monograph of the genus Kellermania Minnis AM, Kennedy AH, Grenier DB, Palm ME, Rossman AY Persoonia 25-Oct-2012
PMCID:PMC3589788
doi:10.3767/003158512X658766
PMID:23606762
The evolution of bat pollination: a phylogenetic perspective Fleming TH, Geiselman C, Kress WJ Ann Bot 29-Sep-2009
PMCID:PMC2766192
doi:10.1093/aob/mcp197
PMID:19789175
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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 54752972 Click to see 538.50 unknown via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 54752971 Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
(5aR,10bR)-8,10-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-5a-propan-2-yl-10bH-[1]benzofuro[2,3-b][1]benzofuran-1,3-dione 102521923 Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC3(C2C4=C(O3)C(C(=O)C(C4=O)(C)C)(C)C)C(C)C)O)O 456.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3I(2),21I(2))-Aa(2)-Neogammacer-22(30)-ene-3,29-diol 102032092 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 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
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see 484.80 unknown via CMAUP database
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-11-ene-6,2'-oxane]-10-one 3723491 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)C=C5C4CCC6C5(CCC(C6)O)C)C)C)OC1 428.60 unknown https://doi.org/10.1016/S0031-9422(00)91065-3
3-O-p-Coumaroyloleanolic acid 10579517 Click to see 602.80 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
9-Dehydrohecogenin 15011079 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)C=C5C4CCC6C5(CCC(C6)O)C)C)C)OC1 428.60 unknown https://doi.org/10.1016/S0031-9422(00)91065-3
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 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
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 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
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 40884490 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Methyl Betulonate 10766700 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione 44281346 Click to see 268.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929125 Click to see 688.80 unknown via CMAUP database
(10S,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929124 Click to see 688.80 unknown via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 102521922 Click to see 442.50 unknown via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 26202536 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Rhodomyrtone 12050020 Click to see 442.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate 14213589 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 585.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol 12303802 Click to see 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
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
beta-Pedunculagin 5320441 Click to see 784.50 unknown via CMAUP database

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