Agave shawii
Details Top
| 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
Suggest a correction!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.
Common names Top
Add a new one! Suggest a correction!| 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
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Agave shawii subsp. goldmaniana | (Trel.) Gentry | Occas. Pap. Calif. Acad. Sci. 130: 93 (1978) |
| Agave shawii subsp. shawii | Unknown |
Germination/Propagation Top
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No germination or propagation data was added yet.
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
Suggest others/fix!| 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)!
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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 |
|---|---|---|---|---|---|
| > 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |