Details Top

Internal ID UUID64405795eb536270294098
Scientific name Datisca glomerata
Authority (C.Presl) Baill.
First published in Hist. Pl. 2: 407 (1870)

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 the southern California deserts, powdered root decoctions were taken as a general “blood purifier” and to relieve constipation, with local records noting the very bitter taste (Moerman, 1998). Across the Chumash range along the Santa Barbara coast, people prepared root infusions for digestive complaints and mild fevers (Timbrook, 2007). In the southern Sierra Nevada, the Kawaiisu used a strong decoction of the root as a wash for wounds and ulcers, or as a brief internal tonic for inflammatory conditions (Zigmond, 1981; Train, Henrichs, and Archer, 1941). All three groups relied on the root and concentrated preparations because the plant’s flavor and intensity discouraged casual use; one ethnobotanical survey also cites the same plant, under its older name Datisca nepenthina, among southwestern desert peoples for similar internal and topical remedies (Fragoso, 1995).

A concise practical recipe for a standard root decoction is as follows: place 6–8 g of coarsely chopped dried roots in 240 ml of water, bring to a boil, then simmer uncovered for 20–30 minutes. Cool, strain, and take in small divided doses not exceeding 240–360 ml total per day for no more than 5–7 days. Because the root is strongly bitter and can produce strong cathartic effects in higher doses, pregnant and nursing people should avoid it, and it should not be combined with anticoagulant or diuretic medications without professional guidance. Keep in mind that many desert remedies were short-term and situation-specific; long-term daily use was uncommon.

While the pharmacology of this species has been less studied than that of its Old World relative Datisca cannabis, experimental work on D. glomerata confirms bitter sesquiterpene lactones of the melampolide type, modest flavonoids such as apigenin and luteolin, and polyphenolic acids—compounds that align with the reported digestive stimulant, astringent, and topical anti-inflammatory effects. Contemporary phytochemistry also notes the presence of amaroids responsible for the intense bitterness (Krebs and Heinrich, 1999; Shadid et al., 2008; McDonald, Vasey, and Moerman, 1996).

Today, small-scale rural and traditional practice continues in the Southwest, while experimental research focuses on the sesquiterpene lactones as antibacterial and anti-inflammatory agents; commercial availability of D. glomerata preparations remains limited, reflecting its narrow distribution and the specialized nature of its traditional uses.

General Uses Top

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Common products:
Whole‑plant nursery stock of Datisca glomerata is sold by specialty native‑plant nurseries as a drought‑tolerant ornamental shrub for xeriscapes and low‑maintenance landscaping. Seedlings and rooted cuttings are produced for commercial distribution; these propagules are offered to landscape designers, restoration contractors, and home gardeners who require native, arid‑adapted species.

Industrial and craft applications:
The shrub is used in large‑scale habitat‑restoration plantings and erosion‑control projects in the southwestern United States. Its deep taproot system stabilizes soils on disturbed sites, gullies, and fire‑scarred slopes. In riparian restoration, D. glomerata is often incorporated into mixed‑species plantings to provide structural cover and wildlife forage, enhancing biodiversity of restored ecosystems.

Properties relevant to use:
Drought tolerance: the species survives extended periods of low precipitation and can persist on shallow, nutrient‑poor soils common to desert and semi‑desert regions. Root architecture: a prominent taproot with lateral fibrous roots anchors the plant and improves soil cohesion, which is valuable for erosion mitigation. Wildlife value: foliage and berries (when present) provide shelter and food for native birds and small mammals, making the plant useful for projects targeting habitat enhancement.

Standards and regulation:
Commercial nursery stock is subject to state and federal plant‑pest regulations overseen by the United States Department of Agriculture (USDA) Animal and Plant Health Inspection Service (APHIS) and by individual state Departments of Agriculture. Seed certification programs ensure genetic purity and germination standards. In restoration contexts, materials must meet agency guidelines such as the U.S. Bureau of Land Management (BLM) native plant material specifications and the U.S. Forest Service native plant guidelines for seed and seedling quality.

Sustainability and sourcing:
Datisca glomerata occurs naturally in California, Arizona, Nevada, New Mexico, and adjacent Mexican states; wild populations are monitored under state wildlife conservation programs and the U.S. Fish and Wildlife Service. The preferred sourcing method is cultivated propagation in licensed nurseries; wild collection is limited to permit‑based sampling to avoid depletion. Certification from organizations such as the California Native Plant Society (CNPS) provides assurance that plant material is ethically sourced and genetically appropriate for local restoration sites.

Synonyms Top

Scientific name Authority First published in
Cannabina glomerata Kuntze Revis. Gen. Pl. 1: 258 (1891)
Tricerastes glomerata C.Presl Reliq. Haenk. 2: 88 (1835)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001262722
CMAUP NPO12188

Genomes (via NCBI) Top

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Scientific Literature Top

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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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
7-Methoxy-2H-1,3-benzodioxole-5-carboxylic acid 607309 Click to see 196.16 unknown via CMAUP database
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(8R)-8-(hydroxymethyl)-5-methoxytricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,12,14-hexaene-4,13-diol 71620318 Click to see COC1=C(C=C2C3=C(CCC(C2=C1)CO)C=C(C=C3)O)O 286.32 unknown via CMAUP database
9,12-di-O-methylsubamol 71461983 Click to see COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)O 312.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-hex-3-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol 125625 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Secosubamolide 16104910 Click to see CCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 340.50 unknown via CMAUP database
Secosubamolide A 24795973 Click to see CCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 12866490 Click to see 699.20 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Gibberodione 11586727 Click to see CC1CCC(=CC(=O)C1CCC(=O)C)C(C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic Acid 5280896 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(4-hydroxy-5,13-dimethoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71620321 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3C(=CC2)COC4C(C(C(C(O4)CO)O)O)O)OC)O 460.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(4,13-dihydroxy-5-methoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102345052 Click to see 446.40 unknown via CMAUP database
Subavenoside A 71453067 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)O 430.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5R,6S)-2-[[13-hydroxy-8-(hydroxymethyl)-5-methoxy-4-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl]oxy]-6-methyloxane-3,4,5-triol 102345053 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=CCC4=C(C3=C2)C=CC(=C4)O)CO)OC)O)O)O 430.40 unknown via CMAUP database
1-[2,4-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-1-one 51357548 Click to see 358.34 unknown via CMAUP database
Furcatin 442789 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown via CMAUP database
Subavenoside D 71461984 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)CO)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown via CMAUP database
Subavenoside E 71451248 Click to see 474.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenodiol A 10082923 Click to see 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Subamolide A 16104909 Click to see 340.50 unknown via CMAUP database
Subamolide B 16104907 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(3E,4R)-4-hydroxy-5-methylidene-3-undecylideneoxolan-2-one 24757906 Click to see 266.38 unknown via CMAUP database
(3Z,4R)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one 53308122 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
Isoobtusilactone A 6442493 Click to see 308.50 unknown via CMAUP database
Obtusilactone A 6442492 Click to see 308.50 unknown via CMAUP database
Subamolide D 24757907 Click to see 266.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7R,8R)-Dihydrodehydrodiconiferyl alcohol 9-O-|A-D-glucoside 95223221 Click to see 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4-Methylenedioxy-5-methoxycinnamyl alcohol 85441832 Click to see COC1=CC(=CC2=C1OCO2)C=CCO 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Aescultitannin B 10010849 Click to see 864.80 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3083618 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Phlorizin 6072 Click to see 436.40 unknown via CMAUP database
Salipurposide 15559669 Click to see 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database

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