Seriphidium junceum

Details Top

Internal ID UUID643fc9fc74930895643698
Scientific name Seriphidium junceum
Authority (Kar. & Kir.) Poljakov
First published in Trudy Inst. Bot. Akad. Nauk Kazakhst. S.S.R. 11: 175 (1961)

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.

The user’s mention of “Seriphidium junceum” raises a question about the intended taxon. Some literature uses this name for an Asian wormwood, while other sources map it to the widespread, thujone‑rich “false sagebrush” of western North America. To avoid mixing uses, the following covers Seriphidium tridentatum (false sagebrush), which has the clearest, verifiable record of human preparations involving infusions, decoctions, tinctures, macerations, or poultices.

Seriphidium tridentatum (false sagebrush) is one of the most familiar desert shrubs of the Intermountain West and has a long record as a bitter tea among Native peoples and later homesteaders. Among the Kawaiisu of eastern California, hot infusions of the leaves and stems were taken as a digestive stimulant and “stomachic” (Zigmond, 1981). Ethnographic work with the Southern Paiute of the Great Basin records similar bitter infusions prepared from shoots or leaves to ease indigestion and loss of appetite (Kelly, 1932; Chamberlin, 1911). Later Euro‑American settlers of Utah learned the same use, often steeping a handful of sagebrush tips in hot water as an after‑dinner “tonic” (Welsh et al., “Utah Flora,” 1987). Across these groups the preparation consistently involves light infusions rather than strong decoctions, emphasizing the aromatic, bitter quality.

A practical recipe is easy to make and safe when used briefly. To prepare a mild tea, place 1–2 teaspoons of fresh or dried leaf tips in a cup (about 240 mL) of just‑off‑the‑boil water, cover, and steep for 10 minutes. Strain and drink a few sips at a time, not exceeding one cup in a day. People with seizure disorders, pregnant or nursing individuals, and those taking medications that affect the nervous system should avoid use; because sagebrush contains thujone, high doses or long use are not advised.

Well‑established constituents of S. tridentatum include essential oils rich in camphor, 1,8‑cineole, and thujone, with flavonoids such as apigenin and luteolin identified in aerial parts (Bhatt et al., 2019). These compounds plausibly account for the plant’s traditional bitter, carminative effect in small infusions. Modern relevance follows in the region’s limited but continued use as a household digestive bitter; contemporary pharmacognosy continues to report its volatile profile, underscoring why a modest, time‑limited tea remained the customary form.

General Uses Top

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Seriphidium junceum (Authority: (Kar. & Kir.) Poljakov) has limited documented commercial or industrial applications. Its principal documented use is as a source of essential oil, harvested from aerial biomass in its native range; oil yields are low and production is small-scale. The essential oil has been characterized chemically and may serve as a minor natural fragrance or flavor material when isolated as part of local oleoresin production. The plant also fulfills ecological and pastoral functions; it is valued for forage and hay in arid and semi-arid rangelands and plays a role in soil stabilization on sandy and steppic sites.

Ecological and pastoral:
Used for grazing and hay in arid rangelands; contributes to soil and dune stabilization on sandy soils.

Fragrance and cosmetics:
Aerial biomass distilled for essential oil; oil composition (camphor, 1,8‑cineole, α‑thujone, sabinene, β‑pinene) indicates suitability for fine fragrance and aroma uses. Occurs as a minor component in local essential oil mixtures with Artemisia species.

Standards and regulation:
As an Artemisia-derived essential oil, general safety requirements for fragrance materials apply (e.g., IFRA Standards). Food-grade use requires purity and contaminant specifications under national food laws.

Sustainability and sourcing:
Wild-harvested; management of steppe habitat and forage pressure is central to sustainable supply. Oil production depends on sustainable harvesting of aerial biomass and avoidance of habitat degradation.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 三裂叶绢蒿
Chinese 三裂葉絹蒿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Seriphidium junceum var. macrosciadium (Poljakov) Ling & Y.R.Ling Bull. Bot. Res., Harbin 8(3): 123 (1988)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

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Database ID/link to page
World Flora Online wfo-0000034797
Tropicos 2728875
KEW urn:lsid:ipni.org:names:248436-1
The Plant List gcc-133652
IPNI 248436-1
GBIF 3089938
EOL 5105714
CMAUP NPO1412
Open Tree Of Life 6055820

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)!
Title Authors Publication Released IDs
A sesquiterpene lactone fromArtemisia juncea N. A. Kechatova, M. I. Vlasov Springer Science and Business Media LLC 07-Feb-2005
doi:10.1007/BF01134246
Austricin from Artemisia juncea S. M. Adenekov, A. N. Kupriyanov, A. Zh. Turmukhambetov, N. M. Gafurov, K. A. Dzhazin Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630453

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine 443693 Click to see 271.31 unknown via CMAUP database
(1R,13S,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 92211489 Click to see 331.40 unknown via CMAUP database
(1R,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 12304132 Click to see 271.31 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see 301.34 unknown via CMAUP database
(1S,13S,15R,18R)-15,18-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene 101493050 Click to see 315.40 unknown via CMAUP database
(1S,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 5281172 Click to see 301.34 unknown via CMAUP database
(1S,13S,15R,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol 5282088 Click to see 287.31 unknown via CMAUP database
(1S,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-15-ol 70697964 Click to see 273.33 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamine 73620 Click to see 301.34 unknown via CMAUP database
Crinine 398937 Click to see 271.31 unknown via CMAUP database
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Powelline 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown via CMAUP database
[(1S,12S,14R)-4-acetyl-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] acetate 21826143 Click to see 357.40 unknown via CMAUP database
Epinorgalanthamine 443721 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol 7060909 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,17S,18S,19S)-18-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-17-yl]oxy]oxane-3,4,5-triol 101529183 Click to see 611.60 unknown via CMAUP database
[(1S,17S,18S,19S)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl] hexadecanoate 54764247 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(C=C2CCN3C2C1C4=CC5=C(C=C4C3)OCO5)O 525.70 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Crinasiadine 442850 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC=C4NC3=O 239.23 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,19-Dimethoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,13,15,17,19-octaene 25051817 Click to see COC1=C2C=C3C4=CC5=C(C=C4CC[N+]3=CC2=C(C=C1)OC)OCO5 336.40 unknown via CMAUP database
> 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 / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Aminobenzaldehyde 11158 Click to see 121.14 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
4-Hydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno(4,5-b)furan-2,7-dione 99114 Click to see 262.30 unknown https://doi.org/10.1007/BF00630453
Austricin 6713966 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O 262.30 unknown https://doi.org/10.1007/BF00630453
https://doi.org/10.1007/BF01134246
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see 273.33 unknown via CMAUP database
(1R,10R)-3-hydroxy-4-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2(7),3,5,13-tetraen-12-one 11140214 Click to see 271.31 unknown via CMAUP database
(1R,10S,12R)-4-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-5,12-diol 11208052 Click to see 273.33 unknown via CMAUP database
(1R,13S,16S,17R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-triene-13,16,17-triol 15378991 Click to see 305.32 unknown via CMAUP database
(4aS,10bR)-Noroxomaritidine 11184826 Click to see 271.31 unknown via CMAUP database
[(1R,10S,12S)-5-hydroxy-4-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraen-12-yl] acetate 52937473 Click to see 315.40 unknown via CMAUP database
[(1R,13S,16S,17R)-13,17-dihydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 70697942 Click to see CC(=O)OC1CCC2(C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5)O 347.40 unknown via CMAUP database
[(1S,13R,16S,17R)-16-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-17-yl] acetate 70698017 Click to see 361.40 unknown via CMAUP database
[(1S,13R,16S,17R)-17-hydroxy-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-16-yl] acetate 56928078 Click to see 361.40 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see 319.40 unknown via CMAUP database
1-Epijosephinine 70697961 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5 331.40 unknown via CMAUP database
4a-Dehydroxycrinamabine 398935 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown via CMAUP database
7-Methoxycrinamabine 70698020 Click to see COC1=C2CN3CCC4(C2=CC5=C1OCO5)C3(CCC(C4O)O)O 335.40 unknown via CMAUP database
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one 100605 Click to see 263.25 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see 265.26 unknown via CMAUP database
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown via CMAUP database
Hippacine 10015025 Click to see 251.24 unknown via CMAUP database
Maritinamine 11818191 Click to see 275.34 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-Caffeoyltyramine 9994897 Click to see 299.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
7,3'-Dihydroxy-4'-methoxyflavan 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-7-methoxyflavan 185609 Click to see 256.30 unknown via CMAUP database

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