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
Suggest a correction!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.
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Chinese | 三裂叶绢蒿 |
| Chinese | 三裂葉絹蒿 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Seriphidium junceum var. macrosciadium | (Poljakov) Ling & Y.R.Ling | Bull. Bot. Res., Harbin 8(3): 123 (1988) |
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-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 |
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| 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 |
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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 |
|---|---|---|---|---|---|
| > 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |