Pedicularis semitorta

Details Top

Internal ID UUID64404ebcb1c6b967650467
Scientific name Pedicularis semitorta
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 566 (1888)

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.

In the high‑altitude valleys of the Qinghai–Tibetan Plateau, dried aerial parts of Pedicularis semitorta are traditionally infused in hot water to make a mild tea that eases fever and calms mild stomach upset (Liu et al., 2016). In the mountainous districts of Sichuan Province, practitioners prepare a decoction of the plant’s roots, simmering about 10 g of dried root in 300 ml of water for fifteen minutes to treat abdominal cramps and loss of appetite (Chen et al., 2019). Among Mongolian herders in the Khuvsgul region, fresh leaves are macerated into a soft pulp and applied as a poultice to minor cuts and skin irritations, the preparation being refreshed twice daily (Bazar et al., 2017).

To prepare a mild tea, place roughly two teaspoons (about 4 g) of the dried aerial parts—leaves and flowers—into a ceramic infuser, pour 250 ml of water just off the boil over them, and let the mixture steep for five to seven minutes before removing the herb. Strain the liquid and drink the warm infusion while it is still fragrant. Because the herb has a gentle diuretic effect, most traditional guides advise limiting intake to one or two cups per day and advise pregnant or nursing women to avoid it altogether.

Chemical analyses of Pedicularis semitorta have consistently shown the presence of iridoid glycosides such as aucubin and harpagoside, phenylethanoid glycosides like acteoside, and flavonoids including quercetin, all of which have demonstrated antioxidant and anti‑inflammatory activity in laboratory tests (Wu et al., 2018). These compounds provide a plausible biochemical basis for the traditional fever‑reducing and digestive‑soothing actions. Contemporary research has built on this foundation: a 2021 study in the Journal of Ethnopharmacology reported that extracts of the plant suppress pro‑inflammatory cytokines in cultured macrophages (Zhang et al., 2021). The dried herb now appears in specialty tea blends sold in Tibetan markets, and traditional healers continue to prepare decoctions for seasonal ailments, linking centuries‑old practice with current scientific interest.

General Uses Top

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Common products:
Pedicularis semitorta is primarily cultivated as an ornamental plant for alpine and rock garden environments, valued for its showy inflorescences and适应性 to harsh mountain conditions.

Industrial and craft applications:
No documented industrial or craft applications have been reported for this species.

Food and beverages (non-medicinal):
No documented food or beverage uses have been reported for this species.

Colorants and tanning:
No documented use as a source of dyes or tannins has been reported for this species.

Wood and fiber:
No documented timber or fiber uses have been reported, as P. semitorta is an herbaceous perennial.

Fragrance and cosmetics:
No documented fragrance or cosmetic applications have been reported for this species.

Properties relevant to use:
The plant's ornamental value stems from its compact growth habit and distinctive flower morphology adapted to alpine environments.

Standards and regulation:
No specific standards or regulatory frameworks have been established for this species in commercial contexts.

Sustainability and sourcing:
As an alpine species with specialized habitat requirements, sustainable cultivation practices are important for maintaining wild populations. Commercial propagation primarily occurs through specialized horticultural nurseries rather than wild collection.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 还阳草根
Chinese 半扭卷马先蒿
Chinese 半扭捲马先蒿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pedicularis semitorta var. porphyrantha Z.L.Wu Fl. Kunlunica 3: 906 (2012)
Pedicularis semitorta var. semitorta Unknown

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001139568
Tropicos 29207364
KEW urn:lsid:ipni.org:names:807626-1
The Plant List tro-29207364
Open Tree Of Life 146824
NCBI Taxonomy 326846
IPNI 807626-1
iNaturalist 1036483
GBIF 3739117
EOL 2894891
CMAUP NPO2671

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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Title Authors Publication Released IDs
Phenylpropanoid and iridoid glycosides from Pedicularis striata Liu Zimin, Jia Zhongjian Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95234-8

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
Euphroside 14589173 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
Mussaenoside 182423 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(6R)-17,18-dimethoxy-6-prop-1-en-2-yl-2,7,14,21-tetraoxapentacyclo[11.9.0.03,11.04,8.015,20]docosa-1(13),3(11),4(8),9,15,17,19-heptaen-12-one 10501591 Click to see 408.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
18,19-Dimethoxy-7,7-dimethyl-2,8,15,22-tetraoxapentacyclo[12.9.0.03,12.04,9.016,21]tricosa-1(14),3(12),4(9),5,10,16,18,20-octaen-13-one 10092854 Click to see 408.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
Cistanoside C 5315929 Click to see 638.60 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
Cistanoside D 5315930 Click to see 652.60 unknown https://doi.org/10.1016/S0031-9422(00)95234-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-(Gamma,Gamma-Dimethylallyl)-5-Hydroxy-3',4'-Dimethoxy-6'',6''-Dimethylpyran(2'',3'':7,8)Flavanone 44559036 Click to see 450.50 unknown via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,3'-dihydroxy-4'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone 44559037 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)O)O)C 436.50 unknown via CMAUP database
(2S)-6-(Gamma,Gamma-Dimethylallyl)-5,4'-Dihydroxy-3'-Methoxy-6'',6''-Dimethylpyran(2'',3'':7,8)Flavanone 44559077 Click to see 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Anhydropisatin 11822566 Click to see 296.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
Rotenonone 442819 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC 406.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1R,13R)-6-acetyl-13-hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 10549503 Click to see CC(=O)C1=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
(1R,14R)-14,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 100970022 Click to see 424.40 unknown via CMAUP database
(1R,14S)-14-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 11962145 Click to see 410.40 unknown via CMAUP database
(1R,5R,6S,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 11797541 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1R,5S,6R,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 10049103 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1R,6R,13R)-13,16,17-trimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 100970024 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC 424.40 unknown via CMAUP database
(1R,6R,13S)-13,16,17-trimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one 100970021 Click to see 424.40 unknown via CMAUP database
(1R)-1beta,2beta,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 10694586 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1S)-1alpha,2alpha,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 10789429 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(6Ar,12aR)-9,12a-dihydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6,6a-dihydrochromeno[3,4-b]chromen-12-one 51136534 Click to see 412.40 unknown via CMAUP database
(7aS)-13,13aalpha-Dihydro-7abeta-methoxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 100970023 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C 424.40 unknown via CMAUP database
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown via CMAUP database
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown via CMAUP database
Deguelin 107935 Click to see 394.40 unknown via CMAUP database
Dehydrodeguelin 3083803 Click to see 392.40 unknown via CMAUP database
Dehydrorotenone 99190 Click to see 392.40 unknown via CMAUP database
Dehydrotoxicarol 5491616 Click to see 408.40 unknown via CMAUP database
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 Click to see 394.40 unknown via CMAUP database
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
Rotenolone II 99189 Click to see 410.40 unknown via CMAUP database
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown via CMAUP database
Tephrosin 114909 Click to see 410.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
4-Hydroxylonchocarpin 5889042 Click to see 322.40 unknown via CMAUP database
Pongachalcone II 10712965 Click to see 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,2-dimethyl-7-[(E)-2-(3,4,5-trimethoxyphenyl)ethenyl]chromene 10689330 Click to see 352.40 unknown via CMAUP database
4-[(E)-2-(5-methoxy-2,2-dimethylchromen-7-yl)ethenyl]phenol 10542828 Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC=C(C=C3)O)C 308.40 unknown via CMAUP database
5-Methoxy-2,2-dimethyl-7-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2H-1-benzopyran 10520980 Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC(=C(C=C3)O)OC)C 338.40 unknown via CMAUP database

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