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Pedicularis chinensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404ecc43334003568948
Scientific name Pedicularis chinensis
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 24: 57 (1877)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pedicularis chinensis f. erubescens P.C.Tsoong Fl. Reipubl. Popularis Sin. 68: 419 (1963)

Common names Top

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Language Common/alternative name
Chinese 中国马先蒿
Chinese 鹅首马先蒿

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001139792
Tropicos 29207623
KEW urn:lsid:ipni.org:names:806905-1
The Plant List tro-29207623
Open Tree Of Life 339911
NCBI Taxonomy 399715
IPNI 806905-1
iNaturalist 922286
GBIF 3725425
EOL 2894678

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Comprehensive Analysis of the Complete Mitochondrial Genome of Rehmannia chingii: An Autotrophic Species in the Orobanchaceae Family Han Y, Feng YL, Wang J, Zhu SS, Jin XJ, Wu ZQ, Zhang YH Genes (Basel) 15-Jan-2024
PMCID:PMC10815111
doi:10.3390/genes15010098
PMID:38254987
Assessment of the vegetation sensitivity index in alpine meadows with a high coverage and toxic weed invasion under grazing disturbance Hu Y, Gou X, Tsunekawa A, Cheng Y, Hou F Front Plant Sci 23-Nov-2022
PMCID:PMC9727404
doi:10.3389/fpls.2022.1068941
PMID:36507459
Search of anti-allodynic compounds from Plantaginis Semen, a crude drug ingredient of Kampo formula “Goshajinkigan” Toume K, Hou Z, Yu H, Kato M, Maesaka M, Bai Y, Hanazawa S, Ge Y, Andoh T, Komatsu K J Nat Med 12-Jun-2019
PMCID:PMC7176603
doi:10.1007/s11418-019-01327-2
PMID:31190267
Iridoids in roots of Pedicularis chinensis Yang Li, Wang Changzeng, Jia Zhongjian Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00354-A

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
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(((1S,4aR,7aS)-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl)oxy)tetrahydro-2H-pyran-3,4,5-triol 10359257 Click to see 330.33 unknown https://doi.org/10.1016/0031-9422(95)00354-A
(2S,3R,4S,5S,6R)-2-[[(1S,3S,4aR,5S,7aS)-3-butoxy-5-hydroxy-7-(hydroxymethyl)-1,3,4,4a,5,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101931836 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00354-A
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5R,7aS)-5-butoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101931838 Click to see 402.40 unknown https://doi.org/10.1016/0031-9422(95)00354-A
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5S,7aS)-5-butoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101931837 Click to see CCCCOC1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO 402.40 unknown https://doi.org/10.1016/0031-9422(95)00354-A
2-(Hydroxymethyl)-6-[[7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]oxane-3,4,5-triol 14081905 Click to see C1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO 330.33 unknown https://doi.org/10.1016/0031-9422(95)00354-A
2-[[3-Butoxy-5-hydroxy-7-(hydroxymethyl)-1,3,4,4a,5,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162879328 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00354-A
2-[[5-Butoxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162908573 Click to see 402.40 unknown https://doi.org/10.1016/0031-9422(95)00354-A
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/10.1016/0031-9422(95)00354-A
Bartsioside 14081907 Click to see C1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO 330.33 unknown https://doi.org/10.1016/0031-9422(95)00354-A
Rhinanthin 348157 Click to see 346.33 unknown https://doi.org/10.1016/0031-9422(95)00354-A
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,5S,7aS)-5-hydroxy-7-(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 10866992 Click to see C1C2C(COC1=O)C(=CC2O)CO 184.19 unknown https://doi.org/10.1016/0031-9422(95)00354-A
5-hydroxy-7-(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 85294993 Click to see 184.19 unknown https://doi.org/10.1016/0031-9422(95)00354-A
Isoiridomyrmecin 120743 Click to see 168.23 unknown https://doi.org/10.1016/0031-9422(95)00354-A
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
4,5-Bis(hydroxymethyl)-3,3a,4,6a-tetrahydrocyclopenta[b]furan-2-one 85303656 Click to see 184.19 unknown https://doi.org/10.1016/0031-9422(95)00354-A
Pedicularislactone 10888602 Click to see 184.19 unknown https://doi.org/10.1016/0031-9422(95)00354-A

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