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Pedicularis muscicola

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64404eb0c0bae285310629
Scientific name Pedicularis muscicola
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 24: 54 (1877)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 马先蒿
Chinese 藓生马先蒿

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
      • China South-central
      • Inner Mongolia
      • Qinghai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001139361
Tropicos 29207117
KEW urn:lsid:ipni.org:names:807374-1
The Plant List tro-29207117
Open Tree Of Life 5793525
NCBI Taxonomy 1348741
IPNI 807374-1
GBIF 3740885

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
Structure modelling of odorant receptor from Aedes aegypti and identification of potential repellent molecules Tiwari V, Sowdhamini R Comput Struct Biotechnol J 06-Mar-2023
PMCID:PMC10066510
doi:10.1016/j.csbj.2023.03.005
PMID:37013002
Taxonomy, comparative genomics of Mullein (Verbascum, Scrophulariaceae), with implications for the evolution of Verbascum and Lamiales Dong X, Mkala EM, Mutinda ES, Yang JX, Wanga VO, Oulo MA, Onjolo VO, Hu GW, Wang QF BMC Genomics 08-Aug-2022
PMCID:PMC9358837
doi:10.1186/s12864-022-08799-9
PMID:35941527
Changes in traditional ecological knowledge of forage plants in immigrant villages of Ningxia, China Ma Y, Luo B, Zhu Q, Ma D, Wen Q, Feng J, Xue D J Ethnobiol Ethnomed 16-Dec-2019
PMCID:PMC6916113
doi:10.1186/s13002-019-0333-0
PMID:31842902
Chemical Constituents of Pedicularis densispica Franch Hong Biao Chu, Guang Zhi Zeng, Mei Ju Zhu, Wen Jun He, Yu Mei Zhang, Ning Hua Tan Walter de Gruyter GmbH 04-Feb-2015
doi:10.1515/ZNB-2011-0613
Chemical constituents of Rhodiola kirilowii Maxim. Lian-Mei Yang, Hong-Zheng Fu Journal of Chinese Pharmaceutical Sciences 10-Oct-2011
doi:10.5246/JCPS.2011.02.019

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate 163021367 Click to see CCCCCCCCCCCCC(CCCCC(CC(=O)OC(CO)CO)OC(=O)C)OC(=O)C 502.70 unknown https://doi.org/10.5246/JCPS.2011.02.019
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1R,4aR,7R,7aR)-7-hydroxy-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 133556235 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.5246/JCPS.2011.02.019
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/10.5246/JCPS.2011.02.019
CID 15726439 15726439 Click to see CC1(C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1515/ZNB-2011-0613
Euphroside 14589173 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.5246/JCPS.2011.02.019
Geniposidic Acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown https://doi.org/10.5246/JCPS.2011.02.019
methyl (1S,4aS,5R,7R,7aR)-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101643005 Click to see CC1CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.5246/JCPS.2011.02.019
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.5246/JCPS.2011.02.019
Pedicularioside 133627 Click to see CC1CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1515/ZNB-2011-0613
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/10.5246/JCPS.2011.02.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sesamoside 3082856 Click to see CC12C3C(OC=C(C3(C(C1O2)O)O)C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.1515/ZNB-2011-0613
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Pedicularioside A 6449948 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)OC4C(C(CO4)(CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 756.70 unknown https://doi.org/10.5246/JCPS.2011.02.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1515/ZNB-2011-0613
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.5246/JCPS.2011.02.019
cis-Martynoside 10349304 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown https://doi.org/10.5246/JCPS.2011.02.019
Martynoside 5319292 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown https://doi.org/10.5246/JCPS.2011.02.019

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