Codonopsis pilosula subsp. tangshen

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Internal ID UUID644035a0ace58402106703
Scientific name Codonopsis pilosula subsp. tangshen
Authority (Oliv.) D.Y.Hong
First published in Novon 20: 423 (2010)

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Common names Top

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Language Common/alternative name
Chinese 党参
Chinese 川党参

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000923313
Tropicos 100366978
KEW urn:lsid:ipni.org:names:77112229-1
The Plant List kew-469012
Open Tree Of Life 141095
NCBI Taxonomy 94284
IPNI 77112229-1
GBIF 6549990
USDA GRIN 464993

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
Codonopsis radix: a review of resource utilisation, postharvest processing, quality assessment, and its polysaccharide composition Liang W, Sun J, Bai G, Qiu D, Li Q, Dong P, Chen Y, Guo F Front Pharmacol 30-Apr-2024
PMCID:PMC11091420
doi:10.3389/fphar.2024.1366556
PMID:38746010
An Inulin-Type Fructan CP-A from Codonopsis pilosula Alleviated 5-Fluorouracil-Induced Intestinal Mucositis via the ERK/MLCK/MLC2 Pathway and Regulation of Gut Microbiota Zhou J, Li D, Wang J, Cheng Z, Wang C, Zhang X, Xu X, Gao J Pharmaceuticals (Basel) 26-Feb-2024
PMCID:PMC10975959
doi:10.3390/ph17030297
PMID:38543083
Zishen Yutai Pills Promote Angiogenesis at the Maternal-Fetal Interface in Recurrent Spontaneous Abortion Mice by Regulating miR-187/VEGF Axis Wang X, Hu H, Yu X, Liang C, Han Y, Chen H, Chu J Drug Des Devel Ther 12-Feb-2024
PMCID:PMC10871043
doi:10.2147/DDDT.S436718
PMID:38370565
Chinese herbal compound for multidrug-resistant or extensively drug-resistant bacterial pneumonia: a meta-analysis and trial sequential analysis with association rule mining to identify core herb combinations Zhao S, Geng Y, Shi J, Qian J, Yang Y, Dai D, Yan Z, Qi W, Yu D, Zhao X Front Pharmacol 20-Dec-2023
PMCID:PMC10761442
doi:10.3389/fphar.2023.1282538
PMID:38174222
Is there a role for traditional and complementary medicines in managing chronic fatigue? a systematic review of randomized controlled trials Li Y, Yang J, Chau CI, Shi J, Chen X, Hu H, Ung CO Front Pharmacol 24-Oct-2023
PMCID:PMC10628447
doi:10.3389/fphar.2023.1266803
PMID:37942489
Integrated widely targeted metabolomics and network pharmacology revealed quality disparities between Guizhou and conventional producing areas of Codonopsis Radix Zhang K, Zhang D, Yang Q, Long L, Xie J, Wang Y, Yao Q, Wu F, Liu S Front Nutr 17-Oct-2023
PMCID:PMC10616484
doi:10.3389/fnut.2023.1271817
PMID:37915621
Revealing the Preventable Effects of Fu-Zheng-Qu-Xie Decoction against Recurrence and Metastasis of Postoperative Early-Stage Lung Adenocarcinoma Based on Network Pharmacology Coupled with Metabolomics Analysis Zhang Y, Ma K, Jiang L, Xu L, Luo Y, Wu J, Li Y ACS Omega 20-Sep-2023
PMCID:PMC10552138
doi:10.1021/acsomega.3c00122
PMID:37810735
Immunomodulatory effects of inulin and its intestinal metabolites Sheng W, Ji G, Zhang L Front Immunol 10-Aug-2023
PMCID:PMC10449545
doi:10.3389/fimmu.2023.1224092
PMID:37638034
A Systematic Review on the Continuous Cropping Obstacles and Control Strategies in Medicinal Plants Zeeshan Ul Haq M, Yu J, Yao G, Yang H, Iqbal HA, Tahir H, Cui H, Liu Y, Wu Y Int J Mol Sci 05-Aug-2023
PMCID:PMC10419402
doi:10.3390/ijms241512470
PMID:37569843
Quality Assessment and Classification of Codonopsis Radix Based on Fingerprints and Chemometrics Liu X, Chen Z, Wang X, Luo W, Yang F Molecules 29-Jun-2023
PMCID:PMC10343490
doi:10.3390/molecules28135127
PMID:37446787
DNA metabarcoding analysis of fungal community on surface of four root herbs Dao Y, Yu J, Yang M, Han J, Fan C, Pang X Chin Herb Med 25-Apr-2023
PMCID:PMC10874771
doi:10.1016/j.chmed.2023.01.003
PMID:38375056
A review of the botany, ethnopharmacology, phytochemistry, analysis method and quality control, processing methods, pharmacological effects, pharmacokinetics and toxicity of codonopsis radix Dong J, Na Y, Hou A, Zhang S, Yu H, Zheng S, Lan W, Yang L Front Pharmacol 06-Apr-2023
PMCID:PMC10117688
doi:10.3389/fphar.2023.1162036
PMID:37089919
Effects of Different Drying Methods on the Drying Characteristics and Quality of Codonopsis pilosulae Slices Yue Y, Zhang Q, Wan F, Ma G, Zang Z, Xu Y, Jiang C, Huang X Foods 20-Mar-2023
PMCID:PMC10048468
doi:10.3390/foods12061323
PMID:36981249
TMT-Based Proteomic Analysis of Continuous Cropping Response in Codonopsis tangshen Oliv. Jiang X, Zhou W, Wang H, You J, Liu W, Zhang M Life (Basel) 13-Mar-2023
PMCID:PMC10052164
doi:10.3390/life13030765
PMID:36983920
Advances in health-promoting effects of natural polysaccharides: Regulation on Nrf2 antioxidant pathway Luo JH, Li J, Shen ZC, Lin XF, Chen AQ, Wang YF, Gong ES, Liu D, Zou Q, Wang XY Front Nutr 16-Feb-2023
PMCID:PMC9978827
doi:10.3389/fnut.2023.1102146
PMID:36875839

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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5R,6R)-2-[(4E,6R,7S,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 154496915 Click to see 396.40 unknown https://doi.org/10.1248/CPB.56.1546
(2R,3R,4S,5S,6R)-2-[(4E,6S,7R,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 93991642 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(90)85053-I
https://doi.org/10.1248/CPB.56.1546
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown https://doi.org/10.1248/CPB.56.1546
2-(1,7-Dihydroxytetradeca-4,12-dien-8,10-diyn-6-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol 372976 Click to see CC=CC#CC#CC(C(C=CCCCO)OC1C(C(C(C(O1)CO)O)O)O)O 396.40 unknown https://doi.org/10.1248/CPB.56.1546
https://doi.org/10.1016/0031-9422(90)85053-I
3-Phenyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 76031018 Click to see 326.30 unknown https://doi.org/10.1248/CPB.56.1546
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(4E,6S,7R,12E)-tetradeca-4,12-dien-8,10-diyne-1,6,7-triol 154496914 Click to see 234.29 unknown https://doi.org/10.1248/CPB.56.1546
4,12-Tetradecadiene-8,10-diyne-1,6,7-triol 372975 Click to see 234.29 unknown https://doi.org/10.1248/CPB.56.1546
Lobetyol 5807986 Click to see CC=CC#CC#CC(C(C=CCCCO)O)O 234.29 unknown https://doi.org/10.1080/14786419.2013.778849
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Astersaponin Hc 162890793 Click to see 1191.30 unknown https://doi.org/10.1248/CPB.56.1546
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1248/CPB.56.1546
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1248/CPB.56.1546
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol 191 Click to see 267.24 unknown https://doi.org/10.1248/CPB.56.1546
9-alpha-Ribofuranosyladenine 448378 Click to see 267.24 unknown https://doi.org/10.1248/CPB.56.1546
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1248/CPB.56.1546
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1248/CPB.36.2726
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3S)-5-[(E)-3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoxy]-3-methyl-5-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid 14135589 Click to see CC(CC(=O)O)(CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC)OC3C(C(C(C(O3)CO)O)O)O 678.60 unknown https://doi.org/10.1002/HLCA.200890213
5-[3-[3,5-Dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoxy]-3-methyl-5-oxo-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid 78410133 Click to see CC(CC(=O)O)(CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC)OC3C(C(C(C(O3)CO)O)O)O 678.60 unknown https://doi.org/10.1002/HLCA.200890213
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1248/CPB.36.2726
https://doi.org/10.1016/0031-9422(90)85053-I
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-3-[(S)-methylsulfinyl]-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]prop-2-enamide 163064027 Click to see 332.40 unknown https://doi.org/10.1248/CPB.56.1546
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1248/CPB.56.1546

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