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Polygonatum stenophyllum

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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 UUID64401fd4a18a8184531397
Scientific name Polygonatum stenophyllum
Authority Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 274 (1859)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polygonatum verticillatum var. stenophyllum (Maxim.) Baker J. Linn. Soc., Bot. 14: 561. 1875

Common names Top

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Language Common/alternative name
Chinese 狭叶黄精

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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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
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000716889
Tropicos 18400723
KEW urn:lsid:ipni.org:names:540235-1
The Plant List kew-284161
Open Tree Of Life 676689
Observations.org 145843
NCBI Taxonomy 261425
IPNI 540235-1
iNaturalist 522319
GBIF 2770000
EOL 1015105
Elurikkus 300201
CMAUP NPO8312

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
Phytochemistry and Pharmacology of Eleutherococcus sessiliflorus (Rupr. & Maxim.) S.Y.Hu: A Review Sun H, Feng J, Sun Y, Sun S, Li L, Zhu J, Zang H Molecules 11-Sep-2023
PMCID:PMC10536541
doi:10.3390/molecules28186564
PMID:37764339
Effects of human activities on Sericinus montela and its host plant Aristolochia contorta Park SH, Kim JH, Kim JG Sci Rep 22-May-2023
PMCID:PMC10202907
doi:10.1038/s41598-023-35607-5
PMID:37217596
Metabolome and transcriptome signatures shed light on the anti-obesity effect of Polygonatum sibiricum Ou X, Wang X, Zhao B, Zhao Y, Liu H, Chang Y, Wang Z, Yang W, Zhang X, Yu K Front Plant Sci 18-Apr-2023
PMCID:PMC10151794
doi:10.3389/fpls.2023.1181861
PMID:37143889
Succession of the Abandoned Rice Fields Restores the Riparian Forest Lim BS, Seol J, Kim AR, An JH, Lim CH, Lee CS Int J Environ Res Public Health 21-Aug-2022
PMCID:PMC9407847
doi:10.3390/ijerph191610416
PMID:36012049
Comparative Analysis of Chloroplast Genome and New Insights Into Phylogenetic Relationships of Polygonatum and Tribe Polygonateae Wang J, Qian J, Jiang Y, Chen X, Zheng B, Chen S, Yang F, Xu Z, Duan B Front Plant Sci 24-Jun-2022
PMCID:PMC9263837
doi:10.3389/fpls.2022.882189
PMID:35812916
The Impacts of Herbal Medicines and Natural Products on Regulating the Hepatic Lipid Metabolism Li S, Xu Y, Guo W, Chen F, Zhang C, Tan HY, Wang N, Feng Y Front Pharmacol 24-Mar-2020
PMCID:PMC7105674
doi:10.3389/fphar.2020.00351
PMID:32265720
The complete chloroplast genome of a traditional medicinal and food plant, Polygonatum humile (Asparagaceae, Asparagales) Lee SY, Zou Y, Liao W, Fan Q Mitochondrial DNA B Resour 23-Sep-2019
PMCID:PMC7706532
doi:10.1080/23802359.2019.1666044
PMID:33365910
Characterization of the complete chloroplast genome of Asparagus setaceus Li JR, Li SF, Wang J, Dong R, Zhu HW, Li N, Deng CL, Gao WJ Mitochondrial DNA B Resour 18-Jul-2019
PMCID:PMC7706555
doi:10.1080/23802359.2019.1643798
PMID:33365661
Complete plastome sequence of Dracaena cambodiana (Asparagaceae): a species considered “Vulnerable” in Southeast Asia Zhu ZX, Mu WX, Wang JH, Zhang JR, Zhao KK, Ross Friedman C, Wang HF Mitochondrial DNA B Resour 21-May-2018
PMCID:PMC7800030
doi:10.1080/23802359.2018.1473740
PMID:33474263
The Biogeographic South-North Divide of Polygonatum (Asparagaceae Tribe Polygonateae) within Eastern Asia and Its Recent Dispersals in the Northern Hemisphere Wang JJ, Yang YP, Sun H, Wen J, Deng T, Nie ZL, Meng Y PLoS One 03-Nov-2016
PMCID:PMC5094755
doi:10.1371/journal.pone.0166134
PMID:27812188
Emodin inhibits tonic tension through suppressing PKCδ-mediated inhibition of myosin phosphatase in rat isolated thoracic aorta Lim KM, Kwon JH, Kim K, Noh JY, Kang S, Park JM, Lee MY, Bae ON, Chung JH Br J Pharmacol 28-Aug-2014
PMCID:PMC4241095
doi:10.1111/bph.12804
PMID:24909118
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Optimization of the method of isolating (25R)-spirost-5-ene-3?,17?-diol (pennogenin) from plant material L. I. Glebko, L. I. Berezhevskaya, Zh. I. Ul'kina, L. I. Strigina, S. A. Zinova Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00602468
Spectrophotometric determination of a spirostane aglycone — Pennogenin — InPolygonatum stenophyllum L. I. Glebko, N. N. Syromolotova, L. I. Strigina, P. G. Gorovoi Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580457
Diosgenin and β-sitosterol from the hypogeal organs ofPolygonatum stenophyllum L. I. Glebko, Zh. I. Ul'kina, L. I. Berezhevskaya, S. A. Zinova, L. I. Strigina, P. G. Gorovoi Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00576234

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
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown via CMAUP database
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-carboxylic acid 101673969 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O 552.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl 7-methyl ester 101673970 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 566.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 7-methyl ester 101673972 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown via CMAUP database
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown via CMAUP database
dimethyl (1S,4aS,7S,7aS)-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-4,7-dicarboxylate 101673971 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown via CMAUP database
Forsythide 15559328 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1007/BF00576234
Pennogenin 12314056 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)O)C)OC1 430.60 unknown https://doi.org/10.1007/BF00602468
https://doi.org/10.1007/BF00565854
https://doi.org/10.1007/BF00576234
https://doi.org/10.1007/BF00580457
Spirost-5-en-3-ol 234096 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1007/BF00576234
Spirost-5-en-3,17-diol 581098 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)O)C)OC1 430.60 unknown https://doi.org/10.1007/BF00576234
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00576234
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00576234
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside F 6442994 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown via CMAUP database
Forsythoside G 101231533 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)OC)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Verbascoside 5281800 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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