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Polygonatum prattii

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 UUID64401fc3f08f9213998630
Scientific name Polygonatum prattii
Authority Baker
First published in Hooker's Icon. Pl. 28: t. 2217 (1892)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Polygonatum delavayi Hua J. Bot. (Morot) 6: 422 (1892)
Polygonatum gentilianum H.Lév. Repert. Spec. Nov. Regni Veg. 12: 287 (1913)

Common names Top

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Language Common/alternative name
Chinese 小玉竹
Chinese 康定玉竹

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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Sow at 4°C for 3 weeks, then increase to 20°C.
sow outdoors immediately; hypogeal germination after 1 year; leaves in second year

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000715961
Tropicos 18406954
KEW urn:lsid:ipni.org:names:540210-1
The Plant List kew-283999
Open Tree Of Life 3995474
NCBI Taxonomy 261421
IPNI 540210-1
iNaturalist 862587
GBIF 2770119
EOL 1014894
CMAUP NPO15771

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
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
Deciphering potential pharmacological mechanism of Sha-Shen-Mai-Dong decoction on primary Sjogren’s syndrome Jiang Y, Zhao X, Yu J, Wang Q, Wen C, Huang L BMC Complement Med Ther 01-Mar-2021
PMCID:PMC7923330
doi:10.1186/s12906-021-03257-7
PMID:33648502
DNA barcoding for the efficient and accurate identification of medicinal polygonati rhizoma in China Jiao J, Huang W, Bai Z, Liu F, Ma C, Liang Z PLoS One 18-Jul-2018
PMCID:PMC6051646
doi:10.1371/journal.pone.0201015
PMID:30021015
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
Steroid glycosides from Polygonatum prattii. Li XC, Yang CR, Matsuura H, Kasai R, Yamasaki K Phytochemistry 01-May-1993
doi:10.1016/0031-9422(93)85541-X
PMID:7763625

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 / Diterpenoids / Colensane and clerodane diterpenoids
(1S,4R,5S,6R,8R)-5-[2-(furan-3-yl)ethyl]-4,5-dimethyl-9-oxatricyclo[6.2.2.01,6]dodec-11-ene-11-carboxylic acid 6325080 Click to see CC1CCC23COC(CC2C1(C)CCC4=COC=C4)C=C3C(=O)O 330.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
15,16-Epoxy-neo-clerodan-1,3,13(16),14-tetraen-18,19-olide 5317151 Click to see 312.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4R,5S,6R)-2-[(2R,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2R,4R,5'R,6S,7S,8R,9S,12S,13R,16R)-8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163067422 Click to see 917.00 unknown https://doi.org/10.1016/0031-9422(93)85541-X
2-[2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163067420 Click to see 917.00 unknown https://doi.org/10.1016/0031-9422(93)85541-X
Pratioside A 44152530 Click to see 917.00 unknown https://doi.org/10.1016/0031-9422(93)85541-X
Pratioside B 44150207 Click to see 1097.20 unknown https://doi.org/10.1016/0031-9422(93)85541-X
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Dodonolide 643656 Click to see CC1CCC2=C(C=CC=CC1(C)CCC3=COC=C3)C(=O)OC2 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown via CMAUP database
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown via CMAUP database
Nepetin 5317284 Click to see 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown via CMAUP database

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