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Stauntonia chinensis

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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 UUID643ffc02eb0f6711988380
Scientific name Stauntonia chinensis
Authority DC.
First published in Syst. Nat. 1: 514 (1817)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stauntonia hainanensis T.C.Chen Fl. Reipubl. Popularis Sin. 29: 307 (2001)
Stauntonia pseudomaculata C.Y.Wu & S.H.Huang Fl. Yunnanica 2: 11 (1979)

Common names Top

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Language Common/alternative name
szy nipaluma-kakuwa, kakowa
Chinese 七叶莲
Chinese 野木瓜
Chinese 假荔枝
Chinese 野木瓜果

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 South-central
      • China Southeast
      • Hainan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000431102
Tropicos 50064696
KEW urn:lsid:ipni.org:names:107613-1
The Plant List kew-2473160
Open Tree Of Life 512531
NCBI Taxonomy 161269
IPNI 107613-1
GBIF 4191606
Wikipedia Stauntonia_chinensis

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
A systematic analysis of anti-diabetic medicinal plants from cells to clinical trials Omale S, Amagon KI, Johnson TO, Bremner SK, Gould GW PeerJ 05-Jan-2023
PMCID:PMC9826616
doi:10.7717/peerj.14639
PMID:36627919
The Hydroethanolic Stem Bark Extract of Tieghemella heckelii (A.Chev.) Pierre ex Dubard (Sapotaceae) Produced N-Methyl-D-Aspartate (NMDA) Receptor-Dependent Analgesia and Attenuates Acute Inflammatory Pain via Disruption of Oxidative Stress Kumatia EK, Appiah-Opong R Evid Based Complement Alternat Med 09-Aug-2021
PMCID:PMC8371650
doi:10.1155/2021/3466757
PMID:34422066
Solanum anguivi Lam. Fruits: Their Potential Effects on Type 2 Diabetes Mellitus Nakitto AM, Muyonga JH, Byaruhanga YB, Wagner AE Molecules 02-Apr-2021
PMCID:PMC8038283
doi:10.3390/molecules26072044
PMID:33918509
The complete chloroplast genome of Stauntonia chinensis and compared analysis revealed adaptive evolution of subfamily Lardizabaloideae species in China Wen F, Wu X, Li T, Jia M, Liu X, Liao L BMC Genomics 06-Mar-2021
PMCID:PMC7937279
doi:10.1186/s12864-021-07484-7
PMID:33676415
Plant Extracts for Type 2 Diabetes: From Traditional Medicine to Modern Drug Discovery Lee J, Noh S, Lim S, Kim B Antioxidants (Basel) 09-Jan-2021
PMCID:PMC7827314
doi:10.3390/antiox10010081
PMID:33435282
Nigella A ameliorates inflammation and intestinal flora imbalance in DSS induced colitis mice Hu X, Xu N, Yang X, Hu X, Zheng Y, Zhang Q AMB Express 04-Oct-2020
PMCID:PMC7533278
doi:10.1186/s13568-020-01114-3
PMID:33011900
Consumption of Cooked Common Beans or Saponins Could Reduce the Risk of Diabetic Complications Calderón Guzmán D, Juárez Olguín H, Veloz Corona Q, Ortiz Herrera M, Osnaya Brizuela N, Barragán Mejía G Diabetes Metab Syndr Obes 02-Oct-2020
PMCID:PMC7537848
doi:10.2147/DMSO.S270564
PMID:33061508
The Potential of Anti-Diabetic Rākau Rongoā (Māori Herbal Medicine) to Treat Type 2 Diabetes Mellitus (T2DM) Mate Huka: A Review Koia JH, Shepherd P Front Pharmacol 30-Jun-2020
PMCID:PMC7339977
doi:10.3389/fphar.2020.00935
PMID:32694996
Identification and quantification of oleanane triterpenoid saponins and potential analgesic and anti-inflammatory activities from the roots and rhizomes of Panax stipuleanatus Shu PP, Li LX, He QM, Pan J, Li XL, Zhu M, Yang Y, Qu Y J Ginseng Res 18-May-2020
PMCID:PMC8020355
doi:10.1016/j.jgr.2020.05.002
PMID:33841011
Update of the list of QPS‐recommended biological agents intentionally added to food or feed as notified to EFSA 10: Suitability of taxonomic units notified to EFSA until March 2019 Koutsoumanis K, Allende A, Alvarez‐Ordóñez A, Bolton D, Bover‐Cid S, Chemaly M, Davies R, De Cesare A, Hilbert F, Lindqvist R, Nauta M, Peixe L, Ru G, Simmons M, Skandamis P, Suffredini E, Cocconcelli PS, Fernández Escámez PS, Maradona MP, Querol A, Suarez JE, Sundh I, Vlak J, Barizzone F, Correia S, Herman L EFSA J 15-Jul-2019
PMCID:PMC7009089
doi:10.2903/j.efsa.2019.5753
PMID:32626372
Analgesic Effects of Triterpenoid Saponins From Stauntonia chinensis via Selective Increase in Inhibitory Synaptic Response in Mouse Cortical Neurons Chen S, Rong Y, Liu M, Cheng S, Liu X, Li X, Yu Y, Yang G, Yang X Front Pharmacol 12-Nov-2018
PMCID:PMC6241161
doi:10.3389/fphar.2018.01302
PMID:30483136
Hypoglycemic and hypolipidemic effects of total saponins from Stauntonia chinensis in diabetic db/db mice Xu J, Wang S, Feng T, Chen Y, Yang G J Cell Mol Med 16-Oct-2018
PMCID:PMC6237556
doi:10.1111/jcmm.13876
PMID:30324705
Development of microsatellite markers for Sargentodoxa cuneata (Lardizabalaceae) using next-generation sequencing technology Sun ZX, Ye LJ, Zhang F, Hu W, Fan DM, Zhang ZY Appl Plant Sci 09-May-2016
PMCID:PMC4873275
doi:10.3732/apps.1600003
PMID:27213128
Regulation of AMP-activated protein kinase by natural and synthetic activators Grahame Hardie D Acta Pharm Sin B 21-Jul-2015
PMCID:PMC4724661
doi:10.1016/j.apsb.2015.06.002
PMID:26904394
ITS2 Secondary Structure Improves Discrimination between Medicinal “Mu Tong” Species when Using DNA Barcoding Zhang W, Yuan Y, Yang S, Huang J, Huang L PLoS One 01-Jul-2015
PMCID:PMC4488503
doi:10.1371/journal.pone.0131185
PMID:26132382

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 / Diterpene glycosides
Yemuoside I 195850 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O 1175.30 unknown https://doi.org/10.1021/NP50076A029
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21577277 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O 1191.30 unknown https://doi.org/10.1080/10286020903479709
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[3-[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 3762229 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O 1191.30 unknown https://doi.org/10.1080/10286020903479709
Cussonoside A 171596 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)O)C)(C)C)O)O)O)CO)O)O)O 943.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.005
HuzhangosideB 13880086 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1337.50 unknown https://doi.org/10.1080/10286020903479709
Kalopanax saponin C 195332 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1383.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.005
Kalopanaxsaponin B 11491905 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1221.40 unknown https://doi.org/10.1080/10286020903479709
Kalopanaxsaponin B;Glycoside L-H2; Hederoside H1 3874518 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1221.40 unknown https://doi.org/10.1080/10286020903479709
Sieboldianoside A 57393816 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1353.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.005
Sieboldianoside B 192585 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1337.50 unknown https://doi.org/10.1080/10286020903479709
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.005

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