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Walsura robusta

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 UUID643ffa48ea101180806679
Scientific name Walsura robusta
Authority Roxb.
First published in Fl. Ind. ed. 1832 , 2: 386 (1832)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Scutinanthe boerlagii Hochr. Pl. Bogor. Exs. : 64 (1904)
Scytalia glabra Buch.-Ham. ex Wall. Numer. List : n.º 8048 E (1847)
Surwala robusta M.Roem. Fam. Nat. Syn. Monogr. 1: 108 (1846)

Common names Top

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Language Common/alternative name
Chinese 割舌树
Chinese 割舌樹

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000418024
Tropicos 20400970
KEW urn:lsid:ipni.org:names:579946-1
The Plant List kew-2450799
Open Tree Of Life 5516731
Observations.org 340754
NCBI Taxonomy 1489958
IPNI 579946-1
iNaturalist 866958
GBIF 3851341
EOL 2874868
Elurikkus 424971
Wikipedia Walsura_robusta

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
Factors influencing the distribution of woody plants in tropical karst hills, south China Hu G, Zhang Z, Wu H, Li L PeerJ 27-Oct-2023
PMCID:PMC10615033
doi:10.7717/peerj.16331
PMID:37908415
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Five new limonoids isolated from Walsura robusta Hou L, Mei CX, Yuan CM, Tang GH, Chen DZ, Zhao Q, He HP, Cao MM, Hao XJ Nat Prod Bioprospect 23-Feb-2023
PMCID:PMC9947198
doi:10.1007/s13659-023-00371-6
PMID:36813988
Recent Developments in Methicillin-Resistant Staphylococcus aureus (MRSA) Treatment: A Review Nandhini P, Kumar P, Mickymaray S, Alothaim AS, Somasundaram J, Rajan M Antibiotics (Basel) 29-Apr-2022
PMCID:PMC9137690
doi:10.3390/antibiotics11050606
PMID:35625250
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Natural Products Targeting the Mitochondria in Cancers Yang Y, He PY, Zhang Y, Li N Molecules 28-Dec-2020
PMCID:PMC7795732
doi:10.3390/molecules26010092
PMID:33379233
The Role of Autophagy in Liver Cancer: Crosstalk in Signaling Pathways and Potential Therapeutic Targets Cui J, Shen HM, Lim LH Pharmaceuticals (Basel) 28-Nov-2020
PMCID:PMC7760785
doi:10.3390/ph13120432
PMID:33260729
Nutrient contents predict the bamboo‐leaf‐based diet of Assamese macaques living in limestone forests of southwest Guangxi, China Li Y, Ma G, Zhou Q, Li Y, Huang Z Ecol Evol 28-Apr-2020
PMCID:PMC7319238
doi:10.1002/ece3.6297
PMID:32607175
Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens Mickymaray S Antibiotics (Basel) 09-Dec-2019
PMCID:PMC6963422
doi:10.3390/antibiotics8040257
PMID:31835403
Methicillin-resistant Staphylococcus aureus (MRSA) and anti-MRSA activities of extracts of some medicinal plants: A brief review Okwu MU, Olley M, Akpoka AO, Izevbuwa OE AIMS Microbiol 15-Apr-2019
PMCID:PMC6642907
doi:10.3934/microbiol.2019.2.117
PMID:31384707
Bioactive A-ring rearranged limonoids from the root barks of Walsura robusta An F, Wang X, Yang M, Luo J, Kong L Acta Pharm Sin B 01-Mar-2019
PMCID:PMC6543057
doi:10.1016/j.apsb.2019.02.009
PMID:31193828
Characterization of Condensed Tannins from Purple Prairie Clover (Dalea purpurea Vent.) Conserved as either Freeze-Dried Forage, Sun-Cured Hay or Silage Peng K, Huang Q, Xu Z, McAllister TA, Acharya S, Mueller-Harvey I, Drake C, Cao J, Huang Y, Sun Y, Wang S, Wang Y Molecules 06-Mar-2018
PMCID:PMC6017389
doi:10.3390/molecules23030586
PMID:29509678
Lack of phylogenetic signals within environmental niches of tropical tree species across life stages Zhang C, Yang J, Sha L, Ci X, Li J, Cao M, Brown C, Swenson NG, Lin L Sci Rep 09-Feb-2017
PMCID:PMC5299423
doi:10.1038/srep42007
PMID:28181524
Discovery of structurally diverse and bioactive compounds from plant resources in China Yang SP, Yue JM Acta Pharmacol Sin 03-Sep-2012
PMCID:PMC4003105
doi:10.1038/aps.2012.105
PMID:22941284
Antioxidant, antibacterial and antigiardial activities of Walsura robusta Roxb. Voravuthikunchai SP, Kanchanapoom T, Sawangjaroen N, Hutadilok-Towatana N Nat Prod Res 01-May-2010
doi:10.1080/14786410902819152
PMID:20461627

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside 10483388 Click to see 582.60 unknown https://doi.org/10.1080/14786410902819152
(2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10031185 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O 582.60 unknown https://doi.org/10.1080/14786410902819152
2-((7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14521083 Click to see 582.60 unknown https://doi.org/10.1080/14786410902819152
> Lipids and lipid-like molecules / Steroids and steroid derivatives / 17-furanylsteroids and derivatives
17-(furan-3-yl)-6,11,15-trihydroxy-4,4,8,10,14-pentamethyl-11,12,15,16-tetrahydro-9H-cyclopenta[a]phenanthrene-3,7-dione 73311290 Click to see 438.50 unknown https://doi.org/10.1021/OL070735+
Walsuronoid B 16724460 Click to see CC1(C(=O)C=CC2(C1=C(C(=O)C3(C2C(CC4=C(CC(C43C)O)C5=COC=C5)O)C)O)C)C 438.50 unknown https://doi.org/10.1021/OL070735+
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1R,2R,4R,6R,7S,9S,10R,11R)-9,17-dihydroxy-1,7,11,15,15-pentamethyl-6-(5-oxo-2H-furan-4-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadeca-12,16-diene-14,18-dione 162890302 Click to see 454.50 unknown https://doi.org/10.1021/OL070735+
(8R,9R,10R,11S,14R,15R)-6,11,15-trihydroxy-4,4,8,10,14-pentamethyl-17-(5-oxo-2H-furan-4-yl)-11,12,15,16-tetrahydro-9H-cyclopenta[a]phenanthrene-3,7-dione 16724461 Click to see 454.50 unknown https://doi.org/10.1021/OL070735+
6,11,15-trihydroxy-4,4,8,10,14-pentamethyl-17-(5-oxo-2H-furan-4-yl)-11,12,15,16-tetrahydro-9H-cyclopenta[a]phenanthrene-3,7-dione 73311291 Click to see CC1(C(=O)C=CC2(C1=C(C(=O)C3(C2C(CC4=C(CC(C43C)O)C5=CCOC5=O)O)C)O)C)C 454.50 unknown https://doi.org/10.1021/OL070735+
9,17-dihydroxy-1,7,11,15,15-pentamethyl-6-(5-oxo-2H-furan-4-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadeca-12,16-diene-14,18-dione 162890301 Click to see CC1(C(=O)C=CC2(C1=C(C(=O)C3(C2C(CC4(C35C(O5)CC4C6=CCOC6=O)C)O)C)O)C)C 454.50 unknown https://doi.org/10.1021/OL070735+
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2R,3S,5S,6R,10R,11R,13R,17S,19S)-3,19-diacetyloxy-6-(furan-3-yl)-17-hydroxy-5,10,14,14-tetramethyl-15,16-dioxapentacyclo[15.2.1.01,13.02,10.05,9]icos-8-en-11-yl] acetate 16723525 Click to see 586.70 unknown https://doi.org/10.1021/OL070735+
[3,19-Diacetyloxy-6-(furan-3-yl)-17-hydroxy-5,10,14,14-tetramethyl-15,16-dioxapentacyclo[15.2.1.01,13.02,10.05,9]icos-8-en-11-yl] acetate 73310828 Click to see CC(=O)OC1CC2C(OOC3(CC(C2(C3)C4C1(C5=CCC(C5(CC4OC(=O)C)C)C6=COC=C6)C)OC(=O)C)O)(C)C 586.70 unknown https://doi.org/10.1021/OL070735+
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922637 Click to see 346.33 unknown https://doi.org/10.1080/14786410902819152
3,4,5-Trimethoxyphenyl beta-D-glucopyranoside 636454 Click to see 346.33 unknown https://doi.org/10.1080/14786410902819152

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