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Symplocos setchuensis

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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 UUID64404f1d4e423628784387
Scientific name Symplocos setchuensis
Authority Brand ex Diels
First published in Bot. Jahrb. Syst. 29: 528 (1900)

Description Top

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Synonyms Top

Scientific name Authority First published in
Symplocos argyi H.Lév. Repert. Spec. Nov. Regni Veg. 10: 431 (1912)
Symplocos glomeratiflora Hayata Icon. Pl. Formosan. 5: 100 (1915)
Dicalix setchuensis (Brand) Migo Bull. Shanghai Sci. Inst. 13: 205 (1943)
Bobua ilicifolia (Hayata) Kaneh. & Sasaki List Pl. Formosa : 331 (1928)
Symplocos acutangula Brand Pflanzenr. , IV, 242: 65 (1901)
Symplocos ilicifolia Hayata Icon. Pl. Formosan. 5: 102 (1915)
Symplocos sinuata Brand Repert. Spec. Nov. Regni Veg. 14: 326 (1916)
Bobua glomeratiflora (Hayata) Kaneh. & Sasaki List Pl. Formosa : 331 (1928)

Common names Top

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Language Common/alternative name
Chinese 四川灰木
Chinese 四川山矾

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
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001141684
Tropicos 30900312
KEW urn:lsid:ipni.org:names:827302-1
Open Tree Of Life 790017
NCBI Taxonomy 210366
IPNI 827302-1
GBIF 3643724
CMAUP NPO30753

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
“Diminishing returns” and leaf area-biomass scaling of ferns in subtropical ecosystems Chen S, Li J, Sun J, Zhong Q, Hu D, Cheng D Front Plant Sci 27-Jun-2023
PMCID:PMC10333482
doi:10.3389/fpls.2023.1187704
PMID:37441171
“Realistic strategies” and neutral processes drive the community assembly based on leaf functional traits in a subtropical evergreen broad‐leaved forest Zhao L, Xiang W, Li J, Liu W, Hu Y, Wu H, Zhang Y, Cheng X, Wang W, Wang W, Ouyang S Ecol Evol 17-Sep-2022
PMCID:PMC9482003
doi:10.1002/ece3.9323
PMID:36177111
Mismatch Between Specific and Genetic Diversity in an Evergreen Broadleaf Forest in Southeast China: A Study Case of 10.24 ha Forest Dynamics Plot of Huangshan Xie L, Chen S, Feng Y, Li Y, Wang L, He L, Huang L, Wu J, Guo K, Ding H, Fang Y Front Plant Sci 31-Jan-2022
PMCID:PMC8841795
doi:10.3389/fpls.2021.706006
PMID:35173745
Plant-derived lignans as potential antiviral agents: a systematic review Xu XY, Wang DY, Li YP, Deyrup ST, Zhang HJ Phytochem Rev 31-May-2021
PMCID:PMC8165688
doi:10.1007/s11101-021-09758-0
PMID:34093097
Short‐term decline of Castanopsis fargesii adult trees promotes conspecific seedling regeneration: The complete process from seed production to seedling establishment Huang L, Zhou L, Wang J, Jin C, Hu S, Qian S, Lin D, Zhao L, Yang Y Ecol Evol 09-Sep-2020
PMCID:PMC7548161
doi:10.1002/ece3.6719
PMID:33072287
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Large Underestimation of Intraspecific Trait Variation and Its Improvements Yang J, Lu J, Chen Y, Yan E, Hu J, Wang X, Shen G Front Plant Sci 13-Feb-2020
PMCID:PMC7031497
doi:10.3389/fpls.2020.00053
PMID:32117390
Multivariate path analysis of the relationships between seedling regeneration and environmental factors beneath a dwarf bamboo understory Qian F, Song H, Chen M, Zeng J, Dang C, Tao J Ecol Evol 03-Sep-2019
PMCID:PMC6787829
doi:10.1002/ece3.5548
PMID:31624551
Effects of root spatial distribution on the elastic-plastic properties of soil-root blocks Li Y, Wang Y, Wang Y, Ma C Sci Rep 11-Apr-2017
PMCID:PMC5429779
doi:10.1038/s41598-017-00924-z
PMID:28400584
Quantifying PM2.5 capture capability of greening trees based on leaf factors analyzing Liang D, Ma C, Wang YQ, Wang YJ, Chen-xi Z Environ Sci Pollut Res Int 19-Sep-2016
PMCID:PMC5099360
doi:10.1007/s11356-016-7687-9
PMID:27646446
Natural Products as Anti-HIV Agents and Role in HIV-Associated Neurocognitive Disorders (HAND): A Brief Overview Kurapati KR, Atluri VS, Samikkannu T, Garcia G, Nair MP Front Microbiol 12-Jan-2016
PMCID:PMC4709506
doi:10.3389/fmicb.2015.01444
PMID:26793166
Chemical Transformation and Biological Studies of Marine Sesquiterpene (S)-(+)-Curcuphenol and Its Analogs Gul W, Hammond NL, Yousaf M, Peng J, Holley A, Hamann MT Biochim Biophys Acta 24-Jul-2007
PMCID:PMC2266081
doi:10.1016/j.bbagen.2007.05.011
PMID:17804167
Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives. Ishida J, Wang HK, Oyama M, Cosentino ML, Hu CQ, Lee KH J Nat Prod 01-Jul-2001
doi:10.1021/NP0101189
PMID:11473435

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
> Alkaloids and derivatives / Harmala alkaloids
Harmalan 160510 Click to see CC1=NCCC2=C1NC3=CC=CC=C23 184.24 unknown https://doi.org/10.1021/NP0101189
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1021/NP0101189
Harmine 5280953 Click to see CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC 212.25 unknown https://doi.org/10.1021/NP0101189
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)- 160521 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1021/NP0101189
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP0101189
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP0101189
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Matairesinol 119205 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1021/NP0101189
> Lignans, neolignans and related compounds / Lignan glycosides
(1R)-1alpha-(3-Hydroxy-4-methoxyphenyl)-4alpha-[3-methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-3aalpha,4,6,6aalpha-tetrahydro-1H,3H-furo[3,4-c]furan 44559931 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1021/NP0101189
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 https://doi.org/10.1021/NP0101189

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Collections Top

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