Illicium simonsii - Unknown
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Internal ID UUID6440551fb9fa2495319322
Scientific name Illicium simonsii
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 480 (1888)

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Synonyms Top

Scientific name Authority First published in
Illicium manipurense Watt ex King Ann. Roy. Bot. Gard. (Calcutta) 3(2): 200 (1891)
Illicium yunnanense (Franch.) Franch. ex Finet & Gagnep. Mém. Soc. Bot. France 4: 29 (1906)
Illicium jiadifengpi var. szechuanense (W.C.Cheng) Y.W.Law & B.N.Chang Fl. Reipubl. Popularis Sin. 30(1): 205 (1996)
Illicium szechuanense W.C.Cheng Icon. Pl. Omeiesium 1: t. 6 (1942)
Illicium griffithii var. yunnanense Franch. Bull. Soc. Bot. France 33: 383. 1886
Illicium fargesii Finet & Gagnep. Mém. Soc. Bot. France 4: 29 (1906)
Illicium fargesii var. szechuanense (W.C.Cheng) Q.Lin Acta Bot. Yunnan. 17: 297 (1995)
Illicium fargesii subsp. szechuanense (W.C.Cheng) Q.Lin Acta Phytotax. Sin. 38: 172 (2000)

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Language Common/alternative name
Arabic إليسيوم سيموني
Arabic ليسوم سيموني
Chinese 土大香
Chinese 野八角
Chinese 四川八角

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001238711
Tropicos 50099220
KEW urn:lsid:ipni.org:names:554541-1
The Plant List tro-50099220
Open Tree Of Life 760826
NCBI Taxonomy 1202800
IUCN Red List 147369287
IPNI 554541-1
iNaturalist 498658
GBIF 3592351

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
Asymmetric Total Synthesis of Illisimonin A Etling C, Tedesco G, Di Marco A, Kalesse M J Am Chem Soc 16-Mar-2023
PMCID:PMC10064331
doi:10.1021/jacs.3c01262
PMID:36926847
Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP Plants (Basel) 13-Nov-2022
PMCID:PMC9696113
doi:10.3390/plants11223070
PMID:36432799
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA Pharmaceuticals (Basel) 11-Nov-2022
PMCID:PMC9699253
doi:10.3390/ph15111392
PMID:36422521
Conical petal epidermal cells, regulated by the MYB transcription factor MIXTA, have an ancient origin within the angiosperms Reed A, Rudall PJ, Brockington SF, Glover BJ J Exp Bot 21-May-2022
PMCID:PMC9467652
doi:10.1093/jxb/erac223
PMID:35596728
Sesquiterpenes and Monoterpenes from the Leaves and Stems of Illicium simonsii and Their Antibacterial Activity Li H, Song X, Li H, Zhu L, Cao S, Liu J Molecules 08-Feb-2022
PMCID:PMC8838251
doi:10.3390/molecules27031115
PMID:35164380
Implementation of the visual aesthetic quality of slope forest autumn color change into the configuration of tree species Mu Y, Lin W, Diao X, Zhang Z, Wang J, Lu Z, Guo W, Wang Y, Hu C, Zhao C Sci Rep 20-Jan-2022
PMCID:PMC8776743
doi:10.1038/s41598-021-04317-1
PMID:35058486
Contiguous Quaternary Carbons: A Selection of Total Syntheses Eggert A, Etling C, Lübken D, Saxarra M, Kalesse M Molecules 24-Aug-2020
PMCID:PMC7504199
doi:10.3390/molecules25173841
PMID:32847075
Anti-Inflammatory Effect of Simonsinol on Lipopolysaccharide Stimulated RAW264.7 Cells through Inactivation of NF-κB Signaling Pathway Li LC, Pan ZH, Ning DS, Fu YX Molecules 06-Aug-2020
PMCID:PMC7463804
doi:10.3390/molecules25163573
PMID:32781605
Cones structure and seed traits of four species of large‐seeded pines: Adaptation to animal‐mediated dispersal Zhang M, Su C, Lu C Ecol Evol 29-Apr-2020
PMCID:PMC7319130
doi:10.1002/ece3.6273
PMID:32607152
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
An Overview of Saturated Cyclic Ethers: Biological Profiles and Synthetic Strategies Lu Q, Harmalkar DS, Choi Y, Lee K Molecules 21-Oct-2019
PMCID:PMC6833478
doi:10.3390/molecules24203778
PMID:31640154
A Novel Hypothesis for the Role of Photosynthetic Physiology in Shaping Macroevolutionary Patterns Yiotis C, McElwain JC Plant Physiol 04-Sep-2019
PMCID:PMC6836816
doi:10.1104/pp.19.00749
PMID:31484680
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
Pharmacologic Effect of Miao Medicine Illicium simonsii Maxim. on Collagen-Induced Arthritis in Rats Zhang QZ, Hu XY, Yao WQ, Wan XL, Liang ZC, Dang RM, Yang ZM, Xia YL Evid Based Complement Alternat Med 11-Oct-2018
PMCID:PMC6201380
doi:10.1155/2018/2398379
PMID:30405736
Identification of Insecticidal Constituents from the Essential Oil from the Aerial Parts Stachys riederi var. japonica Quan M, Liu QZ, Liu ZL Molecules 17-May-2018
PMCID:PMC6099633
doi:10.3390/molecules23051200
PMID:29772795

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
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Isodunnianol 15714606 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)C3=C(C=CC(=C3)CC=C)O)CC=C 398.50 unknown https://doi.org/10.1248/CPB.42.112
Isomagnolone 9993913 Click to see CCC(=O)C1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O 282.30 unknown https://doi.org/10.1248/CPB.42.112
> Benzenoids / Benzene and substituted derivatives / Terphenyls / M-terphenyls
Dunnianol 15714605 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=CC(=C2O)C3=C(C=CC(=C3)CC=C)O)CC=C 398.50 unknown https://doi.org/10.1248/CPB.42.112
Macranthol 180210 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C(=C2)C3=C(C=CC(=C3)CC=C)O)O)CC=C 398.50 unknown https://doi.org/10.1248/CPB.42.112
Simonsinol 10340821 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=CC(=C2O)C3=CC(=C(C=C3)O)CC=C)CC=C 398.50 unknown https://doi.org/10.1248/CPB.42.112
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1248/CPB.42.112
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1248/CPB.42.112
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2R,4R,5R,6S,7R,8R,11S)-4,5,7,11-tetrahydroxy-2,7-dimethylspiro[9-oxatricyclo[6.3.1.01,5]dodecane-6,3'-oxetane]-2',10-dione 44575426 Click to see CC1CC(C2(C13CC(C(C24COC4=O)(C)O)OC(=O)C3O)O)O 328.31 unknown https://doi.org/10.4268/CJCMM20111013
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.4268/CJCMM20111013
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown https://doi.org/10.1021/JF058156B

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