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Illicium jiadifengpi

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 UUID6440544e8c7f6301993664
Scientific name Illicium jiadifengpi
Authority B.N.Chang
First published in Acta Bot. Yunnan. 4: 47 (1982)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Illicium jiadifengpi var. baishanense B.N.Chang & S.H.Ou Guihaia 5: 177 (1985)

Common names Top

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Language Common/alternative name
Arabic ليسوم قشري زائف
Chinese 假地枫皮
Chinese 百山祖八角
Chinese 假地楓皮

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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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-0001228174
Tropicos 50053707
KEW urn:lsid:ipni.org:names:900105-1
The Plant List tro-50053707
Open Tree Of Life 105454
NCBI Taxonomy 1202798
IUCN Red List 152824853
IPNI 900105-1
GBIF 7314066
EOL 5348306

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
Anticoronavirus Evaluation of Antimicrobial Diterpenoids: Application of New Ferruginol Analogues Varbanov M, Philippot S, González-Cardenete MA Viruses 09-Jun-2023
PMCID:PMC10301393
doi:10.3390/v15061342
PMID:37376641
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Potential of diterpene compounds as antivirals, a review Wardana AP, Aminah NS, Rosyda M, Abdjan MI, Kristanti AN, Tun KN, Choudhary MI, Takaya Y Heliyon 12-Aug-2021
PMCID:PMC8359577
doi:10.1016/j.heliyon.2021.e07777
PMID:34405122
Neottia wuyishanensis (Orchidaceae: Neottieae), a new species from Fujian, China Chen BH, Jin XH Plant Divers 04-Feb-2021
PMCID:PMC8591140
doi:10.1016/j.pld.2021.01.008
PMID:34816068
Change the channel: CysLoop receptor antagonists from Nature Tong G, Baker MA, Shenvi RA Pest Manag Sci 22-Nov-2020
PMCID:PMC8087819
doi:10.1002/ps.6166
PMID:33135373
The search for, and chemistry and mechanism of, neurotrophic natural products Fukuyama Y, Kubo M, Harada K J Nat Med 08-Jul-2020
PMCID:PMC7456418
doi:10.1007/s11418-020-01431-8
PMID:32643028
The largest early-diverging angiosperm family is mostly pollinated by ovipositing insects and so are most surviving lineages of early angiosperms Luo SX, Zhang LJ, Yuan S, Ma ZH, Zhang DX, Renner SS Proc Biol Sci 03-Jan-2018
PMCID:PMC5784199
doi:10.1098/rspb.2017.2365
PMID:29298936
Bio-Guided Isolation of Methanol-Soluble Metabolites of Common Spruce (Picea abies) Bark by-Products and Investigation of Their Dermo-Cosmetic Properties Angelis A, Hubert J, Aligiannis N, Michalea R, Abedini A, Nuzillard JM, Gangloff SC, Skaltsounis AL, Renault JH Molecules 21-Nov-2016
PMCID:PMC6272914
doi:10.3390/molecules21111586
PMID:27879645
The antiviral effect of jiadifenoic acids C against coxsackievirus B3 Ge M, Wang H, Zhang G, Yu S, Li Y Acta Pharm Sin B 16-Jul-2014
PMCID:PMC4629087
doi:10.1016/j.apsb.2014.06.008
PMID:26579396
Total Synthesis of Jiadifenolide Paterson I, Xuan M, Dalby SM Angew Chem Int Ed Engl 23-May-2014
PMCID:PMC4320761
doi:10.1002/anie.201404224
PMID:24861364
An Enantiospecific Synthesis of Jiadifenolide Siler DA, Mighion JD, Sorensen EJ Angew Chem Int Ed Engl 23-Apr-2014
PMCID:PMC4153357
doi:10.1002/anie.201402335
PMID:24757120
Neurotrophic Natural Products: Chemistry and Biology Xu J, Lacoske MH, Theodorakis EA Angew Chem Int Ed Engl 18-Dec-2013
PMCID:PMC3945720
doi:10.1002/anie.201302268
PMID:24353244
The first examples of seco-prezizaane-type norsesquiterpenoids with neurotrophic activity from Illicium jiadifengpi Miwa Kubo, Kana Kobayashi, Jian-Mei Huang, Kenichi Harada, Yoshiyasu Fukuyama Elsevier BV 11-Jan-2012
doi:10.1016/J.TETLET.2011.12.107
Enantioselective Synthesis of (−)-Jiadifenin, a Potent Neurotrophic Modulator Trzoss L, Xu J, Lacoske MH, Mobley WC, Theodorakis EA Org Lett 03-Aug-2011
PMCID:PMC3163030
doi:10.1021/ol201742j
PMID:21812392
Enantioselective Total Synthesis of (−)-Jiadifenolide Xu J, Trzoss L, Chang WK, Theodorakis EA Angew Chem Int Ed Engl 11-Mar-2011
PMCID:PMC3159889
doi:10.1002/anie.201100313
PMID:21400650

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 / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1021/NP010571K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2R,3S,7R,8S,11R,13R,14S)-2,7-dihydroxy-3,14-dimethyl-5,9,12-trioxapentacyclo[6.6.1.12,13.01,11.03,7]hexadecane-6,10-dione 162939033 Click to see CC1C2CC3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O 310.30 unknown https://doi.org/10.1021/OL9021029
(1R,2R,4R,5R,6S,10R,11R,14R)-4,5,10,14-tetrahydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione 162980859 Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O 328.31 unknown https://doi.org/10.1021/OL9021029
(1R,2R,4S,6S,7S,11R,12S,15R)-6,11,15-trihydroxy-2,7-dimethyl-3,9,13-trioxapentacyclo[10.3.1.01,6.02,4.07,11]hexadecane-10,14-dione 163029090 Click to see 326.30 unknown https://doi.org/10.1021/OL9021029
(1R,2R,5R,6S,10R,11R,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione 45269136 Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O 312.31 unknown https://doi.org/10.1021/OL9021029
https://doi.org/10.1021/NP010571K
(1R,2R,6R,10R,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione 11522412 Click to see 308.28 unknown https://doi.org/10.1021/NP010571K
(1R,2S,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione 163186509 Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O 308.28 unknown https://doi.org/10.1021/NP010571K
(1R,2S,3R,5S,6S,10R,11R)-3,5,10-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.2.1.01,5.06,10]tetradecane-9,13-dione 57330139 Click to see CC1C(CC2(C13CC(C4(C2(COC4=O)C)O)OC3=O)O)O 298.29 unknown https://doi.org/10.1016/J.TETLET.2011.12.107
(1R,2S,3R,6R,10R,11R,14R)-3,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-9,13-dione 21629990 Click to see 310.30 unknown https://doi.org/10.1021/NP010571K
(1R,2S,5R,6S,10R,11S,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-3-ene-9,13-dione 162942090 Click to see 310.30 unknown https://doi.org/10.1021/NP010571K
(1R,2S,6R,10R,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione 11659544 Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O 308.28 unknown https://doi.org/10.1021/NP010571K
(1S,2R,4R,5R,6S,10R,11S,14R)-4,5,10,14-tetrahydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione 162980861 Click to see 328.31 unknown https://doi.org/10.1021/NP010571K
(1S,2R,4S,6R,9R,10R,14S,15R)-10,15-dihydroxy-2,14-dimethyl-5,8,12-trioxapentacyclo[7.6.1.01,6.04,15.010,14]hexadecane-7,11-dione 44542226 Click to see 310.30 unknown https://doi.org/10.1021/OL9021029
(1S,2R,5R,6S,10R,11S,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione 21672428 Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O 312.31 unknown https://doi.org/10.1021/NP010571K
(1S,2S,5R,6S,10R,11R,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-3,9,13-trione 14564520 Click to see 326.30 unknown https://doi.org/10.1021/NP010571K
https://doi.org/10.1021/OL9021029
10,15-Dihydroxy-2,14-dimethyl-5,8,12-trioxapentacyclo[7.6.1.01,6.04,15.010,14]hexadecane-7,11-dione 75046197 Click to see CC1CC2C3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O 310.30 unknown https://doi.org/10.1021/OL9021029
2,7-Dihydroxy-3,14-dimethyl-5,9,12-trioxapentacyclo[6.6.1.12,13.01,11.03,7]hexadecane-6,10-dione 162939032 Click to see 310.30 unknown https://doi.org/10.1021/OL9021029
4,7a-Methano-1H,3H-cyclopenta[e]furo[3,4-c]oxocin-3,6(7H)-dione, heptahydro-3a,7,10,10a-tetrahydroxy-8,10b-dimethyl- 494843 Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O 328.31 unknown https://doi.org/10.1021/OL9021029
https://doi.org/10.1021/NP010571K
5,10,14-Trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-3,9,13-trione 14564519 Click to see 326.30 unknown https://doi.org/10.1021/OL9021029
5,10,14-Trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione 15600080 Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O 312.31 unknown https://doi.org/10.1021/OL9021029
6,11,15-Trihydroxy-2,7-dimethyl-3,9,13-trioxapentacyclo[10.3.1.01,6.02,4.07,11]hexadecane-10,14-dione 163029089 Click to see 326.30 unknown https://doi.org/10.1021/OL9021029
6,9-Dihydroxy-2,11-dimethyl-4,8,14-trioxapentacyclo[7.4.2.17,10.01,10.02,6]hexadecane-5,15-dione 75046196 Click to see CC1CCC23C14CC(C5(C2(COC5=O)C)O)OC4(C(=O)O3)O 310.30 unknown https://doi.org/10.1021/OL9021029
Jiadifenolide 44542225 Click to see 310.30 unknown https://doi.org/10.1021/OL9021029
Majucin 3086559 Click to see 328.31 unknown https://doi.org/10.1021/NP010571K
> Organoheterocyclic compounds / Lactones / Delta valerolactones
1,2-Dehydroneomajucin 11141421 Click to see 310.30 unknown https://doi.org/10.1021/NP010571K
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aR,4R,8aS,8bR)-3a,4-dihydroxy-6,8b-dimethyl-4,5,8,8a-tetrahydro-1H-cyclopenta[e][2]benzofuran-3,7-dione 101792613 Click to see 252.26 unknown https://doi.org/10.1016/J.TETLET.2011.12.107
> Organoheterocyclic compounds / Oxepanes
Jiadifenin 11544617 Click to see 338.31 unknown https://doi.org/10.1021/NP010571K
methyl rel-(3aR,4R,6S,6aR,7R,9bR)-3a,6-dihydroxy-7,9b-dimethyl-3,8-dioxo-1,3a,4,7,8,9b-hexahydro-3H-4,6a-methanocyclopenta[c]furo[3,4-e]oxepine-6-carboxylate 636731 Click to see 338.31 unknown https://doi.org/10.1021/NP010571K

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