PlantaeDB Logo
Login Sign-up

Illicium tashiroi

We don't have an image yet. Upload an image!

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 UUID6440551f1ada2636233347
Scientific name Illicium tashiroi
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 479 (1888)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Illicium randaiense Hayata Icon. Pl. Formosan. 9: 2 (1920)
Illicium anisatum var. tashiroi (Maxim.) E.Walker J. Jap. Bot. 46: 67 (1971)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic إليسيوم طاشيروي
Arabic ليسوم طاشيروي
Chinese 峦大八角
Chinese 東亞八角

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001238706
Tropicos 50099215
KEW urn:lsid:ipni.org:names:554547-1
The Plant List tro-50099215
Open Tree Of Life 7580788
NCBI Taxonomy 2803501
IPNI 554547-1
GBIF 3592311
EOL 5348347

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
Enantioselective para-Claisen Rearrangement for the Synthesis of Illicium-Derived Prenylated Phenylpropanoids Homer JA, De Silvestro I, Matheson EJ, Stuart JT, Lawrence AL Org Lett 15-Apr-2021
PMCID:PMC8155563
doi:10.1021/acs.orglett.1c00620
PMID:33856817
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
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
Studies on the constituents of the plants of Illicium species. II. Structures of phenolic components. KENICHI YAKUSHIJIN, TOMOKO TOHSHIMA, RIKA SUZUKI, HIROYUKI MURATA, SHENGTEN LU, HIROSHI FURUKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.2879
Studies on the constituents of the plants of illicium species. III. Structure elucidations of novel phytoquinoids, illicinones and illifunones from Illicium tashiroi Maxim. and I. arborescens Hayata. KENICHI YAKUSHIJIN, TOMOKO TOHSHIMA, EIJI KITAGAWA, RIKA SUZUKI, JUNKO SEKIKAWA, TAKAYUKI MORISHITA, HIROYUKI MURATA, SHENGTEN LU, HIROSHI FURUKAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.11
Systematic review of herbals as potential anti-inflammatory agents: Recent advances, current clinical status and future perspectives Beg S, Swain S, Hasan H, Barkat MA, Hussain MS Pharmacogn Rev 01-Jul-2011
PMCID:PMC3263046
doi:10.4103/0973-7847.91102
PMID:22279370
Biomimetic total synthesis of tricycloillicinone and mechanistic studies toward the rearrangement of prenyl phenyl ethers Lei X, Dai M, Hua Z, Danishefsky SJ Tetrahedron Lett 03-Nov-2008
PMCID:PMC2632774
doi:10.1016/j.tetlet.2008.07.184
PMID:19890380
Tashironin, a plausible biosynthetic precursor of anisatin-type sesquiterpenes Yoshiyasu Fukuyama, Naomi Shida, Mitsuaki Kodama Elsevier BV 01-May-2003
doi:10.1016/0040-4039(94)02258-D
Prenylated C6-C3 compounds from Illicium tashiroi Yoshiyasu Fukuyama, Naomi Shida, Toshinori Sakurai, Mitsuaki Kodama Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97566-6
Structure of illicinolide A, a novel sesquiterpene lactone from the bark of Illicium tashiroi Yoshiyasu Fukuyama, Naomi Shida, Mitsuaki Kodama, Masaru Kido, Masakazu Nagasawa Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)97914-0
Prenylated C6-C3 compounds from Illicium tashiroi Yoshiyasu Fukuyama, Naomi Shida, Yuuko Hata, Mitsuaki Kodama Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89750-2
Prenylated C6C3 compounds related to illicinone E fromIllicium tashiroi Yoshiyasu Fukuyama, Naomi Shida, Yuuko Hata, Sayoko Anzaki, Mitsuaki Kodama Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89586-2
Illicinolides A and B, novel sesquiterpene lactones from the wood of Illicium tashiroi Yoshiyasu Fukuyama, Naomi Shida, Mitsuaki Kodama, Masaru Kido, Masakazu Nagasawa, Michiharu Sugawara Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)90176-0
Bicycloillicinone asarone acetal: a novel prenylated C6-C3 compound increasing choline acetyltransferase (ChAT) activity from Illicium tashiroi. Fukuyama Y, Hata Y, Kodama M Planta Med 01-Jun-1997
doi:10.1055/S-2006-957675
PMID:9225616
Tricycloillicinone, a novel prenylated c6-c3 compound increasing choline acetyltransferase (ChAT) activity, isolated from Illicium tashiroi. Fukuyama Y, Shida N, Kodama M, Chaki H, Yugami T Chem Pharm Bull (Tokyo) 01-Dec-1995
doi:10.1248/CPB.43.2270
PMID:8582027

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Isodunnianin 192340 Click to see CC1CC(C2(C13CC(C(C2(COC(=O)C3)C)(C)O)OC(=O)C4=CC=CC=C4)O)OC(=O)C 446.50 unknown https://doi.org/10.1055/S-2006-959640
Tashironin 16729380 Click to see CC1CCC2(C13CC(=O)C4(C2(COC4(C3O)OC(=O)C5=CC=CC=C5)C)C)O 386.40 unknown https://doi.org/10.1016/0040-4039(94)02258-D
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Illicinone H 101672250 Click to see CC(C)(C=CC1(CC(C(=O)C=C1OC)CC=C)O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)89750-2
Tricycloillicinone 10538380 Click to see CC1(C2CC34CC2(CC1=C)C(=O)C=C3OCO4)C 246.30 unknown https://doi.org/10.1248/CPB.43.2270
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(1R,3R,4R,6R,11R)-11-(2-hydroxypropan-2-yl)-4-prop-2-enyl-7,9,10-trioxatricyclo[4.3.3.01,6]dodecan-3-ol 101678883 Click to see CC(C)(C1CC23CC(C(CC2(O1)OCO3)O)CC=C)O 284.35 unknown https://doi.org/10.1016/S0031-9422(00)89586-2
(1R,6S,11R)-11-(2-hydroxypropan-2-yl)-4-prop-2-enyl-7,9,10-trioxatricyclo[4.3.3.01,6]dodec-4-en-3-one 101635448 Click to see CC(C)(C1CC23C=C(C(=O)CC2(O1)OCO3)CC=C)O 280.32 unknown https://doi.org/10.1016/S0031-9422(00)97566-6
(1R,6S,11R)-11-(2-methoxypropan-2-yl)-4-prop-2-enyl-7,9,10-trioxatricyclo[4.3.3.01,6]dodec-4-en-3-one 101635449 Click to see CC(C)(C1CC23C=C(C(=O)CC2(O1)OCO3)CC=C)OC 294.34 unknown https://doi.org/10.1016/S0031-9422(00)97566-6
> Organoheterocyclic compounds / Benzodioxoles
(1S,8S,9S,11S)-9-(2-hydroxypropan-2-yl)-11-(5-methoxy-6-prop-2-enyl-1,3-benzodioxol-2-yl)-8-prop-2-enyl-2,4-dioxatricyclo[6.2.1.01,5]undec-5-en-7-one 101707022 Click to see CC(C)(C1CC23C(C1(C(=O)C=C2OCO3)CC=C)C4OC5=C(O4)C=C(C(=C5)CC=C)OC)O 454.50 unknown https://doi.org/10.1055/S-2006-957675
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown https://doi.org/10.1248/CPB.31.2879
> Organoheterocyclic compounds / Benzofurans
(2R,3aR,5S,7aS)-3a,7a-dihydroxy-2-(2-hydroxypropan-2-yl)-5-prop-2-enyl-3,4,5,7-tetrahydro-2H-1-benzofuran-6-one 101672251 Click to see CC(C)(C1CC2(CC(C(=O)CC2(O1)O)CC=C)O)O 270.32 unknown https://doi.org/10.1016/S0031-9422(00)89750-2
(2R,3aR,5S)-3a-hydroxy-2-(2-hydroxypropan-2-yl)-5-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one 101602691 Click to see CC(C)(C1CC2(CC(C(=O)C=C2O1)CC=C)O)O 252.31 unknown https://doi.org/10.1248/CPB.32.11
(2R,3aR,5S)-3a-hydroxy-2-(2-methoxypropan-2-yl)-5-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one 101672252 Click to see CC(C)(C1CC2(CC(C(=O)C=C2O1)CC=C)O)OC 266.33 unknown https://doi.org/10.1016/S0031-9422(00)89750-2
(2R,3aS,5R)-2-(2-chloropropan-2-yl)-3a-hydroxy-5-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one 101672253 Click to see CC(C)(C1CC2(CC(C(=O)C=C2O1)CC=C)O)Cl 270.75 unknown https://doi.org/10.1016/S0031-9422(00)89750-2
> Organoheterocyclic compounds / Dioxolanes / 1,3-dioxolanes
(7aS)-7a-(3-methylbut-2-enyl)-6-prop-2-enyl-1,3-benzodioxol-5-one 101976765 Click to see CC(=CCC12C=C(C(=O)C=C1OCO2)CC=C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)97566-6
(7aS)-7a-[(E)-3-hydroxy-3-methylbut-1-enyl]-6-prop-2-enyl-1,3-benzodioxol-5-one 101672376 Click to see CC(C)(C=CC12C=C(C(=O)C=C1OCO2)CC=C)O 262.30 unknown https://doi.org/10.1016/S0031-9422(00)89750-2
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Illicinolide A 183093 Click to see CC1C(C(C2(C13CC(C4C2(C(C(OC4)OC)O)C)OC3=O)O)O)O 344.36 unknown https://doi.org/10.1016/S0040-4020(01)90176-0
https://doi.org/10.1016/S0040-4039(00)97914-0

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.