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Litsea akoensis

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 UUID6440474385ce9827815044
Scientific name Litsea akoensis
Authority Hayata
First published in J. Coll. Sci. Imp. Univ. Tokyo 30(1): 245 (1911)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Actinodaphne akoensis (Hayata) Tang S.Liu & J.C.Liao Sci. Ann. Taiwan Mus. 14: 5 (1971)
Cylicodaphne akoensis (Hayata) Nakai J. Jap. Bot. 14: 192 (1938)
Tetradenia akoensis (Hayata) Makino & Nemoto Fl. Japan., ed. 2 (Makino & Nemoto) 373. 1931

Common names Top

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Language Common/alternative name
Chinese 屏东木姜子
Chinese 屏東木薑子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Litsea akoensis var. akoensis 3257433 Unknown
Litsea akoensis var. sasakii (Kamik.) J.C.Liao Taxon. Rev. Fam. Lauraceae Taiwan : 84 (1988)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070639
Tropicos 17801732
KEW urn:lsid:ipni.org:names:465492-1
The Plant List tro-17801732
Open Tree Of Life 5699247
NCBI Taxonomy 1898874
IUCN Red List 157146408
IPNI 465492-1
iNaturalist 571327
GBIF 7304374
EOL 5397144

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
Structures and Biological Activities of Secondary Metabolites from Xylaria spp. Chen W, Yu M, Chen S, Gong T, Xie L, Liu J, Bian C, Huang G, Zheng C J Fungi (Basel) 29-Feb-2024
PMCID:PMC10971283
doi:10.3390/jof10030190
PMID:38535199
Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR RSC Adv 13-Oct-2022
PMCID:PMC9558262
doi:10.1039/d2ra04884a
PMID:36320761
Chemical analysis and anticancer activity of sesterterpenoid from an endophytic fungus Hypomontagnella monticulosa Zg15SU and its host Zingiber griffithii Baker Lutfia A, Munir E, Yurnaliza Y, Basyuni M Heliyon 16-Feb-2021
PMCID:PMC7900702
doi:10.1016/j.heliyon.2021.e06292
PMID:33665446
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Naturally Occurring Isocoumarins Derivatives from Endophytic Fungi: Sources, Isolation, Structural Characterization, Biosynthesis, and Biological Activities Noor AO, Almasri DM, Bagalagel AA, Abdallah HM, Mohamed SG, Mohamed GA, Ibrahim SR Molecules 17-Jan-2020
PMCID:PMC7024277
doi:10.3390/molecules25020395
PMID:31963586
Wild edible plants collected by Hani from terraced rice paddy agroecosystem in Honghe Prefecture, Yunnan, China Luo B, Liu B, Zhang H, Zhang H, Li X, Ma L, Wang Y, Bai Y, Zhang X, Li J, Yang J, Long C J Ethnobiol Ethnomed 27-Nov-2019
PMCID:PMC6882008
doi:10.1186/s13002-019-0336-x
PMID:31775804
Volatiles from the xylarialean fungus Hypoxylon invadens Dickschat JS, Wang T, Stadler M Beilstein J Org Chem 29-Mar-2018
PMCID:PMC5905279
doi:10.3762/bjoc.14.62
PMID:29719571
Characteristics of tropical human-modified forests after 20 years of natural regeneration Loo LC, Song GZ, Chao KJ Bot Stud 30-Aug-2017
PMCID:PMC5578950
doi:10.1186/s40529-017-0190-x
PMID:28861854
Antioxidant and antimicrobial properties of Litsea elliptica Blume and Litsea resinosa Blume (Lauraceae) Wong MH, Lim LF, Ahmad FB, Assim ZB Asian Pac J Trop Biomed 01-May-2014
PMCID:PMC3985054
doi:10.12980/APJTB.4.2014C1129
PMID:25182724
Secondary Metabolites from the Stem Bark of <i>Litsea akoensis</i> and Their Cytotoxic Activity Su‐Yen Chang, Ming‐Jen Cheng, Yueh‐Hsiung Kuo, Shiow‐Ju Lee, Hsun‐Shuo Chang, Ih‐Sheng Chen Wiley 10-Jul-2008
doi:10.1002/HLCA.200890125
Cytotoxic butanolides from Litsea akoensis Ih-Sheng Chen, I-Lun Lai-Yaun, Chang-Yih Duh, Ian-Lih Tsai Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00129-0

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 / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3E,4S,5R)-3-[(E,11R)-11,14-dihydroxytetradec-12-enylidene]-4-hydroxy-5-methyloxolan-2-one 163002911 Click to see 340.50 unknown https://doi.org/10.1002/HLCA.200890125
(3E,4S,5R)-3-[(E,13S)-13,14-dihydroxytetradec-11-enylidene]-4-hydroxy-5-methyloxolan-2-one 162909586 Click to see 340.50 unknown https://doi.org/10.1002/HLCA.200890125
3-(11,14-Dihydroxytetradec-12-enylidene)-4-hydroxy-5-methyloxolan-2-one 74350114 Click to see 340.50 unknown https://doi.org/10.1002/HLCA.200890125
3-(13,14-Dihydroxytetradec-11-enylidene)-4-hydroxy-5-methyloxolan-2-one 74350113 Click to see 340.50 unknown https://doi.org/10.1002/HLCA.200890125
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2R)-2-methyl-4-[(E)-tetradec-1-enyl]-2H-furan-5-one 11162159 Click to see 292.50 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
(2R)-4-[(E)-dodec-1-en-11-ynyl]-2-methyl-2H-furan-5-one 14524506 Click to see 260.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
4-dodec-1-en-11-ynyl-2-methyl-2H-furan-5-one 75072234 Click to see CC1C=C(C(=O)O1)C=CCCCCCCCCC#C 260.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
Akolactone A 10085746 Click to see 292.50 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
Akolactone B 44566941 Click to see CC1C=C(C(=O)O1)C=CCCCCCCCCC=CC=C 288.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
Hamabiwalactone A 44566940 Click to see 260.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,4S,5R)-3-[10-[(3S)-3,6-dihydro-1,2-dioxin-3-yl]decylidene]-4-hydroxy-5-methyloxolan-2-one 162881421 Click to see 338.40 unknown https://doi.org/10.1002/HLCA.200890125
(3E,4S,5R)-3-dodec-11-ynylidene-4-hydroxy-5-methyloxolan-2-one 9970799 Click to see 278.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
(3E,4S,5R)-4-hydroxy-5-methyl-3-[(11E)-tetradeca-11,13-dienylidene]oxolan-2-one 100913703 Click to see 306.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
(3E,4S,5R)-4-hydroxy-5-methyl-3-tetradecylideneoxolan-2-one 11722947 Click to see 310.50 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
(3Z,4S,5R)-3-[10-[(3S)-3,6-dihydro-1,2-dioxin-3-yl]decylidene]-4-hydroxy-5-methyloxolan-2-one 162881422 Click to see 338.40 unknown https://doi.org/10.1002/HLCA.200890125
(3Z,4S,5R)-4-hydroxy-5-methyl-3-tetradecylideneoxolan-2-one 10018302 Click to see 310.50 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
(E,13E)-13-[(4S,5R)-4-hydroxy-5-methyl-2-oxooxolan-3-ylidene]tridec-2-enal 162910918 Click to see CC1C(C(=CCCCCCCCCCC=CC=O)C(=O)O1)O 308.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
3-[10-(3,6-Dihydro-1,2-dioxin-3-yl)decylidene]-4-hydroxy-5-methyloxolan-2-one 74350112 Click to see 338.40 unknown https://doi.org/10.1002/HLCA.200890125
3-Dodec-11-ynylidene-4-hydroxy-5-methyloxolan-2-one 73097479 Click to see 278.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
4-Hydroxy-5-methyl-3-tetradecylideneoxolan-2-one 72790665 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)C)O 310.50 unknown https://doi.org/10.1016/S0031-9422(98)00129-0
> Organoheterocyclic compounds / Tetrahydrofurans
(E,13E)-13-[(4S,5R)-4-hydroxy-5-methyloxolan-3-ylidene]tridec-2-enal 100913704 Click to see 294.40 unknown https://doi.org/10.1016/S0031-9422(98)00129-0

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