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Litsea hypophaea

Litsea hypophaea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644047441431f145911660
Scientific name Litsea hypophaea
Authority Hayata
First published in Icon. Pl. Formosan. 5: 167 (1915)

Description Top

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Synonyms Top

Scientific name Authority First published in
Actinodaphne pedicellata Hayata J. Coll. Sci. Imp. Univ. Tokyo 22: 351 (1906)
Fiwa hypophaea (Hayata) Nakai J. Jap. Bot. 14: 192 (1938)
Fiwa pedicellata (Hayata) Nakai J. Jap. Bot. 14: 193 (1938)
Litsea krukovii Kosterm. Reinwardtia 9: 108 (1974)
Litsea kostermansii C.E.Chang Fl. Taiwan 2: 441 (1976)
Litsea taiwaniana Kamik. Bull. Kagoshima Imp. Coll. Agric. Forest (25 Anniv.) 1: 140 1934
Tetradenia hypophaea (Hayata) Makino & Nemoto Fl. Japan., ed. 2 (Makino & Nemoto) 375. 1931

Common names Top

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Language Common/alternative name
Chinese 小梗木薑子
Chinese 黃肉樹
Chinese 黄肉树

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-0001070650
Tropicos 17801756
KEW urn:lsid:ipni.org:names:465744-1
The Plant List tro-17801756
Open Tree Of Life 559683
NCBI Taxonomy 453235
IUCN Red List 153110564
IPNI 465744-1
iNaturalist 632265
GBIF 4175715
EOL 5397423

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
In silico investigation on the inhibitory effect of fungal secondary metabolites on RNA dependent RNA polymerase of SARS-CoV-II: A docking and molecular dynamic simulation study Ebrahimi KS, Ansari M, Hosseyni Moghaddam MS, Ebrahimi Z, salehi Z, Shahlaei M, Moradi S Comput Biol Med 05-Jul-2021
PMCID:PMC8256662
doi:10.1016/j.compbiomed.2021.104613
PMID:34242870
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
Secondary metabolites from the roots of Litsea hypophaea and their antitubercular activity. Pan PC, Cheng MJ, Peng CF, Huang HY, Chen JJ, Chen IS J Nat Prod 28-May-2010
doi:10.1021/NP100022S
PMID:20384293

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/NP100022S
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate 70164 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC 212.20 unknown https://doi.org/10.1021/NP100022S
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1021/NP100022S
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1021/NP100022S
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1021/NP100022S
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1S,2S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-N,3-N-bis[2-(4-hydroxyphenyl)ethyl]-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxamide 163043959 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)NCCC4=CC=C(C=C4)O)C(=O)NCCC5=CC=C(C=C5)O 684.70 unknown https://doi.org/10.1021/NP100022S
7-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-N2,N3-bis(4-hydroxyphenethyl)-6-methoxy-1,2-dihydronaphthalene-2,3-dicarboxamide 73022545 Click to see COC1=C(C=CC(=C1)C2C(C(=CC3=CC(=C(C=C23)O)OC)C(=O)NCCC4=CC=C(C=C4)O)C(=O)NCCC5=CC=C(C=C5)O)O 624.70 unknown https://doi.org/10.1021/NP100022S
7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-N,3-N-bis[2-(4-hydroxyphenyl)ethyl]-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxamide 46888126 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)NCCC4=CC=C(C=C4)O)C(=O)NCCC5=CC=C(C=C5)O 684.70 unknown https://doi.org/10.1021/NP100022S
Cannabisin D 44584134 Click to see COC1=C(C=CC(=C1)C2C(C(=CC3=CC(=C(C=C23)O)OC)C(=O)NCCC4=CC=C(C=C4)O)C(=O)NCCC5=CC=C(C=C5)O)O 624.70 unknown https://doi.org/10.1021/NP100022S
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1021/NP100022S
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1021/NP100022S
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1021/NP100022S
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(3E,4R,5S)-3-decylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 46834842 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP100022S
(3E,4R,5S)-3-dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 46830514 Click to see CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC 310.40 unknown https://doi.org/10.1021/NP100022S
(3E,4R,5S)-3-dodecylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 46834840 Click to see CCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 312.40 unknown https://doi.org/10.1021/NP100022S
(3Z,4R,5S)-3-decylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 46834843 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP100022S
(3Z,4R,5S)-3-dodecylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 46834841 Click to see CCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 312.40 unknown https://doi.org/10.1021/NP100022S
(3Z,4R,5S)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one 46834845 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown https://doi.org/10.1021/NP100022S
3-Decylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 75216090 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP100022S
3-Dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 75214750 Click to see CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC 310.40 unknown https://doi.org/10.1021/NP100022S
3-Dodecylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 75216089 Click to see CCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 312.40 unknown https://doi.org/10.1021/NP100022S
4-Hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one 162986152 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown https://doi.org/10.1021/NP100022S
Litseakolide L 46834844 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown https://doi.org/10.1021/NP100022S
> Organoheterocyclic compounds / Benzodioxoles
1-(1,3-Benzodioxol-5-yl)-3-(2,4,6-trimethoxyphenyl)propan-2-one 46830515 Click to see COC1=CC(=C(C(=C1)OC)CC(=O)CC2=CC3=C(C=C2)OCO3)OC 344.40 unknown https://doi.org/10.1021/NP100022S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(4-hydroxy-3,5-dimethoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide 25202112 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)NCCC2=CC=C(C=C2)O 343.40 unknown https://doi.org/10.1021/NP100022S
n-Feruloyl-3-methoxytyramine 134313 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1021/NP100022S
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1021/NP100022S
N-trans-feruloylmethoxytyramine 5352115 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1021/NP100022S
N-Trans-Sinapoyltyramine 25245053 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)NCCC2=CC=C(C=C2)O 343.40 unknown https://doi.org/10.1021/NP100022S
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
1-(3,4-Dimethoxyphenyl)-3-(2,4,6-trimethoxyphenyl)propan-2-ol 21722174 Click to see COC1=C(C=C(C=C1)CC(CC2=C(C=C(C=C2OC)OC)OC)O)OC 362.40 unknown https://doi.org/10.1021/NP100022S
2-[3-(3,4-Dimethoxyphenyl)propyl]-1,3,5-trimethoxybenzene 71229208 Click to see COC1=C(C=C(C=C1)CCCC2=C(C=C(C=C2OC)OC)OC)OC 346.40 unknown https://doi.org/10.1021/NP100022S
Hypophaol 46888125 Click to see COC1=C(C=C(C=C1)CC(CC2=C(C=C(C=C2OC)OC)OC)O)OC 362.40 unknown https://doi.org/10.1021/NP100022S

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