Pseudotsuga japonica - Unknown
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Internal ID UUID644001a852562646851484
Scientific name Pseudotsuga japonica
Authority (Shiras.) Beissn.
First published in Mitt. Deutsch. Dendrol. Ges. 5: 62 (1896)

Description Top

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Pseudotsuga japonica, also known as the Japanese Douglas-fir, is a type of conifer found only in Japan. It can reach heights of up to 25 meters and is often referred to as 'Togasawara' in Japanese. This species belongs to the pine family, Pinaceae.

Synonyms Top

Scientific name Authority First published in
Tsuga japonica Shiras. Bot. Mag. (Tokyo) 9: 84 (1895)

Common names Top

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Language Common/alternative name
English japanese douglas-fir
German japanische douglasie
Esperanto japana pseŭdotsugo
Esperanto japana pseŭdocugo
Japanese サワラトガ
Japanese トガサワラ
Lithuanian japoninė pocūgė
Chinese 日本黄杉

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-0000478214
Tropicos 24900685
KEW urn:lsid:ipni.org:names:677138-1
The Plant List kew-2556782
Open Tree Of Life 992628
NCBI Taxonomy 25593
IUCN Red List 31291
IPNI 677138-1
iNaturalist 135507
GBIF 2685851
Freebase /m/02vv0yw
EPPO PSTJA
EOL 1034950
USDA GRIN 30190
Wikipedia Pseudotsuga_japonica
CMAUP NPO13451

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
Morphological and Phylogenetic Characterization of Three Novel Thaxterogaster (Cortinariaceae) Species from China with an Emphasis on Their Subtropical Distribution Xie ML, Feng N, Lin WF, Su WY, Li Y, Yang ZQ J Fungi (Basel) 28-Oct-2023
PMCID:PMC10671986
doi:10.3390/jof9111058
PMID:37998864
Forest characteristics, population structure and growth trends of threatened relict Pseudotsuga forrestii in China Tang CQ, Yao SQ, Han PB, Wen JR, Li S, Peng MC, Wang CY, Matsui T, Li YP, Lu S, He Y Plant Divers 07-Nov-2022
PMCID:PMC10435900
doi:10.1016/j.pld.2022.10.005
PMID:37601542
Identification of the sesquiterpene synthase AcTPS1 and high production of (–)-germacrene D in metabolically engineered Saccharomyces cerevisiae Liu J, Chen C, Wan X, Yao G, Bao S, Wang F, Wang K, Song T, Han P, Jiang H Microb Cell Fact 18-May-2022
PMCID:PMC9115970
doi:10.1186/s12934-022-01814-4
PMID:35585553
Phylogenetic imprint of woody plants on the soil mycobiome in natural mountain forests of eastern China Yang T, Tedersoo L, Soltis PS, Soltis DE, Gilbert JA, Sun M, Shi Y, Wang H, Li Y, Zhang J, Chen Z, Lin H, Zhao Y, Fu C, Chu H ISME J 23-Oct-2018
PMCID:PMC6461945
doi:10.1038/s41396-018-0303-x
PMID:30353037
Biogeography of Coptis Salisb. (Ranunculales, Ranunculaceae, Coptidoideae), an Eastern Asian and North American genus Xiang KL, Erst AS, Xiang XG, Jabbour F, Wang W BMC Evol Biol 24-May-2018
PMCID:PMC5968522
doi:10.1186/s12862-018-1195-0
PMID:29793422
Ectomycorrhizal fungal communities in endangered Pinus amamiana forests Murata M, Kanetani S, Nara K PLoS One 19-Dec-2017
PMCID:PMC5736215
doi:10.1371/journal.pone.0189957
PMID:29261780
Source identification of western Oregon Douglas-fir wood cores using mass spectrometry and random forest classification Finch K, Espinoza E, Jones FA, Cronn R Appl Plant Sci 12-May-2017
PMCID:PMC5435404
doi:10.3732/apps.1600158
PMID:28529831
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
3β-Methoxycycloartan-27-oic Acid and Other Constituents from the Leaves of Pseudotsuga japonica Reiko Tanaka, Yoshikazu Takaoka, Haruhiko Yamaguchi, Shunyo Matsunaga American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50100A014

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(4-Hydroxyphenyl)-2-butanone 21648 Click to see CC(=O)CCC1=CC=C(C=C1)O 164.20 unknown https://doi.org/10.1021/NP50100A014
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP50100A014
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
7beta-Hydroxysitosterol 12309569 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Ikshusterol 161816 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 86311182 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)O 242.22 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see COC1=CC(=CC(=C1O)OC)C(=O)CCO 226.23 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(2S,3R)-3-Ethoxy-2,3-bis(3-methoxy-4-hydroxyphenyl)propane-1-ol 11759831 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)C2=CC(=C(C=C2)O)OC 348.40 unknown via CMAUP database
[4-[(4R,5R)-4-(4-acetyloxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenyl] acetate 21591953 Click to see CC(=O)OC1=C(C=C(C=C1)C2COCOC2C3=CC(=C(C=C3)OC(=O)C)OC)OC 416.40 unknown via CMAUP database
4-[(4S,5S)-4-(4-hydroxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenol 10871293 Click to see COC1=C(C=CC(=C1)C2COCOC2C3=CC(=C(C=C3)O)OC)O 332.30 unknown via CMAUP database

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