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Salix japonica

Salix japonica - 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 UUID6440369484cc5428760108
Scientific name Salix japonica
Authority Thunb.
First published in Syst. Veg. , ed. 14: 879 (1784)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salix fauriei Seemen Beibl. Bot. Jahrb. Syst. 67: 40 (1901)
Salix padifolia Andersson Mem. Amer. Acad. Arts , n.s., 6: 451 (1858)
Salix oldhamiana Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 25 (1867)
Salix viridula Andersson Mem. Amer. Acad. Arts , n.s., 6: 451 (1858)
Salix japonica var. oldhamiana (Miq.) Franch. & Sav. Enum. Pl. Jap. 1: 459 1875
Salix japonica var. pygmaea Franch. & Sav. Enum. Pl. Jap. 1: 459 1875
Salix japonica var. padifolia (Andersson) Seemen Salic. Jap. 45 1903
Salix japonica f. padifolia (Andersson) Koidz. Bot. Mag. (Tokyo) 27: 91 1913
Salix japonica f. oldhamiana (Miq.) Koidz. Bot. Mag. (Tokyo) 27: 91 1913
Salix japonica f. pygmaea (Franch. & Sav.) C.K.Schneid. Pl. Wilson. 3: 132 1916
Salix japonica var. angustifolia Kimura Bot. Mag. (Tokyo) 4: 573 1928
Salix japonica f. fauriei (Seemen) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 15: 416 1940
Salix japonica f. angustifolia (Kimura) Kimura Ecol. Rev. 13: 200 1953

Common names Top

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Language Common/alternative name
Persian بید ژاپنی
Japanese シバヤナギ

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-0000928845
Tropicos 50261985
KEW urn:lsid:ipni.org:names:777889-1
The Plant List kew-5001180
Open Tree Of Life 891398
NCBI Taxonomy 1078600
IPNI 777889-1
GBIF 5581587
Freebase /m/0fps7v
EPPO SAXJA
EOL 5600393
USDA GRIN 32723
Wikipedia Salix_japonica
CMAUP NPO3731

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
Aula Verde (tree room) as a link between art and science to raise public awareness of nature-based solutions Conte A, Pace R, Li Q, Carloni S, Boetzkes A, Passatore L Sci Rep 06-Feb-2024
PMCID:PMC10847515
doi:10.1038/s41598-024-51611-9
PMID:38321108
Conferring High IAA Productivity on Low-IAA-Producing Organisms with PonAAS2, an Aromatic Aldehyde Synthase of a Galling Sawfly, and Identification of Its Inhibitor Hiura T, Yoshida H, Miyata U, Asami T, Suzuki Y Insects 02-Jul-2023
PMCID:PMC10380194
doi:10.3390/insects14070598
PMID:37504604
Insect Gallers and Their Plant Hosts: From Omics Data to Systems Biology Oates CN, Denby KJ, Myburg AA, Slippers B, Naidoo S Int J Mol Sci 18-Nov-2016
PMCID:PMC5133890
doi:10.3390/ijms17111891
PMID:27869732
Phytohormones Related to Host Plant Manipulation by a Gall-Inducing Leafhopper Tokuda M, Jikumaru Y, Matsukura K, Takebayashi Y, Kumashiro S, Matsumura M, Kamiya Y PLoS One 30-Apr-2013
PMCID:PMC3640097
doi:10.1371/journal.pone.0062350
PMID:23638047

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 / Sesquiterpenoids
(1aS,1bS,3R,4R,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol 57394792 Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C 238.37 unknown via CMAUP database
(1aS,1bS,3R,4S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1,1b,2,3,4,5,6,6a-octahydrocyclopropa[a]inden-4-ol 57396552 Click to see CC12CC3CC3(C1CC(C(C2)O)C(C)(C)O)C 238.37 unknown via CMAUP database
(1aS,1bS,3S,5aS,6aS)-3-(2-hydroxypropan-2-yl)-1a,5a-dimethyl-1b,2,3,5,6,6a-hexahydro-1H-cyclopropa[a]inden-4-one 57398335 Click to see CC12CC3CC3(C1CC(C(=O)C2)C(C)(C)O)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,8aR)-8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 57391287 Click to see CC12CCC=C(C1CC(CC2)C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)CO 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 57396551 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 650.80 unknown via CMAUP database
1-oxo-3beta,23-dihydroxyolean-12-en-28-oic acid 28-O-beta-D-glucopyranoside 52952751 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 648.80 unknown via CMAUP database
3beta,22alpha-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside 52950912 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)O 634.80 unknown via CMAUP database
3beta,23-dihydroxyurs-12-en-28-oic acid 28-O-beta-D-glucopyranoside 52950911 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 634.80 unknown via CMAUP database
Arjunglucoside II 52951052 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 650.80 unknown via CMAUP database
hederagenin 28-O-beta-D-glucopyranosyl ester 21120798 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 634.80 unknown via CMAUP database
quadranoside IV 10372074 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3S,4aS,6aS,6aR,6bR,8aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene-1,3-diol 57391286 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C)C)C 442.70 unknown via CMAUP database
1-Oxo-3beta-hydroxyolean-18-ene 52950910 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C)C)C 440.70 unknown via CMAUP database
1-Oxo-3beta,23-dihydroxyolean-12-en-28-oic acid 11134679 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 486.70 unknown via CMAUP database
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
2Alpha,3Alpha,23-Trihydroxyurs-12-En-28-Oic Acid 9898760 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
3-Oxo-23-hydroxyurs-12-en-28-oic acid 14396856 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1C)C)C(=O)O 470.70 unknown via CMAUP database
3beta-Acetoxyolean-18-en-28-oic acid 21594125 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C(=O)O)(C)C)C 498.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Virgatic acid 14489125 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 470.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
Juglanin A 70697839 Click to see COC1=C2C=C(CCC(=O)CCCCC3=C(C(=C(O2)C=C3)OC)O)C=C1 356.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5r)-5-Hydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone 637003 Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O 344.40 unknown via CMAUP database

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