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Salix gilgiana

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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 UUID6440368a4fcf9481901127
Scientific name Salix gilgiana
Authority Seemen
First published in Salic. Jap. : 59 (1903)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salix gymnolepis H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 3: 22 (1906)
Salix miyabeana subsp. gilgiana (Seemen) H.Ohashi J. Jap. Bot. 75(1): 22 (2000):.
Salix miyabeana f. gilgiana (Seemen) H.Ohashi J. Jap. Bot. 75: 22 (2000)

Common names Top

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Language Common/alternative name
English willow
Japanese カワヤナギ
Korean 내버들
Chinese 东亚柳

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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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-0000928434
USDA Plants SAGI3
Tropicos 28300717
KEW urn:lsid:ipni.org:names:777657-1
The Plant List kew-5000649
Open Tree Of Life 1081052
Observations.org 126283
NCBI Taxonomy 75556
IPNI 777657-1
GBIF 5583873
Freebase /m/0fpsfc
EOL 5600210
USDA GRIN 102710
Wikipedia Salix_gilgiana

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
Plant volatiles and priority effects interactively determined initial community assembly of arthropods on multiple willow species Yoneya K, Miki T, Katayama N Ecol Evol 19-Jul-2023
PMCID:PMC10364932
doi:10.1002/ece3.10270
PMID:37492458
Study of Phytochemical Component of Salix Species Fukuziro Fuzikawa, Kunio Nakajima Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.68.5-6_175
Arabidopsis AtDjA3 Null Mutant Shows Increased Sensitivity to Abscisic Acid, Salt, and Osmotic Stress in Germination and Post-germination Stages Salas-Muñoz S, Rodríguez-Hernández AA, Ortega-Amaro MA, Salazar-Badillo FB, Jiménez-Bremont JF Front Plant Sci 25-Feb-2016
PMCID:PMC4766394
doi:10.3389/fpls.2016.00220
PMID:26941772
Molecular Interactions of β-(1→3)-Glucans with Their Receptors Legentil L, Paris F, Ballet C, Trouvelot S, Daire X, Vetvicka V, Ferrières V Molecules 27-May-2015
PMCID:PMC6272582
doi:10.3390/molecules20069745
PMID:26023937
Gastroprotective Effect of the Three Glucuronopyranoside Flavonoids in Rats Im WJ, Nam Y, Park SY, Sohn UD Korean J Physiol Pharmacol 17-Oct-2013
PMCID:PMC3823953
doi:10.4196/kjpp.2013.17.5.411
PMID:24227941
Contrasted patterns of selective pressure in three recent paralogous gene pairs in the Medicago genus (L.) Ho-Huu J, Ronfort J, De Mita S, Bataillon T, Hochu I, Weber A, Chantret N BMC Evol Biol 01-Oct-2012
PMCID:PMC3517903
doi:10.1186/1471-2148-12-195
PMID:23025552
In Silico Characterization of Pectate Lyase Protein Sequences from Different Source Organisms Dubey AK, Yadav S, Kumar M, Singh VK, Sarangi BK, Yadav D Enzyme Res 19-Sep-2010
PMCID:PMC2962914
doi:10.4061/2010/950230
PMID:21048874
Comparative analyses of genotype dependent expressed sequence tags and stress-responsive transcriptome of chickpea wilt illustrate predicted and unexpected genes and novel regulators of plant immunity Ashraf N, Ghai D, Barman P, Basu S, Gangisetty N, Mandal MK, Chakraborty N, Datta A, Chakraborty S BMC Genomics 05-Sep-2009
PMCID:PMC2755012
doi:10.1186/1471-2164-10-415
PMID:19732460
Phenolic compounds of the bark of Salix alba × babylonica V. A. Kompantsev, P. M. Gaidash, A. D. Dauksha Springer Science and Business Media LLC 07-Jul-2008
doi:10.1007/BF00564031
Carbohydrate-Active Enzymes Involved in the Secondary Cell Wall Biogenesis in Hybrid Aspen Aspeborg H, Schrader J, Coutinho PM, Stam M, Kallas Å, Djerbi S, Nilsson P, Denman S, Amini B, Sterky F, Master E, Sandberg G, Mellerowicz E, Sundberg B, Henrissat B, Teeri TT Plant Physiol 01-Mar-2005
PMCID:PMC1065399
doi:10.1104/pp.104.055087
PMID:15734915
Acylated luteolin glucosides from Salix gilgiana Mizuo Mizuno, Masaya Kato, Munekazu Iinuma, Toshiyuki Tanaka, Arika Kimura, Hiroyoshi Ohashi, Hideki Sakai Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84739-1
[Studies on medicinal resources. XXXV. The components of Salix plants (Salicaceae) in Japan. (2). The components of the leaves of Salix matsudana Koidz. f. tortuosa Rehd., and S. gilgiana Seemen (author's transl)]. Morita N, Shimizu M, Arisawa M, Kitanaka S Yakugaku Zasshi 01-Jul-1974
doi:10.1248/YAKUSHI1947.94.7_875
PMID:4474400

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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF00564031
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 21721979 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 21721976 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)O)O 490.40 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
[6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 73829955 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
[6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-phenylprop-2-enoate 73829953 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
[6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 13845966 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)O)O 490.40 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
7-(6-O-Cinnamoyl-beta-D-glucopyranosyloxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-4H-1-benzopyran-4-one 21721977 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)84739-1
https://doi.org/10.1248/YAKUSHI1947.68.5-6_175
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/YAKUSHI1947.94.7_875
https://doi.org/10.1248/YAKUSHI1947.68.5-6_175
https://doi.org/10.1016/S0031-9422(00)84739-1

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