Dianthus japonicus - Unknown
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Internal ID UUID64401697ad91c733337197
Scientific name Dianthus japonicus
Authority Thunb.
First published in Syst. Veg. ed. 14: 417. 1784.

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Synonyms Top

Scientific name Authority First published in
Dianthus japonicus f. albiflorus J.Ohara ex Nakan. in J. Geobot. 16: 116. 1968.
Dianthus ellipticus Turcz. in Bull. Soc. Imp. Naturalistes Moscou 27(2): 369. 1854.
Dianthus nipponicus Makino in Bot. Mag. (Tokyo) 17: 58. 1903.

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Language Common/alternative name
Upper Sorbian japanska nalika
Japanese ハマナデシコ
Chinese 日本石竹
Chinese 滨瞿麦

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000643711
Tropicos 6300081
KEW urn:lsid:ipni.org:names:153487-1
The Plant List kew-2764408
Open Tree Of Life 964898
NCBI Taxonomy 520998
IPNI 927352-1
iNaturalist 635137
GBIF 7267525
Freebase /m/03nq_jl
EPPO DINJA
EOL 5206248
USDA GRIN 434845
Wikipedia Dianthus_japonicus

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Identification of the Plant Family Caryophyllaceae in Korea Using DNA Barcoding Jin DP, Sim S, Park JW, Choi JE, Yoon J, Lim CE, Kim MH Plants (Basel) 22-May-2023
PMCID:PMC10222892
doi:10.3390/plants12102060
PMID:37653977
Restoring Fertility for Novel Interspecific Hybrids between Kalanchoe garambiensis and K. nyikae Using Colchicine Treatment Kuang Y, Lu CH, Hsu FC Plants (Basel) 22-Jan-2021
PMCID:PMC7911985
doi:10.3390/plants10020209
PMID:33499148
Metabolic Profiling of Water-Soluble Compounds from the Extracts of Dark Septate Endophytic Fungi (DSE) Isolated from Scots Pine (Pinus sylvestris L.) Seedlings Using UPLC–Orbitrap–MS Tienaho J, Karonen M, Muilu–Mäkelä R, Wähälä K, Leon Denegri E, Franzén R, Karp M, Santala V, Sarjala T Molecules 25-Jun-2019
PMCID:PMC6630819
doi:10.3390/molecules24122330
PMID:31242564
Plant Growth Promoting Rhizobacteria in Amelioration of Salinity Stress: A Systems Biology Perspective Ilangumaran G, Smith DL Front Plant Sci 23-Oct-2017
PMCID:PMC5660262
doi:10.3389/fpls.2017.01768
PMID:29109733
Plant Growth Promoting Bacteria Associated with Langsdorffia hypogaea-Rhizosphere-Host Biological Interface: A Neglected Model of Bacterial Prospection Felestrino ÉB, Santiago IF, Freitas LD, Rosa LH, Ribeiro SP, Moreira LM Front Microbiol 10-Feb-2017
PMCID:PMC5300976
doi:10.3389/fmicb.2017.00172
PMID:28239369
Low functional diversity promotes niche changes in natural island pollinator communities Hiraiwa MK, Ushimaru A Proc Biol Sci 11-Jan-2017
PMCID:PMC5247496
doi:10.1098/rspb.2016.2218
PMID:28077773
Alleviation of Salt Stress by Enterobacter sp. EJ01 in Tomato and Arabidopsis Is Accompanied by Up-Regulation of Conserved Salinity Responsive Factors in Plants Kim K, Jang YJ, Lee SM, Oh BT, Chae JC, Lee KJ Mol Cells 19-Feb-2014
PMCID:PMC3935623
doi:10.14348/molcells.2014.2239
PMID:24598995
Isolated history of the coastal plant Lathyrus japonicus (Leguminosae) in Lake Biwa, an ancient freshwater lake Ohtsuki T, Kaneko Y, Setoguchi H AoB Plants 09-Aug-2011
PMCID:PMC3176521
doi:10.1093/aobpla/plr021
PMID:22476491
Dianthosaponins A-F, triterpene saponins, flavonoid glycoside, aromatic amide glucoside and γ-pyrone glucoside from Dianthus japonicus. Nakano T, Sugimoto S, Matsunami K, Otsuka H Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.1141
PMID:21881258

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4S,4aR,6aR,6bS,8aR,11R,12aS,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101995928 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)CO 827.00 unknown https://doi.org/10.1248/CPB.59.1141
(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 45272283 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C 1135.20 unknown https://doi.org/10.1248/CPB.59.1141
3-Hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-8a-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 73157028 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)CO 827.00 unknown https://doi.org/10.1248/CPB.59.1141
8a-[6-[[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 56671388 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C 1135.20 unknown https://doi.org/10.1248/CPB.59.1141
8a-[6-[[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxycarbonyl-4,6a,6b,11,11,14b-hexamethyl-3-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 56667913 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C 1267.40 unknown https://doi.org/10.1248/CPB.59.1141
Dianversicoside G 42640292 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)C 1267.40 unknown https://doi.org/10.1248/CPB.59.1141
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
2-[(1R,2R,4aR,4bS,6aS,10aS,12aR)-6a-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxycarbonyl-1-(3-hydroxypropyl)-1,4a,4b,9,9-pentamethyl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysen-2-yl]prop-2-enoic acid 102317032 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CCCO)C(=C)C(=O)O)C)C2C1)C)C(=O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C 1135.20 unknown https://doi.org/10.1248/CPB.59.1141
2-[6a-[6-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxycarbonyl-1-(3-hydroxypropyl)-1,4a,4b,9,9-pentamethyl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysen-2-yl]prop-2-enoic acid 162982717 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CCCO)C(=C)C(=O)O)C)C2C1)C)C(=O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C 1135.20 unknown https://doi.org/10.1248/CPB.59.1141
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-methyl-4-oxopyran-3-yl)oxyoxan-2-yl]methyl benzoate 53496369 Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)COC(=O)C3=CC=CC=C3)O)O)O 392.40 unknown https://doi.org/10.1248/CPB.59.1141
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin-6-C-glucoside-7-O-glucoside 4636593 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.59.1141
Saponarin 441381 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.59.1141

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