Viola hondoensis - Unknown
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Internal ID UUID64404fb2d896b805985435
Scientific name Viola hondoensis
Authority W.Becker & Boissieu
First published in Bull. Herb. Boissier , sér. 2, 8: 739 (1908)

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Synonyms Top

Scientific name Authority First published in
Viola hirta var. japonica Maxim.

Common names Top

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Language Common/alternative name
Japanese アオイスミレ
Chinese 日本球果堇菜
Chinese 本岛球果堇菜

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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Sow at 4°C for 3 weeks, then increase to 20°C.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001144906
Tropicos 33800943
KEW urn:lsid:ipni.org:names:868324-1
The Plant List tro-33800943
Open Tree Of Life 705818
NCBI Taxonomy 316467
IPNI 868324-1
GBIF 5664188
EPPO VIOHO
EOL 2885213
USDA GRIN 429841
CMAUP NPO27878

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
Tectorigenin: A Review of Its Sources, Pharmacology, Toxicity, and Pharmacokinetics Rong J, Fu F, Han C, Wu Y, Xia Q, Du D Molecules 05-Aug-2023
PMCID:PMC10421414
doi:10.3390/molecules28155904
PMID:37570873
A Revised Phylogenetic Classification for Viola (Violaceae) Marcussen T, Ballard HE, Danihelka J, Flores AR, Nicola MV, Watson JM Plants (Basel) 27-Aug-2022
PMCID:PMC9460890
doi:10.3390/plants11172224
PMID:36079606
Cataract Preventive Role of Isolated Phytoconstituents: Findings from a Decade of Research Lim V, Schneider E, Wu H, Pang IH Nutrients 26-Oct-2018
PMCID:PMC6265913
doi:10.3390/nu10111580
PMID:30373159
Ecophysiological roles of abaxial anthocyanins in a perennial understorey herb from temperate deciduous forests Fernández-Marín B, Esteban R, Míguez F, Artetxe U, Castañeda V, Pintó-Marijuan M, Becerril JM, García-Plazaola JI AoB Plants 28-Apr-2015
PMCID:PMC4481727
doi:10.1093/aobpla/plv042
PMID:25922298
Plant Diversity Changes during the Postglacial in East Asia: Insights from Forest Refugia on Halla Volcano, Jeju Island Dolezal J, Altman J, Kopecky M, Cerny T, Janecek S, Bartos M, Petrik P, Srutek M, Leps J, Song JS PLoS One 16-Mar-2012
PMCID:PMC3306376
doi:10.1371/journal.pone.0033065
PMID:22438890
Aldose reductase inhibitors from Viola hondoensis W. Becker et H Boss. Chung IM, Kim MY, Park WH, Moon HI Am J Chin Med 01-Jan-2008
doi:10.1142/S0192415X08006247
PMID:18711775
Aldose reductase inhibitory effect by tectorigenin derivatives from Viola hondoensis. Moon HI, Jung JC, Lee J Bioorg Med Chem 15-Nov-2006
doi:10.1016/J.BMC.2006.07.002
PMID:16870454
A glycosidic isoflavonoid from Viola hondoensis W. BECKER et H. BOISSIEU (Violaceae), and its effect on the expression of matrix metalloproteinase-1 caused by ultraviolet irradiation in cultured human skin fibroblasts. Moon HI, Lee J, Zee OP, Chung JH Biol Pharm Bull 01-Jun-2005
doi:10.1248/BPB.28.1123
PMID:15930761
Isoflavonoid from Viola hondoensis, regulates the expression of matrix metalloproteinase-1 in human skin fibroblasts. Moon HI, Lee J, Kwak JH, Zee OP, Chung JH Biol Pharm Bull 01-May-2005
doi:10.1248/BPB.28.925
PMID:15863909
Triterpenoid saponin from Viola hondoensis W. Becker et H Boss. and their effect on MMP-1 and type I procollagen expression. Moon HI, Chung JH, Lee JK, Zee OP Arch Pharm Res 01-Jul-2004
doi:10.1007/BF02980140
PMID:15356999

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 / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C=C)C 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)OC(=O)C)C 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(=O)C2(C)C)C 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimaric Acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see CC1CCC2C(C1)C2(C)C 138.25 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see CC1(CC2(CCC1C2)C)C 138.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Acutoside A 21606142 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 781.00 unknown https://doi.org/10.1007/BF02980140
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxydaidzein 5280520 Click to see C1=CC(=C(C=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O 270.24 unknown https://doi.org/10.1248/BPB.28.925
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
(3S)-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 93517223 Click to see COC1=C(C=C2C(=C1O)C(=O)C(CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMC.2006.07.002
(3S)-5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 163023979 Click to see COC1=C(C=C2C(=C1O)C(=O)C(CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 626.60 unknown https://doi.org/10.1016/J.BMC.2006.07.002
(3S)-5,7-dihydroxy-6-methoxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162921101 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMC.2006.07.002
5-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 76045301 Click to see COC1=C(C=C2C(=C1O)C(=O)C(CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMC.2006.07.002
5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44452420 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1142/S0192415X08006247
5-Hydroxy-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 163023978 Click to see COC1=C(C=C2C(=C1O)C(=O)C(CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 626.60 unknown https://doi.org/10.1016/J.BMC.2006.07.002
5-Hydroxy-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162916994 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1248/BPB.28.1123
5,7-Dihydroxy-6-methoxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162921100 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMC.2006.07.002
Kakkalide 5490351 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1142/S0192415X08006247
Tectorigenin-7-O-beta-glucosyl-4'-O-beta-glucoside 16126681 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1248/BPB.28.1123
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 6-O-methylated isoflavonoids
(3S)-5,7-dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-2,3-dihydrochromen-4-one 162993209 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/J.BMC.2006.07.002
5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-2,3-dihydrochromen-4-one 131836908 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/J.BMC.2006.07.002
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database

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