Viola philippica - Unknown
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Internal ID UUID643ffb3a7aed9124943402
Scientific name Viola philippica
Authority Cav.
First published in Icon. 6: 19 (1800)

Description Top

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Synonyms Top

Scientific name Authority First published in
Viola edanoii W.Becker Philipp. J. Sci. 19: 722 (1921 publ. 1922)
Viola tosaensis Nakai Bull. Soc. Bot. France 72: 191 (1925)
Viola yedoensis Makino Bot. Mag. (Tokyo) 26: 148 (1912)
Viola alisoviana Kiss Bot. Közlem. 19: 93 (1921)
Viola patrinii var. chinensis Hayata Icon. Pl. Formosan. 6: ? 1916
Viola philippica f. candida (Kitag.) Kitag. Lin. Fl. Manshur. 322 1939
Viola philippica subsp. munda W.Becker Bot. Jahrb. Syst. 54(120): 175 1917
Viola yedoensis f. candida Kitag. Bot. Mag. (Tokyo) 48: 102 1934
Viola alisoviana f. candida (Kitag.) Taken. ? 1: 80 1955
Viola chinensis f. alboviolacea Skvortsov
Viola chinensis f. anomala Skvortsov
Viola chinensis f. communis Skvortsov
Viola chinensis f. dissecta Skvortsov
Viola chinensis f. glabra Skvortsov

Common names Top

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Language Common/alternative name
lzh 紫花地丁
Chinese 野堇菜
Chinese 紫花地丁
Chinese 光瓣堇菜
Chinese 辽堇菜
Chinese 铧头草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Viola philippica var. pseudojaponica (Nakai) Y.S.Chen Fl. China 13: 100 (2007)

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Primorye
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000423757
KEW urn:lsid:ipni.org:names:868955-1
The Plant List kew-2459845
Open Tree Of Life 382889
Observations.org 373276
NCBI Taxonomy 316493
IPNI 868955-1
iNaturalist 491262
GBIF 7296732
EPPO VIOYE
EOL 2889915
Elurikkus 584538
USDA GRIN 429977
CMAUP NPO25302

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
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Lawn or spontaneous groundcover? Residents’ perceptions of and preferences for alternative lawns in Xianyang, China Liang H, Li C, Xue D, Liu J, Jin K, Wang Y, Gao D, Chen Y, Li Y, Qiu L, Gao T Front Psychol 27-Oct-2023
PMCID:PMC10646185
doi:10.3389/fpsyg.2023.1259920
PMID:38022966
Research Progress on Low-Surface-Energy Antifouling Coatings for Ship Hulls: A Review Cao Z, Cao P Biomimetics (Basel) 21-Oct-2023
PMCID:PMC10603911
doi:10.3390/biomimetics8060502
PMID:37887633
Companion Plants of Tea: From Ancient to Terrace to Forest Wu H, Long X, Geng Y Plants (Basel) 25-Aug-2023
PMCID:PMC10490072
doi:10.3390/plants12173061
PMID:37687308
Functional immune boosters; the herb or its dead microbiome? Antigenic TLR4 agonist MAMPs found in 65 medicinal roots and algae’s Mazzio E, Barnes A, Badisa R, Fierros-Romero G, Williams H, Council S, Soliman KF J Funct Foods 29-Jul-2023
PMCID:PMC10469438
doi:10.1016/j.jff.2023.105687
PMID:37654434
An integrated transcriptome and metabolome analysis reveals the gene network regulating flower development in Pogostemon cablin Zhang C, Liu X, Liu Y, Yu J, Yao G, Yang H, Yang D, Wu Y Front Plant Sci 29-Jun-2023
PMCID:PMC10340533
doi:10.3389/fpls.2023.1201486
PMID:37457333
Dandelion (Taraxacum Genus): A Review of Chemical Constituents and Pharmacological Effects Fan M, Zhang X, Song H, Zhang Y Molecules 27-Jun-2023
PMCID:PMC10343869
doi:10.3390/molecules28135022
PMID:37446683
Luteolin Alleviates Liver Fibrosis in Rat Hepatic Stellate Cell HSC-T6: A Proteomic Analysis Batudeligen, Han Z, Chen H, Narisu, Xu Y, Anda, Han G Drug Des Devel Ther 17-Jun-2023
PMCID:PMC10285022
doi:10.2147/DDDT.S402864
PMID:37360572
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Identification of natural peptides from “PlantPepDB” database as anti-SARS-CoV-2 agents: A protein-protein docking approach Bhandu P, Verma H, Raju B, Narendra G, Choudhary S, Singh M, Singh PK, Silakari O Phytomed Plus 31-Mar-2023
PMCID:PMC10065049
doi:10.1016/j.phyplu.2023.100446
PMID:37033295
Analysis of the chloroplast genome and phylogenetic evolution of Bidens pilosa Zhang D, Tu J, Ding X, Guan W, Gong L, Qiu X, Huang Z, Su H BMC Genomics 14-Mar-2023
PMCID:PMC10015693
doi:10.1186/s12864-023-09195-7
PMID:36918765
Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L Phytochem Rev 12-Mar-2023
PMCID:PMC10008214
doi:10.1007/s11101-023-09855-2
PMID:37359711
Electrochemical Characterization of the Antioxidant Properties of Medicinal Plants and Products: A Review Ziyatdinova G, Kalmykova A Molecules 02-Mar-2023
PMCID:PMC10004803
doi:10.3390/molecules28052308
PMID:36903553
Cytotoxic and pro-apoptotic effects of botanical drugs derived from the indigenous cultivated medicinal plant Paris polyphylla var. yunnanensis Yan XX, Zhao YQ, He Y, Disayathanoowat T, Pandith H, Inta A, Yang LX Front Pharmacol 26-Jan-2023
PMCID:PMC9911168
doi:10.3389/fphar.2023.1100825
PMID:36778018
The Potential of Surface-Immobilized Antimicrobial Peptides for the Enhancement of Orthopaedic Medical Devices: A Review Skerlavaj B, Boix-Lemonche G Antibiotics (Basel) 19-Jan-2023
PMCID:PMC9952162
doi:10.3390/antibiotics12020211
PMID:36830122

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
> Alkaloids and derivatives / Harmala alkaloids
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(S)-6,8-Dihydroxy-3-methyl-3,4-dihydroisocoumarin 14353462 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown via CMAUP database
2,4-Dihydroxy-6-(2-oxopropyl)benzoic acid 150898 Click to see CC(=O)CC1=C(C(=CC(=C1)O)O)C(=O)O 210.18 unknown via CMAUP database
> Benzenoids / Phenols / Nitrophenols
4-(2-Hydroxyethyl)-2-nitrophenol 14520116 Click to see C1=CC(=C(C=C1CCO)[N+](=O)[O-])O 183.16 unknown via CMAUP database
4-[(1S)-1-Hydroxyethyl]-2-nitrophenol 92466487 Click to see CC(C1=CC(=C(C=C1)O)[N+](=O)[O-])O 183.16 unknown via CMAUP database
4-Hydroxy-3-nitrobenzyl alcohol 142550 Click to see C1=CC(=C(C=C1CO)[N+](=O)[O-])O 169.13 unknown via CMAUP database
4-Hydroxy-3-nitrophenylacetic acid 447364 Click to see C1=CC(=C(C=C1CC(=O)O)[N+](=O)[O-])O 197.14 unknown via CMAUP database
N-(3-Nitro-4-hydroxyphenethyl)acetamide 14778429 Click to see CC(=O)NCCC1=CC(=C(C=C1)O)[N+](=O)[O-] 224.21 unknown via CMAUP database
> Benzenoids / Tetralins
(3S,4S)-3,4,8-trihydroxytetralin-1-one 21769465 Click to see C1C(C(C2=C(C1=O)C(=CC=C2)O)O)O 194.18 unknown via CMAUP database
(4S)-4,6,8-trihydroxytetralin-1-one 44585560 Click to see C1CC(=O)C2=C(C1O)C=C(C=C2O)O 194.18 unknown via CMAUP database
4-Hydroxyscytalone, cis- 101997321 Click to see C1C(C(C2=C(C1=O)C(=CC(=C2)O)O)O)O 210.18 unknown via CMAUP database
Cis-4-hydroxy-6-deoxyscytalone 42612830 Click to see C1C(C(C2=C(C1=O)C(=CC=C2)O)O)O 194.18 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(9Z,11R,12S,13S,15Z)-11-Hydroxy-12,13-epoxy-9,15-octadecadienoic acid 10935815 Click to see CCC=CCC1C(O1)C(C=CCCCCCCCC(=O)O)O 310.40 unknown via CMAUP database
(9Z,11S,12S,13S,15Z)-11-Hydroxy-12,13-epoxy-9,15-octadecadienoic acid 10957878 Click to see CCC=CCC1C(O1)C(C=CCCCCCCCC(=O)O)O 310.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Cerotate 5461023 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)[O-] 395.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Pyriculariol 44191151 Click to see CC(C(C=CC=CC1=C(C(=CC=C1)O)C=O)O)O 248.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Oryzalexin A 158755 Click to see CC1(C(CCC2(C1CC(=O)C3=CC(CCC32)(C)C=C)C)O)C 302.50 unknown via CMAUP database
Oryzalexin B 176496 Click to see CC1(C2CC(C3=CC(CCC3C2(CCC1=O)C)(C)C=C)O)C 302.50 unknown via CMAUP database
Oryzalexin C 176495 Click to see CC1(C2CC(=O)C3=CC(CCC3C2(CCC1=O)C)(C)C=C)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Stemarane diterpenoids
oryzalexin S 101628275 Click to see CC1=CC2CCC3C(CC(CC3(C24CCC1C4)C)O)(C)CO 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4S,8R,9S,10R,13R,14S,16R)-8-hydroxy-5,5,9,14-tetramethyl-7,15-dioxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-6-one 14634291 Click to see CC1(C2CCC34CC(CCC3C2(C(OC1=O)O)C)C5(C4O5)C)C 320.40 unknown via CMAUP database
(1R,4S,8R,9S,10R,13R,15S)-8,15-dihydroxy-5,5,9-trimethyl-14-methylidene-7-oxatetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 101602034 Click to see CC1(C2CCC34CC(CCC3C2(C(OC1=O)O)C)C(=C)C4O)C 320.40 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Nucleoside and nucleotide analogues / Cyclopentyl nucleosides / 1,3-substituted cyclopentyl nucleosides / 1,3-substituted cyclopentyl purine nucleosides
(1S,2R,3R,5R)-3-(6-aminopurin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol 11254104 Click to see C1C(C(C(C1N2C=NC3=C(N=CN=C32)N)O)O)CO 265.27 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine-proline anhydride 57275499 Click to see CC(C)CC(C(=O)OC(=O)C1CCCN1)N 228.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Sorgoleone 6475682 Click to see COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCC=CCC=C)O 358.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one 12311356 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[(5S)-5-ethyloxolan-2-ylidene]-5-methyloxolane-2,4-dione 21151019 Click to see CCC1CCC(=C2C(=O)C(OC2=O)C)O1 210.23 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
(2S)-4-acetyl-2-[(2R)-butan-2-yl]-3-hydroxy-1,2-dihydropyrrol-5-one 54711000 Click to see CCC(C)C1C(=C(C(=O)N1)C(=O)C)O 197.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Dihydropyriculol 101614935 Click to see CC=CC(C(C=CC1=C(C(=CC=C1)O)CO)O)O 250.29 unknown via CMAUP database
Epidihydropyriculol 101614934 Click to see CC=CC(C(C=CC1=C(C(=CC=C1)O)CO)O)O 250.29 unknown via CMAUP database
Epipyriculol 13873379 Click to see CC=CC(C(C=CC1=C(C(=CC=C1)O)C=O)O)O 248.27 unknown via CMAUP database
Pyriculol 13873378 Click to see CC=CC(C(C=CC1=C(C(=CC=C1)O)C=O)O)O 248.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257926 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258913 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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