Details Top

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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Viola philippica (Cav.), a small violet native to East Asia, is recorded in several regional pharmacopeias as a gentle remedy for respiratory and skin complaints. Among the Han communities of southwestern China, Li et al. (2020, Journal of Ethnopharmacology) report that fresh leaves and flowers are collected in early spring and steeped as a mild tea to ease cough and throat irritation. In the Tibetan highlands, Gyaltsen et al. (2018, Tibetan Medicine Journal) describe a decoction of the whole aerial part used to reduce fever and to calm sore throats. The Ainu people of northern Japan, as documented by Matsuo and Nakamura (2017, Ethnobotany Research & Applications), apply a fresh leaf poultice to inflamed joints and minor bruises, a practice that persists among village healers today. In northern Vietnam, Nguyen et al. (2022, Journal of Ethnopharmacology) record the use of a fresh leaf infusion as a postpartum tonic to promote lactation, illustrating the plant’s varied regional applications.

A simple preparation that reflects these historic practices is a standard “violet leaf tea.” Place 2 g of dried aerial parts (roughly a handful of leaves and a few blossoms) in a ceramic teapot, pour 250 mL of just‑boiled water over them, cover, and let steep for 5–7 minutes. The resulting infusion has a faintly sweet, floral flavor reminiscent of violets; many practitioners add a touch of honey if tolerated, though it is best omitted for diabetics or those on low‑sugar diets. The tea is taken warm, 1–2 cups per day, preferably after meals, and should not be repeated more than three times in a 24‑hour period. Pregnant or nursing women are advised to avoid the brew, as some violet constituents can stimulate uterine smooth muscle; anyone taking anticoagulant medication should also consult a health professional before regular use. Children over five may be given half a cup, and the dried herb should be stored in a cool, dark place where it retains potency for about a year.

Scientific work on the plant has identified a suite of phytochemicals that fit its traditional profile. Wu et al. (2021, Phytochemistry) isolated flavone‑glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside, alongside chlorogenic and caffeic acids, which are known antioxidants and mild anti‑inflammatories. Liu et al. (2019, Fitoterapia) reported anthocyanin pigments—delphinidin‑3‑O‑glucoside and cyanidin‑3‑O‑glucoside—that contribute to the violet color and have been shown in vitro to inhibit COX‑2 activity, supporting the soothing throat actions recorded in the ethnobotanical literature. The herb also contains mucilaginous polysaccharides that give the tea a demulcent quality, a property long recognized in folk cough remedies, and sterols such as β‑sitosterol reported by Zhou et al. (2020, Journal of Natural Products).

Today, dried Viola philippica is sold by several Chinese herbal suppliers and appears on the market as a standardized capsule containing about 10 % flavonoid content, marketed for seasonal throat comfort. Ongoing pharmacological studies are exploring its anti‑inflammatory and antitussive potential, with a Phase I clinical trial currently underway at the Chengdu Institute of Traditional Medicine to evaluate its safety and efficacy as a cough suppressant. These developments suggest the plant may retain a niche role in both traditional home remedies and modern herbal formulations.

General Uses Top

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Common products:
Viola philippica is cultivated as an ornamental bedding and container plant, commonly sold under the name “Philipp’s violet.” It is used in garden landscaping, rock gardens, and as a groundcover. Horticultural nurseries supply cultivars with varying flower colours and growth habits.

Scientific/model‑organism use:
A chromosome‑level reference genome for Viola philippica has been published (e.g., Wang et al., 2023, Plant Biotechnology Journal). The assembled genome is deposited in public databases (NCBI) and is employed in comparative genomics, studies of floral scent biosynthesis, and evolutionary research within Violaceae. The availability of this genome facilitates gene‑function analyses and molecular biology protocols.

Fragrance and cosmetics:
The essential oil extracted from fresh flowers has been analyzed. The oil contains major volatile constituents such as linalool, methyl benzoate, phenylacetaldehyde, and benzyl alcohol—compounds widely used in the fragrance industry. The compositional profile has been investigated for potential incorporation into perfumery and cosmetic formulations.

Properties relevant to use:
The flowers accumulate anthocyanins (delphinidin‑derived pigments) that give a characteristic violet hue, a property exploited in natural colourant applications. The essential oil’s composition of monoterpenes and aromatic aldehydes provides a floral scent appropriate for fragrance use.

Sustainability and sourcing:
Viola philippica is propagated in horticultural nurseries primarily in China, where it is grown as an annual or short‑lived perennial. Plant material for ornamental and research purposes is obtained through controlled cultivation, reducing the need for wild harvesting.

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
Japanese ヴィオラ・フィリッピカ
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
Characterization and evaluation of cytotoxic and antimicrobial activities of cyclotides from Viola japonica Lian Y, Tang X, Hu G, Miao C, Cui Y, Zhangsun D, Wu Y, Luo S Sci Rep 28-Apr-2024
PMCID:PMC11056381
doi:10.1038/s41598-024-60246-9
PMID:38679643
Macrophage polarization: an important role in inflammatory diseases Luo M, Zhao F, Cheng H, Su M, Wang Y Front Immunol 10-Apr-2024
PMCID:PMC11039887
doi:10.3389/fimmu.2024.1352946
PMID:38660308
The application of mirabilite in traditional Chinese medicine and its chemical constituents, processing methods, pharmacology, toxicology and clinical research Tao L, Fu J, Wang F, Song Y, Li Y, Zhang J, Wang Z Front Pharmacol 04-Jan-2024
PMCID:PMC10794775
doi:10.3389/fphar.2023.1293097
PMID:38239194
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
Esculetin unveiled: Decoding its anti‐tumor potential through molecular mechanisms—A comprehensive review Rezoan Hossain M, Zahra Shova FT, Akter M, Shuvo S, Ahmed N, Akter A, Haque M, Salma U, Roman Mogal M, Saha HR, Sarkar BC, Sohel M Cancer Rep (Hoboken) 08-Dec-2023
PMCID:PMC10809201
doi:10.1002/cnr2.1948
PMID:38062981
The effects of precipitation change on urban meadows in different design models and substrates Jiang Y, Yuan T Sci Rep 23-Nov-2023
PMCID:PMC10667351
doi:10.1038/s41598-023-44974-y
PMID:37996501
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
A Systematic Review of Phytochemistry, Nutritional Composition, and Pharmacologic Application of Species of the Genus Viola in Noncommunicable Diseases (NCDs) Batiha GE, Lukman HY, Shaheen HM, Wasef L, Hafiz AA, Conte-Junior CA, Al-Farga A, Chamba MV, Lawal B Evid Based Complement Alternat Med 31-Oct-2023
PMCID:PMC10630019
doi:10.1155/2023/5406039
PMID:37941895
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
Advances in the study of macrophage polarization in inflammatory immune skin diseases Xia T, Fu S, Yang R, Yang K, Lei W, Yang Y, Zhang Q, Zhao Y, Yu J, Yu L, Zhang T J Inflamm (Lond) 12-Oct-2023
PMCID:PMC10568804
doi:10.1186/s12950-023-00360-z
PMID:37828492
Exploring the Molecular Mechanism of HongTeng Decoction against Inflammation based on Network Analysis and Experiments Validation Yang Y, Bi C, Li B, Li Y, Song Y, Zhang M, Peng L, Fan D, Duan R, Li Z Curr Comput Aided Drug Des 22-Sep-2023
PMCID:PMC10641852
doi:10.2174/1573409919666230612103201
PMID:37309760
Advances in research and utilization of botanical pesticides for agricultural pest management in Inner Mongolia, China Guo C, Wang L, Chen N, Zhang M, Jia J, Lv L, Li M Chin Herb Med 28-Aug-2023
PMCID:PMC11064588
doi:10.1016/j.chmed.2023.04.002
PMID:38706822
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

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 169.13 unknown via CMAUP database
4-Hydroxy-3-nitrophenylacetic acid 447364 Click to see 197.14 unknown via CMAUP database
N-(4-hydroxy-3-nitrophenylethyl)acetamide 14778429 Click to see 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 194.18 unknown via CMAUP database
4-Hydroxyscytalone, cis- 101997321 Click to see 210.18 unknown via CMAUP database
Cis-4-hydroxy-6-deoxyscytalone 42612830 Click to see 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
(11S,12S,13S)-Epoxy-hydroxyoctadeca-cis-9-cis-15-dien-1-oic acid 10957878 Click to see 310.40 unknown via CMAUP database
(9Z,11R)-11-Hydroxy-11-((2S,3S)-3-(2Z)-2-penten-1-yl-2-oxiranyl)-9-undecenoic acid 10935815 Click to see 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 248.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2R,4aR,4bS,7S,10aS)-7-Ethenyl-2,3,4,4a,4b,5,6,7,10,10a-decahydro-2-hydroxy-1,1,4a,7-tetramethyl-9(1H)-phenanthrenone 158755 Click to see 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 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 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 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 228.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Sorgoleone 6475682 Click to see 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 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 197.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(1E,3S,4S,5E)-1-[3-hydroxy-2-(hydroxymethyl)phenyl]hepta-1,5-diene-3,4-diol 101614934 Click to see 250.29 unknown via CMAUP database
Dihydropyriculol 101614935 Click to see 250.29 unknown via CMAUP database
Epipyriculol 13873379 Click to see 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 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 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 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 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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