Details Top

Internal ID UUID64401c1188bb1578082155
Scientific name Lilium brownii
Authority F.E.Br. ex Miellez
First published in Cat. Expos. Soc. Hort. Lille : s.p. (1841)

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.

In Traditional Chinese Medicine the dried bulb of Lilium brownii var. viridulum, called bái hē, is routinely taken as a decoction to moisten the lungs, relieve dry cough, thin phlegm and calm the mind. The Chinese Pharmacopoeia (2020) describes a standard preparation of 9–15 g of sliced bulb boiled in 250 mL of water for 20–30 minutes, taken twice daily. The same plant appears in Japanese Kampo practice, where the handbook of Kampo medicine (2015) lists a similar tea made from 12 g of dried bulb simmered in 300 mL of water for 15 minutes, used before bedtime to promote sleep. Among the Hani people of Yunnan, a local ethnobotanical survey (Chen et al., 2012) records a fresh‑bulb poultice: the bulb is mashed and applied directly to minor skin lesions for about 30 minutes before rinsing. These three independent traditions show the use of infusions, decoctions and poultices of the bulb across northern China, the Japanese archipelago and southwest China.

The most common modern preparation is a mild bái hē tea: measure 12 g of dried, sliced bulb, place it in a saucepan with 250 mL of cold water, bring to a gentle boil, then simmer for 15 minutes. The liquid is strained and served warm; the dose is limited to three cups per day. No more than 30 g of the bulb should be used in a single day, and the preparation is not recommended for pregnant women because of a lack of safety data.

Phytochemical analyses of Lilium brownii have identified mucilaginous polysaccharides, steroidal saponins (such as lily saponin A) and flavonoid glycosides, especially quercetin‑3‑O‑glucoside. The polysaccharides give a soothing, demulcent quality that eases throat irritation, while the saponins and flavonoids exhibit anti‑inflammatory and mild bronchodilatory activity in vitro. These constituents are well documented in the literature, including a review by Matsubara et al. (2002) on Lilium bulb chemistry.

Recent laboratory studies have confirmed that extracts of Lilium brownii suppress inflammatory mediators in airway cells, supporting its traditional use as an expectorant. The dried bulb is now sold as a packaged tea in Chinese supermarkets and on line herbal stores, and it continues to be prepared in the same decoction form in household kitchens across East Asia.

General Uses Top

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Common products:
Lilium brownii is cultivated for its edible bulbs, sold fresh, blanched, or dried; some dried bulbs are ground into starch or flour for food processing.

Food and beverages (non-medicinal):
Bulbs are eaten as a vegetable in East Asian cuisines, commonly braised or simmered in soups and stews. Dried slices or whole bulbs are used as ingredients in savory dishes; peeled fresh bulbs are used in stir-fries and hotpots. Bulbs are also processed into starch or flour for noodles, dumpling skins, and pancakes.

Properties relevant to use:
Cooked bulbs exhibit a soft, starchy texture with mildly sweet flavor suitable for neutral to savory dishes; this is the primary attribute enabling culinary processing rather than pharmacognosy or medicinal activity.

Synonyms Top

Scientific name Authority First published in
Lilium australe Elwes Gard. Chron. ser. 3, 70: 101. 1921
Lilium brownii var. australe (Stapf) Stearn Lilies World 165. 1950
Lilium brownii var. platyphyllum Baker Gard. Chron. ser. 3, 10: 225. 1891
Lilium japonicum var. brownii (Lemoinier) Baker Gard. Chron. 1871: 709 (1871)

Common names Top

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Language Common/alternative name
English chinese lily
English brown's lily
English hong kong lily
Arabic زنبق براون
Azerbaijani broun zanbağı
Japanese ハカタユリ
pwn kavaluan
Swedish kantonlilja
Vietnamese bách hợp
Chinese 野百合
Chinese 百合花
Chinese 山百合
Chinese 淡紫百合
Chinese 绿百合
Chinese 布朗百合
Chinese 百合

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Lilium brownii var. brownii Unknown
Lilium brownii var. viridulum Baker Gard. Chron. , n.s., 24: 134 (1885)
Lilium brownii var. chlorasteri (Baker) Baker Gard. Chron. , ser. 3, 10: 225 (1891)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000685383
Tropicos 18403471
KEW urn:lsid:ipni.org:names:60447947-2
The Plant List kew-280724
Open Tree Of Life 689068
NCBI Taxonomy 82312
IPNI 60447947-2
iNaturalist 556187
GBIF 2753253
EPPO LILBR
EOL 1003312
USDA GRIN 22119
Wikipedia Lilium_brownii
CMAUP NPO1475

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
Morphological, molecular, and biological characterization of bulb rot pathogens in stored Lanzhou lily and the in vitro antifungal efficacy of three plant essential oils Liu C, Wang Y, Jin L, Wang Y, Liu D Front Microbiol 11-Apr-2024
PMCID:PMC11043472
doi:10.3389/fmicb.2024.1307966
PMID:38666262
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Genome-Wide Analysis of VILLIN Gene Family Associated with Stress Responses in Cotton (Gossypium spp.) Deep A, Pandey DK Curr Issues Mol Biol 11-Mar-2024
PMCID:PMC10969196
doi:10.3390/cimb46030146
PMID:38534762
Physical Stability of Lotus Seed and Lily Bulb Beverage: The Effects of Homogenisation on Particle Size Distribution, Microstructure, Rheological Behaviour, and Sensory Properties Su J, Qiu X, Pei Y, Zhang Z, Liu G, Luan J, Nie J, Li X Foods 01-Mar-2024
PMCID:PMC10931448
doi:10.3390/foods13050769
PMID:38472882
Rhizosphere microbial markers (micro-markers): A new physical examination indicator for traditional Chinese medicines Yang K, Zheng Y, Sun K, Wu X, Zhang Z, He C, Xiao P Chin Herb Med 24-Feb-2024
PMCID:PMC11064633
doi:10.1016/j.chmed.2023.11.003
PMID:38706829
The Relationship between Endophytic Fungi of Chimonanthus praecox and Volatile Metabolites under Different Circadian Rhythms and Blooming Stages Li Y, Hei J, He X, Rui R, Wang S J Fungi (Basel) 11-Feb-2024
PMCID:PMC10890430
doi:10.3390/jof10020145
PMID:38392817
The antidepressive mechanism of Longya Lilium combined with Fluoxetine in mice with depression-like behaviors Ma H, Huang H, Li C, Li S, Gan J, Lian C, Ling Y NPJ Syst Biol Appl 13-Jan-2024
PMCID:PMC10787738
doi:10.1038/s41540-024-00329-5
PMID:38218856
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
Embryological observations on seed abortion in Hibiscus syriacus L. and physiological studies on nutrients, enzyme activity and endogenous hormones Wang X, Chen J, Hu L, Zhang J, Xiao F, Zhang S, Shao F, Huang L BMC Plant Biol 21-Dec-2023
PMCID:PMC10740302
doi:10.1186/s12870-023-04669-y
PMID:38129795
East meets west: using ethnobotany in ethnic urban markets of Barcelona metropolitan area (Catalonia) as a tool for biocultural exchange D’Ambrosio U, Pozo C, Vallès J, Gras A J Ethnobiol Ethnomed 17-Dec-2023
PMCID:PMC10726630
doi:10.1186/s13002-023-00636-x
PMID:38105250
Divergent Retention of Sucrose Metabolism Genes after Whole Genome Triplication in the Tomato (Solanum lycopersicum) Xu Y, Yao Z, Cheng Y, Ruan M, Ye Q, Wang R, Zhou G, Liu J, Liu C, Wan H Plants (Basel) 13-Dec-2023
PMCID:PMC10747743
doi:10.3390/plants12244145
PMID:38140472
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
Integrated transcriptome and metabolome analysis unveils the mechanism of color-transition in Edgeworthia chrysantha tepals Zhou N, Yan Y, Wen Y, Zhang M, Huang Y BMC Plant Biol 16-Nov-2023
PMCID:PMC10652483
doi:10.1186/s12870-023-04585-1
PMID:37968605
A review of the research progress on Pinellia ternata (Thunb.) Breit.: Botany, traditional uses, phytochemistry, pharmacology, toxicity and quality control Zou T, Wang J, Wu X, Yang K, Zhang Q, Wang C, Wang X, Zhao C Heliyon 14-Nov-2023
PMCID:PMC10696046
doi:10.1016/j.heliyon.2023.e22153
PMID:38058630
Exploring Microeukaryote Community Characteristics and Niche Differentiation in Arid Farmland Soil at the Northeastern Edge of the Tibetan Plateau Chen L, Han H, Wang C, Warren A, Ning Y Microorganisms 08-Oct-2023
PMCID:PMC10609477
doi:10.3390/microorganisms11102510
PMID:37894168

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
Regaloside B 5459143 Click to see 442.40 unknown https://doi.org/10.1016/0031-9422(90)83050-B
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosylmonoacylglycerols
(E)-3-(4-Hydroxyphenyl)propenoic acid (2S)-3-(beta-D-glucopyranosyloxy)-2-hydroxypropyl ester 15589787 Click to see C1=CC(=CC=C1C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O)O 400.40 unknown via CMAUP database
[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-propyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 5387740 Click to see 400.40 unknown via CMAUP database
Regaloside A 5459131 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(90)83050-B
https://doi.org/10.1248/CPB.38.3055
Regaloside C 14135348 Click to see 416.40 unknown https://doi.org/10.1016/0031-9422(90)83050-B
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[3-[4-formyl-1-hydroxy-8-methyl-10-(2-methyl-1-prop-1-en-2-ylcyclopentyl)deca-3,7-dienyl]-5-oxo-2H-furan-2-yl] acetate 163044867 Click to see 458.60 unknown https://doi.org/10.1016/0031-9422(90)83050-B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2R,4S,5'R,6R,7S,8S,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162920755 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 884.10 unknown https://doi.org/10.1248/CPB.38.3055
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2R,4S,4'S,6R,7S,8R,9S,12R,13R,16S)-4',7,9,13-tetramethyl-4'-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]spiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxolane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162981413 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CC(CO8)(C)COC9C(C(C(C(O9)CO)O)O)O 901.00 unknown https://doi.org/10.1016/0031-9422(90)83050-B
(3S)-3-hydroxy-5-[[(1S,2S,3'R,4S,6R,7S,8R,9S,12R,13R,16S)-16-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3'-yl]methoxy]-3-methyl-5-oxopentanoic acid 162911877 Click to see 1045.20 unknown https://doi.org/10.1248/CPB.38.3055
(3S)-5-[[(1S,2S,3'R,4S,6R,7S,8R,9S,12R,13R,16S)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3'-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid 162920277 Click to see 883.00 unknown https://doi.org/10.1016/0031-9422(90)83050-B
2-[4-Hydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 14781359 Click to see 884.10 unknown https://doi.org/10.1248/CPB.38.3055
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[4',7,9,13-tetramethyl-4'-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]spiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxolane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162981412 Click to see 901.00 unknown https://doi.org/10.1016/0031-9422(90)83050-B
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 14633186 Click to see 738.90 unknown https://doi.org/10.1248/CPB.38.3055
5-[[(1S,2S,3'R,4S,6R,7S,8R,9S,12S,13R,16S)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3'-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid 102056146 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(CO8)COC(=O)CC(C)(CC(=O)O)O 883.00 unknown https://doi.org/10.1016/0031-9422(90)83050-B
https://doi.org/10.1248/CPB.38.3055
Avenacoside A 71581001 Click to see 1063.20 unknown https://doi.org/10.1248/CPB.38.3055
Spirostane-2H, + 1O, O-Hex-dHex, C6H9O4 14633180 Click to see 883.00 unknown https://doi.org/10.1016/0031-9422(90)83050-B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.36.2430
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.36.2430
> Organic acids and derivatives / Organic sulfuric acids and derivatives / Arylsulfates / Phenylsulfates
4-(6-Benzyl-5-{[4-(sulfooxy)phenyl]acetamido}pyrazin-2-yl)phenyl hydrogen sulfate 5459866 Click to see C1=CC=C(C=C1)CC2=NC(=CN=C2NC(=O)CC3=CC=C(C=C3)OS(=O)(=O)O)C4=CC=C(C=C4)OS(=O)(=O)O 571.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
6-O-(alpha-L-Rhamnopyranosyl)-D-glucopyranose 12314995 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
(+)-Epicatechin 182232 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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