Details Top

Internal ID UUID64401c111fbe2370301317
Scientific name Lilium auratum
Authority Lindl.
First published in Gard. Chron. 1862: 644 (1862)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Lilium auratum is cultivated on a large scale as an ornamental species; its large, fragrant white flowers with golden rays are a staple in the cut‑flower trade, used for bouquets, wedding arrangements, corporate events, and garden displays. The species commands a significant share of the premium cut‑flower market in Japan, with export to North America and Europe.
- Potted plants and garden specimens are sold for landscape design, seasonal colour, and indoor decoration; breeding programmes focus on hybrids with longer vase life, larger blooms, and increased disease resistance to meet commercial standards.

Fragrance and cosmetics:
- Fresh flowers yield an essential oil whose major constituents are monoterpenes such as linalool (~15 % of total oil) and phenylpropanoids like benzyl alcohol (~8 %); sesquiterpenes (e.g., (E)‑caryophyllene) also contribute. Peer‑reviewed analysis has quantified these components and demonstrated a sweet, floral scent profile that is employed as a natural fragrance component in perfumery, soaps, and scented candles.
- The flower extract (INCI: Lilium auratum flower extract) is listed in the International Cosmetic Ingredient Dictionary and is incorporated into skin‑care and hair‑care formulations for its aromatic and conditioning properties.

Food and beverages (non‑medicinal):
- The mature bulb, known as “yurine” in Japanese cuisine, is harvested fresh, dried, or canned and used in simmered dishes, soups, stir‑fries, and as a base for flour or starch. It is a gluten‑free source of complex carbohydrates, containing approximately 70 % starch, low fat, and trace amounts of vitamin C, giving a firm texture after cooking and a neutral flavour that pairs well with soy‑based sauces.

Properties relevant to use:
- Cut‑flower quality stems from thick, fleshy petals that retain turgidity, giving a vase life of 7–10 days when stored at 2–4 °C and kept in appropriate vase solutions; the essential oil’s fragrance profile, high in linalool and benzyl alcohol, provides sweet, floral notes desirable in perfume blends; bulb starch is dominated by amylose (>30 % of total starch) which gelatinises at moderate temperatures, yielding a smooth, viscous paste used as a thickening agent in food processing.

Sustainability and sourcing:
- Lilium auratum is classified as “Least Concern” on the IUCN Red List and is not listed in CITES; the species is propagated primarily by tissue culture and bulblet division, reducing pressure on wild populations. Commercial production occurs mainly in Japan, with additional cultivation in North America and Europe, where growers follow Good Agricultural and Collection Practices (GACP) and use integrated pest management and controlled‑environment greenhouses to minimise environmental impact.

Synonyms Top

Scientific name Authority First published in
Lilium auratum var. rubrovittatum Duch. J. Soc. Centr. Hort. France 2(4): 483. 1870
Lilium auratum var. rubrum Carrière Rev. Hort. (Paris) 39: 371. 1867
Lilium auratum var. cruentum Burb. Fl. Mag. (London) 14: t. 233. 1876
Lilium auratum var. tricolor Baker Gard. Chron. n.s., 14: 198. 1880
Lilium auratum var. virginale Duch. J. Soc. Centr. Hort. France 2(4): 483. 1870
Lilium auratum var. wittei (Suringar) Elwes Monogr. Lilium t. 16, f. 2 1877

Common names Top

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Language Common/alternative name
English mountain lily
English golden rayed lily of japan
English gold rayed lily
English gold band lily
Arabic زنبق مذهب
Arabic زنبق ذهبي
Bulgarian златиста лилия
Persian سوسن کوهی
Armenian Ոսկեգույն շուշան
Japanese 山百合
Japanese ヤマユリ
Korean 산나리
Malayalam ലിലിയം ഔറാറ്റം
Norwegian Bokmål gullbåndlilje
Swedish stor gullbandslilja
Swedish gullbandslilja
Chinese 鳳來寺百合
Chinese 關東百合
Chinese 镰仓百合
Chinese 鐮倉百合
Chinese 筋百合
Chinese 山百合
Chinese 多武峰百合
Chinese 凤来寺百合
Chinese 关东百合
Chinese 天香百合

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Lilium auratum var. auratum Unknown
Lilium auratum var. platyphyllum Baker Gard. Chron. , n.s., 14: 198 (1880)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000685209
INPN 611053
KEW urn:lsid:ipni.org:names:537467-1
The Plant List kew-280708
Missouri Botanical Garden 282318
Open Tree Of Life 884636
NCBI Taxonomy 78997
IPNI 537467-1
iNaturalist 452268
GBIF 2753106
Freebase /m/08qfzj
EPPO LILAU
EOL 1003309
USDA GRIN 22108
Wikipedia Lilium_auratum

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
Transcriptome Analysis Reveals Coexpression Networks and Hub Genes Involved in Papillae Development in Lilium auratum Zhu Y, Yang J, Liu X, Sun T, Zhao Y, Xiang F, Chen F, He H Int J Mol Sci 19-Feb-2024
PMCID:PMC10889295
doi:10.3390/ijms25042436
PMID:38397114
Embryo Rescue in Plant Breeding Rogo U, Fambrini M, Pugliesi C Plants (Basel) 29-Aug-2023
PMCID:PMC10489947
doi:10.3390/plants12173106
PMID:37687352
Bioreactor systems for micropropagation of plants: present scenario and future prospects Murthy HN, Joseph KS, Paek KY, Park SY Front Plant Sci 19-Apr-2023
PMCID:PMC10154609
doi:10.3389/fpls.2023.1159588
PMID:37152119
Floral Scents in Bee-Pollinated Buckwheat and Oilseed Rape under a Global Warming Scenario Cordeiro GD, Dötterl S Insects 28-Feb-2023
PMCID:PMC10057843
doi:10.3390/insects14030242
PMID:36975927
Floral symmetry: the geometry of plant reproduction Jiang Y, Moubayidin L Emerg Top Life Sci 22-Aug-2022
PMCID:PMC9472818
doi:10.1042/ETLS20210270
PMID:35994008
Near-Hexaploid and Near-Tetraploid Aneuploid Progenies Derived from Backcrossing Tetraploid Parents Hibiscus syriacus × (H. syriacus × H. paramutabilis) Chen H, Contreras RN Genes (Basel) 06-Jun-2022
PMCID:PMC9222940
doi:10.3390/genes13061022
PMID:35741783
Evolutionary effects of geographic and climatic isolation between Rhododendron tsusiophyllum populations on the Izu Islands and mainland Honshu of Japan Yoichi W, Takahashi M, Nagano AJ, Uehara K, Abe H Heredity (Edinb) 02-Mar-2021
PMCID:PMC8102576
doi:10.1038/s41437-021-00417-w
PMID:33654179
Evaluation of sampling effort required to assess pollen species richness on pollinators using rarefaction Nikkeshi A, Hiraiwa MK, Ushimaru A, Hoshizaki K, Makita A, Mizuki I Appl Plant Sci 27-Feb-2021
PMCID:PMC7910805
doi:10.1002/aps3.11411
PMID:33680582
Change in Sucrose Cleavage Pattern and Rapid Starch Accumulation Govern Lily Shoot-to-Bulblet Transition in vitro Wu Y, Ren Z, Gao C, Sun M, Li S, Min R, Wu J, Li D, Wang X, Wei Y, Xia Y Front Plant Sci 14-Jan-2021
PMCID:PMC7840508
doi:10.3389/fpls.2020.564713
PMID:33519832
A Complex Journey: Cell Wall Remodeling, Interactions, and Integrity During Pollen Tube Growth Cascallares M, Setzes N, Marchetti F, López GA, Distéfano AM, Cainzos M, Zabaleta E, Pagnussat GC Front Plant Sci 30-Nov-2020
PMCID:PMC7733995
doi:10.3389/fpls.2020.599247
PMID:33329663
LsGRP1, a class II glycine‐rich protein of Lilium, confers plant resistance via mediating innate immune activation and inducing fungal programmed cell death Lin C, Pan Y, Ye N, Shih Y, Liu F, Chen C Mol Plant Pathol 14-Jul-2020
PMCID:PMC7411634
doi:10.1111/mpp.12968
PMID:32662583
Phenylpropanoid Glycerol Glucosides Attenuate Glucose Production in Hepatocytes Murray AF, Palatini K, Komarnytsky S, Gianfagna TJ, Munafo JP Jr ACS Omega 19-Jun-2019
PMCID:PMC6648405
doi:10.1021/acsomega.9b00751
PMID:31460164
Evolution of Cell Wall Polymers in Tip-Growing Land Plant Gametophytes: Composition, Distribution, Functional Aspects and Their Remodeling Dehors J, Mareck A, Kiefer-Meyer MC, Menu-Bouaouiche L, Lehner A, Mollet JC Front Plant Sci 18-Apr-2019
PMCID:PMC6482432
doi:10.3389/fpls.2019.00441
PMID:31057570
K+ Excretion: The Other Purpose for Puddling Behavior in Japanese Papilio Butterflies Inoue TA, Ito T, Hagiya H, Hata T, Asaoka K, Yokohari F, Niihara K PLoS One 08-May-2015
PMCID:PMC4425484
doi:10.1371/journal.pone.0126632
PMID:25955856
The Metabolic Basis of Pollen Thermo-Tolerance: Perspectives for Breeding Paupière MJ, van Heusden AW, Bovy AG Metabolites 30-Sep-2014
PMCID:PMC4279151
doi:10.3390/metabo4040889
PMID:25271355

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
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3S,3aR,6S,6aR)-6-(3,5-dihydroxy-4-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxybenzene-1,3-diol 163028519 Click to see 390.40 unknown https://doi.org/10.1248/CPB.36.4841
5-[6-(3,5-Dihydroxy-4-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxybenzene-1,3-diol 14284477 Click to see COC1=C(C=C(C=C1O)C2C3COC(C3CO2)C4=CC(=C(C(=C4)O)OC)O)O 390.40 unknown https://doi.org/10.1248/CPB.36.4841
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
7-Ethyl-4,9-dihydroxyundec-7-ene-3,6-dione 135370518 Click to see 242.31 unknown https://doi.org/10.1248/CPB.36.4841
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
[(2S)-3-hydroxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 14284483 Click to see 430.40 unknown https://doi.org/10.1248/CPB.36.4841
[1-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162908656 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
[3-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163000508 Click to see 430.40 unknown https://doi.org/10.1248/CPB.36.4841
b-D-Glucopyranoside,2-hydroxy-1-[[[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]oxy]methyl]ethyl,[S-(E)]- 163020053 Click to see 400.40 unknown https://doi.org/10.1248/CPB.36.4841
Regaloside B 5459143 Click to see 442.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
Regaloside D 14284473 Click to see 400.40 unknown https://doi.org/10.1248/CPB.36.4841
Regaloside H 14542288 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2S)-1-acetyloxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 14542292 Click to see CC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)C=CC2=CC=C(C=C2)O 442.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
[1-Acetyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162929820 Click to see 442.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
> 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 https://doi.org/10.1248/CPB.36.4841
[(2R)-2-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163195584 Click to see 430.40 unknown https://doi.org/10.1248/CPB.36.4841
[(2R)-2-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 15589788 Click to see 400.40 unknown https://doi.org/10.1248/CPB.36.4841
[2-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 72431854 Click to see 430.40 unknown https://doi.org/10.1248/CPB.36.4841
Regaloside A 5459131 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(89)80363-2
Regaloside F 14284479 Click to see 430.40 unknown https://doi.org/10.1248/CPB.36.4841
> 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 CC1CCCC1(CCC(=CCCC(=CCC(C2=CC(=O)OC2OC(=O)C)O)C=O)C)C(=C)C 458.60 unknown https://doi.org/10.1016/0031-9422(89)80363-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(3S,5S,8R,9S,10R,13R,14R,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-10,13-dimethyl-3-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 14542295 Click to see 612.80 unknown https://doi.org/10.1016/0031-9422(89)80363-2
(3S,5S,8R,9S,10R,13R,14R,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 14542294 Click to see 612.80 unknown https://doi.org/10.1016/0031-9422(89)80363-2
17-(2,3-dihydroxy-6-methylheptan-2-yl)-14-hydroxy-10,13-dimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 14542293 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2CC(=O)C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)O)O 612.80 unknown https://doi.org/10.1016/0031-9422(89)80363-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3S,4S,5R,6R)-6-[(2S,3S,4R,5R)-5-(acetyloxymethyl)-4-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-2-(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163187143 Click to see CC(=O)OCC1C(C(C(O1)(CO)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O 736.70 unknown https://doi.org/10.1248/CPB.36.4841
[3,4,5-Trihydroxy-6-[4-hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-2,5-bis(hydroxymethyl)oxolan-2-yl]oxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162860687 Click to see 694.60 unknown https://doi.org/10.1248/CPB.36.4841
[6-[5-(Acetyloxymethyl)-4-hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-2-(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163079568 Click to see 736.70 unknown https://doi.org/10.1248/CPB.36.4841
Securoside A 13916034 Click to see 694.60 unknown https://doi.org/10.1248/CPB.36.4841
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1246/NIKKASHI1948.77.1057
https://doi.org/10.1007/BF00629393
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1246/NIKKASHI1948.77.1057
https://doi.org/10.1007/BF00629393

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