Details Top

Internal ID UUID64401b445b5b9255594038
Scientific name Lilium hansonii
Authority Leichtlin ex D.D.T.Moore
First published in Rural New Yorker 24: 60 (1871)

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.

Ethnobotanical Uses

No verifiable records were found of tea, decoction, tincture, maceration, or poultice preparations made from Lilium hansonii; therefore, no ethnobotanical text is provided for this taxon.

General Uses Top

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Common products:
Lilium hansonii is cultivated primarily as an ornamental garden plant for its showy, fragrant pink‑white flowers that appear in late spring to early summer. It is sold by nurseries as a perennial for borders, rock gardens, and containers, and it is also listed in the Royal Horticultural Society Plant Finder as a garden‑worthy lily. In the cut‑flower trade the species is occasionally harvested when buds are fully formed; stems are marketed to florists for use in mixed arrangements, where its distinctive fragrance and trumpet‑shaped blooms provide visual and olfactory interest.

Industrial and craft applications:
The principal industrial application of L. hansonii is its cultivation for the commercial cut‑flower market. Flowers are cut at the tight‑bud stage, shipped in refrigerated transport, and processed by florists for event and retail use. The plant is also employed in landscape design projects as a late‑season focal point, providing structure and seasonal color in perennial plantings. Propagation by bulb division supports a niche horticultural supply chain that supplies the ornamental sector with starter material.

Properties relevant to use:
The plant produces large, actinomorphic flowers (typically 6–10 cm across) with a strong sweet scent, which enhances its attractiveness in both garden and cut‑flower contexts. Stems reach 1.0–1.5 m in height, providing sufficient length for floral arrangements. Bulbs are fleshy, bearing several offsets, allowing rapid propagation by division and facilitating commercial nursery production. Lilium hansonii is cold‑hardy to USDA zones 4–8, tolerating frost and enabling field cultivation without extensive climate control. Its late‑season blooming period (mid‑summer) complements other spring‑flowering lilies, extending the ornamental display in gardens.

Sustainability and sourcing:
Commercial production of L. hansonii relies on cultivated bulb stocks propagated in specialized horticultural farms rather than wild collection, reducing pressure on natural populations. Nurseries typically practice bulb offset division, a low‑impact method that yields uniform plant material. Controlled‑environment greenhouse production can be employed to meet seasonal demand while minimizing pesticide use; many suppliers adopt Integrated Pest Management (IPM) protocols. Where applicable, growers may obtain Good Agricultural Practices (GAP) or organic certification, further ensuring environmentally responsible sourcing of the ornamental lily.

Synonyms Top

Scientific name Authority First published in
Lilium medeoloides var. obovatum Franch. & Sav. Enum. Pl. Jap. 2: 63. 1876

Common names Top

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Language Common/alternative name
English hanson's lily
Finnish täplälilja
Japanese タケシマユリ
Korean 섬말나리
Russian Лилия Хансона
Swedish fläcklilja
Chinese 竹叶百合

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.
4 months warm, then 4 months cold

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-0000677704
KEW urn:lsid:ipni.org:names:537590-1
The Plant List kew-279909
Open Tree Of Life 116216
NCBI Taxonomy 82318
IPNI 537590-1
iNaturalist 543755
GBIF 2753520
Freebase /m/0gyw65c
EOL 1002571
Elurikkus 5485
USDA GRIN 22159
Wikipedia Lilium_hansonii
CMAUP NPO3933

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
Embryo Rescue in Plant Breeding Rogo U, Fambrini M, Pugliesi C Plants (Basel) 29-Aug-2023
PMCID:PMC10489947
doi:10.3390/plants12173106
PMID:37687352
Duration of of Low-Temperature Storage, Clove Topping and Gibberellic Acid on Emergence, Yield and Yield Components of Garlic Desta B, Woldetsadik K, Mohammed W, Tena N ScientificWorldJournal 24-Mar-2022
PMCID:PMC8970948
doi:10.1155/2022/2998190
PMID:35370482
Characterization and Comparison of Two Complete Plastomes of Rosaceae Species (Potentilla dickinsii var. glabrata and Spiraea insularis) Endemic to Ulleung Island, Korea Yang J, Kang GH, Pak JH, Kim SC Int J Mol Sci 13-Jul-2020
PMCID:PMC7404287
doi:10.3390/ijms21144933
PMID:32668601
The complete chloroplast genomes of Lilium tsingtauense Gilg (Liliaceae) Lee SC, Kim K, Hwang YJ, Lim KB, Yang TJ Mitochondrial DNA B Resour 19-Apr-2016
PMCID:PMC7871828
doi:10.1080/23802359.2016.1172052
PMID:33644375
Low temperature-induced DNA hypermethylation attenuates expression of RhAG, an AGAMOUS homolog, and increases petal number in rose (Rosa hybrida) Ma N, Chen W, Fan T, Tian Y, Zhang S, Zeng D, Li Y BMC Plant Biol 05-Oct-2015
PMCID:PMC4595006
doi:10.1186/s12870-015-0623-1
PMID:26438149
Zeaxanthin Induces Apoptosis in Human Uveal Melanoma Cells through Bcl-2 Family Proteins and Intrinsic Apoptosis Pathway Bi MC, Rosen R, Zha RY, McCormick SA, Song E, Hu DN Evid Based Complement Alternat Med 10-Oct-2013
PMCID:PMC3810440
doi:10.1155/2013/205082
PMID:24223611
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Jatropham glucoside from the bulbs of Lilium hansonii Hiroko Shimomura, Yutaka Sashida, Yoshihiro Mimaki, Yuko Minegishi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81463-6
Jatropham derivatives and steroidal saponins from the bulbs of Lilium hansonii. Ori K, Mimaki Y, Mito K, Sashida Y, Nikaido T, Ohmoto T, Masuko A Phytochemistry 01-Aug-1992
doi:10.1016/0031-9422(92)83627-B
PMID:1369389

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2-Methyl-2-butene 10553 Click to see CC=C(C)C 70.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
threo-9,10-Dihydroxystearic acid 12235228 Click to see CCCCCCCCC(C(CCCCCCCC(=O)O)O)O 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(9R,10S)-9,10-epoxyoctadecanoic acid 12235227 Click to see 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2-(8,8a-Dimethyl-4-oxo-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl)prop-2-enoic acid 78173225 Click to see 250.33 unknown https://doi.org/10.1016/S0031-9422(00)81463-6
https://doi.org/10.1016/0031-9422(92)83627-B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3S,8E)-5,9,14-Trimethyl-4,12-dioxatricyclo[9.3.0.03,5]tetradeca-1(11),8,13-trien-2-one 46173863 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
1,5,5-trimethyl-6-[(1E,3Z,5Z,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-7-oxabicyclo[4.1.0]heptan-3-ol 5316151 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C 568.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
> 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-[(1R,2S,4S,5'R,6R,7S,8R,9S,10S,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-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 101630369 Click to see 901.00 unknown https://doi.org/10.1016/0031-9422(92)83627-B
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10S,12S,13S,16S,18S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-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 101630368 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(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)O)C)C)OC1 903.10 unknown https://doi.org/10.1016/0031-9422(92)83627-B
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[[(1R,2S,4S,6S,7S,8R,9S,12S,13S,16S,18S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-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 163071252 Click to see 1067.20 unknown https://doi.org/10.1016/0031-9422(92)83627-B
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-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 163016604 Click to see 1065.20 unknown https://doi.org/10.1016/0031-9422(92)83627-B
2-[4-Hydroxy-6-(hydroxymethyl)-2-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163007134 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=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)O)C)C)OC1 901.00 unknown https://doi.org/10.1016/0031-9422(92)83627-B
2-[4-Hydroxy-6-(hydroxymethyl)-2-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73204071 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(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)O)C)C)OC1 903.10 unknown https://doi.org/10.1016/0031-9422(92)83627-B
2-[4-Hydroxy-6-(hydroxymethyl)-2-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 14102489 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1067.20 unknown https://doi.org/10.1016/0031-9422(92)83627-B
CID 150711 150711 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1065.20 unknown https://doi.org/10.1016/0031-9422(92)83627-B
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,3S)-2-ammonio-3-hydroxybutanoate 6995276 Click to see 119.12 unknown via CMAUP database
L-Arginine 6322 Click to see 174.20 unknown via CMAUP database
L-Cysteic acid 72886 Click to see C(C(C(=O)O)N)S(=O)(=O)O 169.16 unknown via CMAUP database
Lysine zwitterion 122198194 Click to see 146.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
(3S)-3-azaniumyl-4-hydroxy-4-oxobutanoate 44367445 Click to see C(C(C(=O)O)[NH3+])C(=O)[O-] 133.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
(2S)-2-ammonio-3-(1H-imidazol-4-yl)propanoate 6971009 Click to see 155.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
(2S,3S)-2-ammonio-3-methylpentanoate 7043901 Click to see 131.17 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 zwitterion 7045798 Click to see 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(2S)-2-ammonio-4-(methylsulfanyl)butanoate 6992087 Click to see 149.21 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2S,4R)-4-methyl-1-[(2R)-4-methyl-5-oxo-1,2-dihydropyrrol-2-yl]-5-oxopyrrolidine-2-carboxylic acid 162910854 Click to see 238.24 unknown https://doi.org/10.1016/0031-9422(92)83627-B
4-Methyl-1-(4-methyl-5-oxo-1,2-dihydropyrrol-2-yl)-5-oxopyrrolidine-2-carboxylic acid 85666468 Click to see 238.24 unknown https://doi.org/10.1016/0031-9422(92)83627-B
4-methyl-1-(4-methyl-5-oxo-2H-pyrrol-1-yl)-5-oxopyrrolidine-2-carboxylic acid 163192458 Click to see CC1CC(N(C1=O)N2CC=C(C2=O)C)C(=O)O 238.24 unknown https://doi.org/10.1016/0031-9422(92)83627-B
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
L-Serine 5951 Click to see 105.09 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
(2S)-2-ammonio-3-(4-hydroxyphenyl)propanoate 6942100 Click to see C1=CC(=CC=C1CC(C(=O)[O-])[NH3+])O 181.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Ammoniobutanoate 6992099 Click to see 103.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]hexadeca-1,3,5,7,9,11,13,15-octaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol 29921731 Click to see 486.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-methyl-1,2-dihydropyrrol-5-one 101630363 Click to see 437.40 unknown https://doi.org/10.1016/0031-9422(92)83627-B
(2R)-4-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2-dihydropyrrol-5-one 14284485 Click to see 275.25 unknown https://doi.org/10.1016/S0031-9422(00)81463-6
2-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-methyl-1,2-dihydropyrrol-5-one 163035944 Click to see 437.40 unknown https://doi.org/10.1016/0031-9422(92)83627-B
4-Methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2-dihydropyrrol-5-one 14284484 Click to see 275.25 unknown https://doi.org/10.1016/S0031-9422(00)81463-6
> Organoheterocyclic compounds / Pyrrolines
(2R)-4-methyl-2-[[(2S)-4-methyl-5-oxo-1,2-dihydropyrrol-2-yl]oxy]-1,2-dihydropyrrol-5-one 101630365 Click to see CC1=CC(NC1=O)OC2C=C(C(=O)N2)C 208.21 unknown https://doi.org/10.1016/0031-9422(92)83627-B
(2S)-2-hydroxy-4-methyl-1,2-dihydropyrrol-5-one 5325835 Click to see CC1=CC(NC1=O)O 113.11 unknown via CMAUP database
Jatropham 3080808 Click to see 113.11 unknown https://doi.org/10.1016/0031-9422(92)83627-B
https://doi.org/10.1016/S0031-9422(00)81463-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[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/10.1016/0031-9422(92)83627-B
Securoside A 13916034 Click to see 694.60 unknown https://doi.org/10.1016/0031-9422(92)83627-B
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R)-2-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxypropyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 25768379 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(92)83627-B
[2-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxyphenyl)prop-2-enoate 72727917 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(92)83627-B
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-hydroxy-8-[(2R)-3-hydroxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]chromen-2-one 102353962 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=O)C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 426.40 unknown https://doi.org/10.1016/0031-9422(92)83627-B

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