Lilium henryi - Unknown
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Internal ID UUID64401b430b1e7105523295
Scientific name Lilium henryi
Authority Baker
First published in Gard. Chron. , ser. 3, 4: 660 (1888)

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Synonyms Top

Scientific name Authority First published in
Lilium henryi var. citrinum Wallace Gard. Chron. ser. 3, 100: 69. 1936

Common names Top

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Language Common/alternative name
English henry's lily
Arabic زنبق هنري
German henrys lilie
Finnish heikinlilja
Japanese キカノコユリ
Polish lilia henry’ego
Russian Лилия Генри
Swedish orangelilja
Chinese 湖北百合

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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-0000677671
USDA Plants LIHE6
Tropicos 18403473
KEW urn:lsid:ipni.org:names:537595-1
The Plant List kew-279904
Missouri Botanical Garden 282209
Open Tree Of Life 308590
NCBI Taxonomy 4689
IPNI 537595-1
iNaturalist 554274
GBIF 2753211
Freebase /m/08qz4d
EPPO LILHE
EOL 1002554
USDA GRIN 22163
Wikipedia Lilium_henryi

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
Screening and validation of optimal miRNA reference genes in different developing stages and tissues of Lilium henryi Baker Jin G, Zhang X, Yu S, Du Y, Wang M, Zhao C, Zhang M Sci Rep 17-Jan-2024
PMCID:PMC10794412
doi:10.1038/s41598-024-51562-1
PMID:38233457
Reference genome of the nutrition-rich orphan crop chia (Salvia hispanica) and its implications for future breeding Gupta P, Geniza M, Elser J, Al-Bader N, Baschieri R, Phillips JL, Haq E, Preece J, Naithani S, Jaiswal P Front Plant Sci 14-Dec-2023
PMCID:PMC10757625
doi:10.3389/fpls.2023.1272966
PMID:38162307
A Modified Method for Transient Transformation via Pollen Magnetofection in Lilium Germplasm Zhang M, Ma X, Jin G, Han D, Xue J, Du Y, Chen X, Yang F, Zhao C, Zhang X Int J Mol Sci 18-Oct-2023
PMCID:PMC10607007
doi:10.3390/ijms242015304
PMID:37894985
Identification of Candidate Genes Involved in the Determinism of Pollen Grain Aperture Morphology by Comparative Transcriptome Analysis in Papaveraceae Mazuecos-Aguilera I, Suárez-Santiago VN Plants (Basel) 06-Apr-2023
PMCID:PMC10096813
doi:10.3390/plants12071570
PMID:37050196
Structural regulation and dynamic behaviour of organelles during plant meiosis Koç A, De Storme N Front Cell Dev Biol 25-Oct-2022
PMCID:PMC9640475
doi:10.3389/fcell.2022.925789
PMID:36393860
Mechanism of lily bulb and Rehmannia decoction in the treatment of lipopolysaccharide-induced depression-like rats based on metabolomics study and network pharmacology Chi X, Xue X, Pan J, Wu J, Shi H, Wang Y, Lu Y, Zhang Z, Ma K Pharm Biol 07-Oct-2022
PMCID:PMC9553158
doi:10.1080/13880209.2022.2121843
PMID:36205539
Phylogenetic Analysis of Wild Species and the Maternal Origin of Cultivars in the Genus Lilium Using 114 Plastid Genomes Duan Q, Liu F, Gui D, Fan W, Cui G, Jia W, Zhu A, Wang J Front Plant Sci 22-Jul-2022
PMCID:PMC9355515
doi:10.3389/fpls.2022.865606
PMID:35937320
Specificities and Dynamics of Transposable Elements in Land Plants Mhiri C, Borges F, Grandbastien MA Biology (Basel) 23-Mar-2022
PMCID:PMC9033089
doi:10.3390/biology11040488
PMID:35453688
A Review of the Developmental Processes and Selective Pressures Shaping Aperture Pattern in Angiosperms Albert B, Matamoro-Vidal A, Prieu C, Nadot S, Till-Bottraud I, Ressayre A, Gouyon PH Plants (Basel) 28-Jan-2022
PMCID:PMC8840023
doi:10.3390/plants11030357
PMID:35161338
Caught in the Act: Live-Cell Imaging of Plant Meiosis Prusicki MA, Balboni M, Sofroni K, Hamamura Y, Schnittger A Front Plant Sci 21-Dec-2021
PMCID:PMC8724559
doi:10.3389/fpls.2021.718346
PMID:34992616
The complete chloroplast genome sequence of Veratrum oxysepalum and phylogenetic analysis Chen ZJ, Liu JJ, Zhang YM, Qian ZG, Li GD Mitochondrial DNA B Resour 15-Jun-2021
PMCID:PMC8208108
doi:10.1080/23802359.2021.1940330
PMID:34189269
Comparative chloroplast genome analysis of medicinally important Veratrum (Melanthiaceae) in China: Insights into genomic characterization and phylogenetic relationships Zhang YM, Han LJ, Yang CW, Yin ZL, Tian X, Qian ZG, Li GD Plant Divers 01-Jun-2021
PMCID:PMC8897180
doi:10.1016/j.pld.2021.05.004
PMID:35281123
LINC-complex mediated positioning of the vegetative nucleus is involved in calcium and ROS signaling in Arabidopsis pollen tubes Moser M, Kirkpatrick A, Groves NR, Meier I Nucleus 07-Jul-2020
PMCID:PMC7529407
doi:10.1080/19491034.2020.1783783
PMID:32631106
Volatile composition and classification of Lilium flower aroma types and identification, polymorphisms, and alternative splicing of their monoterpene synthase genes Du F, Wang T, Fan JM, Liu ZZ, Zong JX, Fan WX, Han YH, Grierson D Hortic Res 01-Oct-2019
PMCID:PMC6804824
doi:10.1038/s41438-019-0192-9
PMID:31645964
Transcriptome Sequencing Analysis Provides Insights Into the Response to Fusarium oxysporum in Lilium pumilum He X, Li W, Zhang W, Jin X, Shenkute AG, Aynalem T, Xu S, Wang W Evol Bioinform Online 27-Mar-2019
PMCID:PMC6563521
doi:10.1177/1176934319838818
PMID:31223231

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
7-Ethyl-4,9-dihydroxyundec-7-ene-3,6-dione 135370518 Click to see CCC(C=C(CC)C(=O)CC(C(=O)CC)O)O 242.31 unknown https://doi.org/10.1248/CPB.36.2430
> 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.36.2430
[(2S)-2-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (E)-3-(4-methoxyphenyl)prop-2-enoate 14135344 Click to see COC1=CC=C(C=C1)C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
[2-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 73229554 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1248/CPB.36.2430
[2-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] 3-(4-methoxyphenyl)prop-2-enoate 163038753 Click to see COC1=CC=C(C=C1)C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
Regaloside A 5459131 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.36.2430
Regaloside C 14135348 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1248/CPB.36.2430
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde 163191287 Click to see CC1C2CCC3(C(CCC(C3C2OC1=O)C=O)O)C 266.33 unknown https://doi.org/10.1248/CPB.36.2430
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(3S)-3-hydroxy-5-[[(1S,2S,3'R,4S,6R,7S,8R,9S,12S,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 101674000 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)OC19CCC(CO9)COC(=O)CC(C)(CC(=O)O)O 1045.20 unknown https://doi.org/10.1016/0031-9422(93)85472-4
(3S)-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 162920276 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(93)85472-4
3-Hydroxy-5-[[16-[4-hydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(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 14781355 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)OC19CCC(CO9)COC(=O)CC(C)(CC(=O)O)O 1045.20 unknown https://doi.org/10.1016/0031-9422(93)85472-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Inositol phosphates
Phytic acid 890 Click to see C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O 660.04 unknown https://doi.org/10.1016/0031-9422(86)80065-6
https://doi.org/10.1016/0031-9422(86)80065-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[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-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 162968896 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O)O)O)CO)O)O 856.80 unknown https://doi.org/10.1248/CPB.36.2430
3-O-Feruloyl-6 inverted exclamation marka-O-(4-O-|A-D-glucopyranosylferuloyl)sucrose 101450504 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O)O)O)CO)O)O 856.80 unknown https://doi.org/10.1248/CPB.36.2430
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[2-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 67283061 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O 444.40 unknown https://doi.org/10.1248/CPB.36.2430
[3-Hydroxy-2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 72727916 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(CO)OC(=O)C=CC2=CC(=C(C=C2)O)OC)O 444.40 unknown https://doi.org/10.1248/CPB.36.2430
[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 COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)O)O)O)O 694.60 unknown https://doi.org/10.1248/CPB.36.2430
1,2-Diferuloyl-sn-glycerol 76967301 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(CO)OC(=O)C=CC2=CC(=C(C=C2)O)OC)O 444.40 unknown https://doi.org/10.1248/CPB.36.2430
Glyceryl 1,3-diferulate 14135369 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O 444.40 unknown https://doi.org/10.1248/CPB.36.2430
Securoside A 13916034 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)O)O)O)O 694.60 unknown https://doi.org/10.1248/CPB.36.2430
> 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 COC1=C(C=CC(=C1)C=CC(=O)OCC(COC(=O)C=CC2=CC=C(C=C2)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
[(2S)-1-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxypropan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 162900100 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(CO)OC(=O)C=CC2=CC=C(C=C2)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
[1-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162900099 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(CO)OC(=O)C=CC2=CC=C(C=C2)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
[2-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxyphenyl)prop-2-enoate 72727917 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(COC(=O)C=CC2=CC=C(C=C2)O)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430
[3-Hydroxy-2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxyphenyl)prop-2-enoate 163043173 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC(CO)COC(=O)C=CC2=CC=C(C=C2)O)O 414.40 unknown https://doi.org/10.1248/CPB.36.2430

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