Scientific name	Authority	First published in
Lilium lishmanni	T.Moore	Florist Fruitist Gard. Misc. 1872: 260 (1872)
Lilium leopoldii	hort. ex Baker	J. Linn. Soc., Bot. 14: 233 (1874)
Lilium tigrinum	Ker Gawl.	Bot. Mag. 31: t. 1237 (1809)
Lilium lancifolium var. splendens	(Van Houtte) V.A.Matthews	New Plantsman 7: 126 (1985)
Lilium lancifolium var. fortunei	(Standish) V.A.Matthews	New Plantsman 7: 126 (1985)
Lilium tigrinum var. plenescens	Waugh	Bot. Gaz. 27: 254 (1899)
Lilium tigrinum var. fortunei	Standish	Gard. Chron. 1866: 972 1866
Lilium tigrinum var. splendens	Van Houtte	Fl. Serres 19: t. 1931 1870
Lilium lancifolium var. flaviflorum	Makino	J. Jap. Bot. 8: 43. 1932

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	tiger lily
Afrikaans	tierlelie
German	tigerlilie
German	tiger-lilie
Estonian	tiigerliilia
Persian	لیلیوم لانکیفلیوم
Finnish	tiikerililja
Japanese	オニユリ
Korean	참나리
Malayalam	ടൈഗർ ലില്ലി
Norwegian Nynorsk	tigerlilje
Polish	lilia tygrysia
Russian	Лилия ланцетолистная
Russian	lilium tigrinum
Russian	Лилия тигровая
Swedish	tigerlilja
Vietnamese	hoa loa kèn vằn
Chinese	百合
Chinese	百合子
Chinese	百合花
Chinese	卷丹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

diploid form: A or C. Common triploid does not form seed. Bulbils will transmit virus if parent plant infected

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Manchuria
  - Qinghai
  - Tibet
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Amur
  - Kuril Islands
  - Primorye
  - Sakhalin

Europe click to expand
- Eastern Europe
  - East European Russia
  - South European Russia
- Middle Europe
  - Austria
- Southeastern Europe
  - Bulgaria

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Montana
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - District Of Columbia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000677845
UNII	079XQO23D9
Flora of Alabama	4481
Canadensys	6531
USDA Plants	LILA8
Tropicos	18400283
INPN	105986
KEW	urn:lsid:ipni.org:names:537628-1
The Plant List	kew-279922
Open Tree Of Life	73799
Observations.org	131315
NCBI Taxonomy	79002
Nature Serve	2.154687
IPNI	537628-1
iNaturalist	49524
GBIF	2753380
Freebase	/m/0jqg4
WisFlora	9022
EPPO	LILLA
EOL	251460
Elurikkus	5487
USDA GRIN	104679
Wikipedia	Lilium_lancifolium
CMAUP	NPO4414

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

The traditional uses, pharmacology, and phytochemistry of Peucedanum praeruptorum Dunn

Wang Q, Sun Q, Huang Q, Qin L, Zhu B

Front Pharmacol

03-Apr-2024

PMCID:	PMC11021687
doi:	10.3389/fphar.2024.1352657
PMID:	38633612

The impact of thermal pretreatment on phytochemical profiles and bioactivity of freeze-dried lily bulbs (Lilium lancifolium)

Cai Y, Quan H, Liu Y, Han X, Lu Y, Lan X, Guo X

Food Chem X

15-Mar-2024

PMCID:	PMC10966175
doi:	10.1016/j.fochx.2024.101284
PMID:	38544934

Comparative Pharmacokinetics Research of 13 Bioactive Components of Jieyu Pills in Control and Attention Deficit Hyperactivity Disorder Model Rats Based on UPLC-Orbitrap Fusion MS

Liu X, Wan Y, Sun S, Wang T, Li T, Sun Q, Zhang W, Zhao D, Tian Y, Feng S

Molecules

10-Mar-2024

PMCID:	PMC10976160
doi:	10.3390/molecules29061230
PMID:	38542867

A review of the pharmacological action and mechanism of natural plant polysaccharides in depression

Yang YH, Li CX, Zhang RB, Shen Y, Xu XJ, Yu QM

Front Pharmacol

08-Feb-2024

PMCID:	PMC10883385
doi:	10.3389/fphar.2024.1348019
PMID:	38389919

Endophytic fungi of Tradescantia pallida mediated targeting of Multi-Drug resistant human pathogens

Dhevi V. Sundar R, Arunachalam S

Saudi J Biol Sci

20-Jan-2024

PMCID:	PMC10863426
doi:	10.1016/j.sjbs.2024.103937
PMID:	38352729

Two independent LAMP assays for rapid identification of the serpentine leafminer, Liriomyza huidobrensis (Blanchard, 1926) (Diptera: Agromyzidae) in Australia

Zhu X, Gopurenko D, Holloway JC, Duff JD, Malipatil MB

Sci Rep

15-Dec-2023

PMCID:	PMC10721864
doi:	10.1038/s41598-023-49472-9
PMID:	38097660

Heterologous Production in the Synechocystis Chassis Suggests the Biosynthetic Pathway of Astaxanthin in Cyanobacteria

Liang H, Chen H, Liu X, Wang Z, Li P, Lu S

Antioxidants (Basel)

03-Oct-2023

PMCID:	PMC10604110
doi:	10.3390/antiox12101826
PMID:	37891905

Full-length transcriptome analysis revealed that 2,4-dichlorophenoxyacetic acid promoted in vitro bulblet initiation in lily by affecting carbohydrate metabolism and auxin signaling

Gao C, Zhang L, Xu Y, Liu Y, Xiao X, Cui L, Xia Y, Wu Y, Ren Z

Front Plant Sci

20-Sep-2023

PMCID:	PMC10548195
doi:	10.3389/fpls.2023.1236315
PMID:	37799550

Characterization and Functional Analysis of Chalcone Synthase Genes in Highbush Blueberry (Vaccinium corymbosum)

Zhang Z, Qu P, Hao S, Li R, Zhang Y, Zhao Q, Wen P, Cheng C

Int J Mol Sci

09-Sep-2023

PMCID:	PMC10530253
doi:	10.3390/ijms241813882
PMID:	37762185

mRNA-Seq and miRNA-Seq Analyses Provide Insights into the Mechanism of Pinellia ternata Bulbil Initiation Induced by Phytohormones

Xu W, Fan H, Pei X, Hua X, Xu T, He Q

Genes (Basel)

29-Aug-2023

PMCID:	PMC10531394
doi:	10.3390/genes14091727
PMID:	37761867

Current Studies on Bakanae Disease in Rice: Host Range, Molecular Identification, and Disease Management

An YN, Murugesan C, Choi H, Kim KD, Chun SC

Mycobiology

21-Aug-2023

PMCID:	PMC10498795
doi:	10.1080/12298093.2023.2241247
PMID:	37711983

Neuroendocrine Biomarkers of Herbal Medicine for Major Depressive Disorder: A Systematic Review and Meta-Analysis

Seung HB, Kwon HJ, Kwon CY, Kim SH

Pharmaceuticals (Basel)

18-Aug-2023

PMCID:	PMC10458856
doi:	10.3390/ph16081176
PMID:	37631092

Integrative traditional Chinese medicine treatment for children with obstructive sleep apnea

Lai WY, Wei CC, Lin CH, Hang LW, Shih YH, Huang FW, Yen HR

J Tradit Complement Med

07-Aug-2023

PMCID:	PMC10785241
doi:	10.1016/j.jtcme.2023.08.002
PMID:	38223810

A Systematic Review on the Continuous Cropping Obstacles and Control Strategies in Medicinal Plants

Zeeshan Ul Haq M, Yu J, Yao G, Yang H, Iqbal HA, Tahir H, Cui H, Liu Y, Wu Y

Int J Mol Sci

05-Aug-2023

PMCID:	PMC10419402
doi:	10.3390/ijms241512470
PMID:	37569843

Integrated metagenomics and metabolomics analysis reveals changes in the microbiome and metabolites in the rhizosphere soil of Fritillaria unibracteata

Liu C, Yu J, Ying J, Zhang K, Hu Z, Liu Z, Chen S

Front Plant Sci

04-Aug-2023

PMCID:	PMC10436506
doi:	10.3389/fpls.2023.1223720
PMID:	37600181

Phytochemical Profile Top

Add a new one!

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 COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	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 C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
2,4-Dihydroxy-3-(3-methyl-2-butenyl)-6-methylbenzoic acid methyl ester	11161026	Click to see CC1=CC(=C(C(=C1C(=O)OC)O)CC=C(C)C)O	250.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
(2R)-2,3-Dihydropropyl beta-D-glucopyranoside	15559912	Click to see C(C1C(C(C(C(O1)OCC(CO)O)O)O)O)O	254.23	unknown	https://doi.org/10.1016/0031-9422(82)80087-3
2-(2,3-Dihydroxypropoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	4302177	Click to see C(C1C(C(C(C(O1)OCC(CO)O)O)O)O)O	254.23	unknown	https://doi.org/10.1016/0031-9422(82)80087-3
> 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
[(2S)-2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] 3-(4-hydroxyphenyl)prop-2-enoate	6711430	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 C1=CC(=CC=C1C=CC(=O)OCC(COC2C(C(C(C(O2)CO)O)O)O)O)O	400.40	unknown	via CMAUP database
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	via CMAUP database
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	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3-Methoxy-5-methyl-2-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]phenol	5373218	Click to see CC1=CC(=C(C(=C1)OC)CC=C(C)CCC=C(C)CCC=C(C)C)O	342.50	unknown	via CMAUP database
4-O-Methylgrifolic acid	11531145	Click to see CC1=CC(=C(C(=C1C(=O)O)O)CC=C(C)CCC=C(C)CCC=C(C)C)OC	386.50	unknown	via CMAUP database
Grifolic acid	9976563	Click to see CC1=CC(=C(C(=C1C(=O)O)O)CC=C(C)CCC=C(C)CCC=C(C)C)O	372.50	unknown	via CMAUP database
Grifolin	5372312	Click to see CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O	328.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S,3R,6R)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol	45109816	Click to see CC1=C(C(CC(C1)O)(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	584.90	unknown	via CMAUP database
(2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one	25243952	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	via CMAUP database
(2E,4E,6E,8Z,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one	23258405	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1002/HLCA.19850680627
(2E,4Z,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one	23258403	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1002/HLCA.19850680627
13-cis-Capsanthin	23258406	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1002/HLCA.19850680627
3,3'-Dihydroxy-beta,kappa-caroten-6'-one	4481061	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1002/HLCA.19850680627
6-epi-Karpoxanthin	23258402	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	602.90	unknown	https://doi.org/10.1002/HLCA.19850680627
6-Epikarpoxanthin	131751644	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	602.90	unknown	https://doi.org/10.1007/BF02467511
9-cis-Capsanthin	23258404	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1002/HLCA.19850680627
Capsanthin	5281228	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	584.90	unknown	https://doi.org/10.1007/BF02467511 https://doi.org/10.1002/HLCA.19850680627
Capsanthin 5,6-epoxide	11039295	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC(=O)C3(CC(CC3(C)C)O)C	600.90	unknown	https://doi.org/10.1007/BF02467511
Karpoxanthin	23258401	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	602.90	unknown	https://doi.org/10.1002/HLCA.19850680627
Liliaxanthin	134724340	Click to see CC1=C(C(CC(C1O)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C	600.90	unknown	https://doi.org/10.1002/HLCA.19850680627
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Androstenedione	6128	Click to see CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4=O)C	286.40	unknown	via CMAUP database
Testosterone	6013	Click to see CC12CCC3C(C1CCC2O)CCC4=CC(=O)CCC34C	288.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(25S)-5alpha-cholestan-3beta,6beta,15alpha,16beta,26-pentol	52931335	Click to see CC(CCCC(C)C1C(C(C2C1(CCC3C2CC(C4C3(CCC(C4)O)C)O)C)O)O)CO	452.70	unknown	https://doi.org/10.1002/HLCA.19850680627
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Capsicastrine	21575044	Click to see CC1CCC(NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C)O	577.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5S,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(5'R,9S,13R,16S)-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,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	24893696	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	855.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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	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 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
3-[(1S,4S,6S,9R,10R,13R,14R)-4-hydroxy-6-[(2R,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-9,13-dimethyl-17-oxo-14-tetracyclo[11.3.1.01,10.04,9]heptadecanyl]-2H-furan-5-one	163007798	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC4(C5=O)CCC3(C2)O)C6=CC(=O)OC6)C)C)OC)O	532.70	unknown	https://doi.org/10.1002/HLCA.19850680627
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
Methyl alpha-D-mannopyranoside	101798	Click to see COC1C(C(C(C(O1)CO)O)O)O	194.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
1-[(2R,5R)-2-benzyl-5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]piperazin-1-yl]ethanone	162978355	Click to see CC(=O)N1CC(NCC1CC2=CC=CC=C2)CC3=CC4=C(C(=C3)OC)OCO4	382.50	unknown	https://doi.org/10.1002/HLCA.19850680627
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	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 C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin	73160	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
(+)-Epicatechin	182232	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	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)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
7-Epi-Zeaenol	53355130	Click to see CC1CC=CC(C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O)O	364.40	unknown	via CMAUP database
Cochliomycin A, (rel)-	52952745	Click to see CC1CC=CC2C(C(CC=CC3=C(C(=CC(=C3)OC)O)C(=O)O1)O)OC(O2)(C)C	404.50	unknown	via CMAUP database
Cochliomycin B	52952746	Click to see CC1CC=CC(C2C(CC=CC3=C(C(=CC(=C3)OC)O)C(=O)O1)OC(O2)(C)C)O	404.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues / Zearalenones
5E-7-oxozeaenol	9799061	Click to see CC1CC=CC(=O)C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O	362.40	unknown	via CMAUP database
5Z-7-Oxozeaenol	9863776	Click to see CC1CC=CC(=O)C(C(CC=CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O)O	362.40	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Lilium lancifolium

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top