Lilium lancifolium

Details Top

Internal ID UUID64401b4bb13f5896365000
Scientific name Lilium lancifolium
Authority Thunb.
First published in Trans. Linn. Soc. London 2: 333 (1794)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Fresh cut stems and blossoms of Lilium lancifolium are a major ornamental commodity in floristry; typical commercial stems reach 45–80 cm and are graded by length and bud development.
- Dried lily bulbs, sold under names such as “bai he” in Chinese commerce, are used fresh, boiled, sliced, or ground as a culinary ingredient in East Asian dishes and processed products like lily‑bulb cake.

Food and beverages (non‑medicinal):
- Edible bulbs are used fresh, blanched or stir‑fried in soups (e.g., lily‑bulb pork soup), stews, noodles and vegetable hot pot; they are also a component of congee with lotus seeds.
- Processed forms include rehydrated dried bulbs and milled bulb flour, which acts as a thickening agent for sauces and batters due to its high starch content.

Fragrance and cosmetics:
- Essential oil obtained by steam distillation of fresh Lilium lancifolium flowers contains β‑ocimene, linalool, benzyl alcohol and phenylacetaldehyde, providing a sweet floral note used in fine fragrance blends and low‑dose aromatic compounds in cosmetics.

Properties relevant to use:
- Cut stems show high water uptake and a waxy cuticle, extending vase life to several days under standard preservative conditions.
- Bulbs contain ~25 % amylose (amylose : amylopectin ≈ 25 : 75) and soluble starch, enabling rapid gelatinisation for flour or sauce thickening.
- The oil’s monoterpene and phenylpropanoid profile yields the characteristic sweet‑floral scent exploited in perfumery.
- Lilium lancifolium has a diploid chromosome complement of 2n = 24 with unusually large chromosomes, a trait used in cytogenetic and meiotic studies.

Standards and regulation:
- Commercial cut lilies must meet USDA National Floriculture Grade Standards, which specify stem length categories, bud stage and post‑harvest handling; many exporters follow IFHP guidelines.
- Lily bulbs for food use must comply with national food‑safety regulations (e.g., U.S. FDA Food Code, Chinese Food Safety Law) and may require HACCP‑based processing controls.

Sustainability and sourcing:
- Production is centered in East Asian regions such as China’s Yunnan and Guizhou provinces and Japan’s Hokkaido; bulbs are harvested biennially to allow regeneration and limit soil depletion.
- In temperate zones the species can naturalise and spread, prompting management plans where it is listed as invasive (e.g., certain U.S. states) and encouraging sustainable practices such as crop rotation and soil‑health monitoring.

Synonyms Top

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
Lilium lancifolium var. densum W.Bull Proc. Roy. Hort. Soc. London 4: 176 (1864)
Lilium tigrinum var. erectum G.F.Wilson Gard. Chron. , n.s., 2: 83 (1874)
Lilium lancifolium unranked melpomene Hovey Nursery Cat. (Hovey & co.) 1882: 38 (1882)
Lilium lancifolium unranked album Hovey Nursery Cat. (Hovey & co.) 1882: 38 (1882)

Common names Top

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Language Common/alternative name
English tiger lily
Afrikaans tierlelie
Arabic زنبق النمر
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 lilium tigrinum
Russian Лилия тигровая
Russian Лилия ланцетолистная
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

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) 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.
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
    • 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
    • Eastern Europe
      • East European Russia
      • South European Russia
    • Middle Europe
      • Austria
    • Southeastern Europe
      • Bulgaria
  • Northern America
    • 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

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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
Plantarium 22755

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
Zinc Finger-Homeodomain Transcriptional Factors (ZHDs) in Cucumber (Cucumis sativus L.): Identification, Evolution, Expression Profiles, and Function under Abiotic Stresses Gao Y, Zhu L, An M, Wang Y, Li S, Dong Y, Yang S, Shi K, Fan S, Chen X, Ren H, Liu X Int J Mol Sci 17-Apr-2024
PMCID:PMC11050092
doi:10.3390/ijms25084408
PMID:38673993
Bulbil initiation: a comprehensive review on resources, development, and utilisation, with emphasis on molecular mechanisms, advanced technologies, and future prospects Shu F, Wang D, Sarsaiya S, Jin L, Liu K, Zhao M, Wang X, Yao Z, Chen G, Chen J Front Plant Sci 08-Apr-2024
PMCID:PMC11033377
doi:10.3389/fpls.2024.1343222
PMID:38650701
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
Key anti-freeze genes and pathways of Lanzhou lily (Lilium davidii, var. unicolor) during the seedling stage Tian X, Li J, Chen S PLoS One 21-Mar-2024
PMCID:PMC10956819
doi:10.1371/journal.pone.0299259
PMID:38512835
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
Auxin regulates bulbil initiation by mediating sucrose metabolism in Lilium lancifolium Xin Y, Chen X, Liang J, Wang S, Pan W, Wu J, Zhang M, Zaccai M, Yu X, Zhang X, Wu J, Du Y Hortic Res 23-Feb-2024
PMCID:PMC11069426
doi:10.1093/hr/uhae054
PMID:38706581
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
Research progress on classical traditional Chinese medicine formula Baihe Zhimu (Lilium lancifolium bulb and Anemarrhena asphodeloides rhizome) decoction in the treatment of depression Pan W, Shi H, Zang Z, Meng Q, Cheng Y, Liang L, Zhai Y, Yin G, Sun L, Ma K Heliyon 03-Feb-2024
PMCID:PMC10862512
doi:10.1016/j.heliyon.2024.e25171
PMID:38352746
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
Aphid Resistance Evaluation and Constitutive Resistance Analysis of Eighteen Lilies Shi H, Zhong J, Liang Y, Zhang P, Guo L, Wang C, Tang Y, Lu Y, Sun M Insects 08-Dec-2023
PMCID:PMC10743574
doi:10.3390/insects14120936
PMID:38132609
Unveiling the neuroprotective potential of dietary polysaccharides: a systematic review Guo R, Pang J, Zhao J, Xiao X, Li J, Li J, Wang W, Zhou S, Zhao Y, Zhang Z, Chen H, Yuan T, Wu S, Liu Z Front Nutr 22-Nov-2023
PMCID:PMC10702503
doi:10.3389/fnut.2023.1299117
PMID:38075226
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Retracted: EST–SSR Marker Development and Full-Length Transcriptome Sequence Analysis of Tiger Lily (Lilium lancifolium Thunb) and Biomechanics AB Appl Bionics Biomech 01-Nov-2023
PMCID:PMC10632043
doi:10.1155/2023/9823780
PMID:37946833

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
> 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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 2,4-dihydroxy-6-methyl-3-(3-methylbut-2-enyl)benzoate 11161026 Click to see 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 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 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 via CMAUP database
Regaloside C 14135348 Click to see 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 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 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
(3S,3'R,5R,6S)-beta,beta-Carotene-3,3',5,6(5H,6H)-tetrol 23258402 Click to see 602.90 unknown https://doi.org/10.1002/HLCA.19850680627
13-cis-Capsanthin 23258406 Click to see 584.90 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 584.90 unknown https://doi.org/10.1002/HLCA.19850680627
Capsanthin 5281228 Click to see 584.90 unknown https://doi.org/10.1002/HLCA.19850680627
https://doi.org/10.1007/BF02467511
Capsanthin (Paprika Extract) 4481061 Click to see 584.90 unknown https://doi.org/10.1002/HLCA.19850680627
Capsanthin 5,6-epoxide 11039295 Click to see 600.90 unknown https://doi.org/10.1007/BF02467511
Karpoxanthin 23258401 Click to see 602.90 unknown https://doi.org/10.1002/HLCA.19850680627
Liliaxanthin 134724340 Click to see 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 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 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 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 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 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 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
> 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 404.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues / Zearalenones
(5E)-7-Oxozeaenol 9799061 Click to see 362.40 unknown via CMAUP database
(5Z)-7-Oxozeaenol 9863776 Click to see 362.40 unknown via CMAUP database

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