Lactuca indica - Unknown
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Internal ID UUID643fca8917f3a574031677
Scientific name Lactuca indica
Authority L.
First published in Mant. Pl. : 278 (1771)

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Synonyms Top

Scientific name Authority First published in
Microrhynchus patens DC. Prodr. 7(1): 181 (1838)
Sonchus calyculatus Roxb. ex DC. Prodr. 7(1): 140 (1838)
Lactuca brevirostris var. foliis laciniatis Hemsl. Journal of the Linnean Society, Botany 23: "23, 480" 1888
Prenanthes racemosa Roxb. Fl. Ind. 3: 405 (1832)
Prenanthes patens Wall. Numer. List : n.° 3258 (1831)
Chondrilla sonchifolia Poir. Encycl. , Suppl. 2: 330 (1811)
Lactuca squarrosa (Thunb.) Miq. 189 1866
Lactuca amurensis Regel & Maxim. Index Seminum (LE, Petropolitanus) (1857) 42
Prenanthes indica J.G.Klein ex Poir. Encycl. , Suppl. 2: 330 (1811)
Brachyramphus heyneanus Wight Icon. Pl. Ind. Orient. t. 1146
Lactuca brevirostris Champ. Hook., J. Bot. Kew Miscel. 4 (1852) 237 1852
Lactuca kouyangensis H.Lév. Repert. Spec. Nov. Regni Veg. 8: 450 (1910)
Prenanthes squarrosa Thunb. Syst. Veg. ed. 14 : 715 (1784)
Pterocypsela laciniata (Houtt.) C.Shih Acta Phytotax. Sin. 26(5): 388 (1988): (1988)
Lactuca squarrosa f. runcinata Maxim. Bulletin de l'Academie Imperiale des Sciences de St-Petersbourg 19: 526 1874
Brachyramphus sonchifolius Thwaites Enum. Pl. Zeyl. : 168 (1860)
Lactuca indica var. foliislaciniatis (Hemsl.) Y.Ling Y. Ling in Contr. Inst. Bot. Natl. Acad. Peiping 3. 1935 187 1935
Lactuca amurensis Regel E.A. von Regel, Index Sem. Hort. Petrop.. 1857 42 1857
Lactuca indica var. foliisindivisis (Hemsl.) Y.Ling Y. Ling in Contr. Inst. Bot. Natl. Acad. Peiping 3. 1935 187 1935
Lactuca brevirostris var. foliis indivisis Hemsl. Journal of the Linnean Society, Botany 23: 480 1888
Lactuca cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 8: 450 (1910)
Lactuca squarrosa var. dentata Komar. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 25: 779 1907
Lactuca dracoglossa Makino J. Jap. Bot. vii. 23 (1931).
Brachyramphus sinicus Miq. Journ. Bot. Neerl. 1: 105. 1861
Pterocypsela indivisa (Makino) H.S.Pak Fl. Coreana 7: 349 (1999) (1999)
Lactuca squarrosa (Thunb.) Maxim. Annales Museum Botanicum Lugduno-Batavi 2: 189 1865
Scariola brevirostris (Fenzl) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1962: 46 (1962) (1962)
Lactuca indica var. ldracoglossa (Makino) Kitam.
Chondrilla indica Steud. Nomencl. Bot. : 191 (1821)
Chondrilla squarrosa Poir. Encycl. , Suppl. 2: 332 (1811)
Ammoseris patens D.Dietr. Syn. Pl. iv. 1319
Brachyramphus taraxacoides DC. Prodr. 7(1): 177 (1838)
Pterocypsela indica var. laciniata (Houtt.) H.C.Fu Fl. Intramongolica, ed. 2 4: 821 (1993):.
Lactuca indica var. macrothyrsa Miq. Fl. Ned. Ind. 2 (1856) 109 1856
Lactuca indica var. subintegerrima Miq. Fl. Ned. Ind. 2 (1856) 110 1856
Lactuca squarrosa var. runcinato-pinnatifida Kom. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 25: 779 1907
Lactuca indica var. dentata (Komar.) Chu 438 1959
Lactuca indica var. laciniata Hara Enum. Sperm. Jap. 2 (1952) 220 1952
Lactuca squarrosa var. integrifolia Kom. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 25: 779 1907
Lactuca indica f. indivisa (Maxim.) Hara Enumeratio Spermatophytarum Japonicarum 2: 220 1952
Chondrilla racemosa (Michx.) Poir. Encycl. , Suppl. 2: 331 (1811)
Lactuca indica f. runcinata (Maxim.) Kitam. Memoirs of the College of Science, Kyoto Imperial University. Series B. Biology 23: 137 1956
Prenanthes laciniata Houtt. Handl. Pl.-Kruidk. x. 381
Lactuca mauritiana Poir. Encycl. , Suppl. 3: 292 (1813)
Prenanthes taraxacoides Wall. Numer. List : n.° 3279 (1831)
Lactuca brevirostris Champ. ex Benth. Hooker's J. Bot. Kew Gard. Misc. 4: 237. (1852)
Lactuca indica var. foliis Ling Contributions from the Institute of Botany, National Academy of Peiping 3: 187 1935
Pterocypsela indica (L.) C.Shih Acta Phytotax. Sin. 26(5): 387 (1988): (1988)
Lactuca bialata Griff. Not. Pl. Asiat. 4: 247 (1854)
Lactuca jamaicensis Griseb. Fl. Brit. W. I. : 384 (1861)
Lactuca squarrosa f. indivisa Maxim. Bulletin de l'Academie Imperiale des Sciences de St-Petersbourg 19: 526 1874

Common names Top

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Language Common/alternative name
English indian lettuce
Bulgarian индийска маруля
Czech locika indická
Indonesian sijukkot
Japanese ホソバアキノノゲシ
Japanese アキノノゲシ
Korean 왕고들빼기
Vietnamese bồ công anh ta
Vietnamese bồ công anh việt nam
Vietnamese diếp dại
Vietnamese diếp hoang
Vietnamese bồ công anh
Chinese 野莴苣
Chinese 鵝仔草
Chinese 苦莴苣
Chinese 翅果菊
Chinese 滇羌活
Chinese 山莴苣
Chinese 多裂翅果菊

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Kwazulu-Natal
    • West-central Tropical Africa
      • Central African Republic
    • Western Indian Ocean
      • Comoros
      • Madagascar
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Chita
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000039155
USDA Plants LAIN13
Tropicos 2704298
KEW urn:lsid:ipni.org:names:228047-1
The Plant List gcc-13786
Plantarium 21819
PFAF Lactuca indica
Open Tree Of Life 678386
Observations.org 129126
NCBI Taxonomy 75953
IPNI 228047-1
iNaturalist 69996
GBIF 3140510
Freebase /m/0nbcn_v
EPPO LACIN
EOL 590834
USDA GRIN 21341
Wikipedia Lactuca_indica
CMAUP NPO23670

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
Plant phenolics inhibit focal adhesion kinase and suppress host cell invasion by uropathogenic Escherichia coli Lewis AJ, Richards AC, Mendez AA, Dhakal BK, Jones TA, Sundsbak JL, Eto DS, Rousek AA, Mulvey MA Infect Immun 27-Mar-2024
PMCID:PMC11075462
doi:10.1128/iai.00080-24
PMID:38534100
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
An overview of anti-Hepatitis B virus flavonoids and their mechanisms of action Naderi M, Salavatiha Z, Gogoi U, Mohebbi A Front Cell Infect Microbiol 29-Feb-2024
PMCID:PMC10937540
doi:10.3389/fcimb.2024.1356003
PMID:38487354
Editorial: Plant bioactives: challenges of extraction and processing Rakha A, Shehzad A, Khan K Front Nutr 15-Jan-2024
PMCID:PMC10826700
doi:10.3389/fnut.2024.1357925
PMID:38292247
Impact of cellulose and lignin on restoration of vegetation and soil chemical properties for saline-alkali soil of songnen plain Fu F, Luo J, Zhao L, Yang F, Wang N PLoS One 02-Jan-2024
PMCID:PMC10760773
doi:10.1371/journal.pone.0296366
PMID:38165910
Chemical profile and quantitative comparison of constituents in different medicinal parts of Lactuca indica during varied harvest periods using UPLC-MS/MS method Hao J, Na R, Sun L, Jia Y, Han F, Fu Z, Wang Z, Zhao M, Gao C, Ge G Food Chem X 28-Nov-2023
PMCID:PMC10740015
doi:10.1016/j.fochx.2023.101031
PMID:38144840
Plant Phenolics Inhibit Focal Adhesion Kinase and Suppress Host Cell Invasion by Uropathogenic Escherichia coli Lewis AJ, Richards AC, Mendez AA, Dhakal BK, Jones TA, Sundsbak JL, Eto DS, Mulvey MA bioRxiv 23-Nov-2023
PMCID:PMC10690256
doi:10.1101/2023.11.23.568486
PMID:38045282
Metabolic profiling provides insights into the accumulation patterns of flavonoids and phenolic acids in different parts of Lactuca indica L. Hao J, Ge G, Jia Y, Han F, Zhao M, Wang Z Food Chem X 22-Nov-2023
PMCID:PMC10739775
doi:10.1016/j.fochx.2023.101012
PMID:38144821
Testing biological actions of medicinal plants from northern Vietnam on zebrafish embryos and larvae: Developmental, behavioral, and putative therapeutical effects Tran MH, Nguyen TV, Do HG, Kieu TK, Nguyen TK, Le HD, Guerrero-Limon G, Massoz L, Nivelle R, Zappia J, Pham HT, Nguyen LT, Muller M PLoS One 07-Nov-2023
PMCID:PMC10629648
doi:10.1371/journal.pone.0294048
PMID:37934745
Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E PeerJ 07-Nov-2023
PMCID:PMC10637247
doi:10.7717/peerj.16231
PMID:37953791
Dietary supplementation of Polygonum chinense improves the immunity of Asian seabass, Lates calcarifer (Bloch, 1790) against Vibrio harveyi infection Rashidah AR, Shariff M, Yusoff FM, Ismail IS Fish Shellfish Immunol Rep 01-Oct-2023
PMCID:PMC10563064
doi:10.1016/j.fsirep.2023.100118
PMID:37822351
Evaluation of the Weeds around Capsicum annuum (CA) Cultivation Fields as Potential Habitats of CA-Infecting Viruses Choi MK Plant Pathol J 01-Aug-2023
PMCID:PMC10412962
doi:10.5423/PPJ.OA.04.2023.0066
PMID:37550983
Urinary Tract Infections Caused by Uropathogenic Escherichia coli: Mechanisms of Infection and Treatment Options Zhou Y, Zhou Z, Zheng L, Gong Z, Li Y, Jin Y, Huang Y, Chi M Int J Mol Sci 23-Jun-2023
PMCID:PMC10341809
doi:10.3390/ijms241310537
PMID:37445714
Optimization of ultrasonic-assisted extraction of flavonoids from Lactuca indica L. cv. Mengzao and their antioxidant properties Hao J, Wang Z, Jia Y, Sun L, Fu Z, Zhao M, Li Y, Yuan N, Cong B, Zhao L, Ge G Front Nutr 15-Jun-2023
PMCID:PMC10308084
doi:10.3389/fnut.2023.1065662
PMID:37396124

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Monohexyl Phthalate 90532 Click to see CCCCCCOC(=O)C1=CC=CC=C1C(=O)O 250.29 unknown https://doi.org/10.1248/CPB.59.767
> 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 https://doi.org/10.1021/JF0259415
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1021/JF0259415
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5R,6R)-2-[[(1S,3R,3aS,4S,6S,6aS)-3-hydroxy-1,4-bis(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162973135 Click to see COC1=C(C=CC(=C1)C2C3C(C(OC3O)C4=CC(=C(C=C4)O)OC)C(O2)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown https://doi.org/10.1021/NP0205349
(2S,3R,4S,5S,6R)-2-[[(1S,3R,3aS,4S,6S,6aS)-3-hydroxy-1,4-bis(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 6918761 Click to see COC1=C(C=CC(=C1)C2C3C(C(OC3O)C4=CC(=C(C=C4)O)OC)C(O2)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown https://doi.org/10.1021/NP0205349
2-[[3-Hydroxy-1,4-bis(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75072157 Click to see COC1=C(C=CC(=C1)C2C3C(C(OC3O)C4=CC(=C(C=C4)O)OC)C(O2)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown https://doi.org/10.1021/NP0205349
CID 11103620 11103620 Click to see COC1=C(C=CC(=C1)C2C3C(C(OC3O)C4=CC(=C(C=C4)O)OC)C(O2)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown via CMAUP database
Lactucaside 44566763 Click to see COC1=C(C=CC(=C1)C2C3C(C(OC3O)C4=CC(=C(C=C4)O)OC)C(O2)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown https://doi.org/10.1021/NP0205349
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(1R,3aR,5bR,7aR,9S,11aR,11bR,13aS,13bR)-3a,5b,8,8,11a,13a-hexamethyl-1-propan-2-yl-1,2,3,4,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-yl] acetate 53248450 Click to see CC(C)C1CCC2(C1C3(CCC4C5(CCC(C(C5CCC4(C3=CC2)C)(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aS,9R,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-sulfooxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 162944333 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OS(=O)(=O)O)C)C(=C)C)O)O)O)CO)O)O)O 1007.20 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 12358398 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
(3S,6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol 11611623 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown via CMAUP database
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
https://doi.org/10.1248/CPB.59.767
[(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 51398128 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
alpha-Amyrin acetate 293754 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Bauerenyl acetate 177801 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)OC(=O)C)(C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
beta-Amyrine 15942855 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
CID 5256173 5256173 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)OC(=O)C)(C)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Germanicol acetate 14167342 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97171-1
https://doi.org/10.1248/CPB.59.767
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
https://doi.org/10.1016/S0031-9422(00)97171-1
Taraxerol, acetate 345509 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 468.80 unknown https://doi.org/10.1248/CPB.59.767
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S)-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2S)-2-hydroxy-2-methylbutanoate 9961644 Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)O)O)O 693.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[4-[[9-[[2-(4-hydroxyphenyl)acetyl]oxymethyl]-6-methyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl]oxy]-3,6-dimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[8,7-b]furan-9-yl]methyl 2-(4-hydroxyphenyl)acetate 78422618 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)COC(=O)CC4=CC=C(C=C4)O)C)OC5CC(=C6C(C7C5C(=C)C(=O)O7)C(=CC6=O)COC(=O)CC8=CC=C(C=C8)O)C 804.80 unknown https://doi.org/10.1021/NP0205349
Lactucain C 6918760 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)COC(=O)CC4=CC=C(C=C4)O)C)OC5CC(=C6C(C7C5C(=C)C(=O)O7)C(=CC6=O)COC(=O)CC8=CC=C(C=C8)O)C 804.80 unknown https://doi.org/10.1021/NP0205349
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5R)-3-[(E)-4-(3,4-dihydroxyphenyl)-2-oxobut-3-enyl]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 102477377 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)CC(=O)C=CC2=CC(=C(C=C2)O)O 352.30 unknown https://doi.org/10.1021/NP0205349
(1R,3S,4S,5R)-3-[4-(3,4-dihydroxyphenyl)-2-oxobut-3-enyl]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 162880487 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)CC(=O)C=CC2=CC(=C(C=C2)O)O 352.30 unknown https://doi.org/10.1021/NP0205349
1,3,4-Trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 53420248 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 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 https://doi.org/10.1016/J.BMCL.2007.10.046
3,4-Di-O-Caffeoylquinic acid 3802778 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
3,5-Dicaffeoyl-epi-quinic acid 60150332 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
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 https://doi.org/10.1021/NP0205349
https://doi.org/10.1016/J.BMCL.2007.10.046
Chlorogensaure 12310830 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
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1021/JF0259415
Neochlorogenic acid 5280633 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 https://doi.org/10.1016/J.BMCL.2007.10.046
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,3aS,4R,9aR,9bS)-4-hydroxy-3,6-dimethyl-9-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 133562318 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)COC4C(C(C(C(O4)CO)O)O)O)C)O 440.40 unknown https://doi.org/10.1021/NP0205349
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,5S,5'S,6S,9R)-5'-(furan-3-yl)-4-methylidenespiro[10-oxatricyclo[7.2.1.01,6]dodecane-5,3'-oxolane]-2',11-dione 90662094 Click to see C=C1CCC23CC(CCC2C14CC(OC4=O)C5=COC=C5)OC3=O 328.40 unknown via CMAUP database
(3S,3aR,4S,9aR,9bR)-4-hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 149506489 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)CO)C)O 278.30 unknown https://doi.org/10.1021/NP0205349
4-Hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 14138137 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)CO)C)O 278.30 unknown https://doi.org/10.1021/NP0205349
6,9-dimethyl-3-methylidene-4-[(3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl)oxy]-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2,7-dione 85306611 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC4CC(=C5C(C6C4C(=C)C(=O)O6)C(=CC5=O)C)C 504.60 unknown https://doi.org/10.1021/NP0205349
9-(hydroxymethyl)-4-[[9-(hydroxymethyl)-3,6-dimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl]oxy]-6-methyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2,7-dione 85359944 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)CO)C)OC4CC(=C5C(C6C4C(=C)C(=O)O6)C(=CC5=O)CO)C 536.60 unknown https://doi.org/10.1021/NP0205349
Lactucain A 10896414 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC4CC(=C5C(C6C4C(=C)C(=O)O6)C(=CC5=O)C)C 504.60 unknown https://doi.org/10.1021/NP0205349
Lactucain B 10995096 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)CO)C)OC4CC(=C5C(C6C4C(=C)C(=O)O6)C(=CC5=O)CO)C 536.60 unknown https://doi.org/10.1021/NP0205349
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP0205349
Apigenin-7-olate 25200950 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 269.23 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP0205349
Quercetin-7-olate 46906036 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1021/NP0205349
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 25202164 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1021/NP0205349
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(2-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 162892015 Click to see C1=CC=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
3,4,5-Trihydroxy-6-[5-hydroxy-2-(2-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 14188671 Click to see C1=CC=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1021/NP0205349
https://doi.org/10.1016/J.BMCL.2007.10.046
Luteolin-7-o-glucuronide 13607752 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1021/NP0205349
https://doi.org/10.1016/J.BMCL.2007.10.046
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 22635124 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
Quercetin 5-O-|A-D-glucopyranoside 52946987 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/JF0259415
https://doi.org/10.1021/NP0205349
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163046379 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)O)O)O)CO)O)O 464.40 unknown https://doi.org/10.1021/NP0205349
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 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 https://doi.org/10.1021/NP0205349
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP0205349
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[4,5,6-trihydroxy-3-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163046378 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)O)O)O)CO)O)O 464.40 unknown https://doi.org/10.1021/NP0205349
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2007.10.046
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP0205349
Quercetin 3-O-rhamnoside 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP0205349
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 https://doi.org/10.1021/NP0205349
https://doi.org/10.1016/J.BMCL.2007.10.046
Vitamin P 5293655 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 https://doi.org/10.1016/J.BMCL.2007.10.046
https://doi.org/10.1021/NP0205349
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0259415
https://doi.org/10.1021/NP0205349

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