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Lycopus lucidus

Lycopus lucidus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe1e1aecf8764260059
Scientific name Lycopus lucidus
Authority Turcz. ex Benth.
First published in Prodr. 12: 179 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phytosalpinx lucida Lunell Amer. Midl. Naturalist 5: 2 (1917)

Common names Top

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Language Common/alternative name
Japanese シロネ
Korean 쉽싸리
Russian Зюзник блестящий
Chinese 泽兰
Chinese 地瓜儿苗
Chinese 地笋
Chinese 地笋（地瓜儿苗）
Chinese 地筍
Chinese 地参
Chinese 提娄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Lycopus lucidus var. hirtus (Regel) Makino & Nemoto Fl. Japan , ed. 2: 1019 (1931)
Lycopus lucidus var. lucidus Unknown
Lycopus lucidus var. maackianus Maxim. ex Herder Bull. Soc. Imp. Naturalistes Moscou 61(I): 131 (1885)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Chita
      • Irkutsk
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000231418
UNII 2237I5787N
Canadensys 16987
Tropicos 17603010
Flora of Italy 10044
KEW urn:lsid:ipni.org:names:449660-1
The Plant List kew-115931
Open Tree Of Life 980292
Observations.org 132591
NCBI Taxonomy 516551
IPNI 449660-1
iNaturalist 577962
GBIF 5341460
Freebase /m/0_v697z
EPPO LYALU
USDA GRIN 423464
Wikipedia Lycopus_lucidus
CMAUP NPO21824

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
Phosphorylation: new star of pathogenesis and treatment in steatotic liver disease Lv T, Lou Y, Yan Q, Nie L, Cheng Z, Zhou X Lipids Health Dis 17-Feb-2024
PMCID:PMC10873984
doi:10.1186/s12944-024-02037-9
PMID:38368351
Traditional Chinese Medicine is Associated with the Reduction in Endpoint Events in Patients with Gouty Arthritis: Cohort Study and Association Rule Analysis Chen Y, Liu J, Cong C, Li Y, Hu Y Int J Gen Med 13-Feb-2024
PMCID:PMC10874188
doi:10.2147/IJGM.S451097
PMID:38371521
Preparation, Characterization, and Antioxidant Activities of Extracts from Amygdalus persica L. Flowers Yu Q, Li W, Liang M, Li G, Wu Z, Long J, Yuan C, Mei W, Xia X Molecules 29-Jan-2024
PMCID:PMC10856188
doi:10.3390/molecules29030633
PMID:38338377
Therapeutic Potential and Mechanisms of Rosmarinic Acid and the Extracts of Lamiaceae Plants for the Treatment of Fibrosis of Various Organs Boo YC Antioxidants (Basel) 24-Jan-2024
PMCID:PMC10886237
doi:10.3390/antiox13020146
PMID:38397744
Convergent application of traditional Chinese medicine and gut microbiota in ameliorate of cirrhosis: a data mining and Mendelian randomization study Zhou C, Wei J, Yu P, Yang J, Liu T, Jia R, Wang S, Sun P, Yang L, Xiao H Front Cell Infect Microbiol 06-Nov-2023
PMCID:PMC10657829
doi:10.3389/fcimb.2023.1273031
PMID:38029250
The complete chloroplast genome of Ocimum basilicum L. var. basilicum (Lamiaceae) and its phylogenetic analysis Kirankumar SI, Balaji R, Tanuja, Parani M Mitochondrial DNA B Resour 30-Oct-2023
PMCID:PMC10769543
doi:10.1080/23802359.2023.2275835
PMID:38188439
Prebiotics for depression: how does the gut microbiota play a role? Yang Y, Zhou B, Zhang S, Si L, Liu X, Li F Front Nutr 06-Jul-2023
PMCID:PMC10358272
doi:10.3389/fnut.2023.1206468
PMID:37485386
Dandelion (Taraxacum Genus): A Review of Chemical Constituents and Pharmacological Effects Fan M, Zhang X, Song H, Zhang Y Molecules 27-Jun-2023
PMCID:PMC10343869
doi:10.3390/molecules28135022
PMID:37446683
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Traditional Chinese medicine for heart failure with preserved ejection fraction: clinical evidence and potential mechanisms Fan Y, Yang Z, Wang L, Liu Y, Song Y, Liu Y, Wang X, Zhao Z, Mao J Front Pharmacol 10-May-2023
PMCID:PMC10206212
doi:10.3389/fphar.2023.1154167
PMID:37234711
Purification and identification of oligosaccharides from Cimicifuga heracleifolia Kom. rhizomes Cui L, Wu J, Wang X, Yang X, Ye Z, Mayo KH, Sun L, Zhou Y Food Chem X 06-May-2023
PMCID:PMC10196342
doi:10.1016/j.fochx.2023.100706
PMID:37215199
The potential of Chinese medicines in the treatment of hyperuricemia Tang J, Gao H, Xu Y, Chen J, Wu B Am J Transl Res 15-Apr-2023
PMCID:PMC10182497
PMID:37193181
Use of a Silkworm (Bombyx mori) Larvae By-Product for the Treatment of Atopic Dermatitis: Inhibition of NF-κB Nuclear Translocation and MAPK Signaling Fan M, Choi YJ, Wedamulla NE, Zhang Q, Kim SW, Bae SM, Seok YS, Kim EK Nutrients 05-Apr-2023
PMCID:PMC10097122
doi:10.3390/nu15071775
PMID:37049614
NLRP3 Inflammasome’s Activation in Acute and Chronic Brain Diseases—An Update on Pathogenetic Mechanisms and Therapeutic Perspectives with Respect to Other Inflammasomes Chiarini A, Gui L, Viviani C, Armato U, Dal Prà I Biomedicines 23-Mar-2023
PMCID:PMC10135565
doi:10.3390/biomedicines11040999
PMID:37189617
Modulation of the biological network of lumbar spinal stenosis by Tongdu Huoxue Decoction based on clinical metabolomics Ji L, Huang P, Wang Q, Li X, Li Y Front Mol Biosci 21-Mar-2023
PMCID:PMC10070985
doi:10.3389/fmolb.2023.1074500
PMID:37025656

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
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 44584035 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 278.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate 54675866 Click to see C1=CC(=C(C=C1C(=O)O)O)[O-] 153.11 unknown via CMAUP database
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 / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
(E)-3-[3-[[(Z)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethenyl]oxy]-4-hydroxyphenyl]propenoic acid 1-[(R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethyl] ester 10052949 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)OC(=CC3=CC(=C(C=C3)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown via CMAUP database
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methylpentadecane 15267 Click to see CCCCCCCCCCCCCC(C)C 226.44 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 14-methylpentadecanoate 21205 Click to see CC(C)CCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
Methyl arachidate 14259 Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC 326.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearate 3033836 Click to see CCCCCCCCCCCCCCCCCC(=O)[O-] 283.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol 6992244 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
(S)-1-Octen-3-ol 2724898 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl elaidolinolenate 5367462 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown via CMAUP database
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
Octadecadienoic acid, methyl ester 176473 Click to see CCCCCCCCCCCCCC=CC=CC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E,6E,10E)-6,10-dimethyl-12-(5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal 23424860 Click to see CC1=CC(=O)C=C(C1=O)CC=C(C)CCC=C(C)CCC=C(CCC=C(C)C)C=O 408.60 unknown via CMAUP database
(2Z,6E,10E)-6,10-dimethyl-12-(5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid 9802458 Click to see CC1=CC(=O)C=C(C1=O)CC=C(C)CCC=C(C)CCC=C(CCC=C(C)C)C(=O)O 424.60 unknown via CMAUP database
6-Methyl-2-[11-formyl-3,7,15-trimethyl-2,6,10,14-hexadecatetraene-1-yl]-2,5-cyclohexadiene-1,4-dione 25225126 Click to see CC1=CC(=O)C=C(C1=O)CC=C(C)CCC=C(C)CCC=C(CCC=C(C)C)C=O 408.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(R)-Sargachromenol 51003424 Click to see CC1=CC(=CC2=C1OC(C=C2)(C)CCC=C(C)CCC=C(CCC=C(C)C)C(=O)O)O 424.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,10S,11S,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 3052779 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)CO)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E,19E,21Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,21,23-dodecaenyl]-1,3,3-trimethylcyclohexene 10218186 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)C=CC=C(C)C)C)C 534.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aS,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 11897956 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(6R)-6-[(3R,5S,7R,9S,10S,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid 53477686 Click to see CC(CCCC(C)C(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C 434.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 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 acids and derivatives / Carbothioic S-acids
Pentadecanethioic acid 18413781 Click to see CCCCCCCCCCCCCCC(=O)S 258.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,7-Dimethyl-1-octen-3-ol 86748 Click to see CC(C)CCCC(C)(C=C)O 156.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(a1-2a)Fruf 11005647 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown via CMAUP database
Gal(b1-4)Gal(?1-4)Gal(b1-4)Gal(b1-4)Gal(b1-2b)Fruf 11972400 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6(C(C(C(O6)CO)O)O)CO)CO)CO)CO)CO)O)O)O)O 990.90 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
Ethyl rosmarinate 44437692 Click to see CCOC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 388.40 unknown via CMAUP database
Methyl rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown via CMAUP database
Rosmarinate 5315615 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)prop-2-enoate 54710367 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)[O-] 179.15 unknown via CMAUP database
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
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 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 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 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 / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid 49770232 Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O 364.30 unknown via CMAUP database

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