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Eupatorium lindleyanum

Eupatorium lindleyanum - 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 UUID643fc859411af801918647
Scientific name Eupatorium lindleyanum
Authority DC.
First published in Prodr. [A. P. de Candolle] 5: 180. 1836 [1-10 Oct 1836]

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Eupatorium subtetragonum Miq. J. Bot. Néerl. 1: 99 (1861)
Eupatorium lindleyanum var. trisectifolium Makino Somoku-Dzusetsu, ed. 3, 3: 1059 (1912)
Eupatorium lindleyanum f. aureoreticulatum Makino Journal of Japanese Botany 2(2): 5 1918
Eupatorium lindleyanum f. eglandulosum (Kitam.) Murata & H.Koyama Acta Phytotax. Geobot. 33: 295 (1982)
Eupatorium sachalinense f. aureoreticulatum Makino J. Jap. Bot. 2: 5. 1918
Eupatorium kirilowii Turcz. Bull. Soc. Imp. Naturalistes Moscou 7: 153 (1837)
Eupatorium lindleyanum var. trifoliatum Makino Bot. Mag. (Tokyo) 27: 80 (1913)

Common names Top

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Language Common/alternative name
Azerbaijani lindley asırqalotu
azb لیندلی آسیرقال اوْتو
Chinese 林氏澤蘭
Chinese 林泽兰
Chinese 林泽兰（轮叶泽兰)
Chinese 野马追
Chinese 尖佩兰
Chinese 秤杆升麻
Chinese 轮叶泽兰

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000021725
Tropicos 2702483
KEW urn:lsid:ipni.org:names:206259-1
The Plant List gcc-121007
Open Tree Of Life 680373
Observations.org 132075
NCBI Taxonomy 103753
IPNI 206259-1
iNaturalist 372694
GBIF 5402831
Freebase /m/04jmr4z
EPPO EUPLN
EOL 6203205
USDA GRIN 419691
Wikipedia Eupatorium_lindleyanum
CMAUP NPO851

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
Ferroptosis in Liver Disease: Natural Active Compounds and Therapeutic Implications Wu Z, Zhu Y, Liu W, Balasubramanian B, Xu X, Yao J, Lei X Antioxidants (Basel) 15-Mar-2024
PMCID:PMC10968642
doi:10.3390/antiox13030352
PMID:38539886
Sesquiterpene lactones as emerging biomolecules to cease cancer by targeting apoptosis Hsu CY, Rajabi S, Hamzeloo-Moghadam M, Kumar A, Maresca M, Ghildiyal P Front Pharmacol 11-Mar-2024
PMCID:PMC10961375
doi:10.3389/fphar.2024.1371002
PMID:38529189
Novel Insights on Ferroptosis Modulation as Potential Strategy for Cancer Treatment: When Nature Kills Consoli V, Fallica AN, Sorrenti V, Pittalà V, Vanella L Antioxid Redox Signal 17-Jan-2024
PMCID:PMC10824235
doi:10.1089/ars.2022.0179
PMID:37132605
The characterization of traditional Chinese medicine natures and flavors using network pharmacology integrated strategy Wang H, Wei W, Liu J, Zhang S, Zhao Y, Yu Z J Tradit Complement Med 25-Dec-2023
PMCID:PMC11068986
doi:10.1016/j.jtcme.2023.12.004
PMID:38707921
Invasive and Native Plants Differentially Respond to Exogenous Phosphorus Addition in Root Growth and Nutrition Regulated by Arbuscular Mycorrhizal Fungi Yang X, Shen K, Xia T, He Y, Guo Y, Wu B, Han X, Yan J, Jiao M Plants (Basel) 01-Jun-2023
PMCID:PMC10255820
doi:10.3390/plants12112195
PMID:37299174
Pest categorisation of Coleosporium eupatorii 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, Migheli Q, Vloutoglou I, Maiorano A, Pautasso M, Reignault PL EFSA J 24-May-2023
PMCID:PMC10208091
doi:10.2903/j.efsa.2023.8020
PMID:37234271
Eupalinolide J Inhibits Cancer Metastasis by Promoting STAT3 Ubiquitin-Dependent Degradation Hu H, Bai H, Huang L, Yang B, Zhao H Molecules 31-Mar-2023
PMCID:PMC10096386
doi:10.3390/molecules28073143
PMID:37049904
Different influences of phylogenetically conserved and independent floral traits on plant functional specialization and pollination network structure Xiang G, Jiang Y, Lan J, Huang L, Hao L, Liu Z, Xia J Front Plant Sci 24-Jan-2023
PMCID:PMC9902514
doi:10.3389/fpls.2023.1084995
PMID:36760631
Evolution of the Secondary Metabolites in Invasive Plant Species Chromolaena odorata for the Defense and Allelopathic Functions Kato-Noguchi H, Kato M Plants (Basel) 23-Jan-2023
PMCID:PMC9919186
doi:10.3390/plants12030521
PMID:36771607
Eupalinolide O Induces Apoptosis in Human Triple-Negative Breast Cancer Cells via Modulating ROS Generation and Akt/p38 MAPK Signaling Pathway Zhao Y, Fu L, Chen J, Zhou J, Tian C, Zhou D, Zhu R J Oncol 21-Sep-2022
PMCID:PMC9519309
doi:10.1155/2022/8802453
PMID:36185619
Eupalinolide A induces autophagy via the ROS/ERK signaling pathway in hepatocellular carcinoma cells in vitro and in vivo Zhang Y, Dong F, Cao Z, Wang T, Pan L, Luo W, Ding W, Li J, Jin L, Liu H, Zhang H, Mu J, Han M, Wei Y, Deng X, Liu D, Hao P, Zeng G, Pang Y, Liu G, Zhen C Int J Oncol 15-Sep-2022
PMCID:PMC9507091
doi:10.3892/ijo.2022.5421
PMID:36111510
Regulated cell death (RCD) in cancer: key pathways and targeted therapies Peng F, Liao M, Qin R, Zhu S, Peng C, Fu L, Chen Y, Han B Signal Transduct Target Ther 13-Aug-2022
PMCID:PMC9376115
doi:10.1038/s41392-022-01110-y
PMID:35963853
Neuroinflammation inhibition by small-molecule targeting USP7 noncatalytic domain for neurodegenerative disease therapy Zhang XW, Feng N, Liu YC, Guo Q, Wang JK, Bai YZ, Ye XM, Yang Z, Yang H, Liu Y, Yang MM, Wang YH, Shi XM, Liu D, Tu PF, Zeng KW Sci Adv 10-Aug-2022
PMCID:PMC9365288
doi:10.1126/sciadv.abo0789
PMID:35947662
Integrating UPLC-HR-MS/MS, Network Pharmacology, and Experimental Validation to Uncover the Mechanisms of Jin’gan Capsules against Breast Cancer Qiu J, Zhang Z, Hu A, Zhao P, Wei X, Song H, Yang J, Li Y ACS Omega 07-Aug-2022
PMCID:PMC9386888
doi:10.1021/acsomega.2c01921
PMID:35990498
Eupalinolide B inhibits hepatic carcinoma by inducing ferroptosis and ROS-ER-JNK pathway: Inhibition of Eupalinolide B in hepatic carcinoma Zhang Y, Zhang H, Mu J, Han M, Cao Z, Dong F, Wang T, Pan L, Luo W, Li J, Liu H, Jin L, Ding W, Wei Y, Deng X, Liu D, He X, Pang Y, Mu X, Wu Z, Chen D Acta Biochim Biophys Sin (Shanghai) 18-Jul-2022
PMCID:PMC9827796
doi:10.3724/abbs.2022082
PMID:35866605

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 / Phenols / Benzenediols / Catechols
Ulugbekic acid 101967040 Click to see C1=CC(=C(C=C1CC=C(C=CC2=CC(=C(C=C2)O)O)C(=O)O)O)O 328.30 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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid 264 Click to see CCCC(=O)O 88.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
[(1S,2R,6R,7R,9R,10S,11S,12R,14S)-11-acetyloxy-9-hydroxy-9-(hydroxymethyl)-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-4-hydroxy-2-methylbut-2-enoate 163072964 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2OC(=O)C)O4)C)(CO)O 452.50 unknown https://doi.org/10.1021/NP040023H
[(1S,2R,6R,7R,9R,10S,11S,12R,14S)-11-hydroxy-14-methyl-5-methylidene-4-oxospiro[3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecane-9,2'-oxirane]-7-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 163090431 Click to see CC(=CCO)C(=O)OC1CC2(CO2)C3C(C4C1C(=C)C(=O)O4)C5(C(C3O)O5)C 392.40 unknown https://doi.org/10.1021/NP040023H
[(1S,2R,6R,7R,9R,10S,11S,12R,14S)-9,11-dihydroxy-9-(hydroxymethyl)-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162891972 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2O)O4)C)(CO)O 410.40 unknown https://doi.org/10.1021/NP040023H
Eupalinilide G 11474825 Click to see CC(=CCO)C(=O)OC1CC2(CO2)C3C(C4C1C(=C)C(=O)O4)C5(C(C3O)O5)C 392.40 unknown via CMAUP database
Eupalinilide I 11292780 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2O)O4)C)(CO)O 410.40 unknown via CMAUP database
Eupalinilide J 11328460 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2OC(=O)C)O4)C)(CO)O 452.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,4S,6Z,8S,10E,11aR)-4,8-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 162886776 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/NP040023H
(8-Acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl) 2-(hydroxymethyl)but-2-enoate 75029447 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 420.50 unknown https://doi.org/10.1246/CL.1979.1469
(8-Acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl) 4-hydroxy-2-methylbut-2-enoate 162900111 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1R,2R,4R,6R,8S,9E,11S)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-methylbut-2-enoate 157966603 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1021/NP040023H
[(1R,2R,4R,6S,8R,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 162900114 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1R,2R,4R,6S,8S,9Z,11R)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-(hydroxymethyl)but-2-enoate 162926892 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 378.40 unknown https://doi.org/10.1021/NP040023H
[(1R,2R,4R,6S,8S,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-(hydroxymethyl)but-2-enoate 44582727 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1R,2R,4R,6S,8S,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 162900113 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1R,2R,4S,6R,8S,9E)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-methylbut-2-enoate 6325335 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1021/NP040023H
[(1S,2R,4S,6R,8R,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-(hydroxymethyl)but-2-enoate 162904348 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1S,2R,4S,6R,8S,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-(hydroxymethyl)but-2-enoate 162904349 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(1S,2R,4S,6R,8S,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162900115 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 420.50 unknown https://doi.org/10.1246/CL.1979.1469
[(3aR,4R,6E,9S,10E)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 5318060 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)C)OC(=O)C 404.50 unknown https://doi.org/10.1002/PCA.1170
[(3aR,4S,6E,9S,10E,11aS)-9-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 162959602 Click to see CC=C(C)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)CO 362.40 unknown https://doi.org/10.1021/NP040023H
[(3aS,4R,6Z,9R,10E,11aR)-9-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162930236 Click to see CC1=CC2C(C(CC(=CCC1O)CO)OC(=O)C(=CCO)C)C(=C)C(=O)O2 378.40 unknown https://doi.org/10.1021/NP040023H
eupalinin C 44582728 Click to see CC=C(CO)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)C 420.50 unknown https://doi.org/10.1246/CL.1979.1469
Eupalinolide B 102004890 Click to see CC1=CC2C(C(CC(=CCC1OC(=O)C)COC(=O)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 462.50 unknown via CMAUP database
Eupalinolide B 71463992 Click to see CC1=CC2C(C(CC(=CCC1OC(=O)C)COC(=O)C)OC(=O)C(=CCO)C)C(=C)C(=O)O2 462.50 unknown via CMAUP database
Heliangin 12310409 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown via CMAUP database
Hiyodorilactone B 101316962 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)C)OC(=O)C 404.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,4R,6R,6aS,7S,9aR,9bS)-6-(chloromethyl)-4,6,7-trihydroxy-9-methyl-3-methylidene-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one 162993457 Click to see CC1=CC(C2C1C3C(C(CC2(CCl)O)O)C(=C)C(=O)O3)O 314.76 unknown https://doi.org/10.1021/NP040023H
[(1R,2S,6R,7R,9R,12S,15S)-9-hydroxy-14-methyl-5-methylidene-4-oxo-3,11-dioxatetracyclo[7.5.1.02,6.012,15]pentadec-13-en-7-yl] (E)-4-hydroxy-2-methylbut-2-enoate 163044232 Click to see CC1=CC2C3C1C4C(C(CC3(CO2)O)OC(=O)C(=CCO)C)C(=C)C(=O)O4 376.40 unknown https://doi.org/10.1021/NP040023H
[(1S,2R,6R,7R,9R,10S,11S,12R,14S)-9-(chloromethyl)-9,11-dihydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162984409 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2O)O4)C)(CCl)O 428.90 unknown https://doi.org/10.1021/NP040023H
[(1S,2R,6R,7R,9R,10S,11S,12R,14S)-9-(chloromethyl)-9,11-dihydroxy-14-methyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (Z)-2-methylbut-2-enoate 162979040 Click to see CC=C(C)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2O)O4)C)(CCl)O 412.90 unknown https://doi.org/10.1021/NP040023H
[(3aR,4R,6aS,9S,9aS,9bR)-9-hydroxy-9-methyl-3,6-dimethylidene-2-oxo-3a,4,5,6a,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162981898 Click to see CC(=CCO)C(=O)OC1CC(=C)C2C=CC(C2C3C1C(=C)C(=O)O3)(C)O 360.40 unknown https://doi.org/10.1021/NP040023H
[(3aR,4R,6R,6aS,7S,9aR,9bS)-6-(chloromethyl)-6,7-dihydroxy-9-methyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 162987093 Click to see CC=C(C)C(=O)OC1CC(C2C(C=C(C2C3C1C(=C)C(=O)O3)C)O)(CCl)O 396.90 unknown https://doi.org/10.1021/NP040023H
[(3aR,4R,6R,6aS,7S,9aR,9bS)-6-(chloromethyl)-6,7-dihydroxy-9-methyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 162968535 Click to see CC1=CC(C2C1C3C(C(CC2(CCl)O)OC(=O)C(=CCO)C)C(=C)C(=O)O3)O 412.90 unknown https://doi.org/10.1021/NP040023H
[(3aR,4R,6R,6aS,7S,9aR,9bS)-6,7-dihydroxy-6-(hydroxymethyl)-9-methyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 163004831 Click to see CC1=CC(C2C1C3C(C(CC2(CO)O)OC(=O)C(=CCO)C)C(=C)C(=O)O3)O 394.40 unknown https://doi.org/10.1021/NP040023H
[(3aR,4R,6R,6aS,9S,9aS,9bR)-6-(chloromethyl)-6,9-dihydroxy-9-methyl-3-methylidene-2-oxo-3a,4,5,6a,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162948412 Click to see CC(=CCO)C(=O)OC1CC(C2C=CC(C2C3C1C(=C)C(=O)O3)(C)O)(CCl)O 412.90 unknown https://doi.org/10.1021/NP040023H
[(3aS,4R,6R,6aS,7S,9aR,9bS)-7-acetyloxy-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 163046024 Click to see CC1=CC(C2C1C3C(C(CC2(CCl)O)OC(=O)C(=CCO)C)C(=C)C(=O)O3)OC(=O)C 454.90 unknown https://doi.org/10.1021/NP040023H
Eupachinilide E 21578012 Click to see CC(=CCO)C(=O)OC1CC(C2C(C3C1C(=C)C(=O)O3)C4(C(C2O)O4)C)(CCl)O 428.90 unknown via CMAUP database
Eupalinilide B 11245337 Click to see CC(=CCO)C(=O)OC1CC(=C)C2C=CC(C2C3C1C(=C)C(=O)O3)(C)O 360.40 unknown https://doi.org/10.1021/NP040023H
Eupalinilide C 11417523 Click to see CC1=CC2C3C1C4C(C(CC3(CO2)O)OC(=O)C(=CCO)C)C(=C)C(=O)O4 376.40 unknown https://doi.org/10.1021/NP040023H
Eupalinilide D 11347578 Click to see CC1=CC(C2C1C3C(C(CC2(CCl)O)O)C(=C)C(=O)O3)O 314.76 unknown via CMAUP database
Eupalinilide E 11188671 Click to see CC=C(C)C(=O)OC1CC(C2C(C=C(C2C3C1C(=C)C(=O)O3)C)O)(CCl)O 396.90 unknown https://doi.org/10.1021/NP040023H
Eupalinilide F 11429323 Click to see CC1=CC(C2C1C3C(C(CC2(CO)O)OC(=O)C(=CCO)C)C(=C)C(=O)O3)O 394.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6aR,6bR,8aS,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 12305110 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
Pseudotaraxasterol 604983 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
Urs-20-en-3-ol, (3beta,18alpha,19alpha)- 3034659 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,4S,5S,9R,10S,13R,14S,17R)-4,10,13-trimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11875939 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(3aR,4R,6R,9E,10aS)-6,9-dimethyl-4-[(E)-2-methylbut-2-enoyl]oxy-3-methylidene-2,8-dioxo-3a,4,5,10a-tetrahydrofuro[2,3-e]oxonin-6-yl]acetic acid 162911529 Click to see CC=C(C)C(=O)OC1CC(OC(=O)C(=CC2C1C(=C)C(=O)O2)C)(C)CC(=O)O 392.40 unknown https://doi.org/10.1021/NP040023H
> Organic acids and derivatives / Keto acids and derivatives / Beta-keto acids and derivatives
Butanoic acid, 2-(diethoxyphosphinyl)-3-oxo-, ethyl ester 3032451 Click to see CCOC(=O)C(C(=O)C)P(=O)(OCC)OCC 266.23 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
> Organoheterocyclic compounds / Benzofurans
Euparin 119039 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 216.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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
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
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
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
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 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-] 463.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 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 via CMAUP database
kaempferol 3-O-beta-D-galactoside(1-) 25201364 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)[O-])OC4C(C(C(C(O4)CO)O)O)O)O 447.40 unknown via CMAUP database
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
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown via CMAUP database
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database

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