Comparative Analysis of the Interaction between Different Flavonoids and PDIA3The flavonoid eupatorin inactivates the mitotic checkpoint leading to polyploidy and apoptosis.Flavonoids eupatorin and sinensetin present in Orthosiphon stamineus leaves inhibit inflammatory gene expression and STAT1 activation.Eupatorin-induced cell death in human leukemia cells is dependent on caspases and activates the mitogen-activated protein kinase pathway.Phytochemical Characterization of Veronica officinalis L., V. teucrium L. and V. orchidea Crantz from Romania and Their Antioxidant and Antimicrobial Properties.Evaluation of α-Glucosidase Inhibitory Effect of 50% Ethanolic Standardized Extract of Orthosiphon stamineus Benth in Normal and Streptozotocin-Induced Diabetic RatsAntiproliferative and cytostatic effects of the natural product eupatorin on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism.High-performance Thin-layer Chromatography Method Development, Validation, and Simultaneous Quantification of Four Compounds Identified in Standardized Extracts of Orthosiphon stamineusAnti-inflammatory activity of standardized dichloromethane extract of Salvia connivens on macrophages stimulated by LPS.neo-Clerodane Diterpenoids and Other Constituents of Salvia filipes.A new irregular monoterpene acetate along with eight known compounds with antifungal potential from the aerial parts of Artemisia incisa Pamp (Asteraceae).A novel reverse phase high-performance liquid chromatography method for standardization of Orthosiphon stamineus leaf extracts.Characterization of the interaction between eupatorin and bovine serum albumin by spectroscopic and molecular modeling methods.Eupatorin, a constituent of Merrillia caloxylon.The methoxylated flavones eupatorin and cirsiliol induce CYP1 enzyme expression in MCF7 cells.Isolation of Chemical Constituents of Centaurea virgata Lam. and Xanthine Oxidase Inhibitory Activity of the Plant Extract and Compounds.Trypanocidal and leishmanicidal activities of flavonoids isolated from Stevia satureiifolia var. satureiifolia.Activity of myricetin and other plant-derived polyhydroxyl compounds in human LDL and human vascular endothelial cells against oxidative stress.Eupatorin and Salvigenin Potentiate Doxorubicin-Induced Apoptosis and Cell Cycle Arrest in HT-29 and SW948 Human Colon Cancer CellsMechanism of vasorelaxation induced by eupatorin in the rats aortic ring.Flavonoids-Rich Orthosiphon stamineus Extract as New Candidate for Angiotensin I-Converting Enzyme Inhibition: A Molecular Docking Study.A simple isocratic HPLC method for the simultaneous determination of sinensetin, eupatorin, and 3'-hydroxy-5,6,7,4'-tetramethoxyflavone in Orthosiphon stamineus extracts.Antiproliferative and antiangiogenic effects of flavone eupatorin, an active constituent of chloroform extract of Orthosiphon stamineus leaves.In vitro effect of important herbal active constituents on human cytochrome P450 1A2 (CYP1A2) activityApoptotic and antimetastatic activities of betulin isolated from against non-small cell lung cancer cellsTumor inhibitors. 8. Eupatorin, new cytotoxic flavone from Eupatorium semiserratum[Study on chemical constituents of Achillea alpina]Flavonoids Affect the Light Reaction of Photosynthesis in Vitro and in Vivo as Well as the Growth of PlantsAntioxidant and enzyme inhibitory activities of Plebeian herba (Salvia plebeia R. Br.) under different cultivation conditions
P921
Q28817159-115084E6-EB0F-448F-A75C-174766DAFE3BQ34121234-0990E91E-A977-4736-9B9F-400EC4E74538Q34637654-3CDB47FE-73CC-4DE2-84D4-DD4D2CF8C65BQ35414623-EEA50839-5E3C-4518-A804-D21727D344F8Q36184068-8D62455B-8248-4B5B-97C6-EB78F9134972Q36328893-0B966439-93CC-4388-BDB0-7D14207D5C53Q36787314-9B20D980-874A-4D04-A716-0E39ECB138DEQ37216551-ACC40204-31CE-4287-8699-522B4BFE5537Q38710266-079E335E-DD2E-4E2F-809D-B3BBC315E931Q39344356-B978ACD5-2107-42B9-8762-090A75AA79B8Q39760031-BA924DE2-D8B4-421F-9D30-773C241D4F1FQ42173267-2B1D1A8B-6942-4C97-AE1E-8AA79C9845BFQ42552717-90E979C6-D10B-48FF-86E7-A857D00C4BD0Q44243983-B473A4CA-3F57-4CA2-89CE-E1B5EF22B977Q44584027-2F760214-9ABA-475F-8A52-C871399E783CQ46443627-8FB7F8A8-B738-4BDC-84AF-AC52F322C803Q46578958-417E1E1E-93AD-43CB-A891-6CA254BDEE86Q49150805-A1DB2C39-69FE-4940-9E04-845FED991DE4Q49648615-662060CF-CB6A-48E4-9E96-574A96348690Q50200474-4CC803FD-1B63-4A6C-A713-C674DE75F180Q51332447-E45C181B-2D7A-490D-BDAC-686B197B687CQ53125356-D58398B5-DBAB-4B05-BD3C-00755F33C7BDQ53162830-799EC99D-9452-4B1B-997A-AB7A11922D32Q61953146-E3D19116-B59E-49E3-9829-D9F6323F33DCQ64228170-614EB538-7774-419A-9E93-F6201836428DQ72604258-DCE35104-B972-4FA1-8D85-94A7E28A51F3Q85916154-BD87B7B8-6144-4168-91F9-3809B282F2CEQ86038494-2BC66B7B-B66B-4D85-BDD8-32881634A080Q87095114-4D36DF8E-D7B2-4CC9-AB34-F5A3A8D408B0
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Eupatorin
@de
Eupatorine
@fr
eupatorin
@en
type
label
Eupatorin
@de
Eupatorine
@fr
eupatorin
@en
prefLabel
Eupatorin
@de
Eupatorine
@fr
eupatorin
@en
P592
P661
P662
P683
P2063
LMPK12111239
P2067
P231
P232
P233
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O
P234
1S/C18H16O7/c1-22-12-5-4-9(6-1 ...... 4-3)17(16)21/h4-8,19,21H,1-3H3
P235
KLAOKWJLUQKWIF-UHFFFAOYSA-N
P2566
100.189.469
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P2840
P3117
DTXSID20234704
P592
CHEMBL487402
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3J474AV6MY