Effects of 2,3-Dehydrosilybin and Its Galloyl Ester and Methyl Ether Derivatives on Human Umbilical Vein Endothelial Cells

Journal of Natural Products

Volumn 79, Issue 4, 2016, Pages 812-820

  Karas, Daniel ^a   Gažák, Radek ^b   Valentová, Kateřina ^a,b   Chambers, Christopher S ^b   Pivodová, Veronika ^a   Biedermann, David ^b   Křenková, Alena ^b   Oborná, Ivana ^a   Kuzma, Marek ^b   Cvačka, Josef ^c   Ulrichová, Jitka ^a   Křen, Vladimír ^b  

^a PALACKÝ UNIVERSITY   (Czech Republic)

^b INSTITUTE OF MICROBIOLOGY   (Czech Republic)

^c INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

2,3 DEHYDROSILYBIN; 20 O GALLOYL 2,3 DEHYDROSILYBIN; 20 O METHYL 2,3 DEHYDROSILYBIN; 23 O GALLOYL 2,3 DEHYDROSILYBIN; 3 O GALLOYL 2,3 DEHYDROSILYBIN; 3 O METHYL 2,3 DEHYDROSILYBIN; 3,20 DI O METHYL 2,3 DEHYDROSILYBIN; 3,7 DI O METHYL 2,3 DEHYDROSILYBIN; 5 O METHYL 2,3 DEHYDROSILYBIN; 7 20 DI O METHYL 2,3 DEHYDROSILYBIN; 7 O GALLOYL 2,3 DEHYDROSILYBIN; 7 O METHYL 2,3 DEHYDROSILYBIN; ANTINEOPLASTIC AGENT; ESTER DERIVATIVE; ETHER DERIVATIVE; LUTEOLIN; LUTEOLIN 7 GLUCOSIDE; QUERCETIN; SILIBININ; UNCLASSIFIED DRUG; DEHYDROSILYBIN; GALLIC ACID; SCAVENGER; SILYMARIN;

ANGIOGENESIS; ANTIPROLIFERATIVE ACTIVITY; ARTICLE; CANCER CELL; CARBON NUCLEAR MAGNETIC RESONANCE; CELL MIGRATION; CELL PROLIFERATION; CELL VIABILITY; CONTROLLED STUDY; DRUG CONFORMATION; DRUG SYNTHESIS; ENDOTHELIUM CELL; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR SINGLE QUANTUM COHERENCE; HUMAN; HUMAN CELL; HYDROGEN BOND; IC50; IN VITRO STUDY; PHYSICAL CHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; UMBILICAL VEIN ENDOTHELIAL CELL; CELL SURVIVAL; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS;

CELL SURVIVAL; FREE RADICAL SCAVENGERS; GALLIC ACID; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; METHYL ETHERS; MOLECULAR STRUCTURE; SILYMARIN; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84966937531     PISSN: 01633864     EISSN: 15206025     Source Type: Journal    
DOI: 10.1021/acs.jnatprod.5b00905     Document Type: Article

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