Synthesis and evaluation of electron-rich curcumin analogues
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Perspectives on new synthetic curcumin analogs and their potential anticancer propertiesNovel STAT3 phosphorylation inhibitors exhibit potent growth-suppressive activity in pancreatic and breast cancer cellsSynthesis, characterization and fluorescent properties of water-soluble glycopolymer bearing curcumin pendant residues.Perspectives on chemopreventive and therapeutic potential of curcumin analogs in medicinal chemistry.Lesson learned from nature for the development of novel anti-cancer agents: implication of isoflavone, curcumin, and their synthetic analogs.Preparation, characterization, in vivo pharmacokinetics, and biodistribution of polymeric micellar dimethoxycurcumin for tumor targeting.Degradation of Curcumin: From Mechanism to Biological ImplicationsStructures in solid state and solution of dimethoxy curcuminoids: regioselective bromination and chlorination.Synthesis and antibacterial activity of novel curcumin derivatives containing heterocyclic moiety.Natural and synthetic α,β-unsaturated carbonyls for NF-κB inhibition.Modulation of protein quality control systems by food phytochemicals.Natural Product Inspired N-Terminal Hsp90 Inhibitors: From Bench to Bedside?Antioxidant properties and PC12 cell protective effects of a novel curcumin analogue (2E,6E)-2,6-bis(3,5- dimethoxybenzylidene)cyclohexanone (MCH).Synthesis of Curcuminoids and Evaluation of Their Cytotoxic and Antioxidant Properties.An overview of structure-activity relationship studies of curcumin analogs as antioxidant and anti-inflammatory agents.KSRP/FUBP2 Is a Binding Protein of GO-Y086, a Cytotoxic Curcumin Analogue.PAC, a novel curcumin analogue, has anti-breast cancer properties with higher efficiency on ER-negative cells.Design and synthesis of novel iminothiazinylbutadienols and divinylpyrimidinethiones as ARE inducers.Synthesis and biological evaluation of some novel urea and thiourea derivatives of isoxazolo[4,5-d]pyridazine and structurally related thiazolo[4,5-d]pyridazine as antimicrobial agents.A multimodal, β-amyloid-targeted contrast agent.Mannich Curcuminoids as Potent Anticancer Agents.A novel nanoaggregation detection technique of TNT using selective and ultrasensitive nanocurcumin as a probe
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P2860
Synthesis and evaluation of electron-rich curcumin analogues
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 29 October 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Synthesis and evaluation of electron-rich curcumin analogues
@en
Synthesis and evaluation of electron-rich curcumin analogues.
@nl
type
label
Synthesis and evaluation of electron-rich curcumin analogues
@en
Synthesis and evaluation of electron-rich curcumin analogues.
@nl
prefLabel
Synthesis and evaluation of electron-rich curcumin analogues
@en
Synthesis and evaluation of electron-rich curcumin analogues.
@nl
P2093
P2860
P1476
Synthesis and evaluation of electron-rich curcumin analogues
@en
P2093
Brian S J Blagg
Laura B Peterson
Michael W Amolins
P2860
P304
P356
10.1016/J.BMC.2008.10.057
P407
P577
2008-10-29T00:00:00Z