Synthesis and identification of new 4-arylidene curcumin analogues as potential anticancer agents targeting nuclear factor-κB signaling pathway.
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Natural products possessing protein tyrosine phosphatase 1B (PTP1B) inhibitory activity found in the last decadesPerspectives on new synthetic curcumin analogs and their potential anticancer propertiesCritical role of NF-κB in pancreatic cancerCurcumin Pyrazole and its derivative (N-(3-Nitrophenylpyrazole) Curcumin inhibit aggregation, disrupt fibrils and modulate toxicity of Wild type and Mutant α-SynucleinCurcumin analogue T83 exhibits potent antitumor activity and induces radiosensitivity through inactivation of Jab1 in nasopharyngeal carcinoma(1E,4Z,6E)-5-Hy-droxy-1,7-bis-(2-meth-oxy-phen-yl)-1,4,6-hepta-trien-3-oneNovel harmine derivatives for tumor targeted therapy.The Curcumin Analog C-150, Influencing NF-κB, UPR and Akt/Notch Pathways Has Potent Anticancer Activity In Vitro and In VivoW346 inhibits cell growth, invasion, induces cycle arrest and potentiates apoptosis in human gastric cancer cells in vitro through the NF-κB signaling pathway.Involvement of ROS-p38-H2AX axis in novel curcumin analogues-induced apoptosis in breast cancer cells.Identification of potential pathways involved in the induction of cell cycle arrest and apoptosis by a new 4-arylidene curcumin analogue T63 in lung cancer cells: a comparative proteomic analysis.Curcumin analogues with potent and selective anti-proliferative activity on acute promyelocytic leukemia: involvement of accumulated misfolded nuclear receptor co-repressor (N-CoR) protein as a basis for selective activity.Synthesis of the pyridinyl analogues of dibenzylideneacetone (pyr-dba) via an improved Claisen-Schmidt condensation, displaying diverse biological activities as curcumin analogues.A multimodal, β-amyloid-targeted contrast agent.Facile synthesis of some pyrazoline-based compounds with promising anti-inflammatory activity.Mannich Curcuminoids as Potent Anticancer Agents.Quantitative structure-retention relationship of curcumin and its analogues.Structure guided design and binding analysis of EGFR inhibiting analogues of erlotinib and AEE788 using ensemble docking, molecular dynamics and MM-GBSA
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P2860
Synthesis and identification of new 4-arylidene curcumin analogues as potential anticancer agents targeting nuclear factor-κB signaling pathway.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
Synthesis and identification o ...... r factor-κB signaling pathway.
@en
Synthesis and identification o ...... r factor-κB signaling pathway.
@nl
type
label
Synthesis and identification o ...... r factor-κB signaling pathway.
@en
Synthesis and identification o ...... r factor-κB signaling pathway.
@nl
prefLabel
Synthesis and identification o ...... r factor-κB signaling pathway.
@en
Synthesis and identification o ...... r factor-κB signaling pathway.
@nl
P2093
P2860
P356
P1476
Synthesis and identification o ...... r factor-κB signaling pathway.
@en
P2093
Binhua Zhou
Jianing Huang
Weiyan Shao
Xianzhang Bu
Yinglin Zuo
P2860
P304
P356
10.1021/JM1004545
P407
P577
2010-11-11T00:00:00Z