Design, synthesis, cytoselective toxicity, structure-activity relationships, and pharmacophore of thiazolidinone derivatives targeting drug-resistant lung cancer cells.
about
Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding SitePrediction of promiscuous p-glycoprotein inhibition using a novel machine learning schemeThe novel tubulin polymerization inhibitor MHPT exhibits selective anti-tumor activity against rhabdomyosarcoma in vitro and in vivoReducing Both Pgp Overexpression and Drug Efflux with Anti-Cancer Gold-Paclitaxel NanoconjugatesPharmacophore modeling and in silico toxicity assessment of potential anticancer agents from African medicinal plantsN'-[(2Z)-3-Allyl-4-oxo-1,3-thia-zolidin-2-yl-idene]-5-fluoro-3-phenyl-1H-indole-2-carbohydrazide.Proteome interrogation using nanoprobes to identify targets of a cancer-killing molecule.Thiazolidinedione-based PI3Kα inhibitors: an analysis of biochemical and virtual screening methods.2-Imino-3-(2-nitro-phen-yl)-1,3-thia-zolidin-4-one.Improving both aqueous solubility and anti-cancer activity by assessing progressive lead optimization libraries.Advances in preclinical small molecules for the treatment of NSCLC.Synergistic action by multi-targeting compounds produces a potent compound combination for human NSCLC both in vitro and in vivo.Toward a systematic exploration of nano-bio interactions.Design and synthesis of 2-iminothiazolidin-4-one moiety-containing compounds as potent antiproliferative agents.Synthesis and anticancer activity of Indolin-2-one derivatives bearing the 4-thiazolidinone moiety.(Z)-3-(2-Hy-droxy-eth-yl)-2-(phenyl-imino)-1,3-thia-zolidin-4-one.Ethyl 7-methyl-2-((1-methyl-1H-pyrrol-2-yl)methyl-ene)-3-oxo-5-phenyl-3,5-dihydro-2H-thia-zolo[3,2-a]pyrimidine-6-carboxyl-ateAn Efficient and Facile Synthesis of 1,2,4-Aryl Triazoles and 4-Thiazolidinones Bearing 6-Fluorochroman Nucleus.Machine learning-, rule- and pharmacophore-based classification on the inhibition of P-glycoprotein and NorA.Recent developments with rhodanine as a scaffold for drug discovery.In silico identification of targets for a novel scaffold, 2-thiazolylimino-5-benzylidin-thiazolidin-4-one.In silicoprediction of substrate properties for ABC-multidrug transporters
P2860
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P2860
Design, synthesis, cytoselective toxicity, structure-activity relationships, and pharmacophore of thiazolidinone derivatives targeting drug-resistant lung cancer cells.
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@ast
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@en
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@nl
type
label
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@ast
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@en
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@nl
prefLabel
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@ast
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@en
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@nl
P2093
P50
P356
P1476
Design, synthesis, cytoselecti ...... g-resistant lung cancer cells.
@en
P2093
Aifeng Liu
Bingliang Fang
Hongyu Zhou
Rongshi Li
Shuhong Wu
Shumei Zhai
P304
P356
10.1021/JM7012024
P407
P577
2008-02-08T00:00:00Z