Synthesis and biological evaluation of (hetero)arylmethyloxy- and arylmethylamine-phenyl derivatives as potent P-glycoprotein modulating agents.
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A novel approach for predicting P-glycoprotein (ABCB1) inhibition using molecular interaction fieldsBCRP Inhibition: from Data Collection to Ligand-Based Modeling.Subtle Structural Differences Trigger Inhibitory Activity of Propafenone Analogues at the Two Polyspecific ABC Transporters: P-Glycoprotein (P-gp) and Breast Cancer Resistance Protein (BCRP).Development of classification models for identifying "true" P-glycoprotein (P-gp) inhibitors through inhibition, ATPase activation and monolayer efflux assays.Three- and four-class classification models for P-glycoprotein inhibitors using counter-propagation neural networks.Synthesis and In Vivo Imaging of N-(3-[11C]Methoxybenzyl)-2-(3-Methoxyphenyl)ethylaniline as a Potential Targeting Agent for P-glycoprotein.
P2860
Synthesis and biological evaluation of (hetero)arylmethyloxy- and arylmethylamine-phenyl derivatives as potent P-glycoprotein modulating agents.
description
2008 nî lūn-bûn
@nan
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
2008年论文
@zh
2008年论文
@zh-cn
name
Synthesis and biological evalu ...... lycoprotein modulating agents.
@en
type
label
Synthesis and biological evalu ...... lycoprotein modulating agents.
@en
prefLabel
Synthesis and biological evalu ...... lycoprotein modulating agents.
@en
P2093
P356
P1476
Synthesis and biological evalu ...... lycoprotein modulating agents.
@en
P2093
Aldo Balsamo
Francesco Berardi
Michael Vanni
Nicola Antonio Colabufo
Roberto Perrone
P304
P356
10.1021/JM701267Q
P407
P577
2008-02-08T00:00:00Z