14 articles for KJ Shin
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Identification and characterization of potent, selective and metabolically stable IKKß inhibitor.
The Catholic University of Korea
Discovery of a potent enoyl-acyl carrier protein reductase (FabI) inhibitor suitable for antistaphylococcal agent.
The Catholic University of Korea
Synthesis and structure-activity relationships of tri-substituted thiazoles as RAGE antagonists for the treatment of Alzheimer's disease.
Korea Institute of Science and Technology
Discovery of potent and selective rhodanine type IKKß inhibitors by hit-to-lead strategy.
Korea University
Methanocarba analogues of purine nucleosides as potent and selective adenosine receptor agonists.
National Institute of Diabetes
Synthesis and biological evaluation of 4-piperidinecarboxylate and 4-piperidinecyanide derivatives for T-type calcium channel blockers.
Korea Institute of Science and Technology
Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors.
Korea Institute of Science and Technology
IKKbeta inhibitors identification part II: ligand and structure-based virtual screening.
Institute of Science and Technology
Synthesis and evaluation of alpha,alpha'-disubstituted phenylacetate derivatives for T-type calcium channel blockers.
Institute of Science and Technology
Thiazolidine-2,4-dione-based irreversible allosteric IKK-β kinase inhibitors: Optimization into in vivo active anti-inflammatory agents.
Korea Institute of Science & Technology (Kist)
Successful reduction of off-target hERG toxicity by structural modification of a T-type calcium channel blocker.
The Catholic University of Korea
Small molecules that protect against β-amyloid-induced cytotoxicity by inhibiting aggregation of β-amyloid.
Korea Institute of Science and Technology
Bis-styrylpyridine and bis-styrylbenzene derivatives as inhibitors for Abeta fibril formation.
Korea Institute of Science and Technology