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Structural and biological studies on bacterial nitric oxide synthase inhibitorsNitric Oxide Synthase Inhibitors That Interact with Both Heme Propionate and Tetrahydrobiopterin Show High Isoform SelectivityThe Mobility of a Conserved Tyrosine Residue Controls Isoform-Dependent Enzyme–Inhibitor Interactions in Nitric Oxide SynthasesElectrostatic Control of Isoform Selective Inhibitor Binding in Nitric Oxide SynthaseSerotonergic signalling suppresses ataxin 3 aggregation and neurotoxicity in animal models of Machado-Joseph disease.Synthesis and biological evaluation of a library of resveratrol analogues as inhibitors of COX-1, COX-2 and NF-kappaB.Development of nitric oxide synthase inhibitors for neurodegeneration and neuropathic pain.CaV1.3-selective L-type calcium channel antagonists as potential new therapeutics for Parkinson's disease.Synthesis of mevalonate- and fluorinated mevalonate prodrugs and their in vitro human plasma stability.Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2.Structure-based design of bacterial nitric oxide synthase inhibitors.Nitric Oxide Synthase as a Target for Methicillin-Resistant Staphylococcus aureus.2-Aminopyridines with a Truncated Side Chain To Improve Human Neuronal Nitric Oxide Synthase Inhibitory Potency and SelectivityPhenyl Ether- and Aniline-Containing 2-Aminoquinolines as Potent and Selective Inhibitors of Neuronal Nitric Oxide Synthase.Inhibitor Bound Crystal Structures of Bacterial Nitric Oxide Synthase.Regulation of aldosterone secretion by Cav1.3.Microwave-assisted protection of primary amines as 2,5-dimethylpyrroles and their orthogonal deprotection.Antagonism of 4-substituted 1,4-dihydropyridine-3,5-dicarboxylates toward voltage-dependent L-type Ca2+ channels Ca V 1.3 and Ca V 1.2.Correction to Phenyl Ether- and Aniline-Containing 2-Aminoquinolines as Potent and Selective Inhibitors of Neuronal Nitric Oxide Synthase.Paralog Specificity Determines Subcellular Distribution, Action Mechanism, and Anticancer Activity of TRAP1 Inhibitors.Exploring G Protein-Coupled Receptors (GPCRs) Ligand Space via Cheminformatics Approaches: Impact on Rational Drug Design.Evolution of In Silico Strategies for Protein-Protein Interaction Drug DiscoveryCF₃-Substituted Mollugin 2-(4-Morpholinyl)-ethyl ester as a Potential Anti-inflammatory Agent with Improved Aqueous Solubility and Metabolic StabilityMetal-Free Synthesis of N-Aryl-Substituted Azacycles from Cyclic Ethers Using POCl3Casein kinase-1γ1 and 3 stimulate tumor necrosis factor-induced necroptosis through RIPK3Physiological involvement of presynaptic L-type voltage dependent calcium channels in GABA release of cerebellar molecular layer interneurons
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Soosung Kang
@ast
Soosung Kang
@en
Soosung Kang
@es
Soosung Kang
@nl
Soosung Kang
@sl
type
label
Soosung Kang
@ast
Soosung Kang
@en
Soosung Kang
@es
Soosung Kang
@nl
Soosung Kang
@sl
prefLabel
Soosung Kang
@ast
Soosung Kang
@en
Soosung Kang
@es
Soosung Kang
@nl
Soosung Kang
@sl
P106
P1153
57199508507
P31
P496
0000-0001-7016-2417