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検索結果 1 - 20 結果 / 32 検索語 '((((eum j) OR (mur j))) OR (((eun ju) OR (eun jung)))) ((med chem) OR (od chem))', 処理時間: 0.87秒 結果の絞り込み
Synthesis and SAR of Thiazolylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors
Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries

Tat-DJ-1 inhibits oxidative stress-mediated RINm5F cell death through suppression of NF-κB and MAPK activation
Non-proteinogenic amino acids in the pThr-2 position of a pentamer peptide that confer high binding affinity for the polo box domain (PBD) of polo-like kinase 1 (Plk1)

Effects on Polo-like Kinase 1 Polo-box Domain Binding Affinities of Peptides Incurred by Structural Variation at the Phosphoamino Acid Position
Probing Binding Modes of Small Molecule Inhibitors to the Polo-Box Domain of Human Polo-like Kinase 1

Effect of cinnamamides on atopic dermatitis through regulation of IL-4 in CD4(+) cells
Optimizing Thiadiazole Analogues of Resveratrol vs. Three Chemopreventive Targets

Optimization of Thiazole Analogues of Resveratrol for Induction of NAD(P)H:quinone Reductase 1 (QR1)
Epimeric methylsulfinyladenosine derivatives from the marine ascidian Herdmania momus

Structure-activity relationships and docking studies of synthetic 2-arylindole derivatives determined with aromatase and quinone reductase 1
Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents

OGA inhibition by GlcNAc-selenazoline
Selective Synthesis and Biological Evaluation of Sulfate-Conjugated Resveratrol Metabolites

Potential Chemopreventive Agents Based on the Structure of the Lead Compound 2-Bromo-1-hydroxyphenazine, Isolated from Streptomyces sp., Strain CNS284
Identification, Synthesis, and Biological Evaluation of the Metabolites of 3-Amino-6-(3'-aminopropyl)-5H-indeno[1,2-c]isoquinoline-5,11-(6H)dione (AM6-36), a Promising Rexinoid Lead Compound for the Development of Cancer Chemotherapeutic and Chemopreventive Agents

Identification of a New Heterocyclic Scaffold for Inhibitors of the Polo-Box Domain of Polo-like Kinase 1
Identification of 6′-β-fluoro-homoaristeromycin as a potent inhibitor of chikungunya virus replication

Design, synthesis and biological evaluation of 2-aminoquinazolin-4(3H)-one derivatives as potential SARS-CoV-2 and MERS-CoV treatments
A POTENT AND SELECTIVE INHIBITOR TARGETING HUMAN AND MURINE 12/15-LOX

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