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A mostrar 1 - 20 resultados de 388 para a pesquisa '((((eur j) OR (eun a))) OR (((eun au) OR (eun ah)))) med chem', tempo de pesquisa: 0.29seg Refinar resultados
Structure–Activity Studies of Divin: An Inhibitor of Bacterial Cell Division
Simultaneous determination of methylcarbamate and ethylcarbamate in fermented foods and beverages by derivatization and GC-MS analysis

Structure Activity Relationships of 1,4-Dihydropyridines That Act as Enhancers of the Vanilloid Receptor 1 (TRPV1)
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)

(S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5
Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X(7) receptor

Synthesis, characterization and antineoplastic activity of bis-aziridinyl dimeric naphthoquinone - a novel class of compounds with potent activity against acute myeloid leukemia cells
Corrigendum to “Synthesis and cytotoxic activity of novel Aring cleaved ursolic acid derivatives in human nonsmall cell lung cancer cells” [Eur. J. Med. Chem. 123 (2016) 317–331]

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

Synthesis and SAR of Thiazolylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors
OGA inhibition by GlcNAc-selenazoline

Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles
Anticancer Properties of Halogenated Pyrrolo[3,2-d]pyrimidines with Decreased Toxicity Via N5 Substitution

Jostling for Position: Optimizing Linker Location in the Design of Estrogen Receptor-targeting PROTACs
Optimizing Thiadiazole Analogues of Resveratrol vs. Three Chemopreventive Targets

Structural Basis of Wee Kinases Functionality and Inactivation by Diverse Small Molecule Inhibitors
Optimization of Thiazole Analogues of Resveratrol for Induction of NAD(P)H:quinone Reductase 1 (QR1)

Polymer-Protein Hydrogel Nanomatrix for Stabilization of Indocyanine Green towards Targeted Fluorescence and Photoacoustic Bio-imaging
Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia Pestis Outer Protein H (YopH) Phosphatase, ,

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