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A mostrar 1 - 20 resultados de 43 para a pesquisa '((mur j) OR (((eun a) OR (eun ai)))) med chem', tempo de pesquisa: 0.89seg 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
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, ,
Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents

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