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A mostrar 221 - 240 resultados de 393 para a pesquisa '((((((kuru OR kurt) OR kuria) j) OR (eus j))) OR (sun j)) ((med chem) OR (od chem))', tempo de pesquisa: 2.52seg Refinar resultados
Synthesis, pharmacology and molecular docking on multifunctional tacrine-ferulic acid hybrids as cholinesterase inhibitors against Alzheimer’s disease
Ultrasound-assisted lipase-catalyzed synthesis of D-isoascorbyl palmitate: process optimization and Kinetic evaluation

Discovery of NCT-501, a Potent and Selective Theophylline-Based Inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1)
Computer-Aided Discovery and Characterization of Novel Ebola Virus Inhibitors

The Structure Activity Relationship of Urea Derivatives as Anti-Tuberculosis Agents
Discovery of a Potent Class of PI3Kα Inhibitors with Unique Binding Mode via Encoded Library Technology (ELT)

Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic template
Facilely Accessible Quinoline Derivatives as Potent Antibacterial Agents

Potent Non-Nucleoside Inhibitors of the Measles Virus RNA-Dependent RNA Polymerase Complex
Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria

Design, Synthesis, and Preclinical Evaluations of Novel 4-Substituted 1,5-Diarylanilines as Potent HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) Drug Candidates
Potential anti-neuroinflammatory NF-кB inhibitors based on 3,4-dihydronaphthalen-1(2H)-one derivatives

Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8
Solid-Phase Synthesis and Biological Evaluation of a Uridinyl Branched Peptide Urea Library

Design, Synthesis and Evaluation of Tricyclic, Conformationally Constrained Small-Molecule Mimetics of Second Mitochondria-derived Activator of Caspases
7-(Pyrazol-4-yl)-3H-imidazo[4,5-b]pyridine-based derivatives for kinase inhibition: Co-crystallisation studies with Aurora-A reveal distinct differences in the orientation of the pyrazole N1-substituent

Asymmetric Synthesis of Conformationally Constrained Fingolimod Analogues—Discovery of an Orally Active Sphingosine 1-Phosphate Receptor Type-1 Agonist and Receptor Type-3 Antagonist
Design, synthesis and biological evaluation of photoaffinity probes of antiangiogenic homoisoflavonoids

Discovery of Soluble Epoxide Hydrolase Inhibitors from Chemical Synthesis and Natural Products
Synthesis, Structure–Activity Relationship Studies, and Antibacterial Evaluation of 4-Chromanones and Chalcones, as Well as Olympicin A and Derivatives

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