Structure activity Relationship

A novel amino-benzosuberone derivative is a picomolar inhibitor of mammalian aminopeptidase N/CD13

Organic Chemistry / Kinetics / Enzyme Inhibitors / Kidney / Animals / Aeromonas / Swine / Bioorganic and medicinal Chemistry / Structure activity Relationship / Low molecular weight / Molecular Structure / Aeromonas / Swine / Bioorganic and medicinal Chemistry / Structure activity Relationship / Low molecular weight / Molecular Structure

Hollow Silica Nanocontainers as Drug Delivery Vehicles

Drug delivery / Multidisciplinary / Silica / Drug Delivery Systems / Nanocapsules / Doxorubicin / Langmuir / Structure activity Relationship / Silicon Dioxide / Ferric Compounds / Doxorubicin / Langmuir / Structure activity Relationship / Silicon Dioxide / Ferric Compounds

2-Alkyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoles as novel 5-HT6 receptor agonists

Organic Chemistry / Cell line / Humans / cyclic AMP / Serotonin Receptors / Radioligand Assay / Pyridines / Structure activity Relationship / Radioligand Assay / Pyridines / Structure activity Relationship

A Novel Potent Nicotinamide Phosphoribosyltransferase Inhibitor Synthesized via Click Chemistry

Organic Chemistry / Medicinal Chemistry / Enzyme Inhibitors / Autophagy / Humans / Animals / Medicinal / Structure activity Relationship / Protein Binding / Antineoplastic Agents / Alkynes / Animals / Medicinal / Structure activity Relationship / Protein Binding / Antineoplastic Agents / Alkynes

Artificial neural networks for computer-based molecular design

Back Propagation / Radial Basis Function / Computer Aided Design / Neural Network / Sequence Analysis / Dimension Reduction / Software / Drug Design / Quantitative Structure Activity Relationship / Feature Extraction / Adaptive Resonance Theory / Principle component analysis / Target Identification / Associative Memory / Least Mean Square / Three Dimensional / Molecular Conformation / Structure activity Relationship / Artificial Neural Network / Biochemistry and cell biology / Molecular Structure / Dimension Reduction / Software / Drug Design / Quantitative Structure Activity Relationship / Feature Extraction / Adaptive Resonance Theory / Principle component analysis / Target Identification / Associative Memory / Least Mean Square / Three Dimensional / Molecular Conformation / Structure activity Relationship / Artificial Neural Network / Biochemistry and cell biology / Molecular Structure

Identification of [(naphthalene-1-carbonyl)-amino]-acetic acid derivatives as nonnucleoside inhibitors of HCV NS5B RNA dependent RNA polymerase

Organic Chemistry / Enzyme Inhibitors / High throughput screening / Iterative Design / Enzyme / Acetic Acid / Structure activity Relationship / RNA Dependent RNA Polymerase / Acetic Acid / Structure activity Relationship / RNA Dependent RNA Polymerase

Design and synthesis of 2,3,4,9-tetrahydro-1H-carbazole and 1,2,3,4-tetrahydro-cyclopenta[b]indole derivatives as non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA polymerase

Organic Chemistry / Drug Design / Hepatitis C Virus / Enzyme / Microbial Sensitivity Tests / Structure activity Relationship / RNA Dependent RNA Polymerase / Antiviral Agents / Molecular Structure / Structure activity Relationship / RNA Dependent RNA Polymerase / Antiviral Agents / Molecular Structure

Synthesis of novel indenoquinoxaline derivatives as potent α-glucosidase inhibitors

Organic Chemistry / Enzyme Inhibitors / Magnetic Resonance Spectroscopy / Fourier transform infrared spectroscopy / Oral Hypoglycemic Agents / Bioorganic and medicinal Chemistry / Imidazoles / Structure activity Relationship / Molecular Structure / Acarbose / Bioorganic and medicinal Chemistry / Imidazoles / Structure activity Relationship / Molecular Structure / Acarbose

Synthesis of spiro[isobenzofuran-1(3H),4\'-piperidines as potential central nervous system agents. 2. Compounds containing a heteroatom attached to nitrogen

Organic Chemistry / Medicinal Chemistry / Methods / Mice / Animals / Structure activity Relationship / Piperidines / Tetrabenazine / Structure activity Relationship / Piperidines / Tetrabenazine

Development of Pyridopyrimidines as Potent Akt1/2 Inhibitors

Organic Chemistry / Cancer / Levels of selection / Signal Transduction / Cell line / In Vitro / Humans / Amines / Caspase / Akt / Bioorganic and medicinal Chemistry / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Selectivity / Piperidines / In Vitro / Humans / Amines / Caspase / Akt / Bioorganic and medicinal Chemistry / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Selectivity / Piperidines

Enzymes Assembled from Aquifex aeolicus and Escherichia coli Leucyl-tRNA Synthetases †

Biochemistry / Molecular Evolution / Kinetics / Horizontal Gene Transfer / Mutation / Escherichia coli / Enzyme / Amino Acid Profile / Structure activity Relationship / Hot Temperature / Biochemistry and cell biology / Escherichia coli / Enzyme / Amino Acid Profile / Structure activity Relationship / Hot Temperature / Biochemistry and cell biology

Flavonol glycosides from Nitraria retusa

Phytochemistry / NMR Spectroscopy / Flavonoids / Biological Sciences / Plants / CHEMICAL SCIENCES / Flavonols / Structure activity Relationship / Glycosides / Plant Leaves / CHEMICAL SCIENCES / Flavonols / Structure activity Relationship / Glycosides / Plant Leaves

Cyanopyridyl containing 1,4-dihydroindeno[1,2-c]pyrazoles as potent checkpoint kinase 1 inhibitors: Improving oral biovailability

Organic Chemistry / Hydrogen / Pharmacokinetics / DNA damage / Signal Transduction / In Vitro / Protein Kinases / Mice / Animals / Bioavailability / In Vivo / Rats / Pyridines / Bioorganic and medicinal Chemistry / Pyrazoles / Cyanides / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Molecular Structure / In Vitro / Protein Kinases / Mice / Animals / Bioavailability / In Vivo / Rats / Pyridines / Bioorganic and medicinal Chemistry / Pyrazoles / Cyanides / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Molecular Structure

Cyanopyridyl containing 1,4-dihydroindeno[1,2- c]pyrazoles as potent checkpoint kinase 1 inhibitors: Improving oral biovailability

Organic Chemistry / Hydrogen / Pharmacokinetics / DNA damage / Signal Transduction / In Vitro / Protein Kinases / Mice / Animals / Bioavailability / In Vivo / Rats / Pyridines / Bioorganic and medicinal Chemistry / Pyrazoles / Cyanides / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Molecular Structure / In Vitro / Protein Kinases / Mice / Animals / Bioavailability / In Vivo / Rats / Pyridines / Bioorganic and medicinal Chemistry / Pyrazoles / Cyanides / Structure activity Relationship / Chemical Synthesis / Protein Kinase Inhibitors / Molecular Structure

Structural aspects of ganglioside-containing membranes

Chemical Engineering / Membranes / Kinetics / Biological Sciences / Physical sciences / Scaling up / Glass Transition / Surface Structure / Biological systems / Model System / Three Dimensional / Structure activity Relationship / Gangliosides / Membrane Fluidity / Biochemistry and cell biology / Molecular Structure / Scaling up / Glass Transition / Surface Structure / Biological systems / Model System / Three Dimensional / Structure activity Relationship / Gangliosides / Membrane Fluidity / Biochemistry and cell biology / Molecular Structure

Novel Antibacterial Class: A Series of Tetracyclic Derivatives

Organic Chemistry / Medicinal Chemistry / Streptococcus pneumoniae / Humans / Anti-Bacterial Agents / Medicinal / Microbial Sensitivity Tests / B Lymphocytes / Structure activity Relationship / Protein Biosynthesis / Medicinal / Microbial Sensitivity Tests / B Lymphocytes / Structure activity Relationship / Protein Biosynthesis

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