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Daneshyari Medicine and Dentistry (General) Journas Latest Articles

Medicine and Dentistry (General) Research Articles

Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: peptidomimetic replacement of the P2 α-amino acid by a α-hydroxy acid
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Synthesis and SAR studies of 3-phenoxypropyl piperidine analogues as ORL1 (NOP) receptor agonists
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Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V, and IX with anions isosteric and isoelectronic with sulfate, nitrate, and carbonate
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Synthesis and biological evaluation of 3-benzyl-1-methyl- and 1-methyl-3-phenyl-isothioureas as potential inhibitors of iNOS
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Synthesis of alkyne derivatives of a novel triazolopyrazine as A2A adenosine receptor antagonists
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Hybridization dependent cleavage of internally modified disulfide-peptide nucleic acids
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Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure-activity relationship studies
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Synthesis and evaluation of azalanstat analogues as heme oxygenase inhibitors
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New derivatives of 1α,25-dihydroxy-19-norvitamin D3 with two substituents at C-2: synthesis and biological activity
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Synthesis and SAR of 4-(3-hydroxyphenylamino)pyrrolo[2,1-f][1,2,4]triazine based VEGFR-2 kinase inhibitors
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Synthesis and in vitro antitrypanosomal activity of novel Nifurtimox analogues
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Efficient synthesis of bicyclic oxazolino- and thiazolino[3,2-c]pyrimidine-5,7-diones and its application to the synthesis of GnRH antagonists
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Discovery and investigation of a novel class of thiophene-derived antagonists of the human glucagon receptor
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Synthesis and in vitro selective anti-Helicobacter pylori activity of pyrazoline derivatives
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Chiral polyamines from reduction of polypeptides: asymmetric pyridoxamine-mediated transaminations
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(R)-2-(4-Phenylbutyl)dihydrobenzofuran derivatives as melatoninergic agents
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cis-6-Oxo-hexahydro-2-oxa-1,4-diazapentalene and cis-6-oxo-hexahydropyrrolo[3,2-c]pyrazole based scaffolds: design rationale, synthesis and cysteinyl proteinase inhibition
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Benzodipyrazoles: a new class of potent CDK2 inhibitors
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Effects of suberoylanilide hydroxamic acid and trichostatin A on induction of cytochrome P450 enzymes and benzo[a]pyrene DNA adduct formation in human cells
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Design and synthesis of highly active Alzheimer's β-secretase (BACE1) inhibitors, KMI-420 and KMI-429, with enhanced chemical stability
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Discovery of novel tetrahydroisoquinoline derivatives as potent and selective factor Xa inhibitors
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Discovery of (2S)-N-[(1R)-2-[4-cyclohexyl-4-[[(1,1-dimethylethyl)amino]carbonyl]-1-piperidinyl]-1-[(4-fluorophenyl)methyl]-2-oxoethyl]-4-methyl-2-piperazinecarboxamide (MB243), a potent and selective melanocortin subtype-4 receptor agonist
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Enzymatic syntheses and selective hydrolysis of O-β-d-galactopyranosides using a marine mollusc β-galactosidase
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A comparative binding study of BIV Tat peptide against its TAR RNA duplex, RNA-DNA heteroduplex and DNA duplex
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Aminothiazole inhibitors of HCV RNA polymerase
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Benzimidazole derivatives as novel nonpeptide luteinizing hormone-releasing hormone (LHRH) antagonists. Part 1: Benzimidazole-5-sulfonamides
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Potent Kv1.3 inhibitors from correolide-modification of the C18 position
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Novel estimation of lipophilicity using 13C NMR chemical shifts as molecular descriptor
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3D QSAR studies on GSK-3 inhibition by aloisines
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Identification of a novel class of androgen receptor antagonists based on the bicyclic-1H-isoindole-1,3(2H)-dione nucleus
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N1-arylsulfonyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives are potent and selective 5-HT6 receptor antagonists
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Identification of a potent non-hydroxamate histone deacetylase inhibitor by mechanism-based drug design
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Tubulin-polymerization inhibitors derived from thalidomide
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Trypanocidal activity of (−)-cubebin derivatives against free amastigote forms of Trypanosoma cruzi
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Detection of aptamer-protein interactions using QCM and electrochemical indicator methods
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The identification and optimization of a N-hydroxy urea series of flap endonuclease 1 inhibitors
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Identification of agonists and antagonists of the human melanocortin-4 receptor from piperazinebenzylamines
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Specific recognition of napthyridine-based ligands toward guanine-containing bulges in RNA duplexes and RNA-DNA heteroduplexes
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Possible role of hydroxyl radicals in the oxidative degradation of folic acid
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Structure-based design, synthesis and biochemical testing of novel and potent Smac peptido-mimetics
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N-Arylalkylpiperidine urea derivatives as CC chemokine receptor-3 (CCR3) antagonists
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Increased catalytic activity of protein disulfide isomerase using aromatic thiol based redox buffers
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Non-peptidic small molecule inhibitors of XIAP
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3,4-Dihydro-2H-benzoxazinones are 5-HT1A receptor antagonists with potent 5-HT reuptake inhibitory activity
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4-(2-Pyridyl)piperazine-1-benzimidazoles as potent TRPV1 antagonists
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Synthesis of 9-(2-β-C-methyl-β-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication
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Discovery and structure-activity relationships of novel selective norepinephrine and dual serotonin/norepinephrine reuptake inhibitors
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Novel isoindoline compounds for potent and selective inhibition of prolyl dipeptidase DPP8
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Pyrrolidinohydroquinazolines--a novel class of CCR3 modulators
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A new bactericidal lead structure for the protection of materials
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Synthesis and incorporation into DNA fragments of the artificial nucleobase, 2-amino-8-oxopurine
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1,3-Dioxo-4-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines as potent caspase-3 inhibitors
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Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): synthesis and initial structure-activity relationships
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Novel and potent cyclic cyanamide-based cathepsin K inhibitors
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Design, synthesis, biological evaluation and molecular docking of curcumin analogues as antioxidant, cyclooxygenase inhibitory and anti-inflammatory agents
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QSAR-by-NMR: quantitative insights into structural determinants for binding affinity by analysis of 1H/15N chemical shift differences in MMP-3 ligands
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18F-Labeled sufentanil for PET-imaging of μ-opioid receptors
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Synthesis of a novel plant growth promoter from gallic acid
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Kinetic model studies on the chemical ligation of oligonucleotides via hydrazone formation
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Exploring the active site of phenylethanolamine N-methyltransferase with 3-hydroxyethyl- and 3-hydroxypropyl-7-substituted-1,2,3,4-tetrahydroisoquinolines
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2,3-Dimethoxy-5-methyl-1,4-benzoquinones and 2-methyl-1,4-naphthoquinones: glycation inhibitors with lipid peroxidation activity
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Synthesis and biological properties of novel sphingosine derivatives
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Synthesis and evaluation of novel peripherally restricted κ-opioid receptor agonists
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Fluorescent metal ion indicators based on benzoannelated crown systems: a green fluorescent indicator for intracellular sodium ions
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Syntheses and properties of the major hydroxy metabolites in humans of blonanserin AD-5423, a novel antipsychotic agent
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Spiro-annulation of barbituric acid derivatives and its analogs by ring-closing metathesis reaction
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Synthesis and biological activity evaluation of lignan lactones derived from (−)-cubebin
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Synthesis of mono-glucose-branched cyclodextrins with a high inclusion ability for doxorubicin and their efficient glycosylation using Mucor hiemalis endo-β-N-acetylglucosaminidase
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Identification of nonpeptidic small-molecule inhibitors of interleukin-2
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QSAR of estrogen receptor modulators: exploring selectivity requirements for ERα versus ERβ binding of tetrahydroisoquinoline derivatives using E-state and physicochemical parameters
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A rate determining step change in the pre-steady state of acetylcholinesterase inhibitions by 1,n-alkane-di-N-butylcarbamates
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Recognition of stable protein mutants with 3D stochastic average electrostatic potentials
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A model system for [NiFe] hydrogenase maturation studies: Purification of an active site-containing hydrogenase large subunit without small subunit
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The structure of the Ni–Fe site in the isolated HoxC subunit of the hydrogen-sensing hydrogenase from Ralstonia eutropha
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Raver2, a new member of the hnRNP family
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Synthesis and SAR of diazepine and thiazepine TACE and MMP inhibitors
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Synthesis of the naphthalene-derived inhibitors against Cdc25A dual-specificity protein phosphatase and their biological activity
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2-Alkoxydihydrocinnamates as PPAR agonists. Activity modulation by the incorporation of phenoxy substituents
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Identified a morpholinyl-4-piperidinylacetic acid derivative as a potent oral active VLA-4 antagonist
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Isosteric ramatroban analogs: selective and potent CRTH-2 antagonists
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Further studies on ethenyl and ethynyl-4-phenylamino-3-quinolinecarbonitriles: identification of a subnanomolar Src kinase inhibitor
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A two-state homology model of the hERG K+ channel: application to ligand binding
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A chromism-based assay (CHROBA) technique for in situ detection of protein kinase activity
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Synthesis and fluorescence studies of thiazole orange tethered onto oligonucleotide: development of a self-contained DNA biosensor on a fiber optic surface
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1-(1-Naphthyl)piperazine as a novel template for 5-HT6 serotonin receptor ligands
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Design, synthesis and structure-activity relationship studies of hexahydropyrazinoquinolines as a novel class of potent and selective dopamine receptor 3 (D3) ligands
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Discovery and SAR studies of a novel series of noncovalent cathepsin S inhibitors
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Potent and selective [2-imidazol-1-yl-2-(6-alkoxy-naphthalen-2-yl)-1-methyl-ethyl]-dimethyl-amines as retinoic acid metabolic blocking agents (RAMBAs)
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Electrostatic influence of active-site waters on the nucleophilic aromatic substitution catalyzed by 4-chlorobenzoyl-CoA dehalogenase
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Melanocortin subtype-4 receptor agonists containing a piperazine core with substituted aryl sulfonamides
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iPF2α-III-17,18,19,20-d4: Total synthesis and metabolism
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Novel and potent NPY5 receptor antagonists derived from virtual screening and iterative parallel chemistry design
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Design, synthesis, and biological activity of novel PPARγ ligands based on rosiglitazone and 15d-PGJ2
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Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases
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Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Wee1
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Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V and IX with complex fluorides, chlorides and cyanides
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Design, synthesis, and structure-activity relationships of tetrahydroquinoline-based farnesyltransferase inhibitors
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Structure-activity relationship study of novel tissue transglutaminase inhibitors
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Structure-based design of derivatives of tyropeptin A as the potent and selective inhibitors of mammalian 20S proteasome
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Structure-based design, synthesis, and biological evaluation of novel 1,4-diazepines as HDM2 antagonists
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