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Daneshyari Medicine and Dentistry (General) Journas Latest Articles

Medicine and Dentistry (General) Research Articles

Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists
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Synthesis and antibacterial activity of a novel series of DNA gyrase inhibitors: 5-[(E)-2-arylvinyl]pyrazoles
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Analogs of a potent maxi-K potassium channel opener with an improved inhibitory profile toward cytochrome P450 isozymes
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Boro-norleucine as a P1 residue for the design of selective and potent DPP7 inhibitors
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Antiviral 6-amino-quinolones: Molecular basis for potency and selectivity
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2-Alkyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoles as novel 5-HT6 receptor agonists
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4-Phenyl-1,2,3,6-tetrahydropyridine, an excellent fragment to improve the potency of PARP-1 inhibitors
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Cyclic sulfamide γ-secretase inhibitors
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Novel, selective indole-based ECE inhibitors: Lead optimization via solid-phase and classical synthesis
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Correlation of cytotoxic activity of betulinines and their hydroxy analogues
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Hepatitis C virus NS3-4A serine protease inhibitors: SAR of P2′ moiety with improved potency
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Synthesis and in vitro pharmacological studies of C(4) modified salvinorin A analogues
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Carbonic anhydrase inhibitors: Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with benzo[b]thiophene 1,1-dioxide sulfonamides
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3-(2-Aminoethyl)pyridine analogs as α4β2 nicotinic cholinergic receptor ligands
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Carbonic anhydrase inhibitors: Inhibition of the tumor-associated isozymes IX and XII with a library of aromatic and heteroaromatic sulfonamides
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Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 1
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Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 2
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Synthesis and evaluation of 18F-labeled dopamine D3 receptor ligands as potential PET imaging agents
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Activity and QSAR study of baogongteng A and its derivatives as muscarinic agonists
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Synthesis of [1,2,4]triazolo[1,5-a]pyrazines as adenosine A2A receptor antagonists
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Novel 3,4-diarylpyrazolines as potent cannabinoid CB1 receptor antagonists with lower lipophilicity
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The discovery of fluoropyridine-based inhibitors of the Factor VIIa/TF complex
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Total and semisynthesis and in vitro studies of both enantiomers of 20-fluorocamptothecin
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Parallel synthesis and biological evaluation of 5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidin-4(3H)-one cytotoxic agents selective for p21-deficient cells
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Novel C2–C3′ N-peptide linked macrocyclic taxoids. Part 1: Synthesis and biological activities of docetaxel analogues with a peptide side chain at C3′
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Acyclic cyanamide-based inhibitors of cathepsin K
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A strategy to profile prime and non-prime proteolytic substrate specificity
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Tethered phytic acid as a probe for measuring phytase activity
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Inhibition of hydrogen peroxide-induced necrotic cell death with 3-amino-2-indolylmaleimide derivatives
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Structure–activity relationship of N-methyl-bisindolylmaleimide derivatives as cell death inhibitors
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Discovery of diphenylcarbamate derivatives as highly potent and selective IP receptor agonists: Orally active prostacyclin mimetics. Part 3
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Beta-lactam compounds as apparently uncompetitive inhibitors of HIV-1 protease
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A new orally bioavailable dual adenosine A2B/A3 receptor antagonist with therapeutic potential
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Quaternary salts of 4,3′ and 4,4′ bis-pyridinium monooximes: Synthesis and biological activity
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Total asymmetric synthesis of (−)-conduramine B-1 and of its enantiomer. N-Benzyl derivatives of conduramine B-1 are β-glucosidase inhibitors
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Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors
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4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17β-hydroxysteroid dehydrogenase. Part 2. SAR
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Discovery of potent and selective orally bioavailable β-substituted phenylalanine derived dipeptidyl peptidase IV inhibitors
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An efficient synthesis of argifin: A natural product chitinase inhibitor with chemotherapeutic potential
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Synthesis of a small library of diketopiperazines as potential inhibitors of calpain
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Stereospecific synthesis and mass spectrometry of 5,6-trans-epoxy-8Z,11Z,14Z-eicosatrienoic acid
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Exploiting a basic chemosensitizing pharmacophore hypothesis. Part 1: Synthesis and biological evaluation of novel arylbromide and bicyclic chemosensitizers against drug-resistant malaria parasites
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Synthesis of [18F]SU11248, a new potential PET tracer for imaging cancer tyrosine kinase
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Synthesis and antiamoebic activity of new oxime ether derivatives containing 2-acetylpyridine/2-acetylfuran
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8-Piperazinyl-2,3-dihydropyrrolo[3,2-g]isoquinolines: Potent, selective, orally bioavailable 5-HT1 receptor ligands
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Biphenyl-indanones: Allosteric potentiators of the metabotropic glutamate subtype 2 receptor
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Acetylenic TACE inhibitors. Part 2: SAR of six-membered cyclic sulfonamide hydroxamates
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Ligands with dual vitamin D3-agonistic and androgen-antagonistic activities
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Synthesis and evaluation of tricyclic pyrrolopyrimidinones as dipeptide mimetics: Inhibition of interleukin-1β-converting enzyme
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Structural elucidation of A-74528, an inhibitor for 2′,5′-phosphodiesterase isolated from Streptomyces sp.
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Synthesis and antimicrobial activity of 5-hydroxymethyl- 8-methyl-2-(N-arylimino)-pyrano[2,3-c]pyridine-3-(N-aryl)-carboxamides
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Deoxyribosyl analogues of methionyl and isoleucyl sulfamate adenylates as inhibitors of methionyl-tRNA and isoleucyl-tRNA synthetases
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Sialyl Lewisx analogs based on a quinic acid scaffold as the fucose mimic
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Design, synthesis, and evaluation of dioxane-based antiviral agents targeted against the Sindbis virus capsid protein
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Estrogen receptor β selective ligands: Discovery and SAR of novel heterocyclic ligands
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A novel one-pot three-component reaction: Synthesis of triheterocyclic 4H-pyrimido[2,1-b]benzazoles ring systems
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Antioxidant and cytotoxic activities of xanthones from Cudrania tricuspidata
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Cyclohexyl-linked tricyclic isoxazoles are potent and selective modulators of the multidrug resistance protein (MRP1)
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Molecular docking and 3D-QSAR on 2-(oxalylamino) benzoic acid and its analogues as protein tyrosine phosphatase 1B inhibitors
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Angiogenesis inhibitors derived from thalidomide
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Preparation of human Melanocortin-4 receptor agonist libraries: Linear peptides X-Y-DPhe7-Arg8-Trp(or 2-Nal)9-Z-NH2
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Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strains
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Toll-like receptor 2 antagonists. Part 1: Preliminary SAR investigation of novel synthetic phospholipids
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(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors
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Discovery of novel 1-arylmethyl pyrrolidin-2-yl ethanol amines as calcium-sensing receptor antagonists
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Synthesis and evaluation of novel 8,6-fused bicyclic peptidomimetic compounds as interleukin-1β converting enzyme inhibitors
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Synthesis and structure–activity relationships of novel benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II
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Synthesis, spectral studies and in vitro assessment for antiamoebic activity of new cyclooctadiene ruthenium(II) complexes with 5-nitrothiophene-2-carboxaldehyde thiosemicarbazones
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N-8-Substituted benztropinamine analogs as selective dopamine transporter ligands
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Novel triazole based inhibitors of Ras farnesyl transferase
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Selection of 5′-untranslated sequences that enhance initiation of translation in a cell-free protein synthesis system from wheat embryos
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Synthesis and in vitro anti-hepatitis B and C virus activities of ring-expanded ('fat') nucleobase analogues containing the imidazo[4,5-e][1,3]diazepine-4,8-dione ring system
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Photoisomerization as a trigger for Bergman cyclization: Synthesis and reactivity of azoenediynes
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Factors affecting the protease activity of venom from jellyfish Rhopilema esculentum Kishinouye
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Screening of electrophilic compounds yields an aziridinyl peptide as new active-site directed SARS-CoV main protease inhibitor
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3,3-Bisaryloxindoles as mineralocorticoid receptor antagonists
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Identification of a potent and selective 5-HT1B receptor antagonist
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Diamino-C,N-diarylpyridine positional isomers as inhibitors of lysophosphatidic acid acyltransferase-β
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Bioisosteric phentolamine analogs as potent α-adrenergic antagonists
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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold
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Neamine dimers targeting the HIV-1 TAR RNA
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Selective interaction between tylophorine B and bulged DNA
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Geometry, topology, and atom-weights assembly descriptors to predicting A1 adenosine receptors agonists
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5-Lipoxygenase inhibitors: convenient synthesis of 4-[3-(4-heterocyclylphenylthio)phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxamide analogues
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Synthesis and evaluation of 3D templates based on a taxane skeleton to circumvent P-glycoprotein-associated multidrug resistance of cancer
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Macrolactonization catalyzed by the terminal thioesterase domain of the nonribosomal peptide synthetase responsible for lichenysin biosynthesis
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Discovery of 4-(dimethylamino)quinazolines as potent and selective antagonists for the melanin-concentrating hormone receptor 1
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Structure–activity relationships of arylbenzofuran H3 receptor antagonists
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Virtual screening to identify lead inhibitors for bacterial NAD synthetase (NADs)
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Redefining the structure–activity relationships of 2,6-methano-3-benzazocines. Part 3: 8-Thiocarboxamido and 8-thioformamido derivatives of cyclazocine
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4-Alkyl and 4,4′-dialkyl 1,2-bis(4-chlorophenyl)pyrazolidine-3,5-dione derivatives as new inhibitors of bacterial cell wall biosynthesis
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In vitro advanced antimycobacterial screening of isoniazid-related hydrazones, hydrazides and cyanoboranes: Part 14
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Structure-based design of protein tyrosine phosphatase-1B inhibitors
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Synthesis and biological evaluation of new biphalin analogues with non-hydrazine linkers
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Discovery of novel conformationally constrained tropane-based biaryl and arylacetylene ligands as potent and selective norepinephrine transporter inhibitors and potential antidepressants
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Site-specific immobilization of proteins in a microarray using intein-mediated protein splicing
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1-((S)-γ-Substituted prolyl)-(S)-2-cyanopyrrolidine as a novel series of highly potent DPP-IV inhibitors
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Structure–activity relationship of a series of cyclohexylpiperidines bearing an amide side chain as antagonists of the human melanocortin-4 receptor
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Identification of aminopiperidine benzamides as MCHr1 antagonists
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(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: Further optimisation as highly potent and selective MSK-1-inhibitors
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