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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Identification of 6-substituted 4-arylsulfonyl-1,4-diazepane-2,5-diones as a novel scaffold for human chymase inhibitors
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Synthesis and biological evaluation of 7-azaindole derivatives, synthetic cytokinin analogues
Fulltext Access 4 Pages 2007
Studies on acyl pyrrolidine inhibitors of HCV RNA-dependent RNA polymerase to identify a molecule with replicon antiviral activity
Fulltext Access 4 Pages 2007
Self-aggregation of zinc chlorophylls possessing perfluoroalkyl chains in fluorous solvents: Selective extraction of the self-aggregates with fluorous phase and accelerated formation of the ordered supramolecules in this phase
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A long-acting selective neuropeptide Y2 receptor PEGylated peptide agonist reduces food intake in mice
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Degradation of DNA by bisulfite treatment
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Design of LFA-1 antagonists based on a 2,3-dihydro-1H-pyrrolizin-5(7aH)-one scaffold
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N-Hydroxythiosemicarbazones: Synthesis and in vitro antitubercular activity
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Neuroprotective effects of kobophenol A against the withdrawal of tropic support, nitrosative stress, and mitochondrial damage in SH-SY5Y neuroblastoma cells
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Isoform selective inhibition of STAT1 or STAT3 homo-dimerization via peptidomimetic probes: Structural recognition of STAT SH2 domains
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Polypseudorotaxanes of pegylated insulin with cyclodextrins: Application to sustained release system
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3,4-Dihydro-2H-benzo[1,4]oxazine derivatives as 5-HT6 receptor antagonists
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Synthesis of furanosyl α-C-glycosides derived from 4-chloro-4-deoxy-α-d-galactose and their cytotoxic activities
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Thyroid receptor ligands. Part 7: Indirect antagonists of the thyroid hormone receptor with improved affinity
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Synthesis and biological activity of naphthalene analogues of phenstatins: Naphthylphenstatins
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A cell-permeable inhibitor and activity-based probe for the caspase-like activity of the proteasome
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Synthesis and evaluation of 2′-substituted cyclobutyl nucleosides and nucleotides as potential anti-HIV agents
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Discovery of 1-(4-phenoxypiperidin-1-yl)-2-arylaminoethanone stearoyl-CoA desaturase 1 inhibitors
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Rational design of a novel, potent, and orally bioavailable cyclohexylamine DPP-4 inhibitor by application of molecular modeling and X-ray crystallography of sitagliptin
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Benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulfonamides as inhibitors of carbonic anhydrase
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Squalene-derived flexible linkers for bioactive peptides
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Discovery of new C3aR ligands. Part 2: Amino-piperidine derivatives
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Discovery of new C3aR ligands. Part 1: Arginine derivatives
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Discovery and SAR development of thienopyridones: A class of small molecule AMPK activators
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Synthesis and antibacterial activity of some novel chiral fluorophoric biscyclic macrocycles
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Development of new pyrrolopyrimidine-based inhibitors of Janus kinase 3 (JAK3)
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Novel membrane-localizing TEMPO derivatives for measurement of cellular oxidative stress at the cell membrane
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N-Alkyl-N-alkyloxycarbonylaminomethyl (NANAOCAM) prodrugs of carboxylic acid containing drugs
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4-[6-(2-Aminoethyl)naphthalen-2-yl]benzonitriles are potent histamine H3 receptor antagonists with high CNS penetration
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Ac2-DPD, the bis-(O)-acetylated derivative of 4,5-dihydroxy-2,3-pentanedione (DPD) is a convenient stable precursor of bacterial quorum sensing autoinducer AI-2
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Synthesis and evaluation of novel chromogenic aminopeptidase substrates for microorganism detection and identification
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Dopamine/serotonin receptor ligands. Part 15: Oxygenation of the benz-indolo-azecine LE 300 leads to novel subnanomolar dopamine D1/D5 antagonists
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Inhibition of Src kinase activity by 7-ethynyl-4-phenylamino-3-quinolinecarbonitriles: Identification of SKS-927
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Novel antiproliferative analogs of the Taq DNA polymerase inhibitor catalpol
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3-Hydroxychromones as cyclin-dependent kinase inhibitors: Synthesis and biological evaluation
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High-throughput screening affords novel and selective trypanothione reductase inhibitors with anti-trypanosomal activity
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Identification of arylsulfonamides as Aquaporin 4 inhibitors
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A novel diketo phosphonic acid that exhibits specific, strand-transfer inhibition of HIV integrase and anti-HIV activity
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Design and evaluation of a potential mutagen for Hepatitis C virus
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Thienopyridine urea inhibitors of KDR kinase
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Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents
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5-((1H-Pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5
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Synthesis and evaluation of aryl thioxothiazolidinone inhibitors of ADAMTS-5 (Aggrecanase-2)
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Synthesis and antibacterial evaluation of a novel series of rifabutin-like spirorifamycins
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A new visual screening assay for catalytic antibodies with retro-aldol retro-Michael activity
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Synthesis of new xanthone analogues and their biological activity test—Cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study
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Rational design and synthesis of novel nucleotide anti-Giardia agents
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Novel mitochondria-localizing TEMPO derivative for measurement of cellular oxidative stress in mitochondria
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Comparison of the in vitro apparent permeability and stability of opioid mimetic compounds with that of the native peptide
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N-Benzyl-N-(tetrahydro-2H-pyran-4-yl)pyrrolidin-3-amines as selective dual serotonin/noradrenaline reuptake inhibitors
Fulltext Access 4 Pages 2007
Preparation, characterization and in vivo conversion of new water-soluble sulfenamide prodrugs of carbamazepine
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Synthesis and reactivity of azobenzene-based bispropargyl sulfones: Interesting comparison between cyclic and acyclic systems
Fulltext Access 4 Pages 2007
Proinsecticide candidates N-(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl derivatives of imidacloprid and 1-chlorothiazolylmethyl-2-nitroimino-imidazolidine
Fulltext Access 4 Pages 2007
Induction of GRP78 by valproic acid is dependent upon histone deacetylase inhibition
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Synthesis and SAR of tetrahydropyrrolo[1,2-b][1,2,5]thiadiazol-2(3H)-one 1,1-dioxide analogues as highly potent selective androgen receptor modulators
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Gypsophin: A novel α-glucosidase inhibitory cyclic peptide from the roots of Gypsophila oldhamiana
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Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase
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Synthesis, cytotoxicity, and antiviral activities of new neolignans related to honokiol and magnolol
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Rational design of 7-arylquinolines as non-competitive metabotropic glutamate receptor subtype 5 antagonists
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Aminopyrrolidineamide inhibitors of site-1 protease
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Efficient synthesis and in vitro cytostatic activity of 4-substituted triazolyl-nucleosides
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Synthesis and cytotoxic activity of various 5-[alkoxy-(4-nitro-phenyl)-methyl]-uracils in their racemic form
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Synthesis of novel phytosphingosine derivatives and their preliminary biological evaluation for enhancing radiation therapy
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Synthesis and antibacterial activity of novel fluoroquinolones containing substituted piperidines
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3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109b
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A phosphorylated prodrug for the inhibition of Pin1
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Potent achiral agonists of the ghrelin (growth hormone secretagogue) receptor. Part I: Lead identification
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Synthesis and evaluation of novel pyrazolidinone analogs of PGE2 as EP2 and EP4 receptors agonists
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Dipeptidyl α-fluorovinyl Michael acceptors: Synthesis and activity against cysteine proteases
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Preparation of carbohydrate–oligonucleotide conjugates using the squarate spacer
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Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists
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Identifying common metalloprotease inhibitors by protein fold types using Fourier Transform Mass Spectrometry
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Phenylpiperidine-benzoxazinones as urotensin-II receptor antagonists: Synthesis, SAR, and in vivo assessment
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Discovery of novel non-cytotoxic salicylhydrazide containing HIV-1 integrase inhibitors
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Synthesis and structure–activity relationships of second-generation hydroxamate botulinum neurotoxin A protease inhibitors
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Benzopyrans as selective estrogen receptor β agonists (SERBAs). Part 4: Functionalization of the benzopyran A-ring
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Novel substituted tetrahydrotriazaacenaphthylene derivatives as potent CRF1 receptor antagonists
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Studies on a series of potent, orally bioavailable, 5-HT1 receptor ligands
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Synthesis, resolution, and antiplatelet activity of 3-substituted 1(3H)-isobenzofuranone
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Cyanine dye conjugates as probes for live cell imaging
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A minimalistic approach to identify substrate binding features in B1 Metallo-β-lactamases
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Optimized synthesis of aminooxy-peptides as glycoprobe precursors for surface-based sugar–protein interaction studies
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Synthesis and antimicrobial activity of 7-fluoro-3-aminosteroids
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Development of oligoarginine–drug conjugates linked to new peptidic self-cleavable spacers toward effective intestinal absorption
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Tetrapeptide inhibitors of the glutamate vesicular transporter (VGLUT)
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Synthesis of fluorescent and photoaffinity-labeled derivatives of bisphenol A and their inhibitory activity toward hypoxic expression of erythropoietin
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Antiviral 2,5-disubstituted imidazo[4,5-c]pyridines: Further optimization of anti-hepatitis C virus activity
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Rapid synthesis of VX-745: p38 MAP kinase inhibition in Werner syndrome cells
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An atom efficient, solvent-free, green synthesis and antimycobacterial evaluation of 2-amino-6-methyl-4-aryl-8-[(E)-arylmethylidene]-5,6,7,8-tetrahydro-4H-pyrano[3,2-c]pyridine-3-carbonitriles
Fulltext Access 4 Pages 2007
Unique spirocyclopiperazinium salt. Part 4: Modification of dispirocyclopiperazinium (DSPZ) salts as analgesics
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Fluorine-containing aryloxyethyl thiocyanate derivatives are potent inhibitors of Trypanosoma cruzi and Toxoplasma gondii proliferation
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Membrane permeable esterase-activated fluorescent imaging probe
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Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety
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Synthesis and SAR of novel conformationally restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 2: Amino substitutions on heterocyclic D-ring system
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Selective oxidation of sulfides to sulfoxides catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen
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Human serum albumin binding assay based on displacement of a non selective fluorescent inhibitor
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Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis
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Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide
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Inhibitors of anthrax lethal factor
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Synthesis of symmetrical C- and pseudo-symmetrical O-linked disaccharide analogs for arabinosyltransferase inhibitory activity in Mycobacterium tuberculosis
Fulltext Access 4 Pages 2007
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