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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

N-Hydroxy sulfonimidamides as new nitroxyl (HNO) donors
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Synthesis and in vitro pharmacological studies of new C(2) modified salvinorin A analogues
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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety
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2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: The successful reduction of hERG activity. Part 2
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Structural biology of G protein-coupled receptors
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Instructions to contributors
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QSAR for phospholipase A2 inhibitions by 1-acyloxy-3-N-n-octylcarbamyl-benzenes
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Quorum sensing in Vibrio harveyi: probing the specificity of the LuxP binding site
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2,3-Diaminopyridine as a platform for designing structurally unique nonpeptide bradykinin B1 receptor antagonists
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New pyrazolo[1′,5′:1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective PDE5 inhibitors
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Equipotent activity in both enantiomers of a series of ketopiperazine-based renin inhibitors
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Stereospecific deuteration of 2-deoxyerythrose 4-phosphate using 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase
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N-DEVD-N′-morpholinecarbonyl-rhodamine 110: novel caspase-3 fluorogenic substrates for cell-based apoptosis assay
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Inhibition of tumor cell proliferation by thieno[2,3-d]pyrimidin-4(1H)-one-based analogs
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Hypoxia-selective activation of 5-fluorodeoxyuridine prodrug possessing indolequinone structure: radiolytic reduction and cytotoxicity characteristics
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A new development of matrix metalloproteinase inhibitors: twin hydroxamic acids as potent inhibitors of MMPs
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Synthesis and photochemotherapeutic activity of thiopyrano[2,3-e]indol-2-ones
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Oximinoarylsulfonamides as potent HIV protease inhibitors
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Reduction of a 4-pyrrole phenylacyl-containing peptide with trifluoroacetic acid–triisopropylsilane–phenol–H2O during solid-phase peptide synthesis and its protein kinase C α inhibitory activity
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Solid-phase synthesis of naphthylamidines as factor VIIa/tissue factor inhibitors
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Observations on the reactivity of thiyl radicals derived from 3,6-epidithiodiketopiperazine-2,5-diones and related congeners
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Phthalazinones. Part 1: The design and synthesis of a novel series of potent inhibitors of poly(ADP-ribose)polymerase
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NMDA-NR2B subtype selectivity of stereoisomeric 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
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3-Acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors: synthesis and biological evaluation
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Synthesis and assay of isoquinoline derivatives as HIV-1 Tat–TAR interaction inhibitors
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Design, synthesis and activity of novel derivatives of Oxybutynin and Tolterodine
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Discovery of 3-OH-3-methylpipecolic hydroxamates: Potent orally active inhibitors of aggrecanase and MMP-13
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Inhibitors of the inducible microsomal prostaglandin E2 synthase (mPGES-1) derived from MK-886
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Instructions to contributors
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Synthesis and evaluation of potential inhibitors of eIF4E cap binding to 7-methyl GTP
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DNA photocleavage and biological activity of a pyrene dihydrodioxin
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Fluorescence resonance energy transfer studies of aminoglycoside binding to a T box antiterminator RNA
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A proof of the specificity of kanamycin-ribosomal RNA interaction with designed synthetic analogs and the antibacterial activity
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Quinazolines revisited: search for novel anxiolytic and GABAergic agents
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Synthesis of sphingomyelin sulfur analogue and its behavior toward sphingomyelinase
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6-(2-Furanyl)-9H-purin-2-amine derivatives as A2A adenosine antagonists
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Synthesis and opioid receptor binding properties of a highly potent 4-hydroxy analogue of naltrexone
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Discovery, synthesis and biological evaluation of novel glucokinase activators
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A colorimetric titration method for quantification of millimolar glucose in a pH 7.4 aqueous phosphate buffer
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Synthesis, in vitro, and in vivo antibacterial activity of nocathiacin I thiol-Michael adducts
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Inhibitory activities against topoisomerase I and II by isoaurostatin derivatives and their structure–activity relationships
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Dependence of reactivity of a novel 2,6-diamino pyridine-based enediyne on the extent of salt formation with external acids: a possible implication in pH based drug design
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A general carbometalation, three component coupling strategy for the synthesis of α,β-unsaturated γ-sultines including thio-rofecoxib, a selective COX-2 inhibitor
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Inosine substitutions demonstrate that intramolecular DNA quadruplexes adopt different conformations in the presence of sodium and potassium
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Instructions to contributors
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Effects of B group vitamins on reactions of various α-hydroxyl-containing organic radicals
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Structure-based design and synthesis of novel non-zinc chelating MMP-12 inhibitors
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Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyrimidines
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Synthesis and structural modeling of the amphiphilic siderophore rhizobactin-1021 and its analogs
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Hydrophobicity in the design of P2/P2′ tetrahydropyrimidinone HIV protease inhibitors
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Synthesis and structure–activity relationship of imidazo[1,2-a]benzimidazoles as corticotropin-releasing factor 1 receptor antagonists
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Design, synthesis, and bioavailability evaluation of coumarin-based prodrug of meptazinol
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Insecticidal activity of proteinous venom from tentacle of jellyfish Rhopilema esculentum Kishinouye
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Design, synthesis, and enzymatic property of a sulfur-substituted analogue of trigalacturonic acid
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Solid support synthesis of 6-aryl-2-substituted pyrimidin-4-yl phenols as anti-infective agents
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The synthesis and 16S A-site rRNA recognition of carbohydrate-free aminoglycosides
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The synthesis and biological evaluation of dopamine transporter inhibiting activity of substituted diphenylmethoxypiperidines
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Solid-phase synthesis and anti-infective activity of a combinatorial library based on the natural product anisomycin
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Contribution of site-specific PEGylation to the dipeptidyl peptidase IV stability of glucose-dependent insulinotropic polypeptide
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1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles
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Controllable selective synthesis of a polymerizable prodrug of cytarabine by enzymatic and chemical methods
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Influence of acid surrogates toward potency of VLA-4 antagonist
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Utilizing the intramolecular Fukuyama–Mitsunobu reaction for a flexible synthesis of novel heterocyclic scaffolds for peptidomimetic drug design
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Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents
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New HIV-1 replication inhibitors of the styryquinoline class bearing aroyl/acyl groups at the C-7 position: Synthesis and biological activity
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SAR studies of 2-arylthiazolidine-4-carboxylic acid amides: A novel class of cytotoxic agents for prostate cancer
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O-Methylglucogalloyl esters: Synthesis and evaluation of their antimycotic activity
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Novel peptide derivatives of bleomycin A5: Synthesis, antitumor activity and interaction with DNA
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Diprolyl nitriles as potent dipeptidyl peptidase IV inhibitors
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Instructions to contributors
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Design and synthesis of new bis-pyridinium oxime reactivators for acetylcholinesterase inhibited by organophosphorous nerve agents
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Synthesis and structure–activity relationship of 3-phenyl-3H-quinazolin-4-one derivatives as CXCR3 chemokine receptor antagonists
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New inhibitors of rabbit muscle triose-phosphate isomerase
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Biological evaluation of Tyr6 and Ser7 modified drosocin analogues
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Novel 2-N,N-dimethylaminomethyl-2,3,3a,12b-tetrahydrodibenzo[b,f]furo[2,3-d]oxepin derivatives displaying combined norepinephrine reuptake inhibition and 5-HT2A/2C receptor antagonism
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Synthesis of desthio prenylcysteine analogs: Sulfur is important for biological activity
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Design, synthesis, and evaluation of novelly substituted benzimidazole compounds as angiotensin II receptor antagonists
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Synthesis and in vitro study of novel 7-O-acyl derivatives of Oroxylin A as antibacterial agents
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In vitro antiproliferative activity against human colon cancer cell lines of representative 4-thiazolidinones. Part I
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Generation of reactive oxygen species by a persulfide (BnSSH)
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Synthesis and evaluation of photolabile insulin prodrugs
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Self-assembly of bivalent protein-binding agents based on oligonucleotide-linked organic fragments
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Cyclic urea derivatives as potent NK1 selective antagonists
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Synthesis, structure–activity relationships, and anxiolytic activity of 7-aryl-6,7-dihydroimidazoimidazole corticotropin-releasing factor 1 receptor antagonists
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Lead optimization of 4-(dimethylamino)quinazolines, potent and selective antagonists for the melanin-concentrating hormone receptor 1
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Structure–activity relationship studies of salubrinal lead to its active biotinylated derivative
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Design, synthesis, and evaluation of 2-phenoxy-indan-1-one derivatives as acetylcholinesterase inhibitors
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Toward high yield synthesis of peptide–oligonucleotide chimera through a disulfide bridge: A simplified method for oligonucleotide activation
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Synthesis, in vivo and in vitro biological activity of novel azaline B analogs
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Synthesis of (2R,3S) 3-amino-4-mercapto-2-butanol, a threonine analogue for covalent inhibition of sortases
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3-[Substituted]-5-(5-pyridin-2-yl-2H-tetrazol-2-yl)benzonitriles: Identification of highly potent and selective metabotropic glutamate subtype 5 receptor antagonists
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Design, synthesis, and antiproliferative activity of some novel aminosubstituted xanthenones, able to overcome multidrug resistance toward MES-SA/Dx5 cells
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Synthesis and HIV-1 integrase inhibitory activities of caffeic acid dimers derived from Salvia officinalis
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Synthesis of a novel prodrug of 3-(4′-geranyloxy-3′-methoxyphenyl)-2-trans-propenoic acid for colon delivery
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Polymer supported carbodiimide strategy for the synthesis of N-acylated derivatives of deoxy- and ribo purinenucleosides using active esters
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Synthesis and biological activities of novel aryl indole-2-carboxylic acid analogs as PPARγ partial agonists
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Modulators of the human CCR5 receptor. Part 2: SAR of substituted 1-(3,3-diphenylpropyl)-piperidinyl phenylacetamides
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(4-Substituted-phenyl)-(5H-10,11-dihydro-pyrrolo [2,1-c][1,4] benzodiazepin-10-yl)-methanone derivatives as vasopressin receptor modulators
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Solid-phase binding assays of peptides using EGFP-Src SH2 domain fusion protein and biotinylated Src SH2 domain
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Synthesis and biological activities of aryl-ether-, biaryl-, and fluorene-aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT-2
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