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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Photoreactive threading agent that specifically binds to abasic sites in DNA
Fulltext Access 4 Pages 2006
Design, synthesis, and SAR studies on a series of 2-pyridinylpiperazines as potent antagonists of the melanocortin-4 receptor
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Highly selective and potent agonists of sphingosine-1-phosphate 1 (S1P1) receptor
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New pyrrolopyrimidin-6-yl benzenesulfonamides: Potent A2B adenosine receptor antagonists
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BACE-1 inhibition by a series of ψ[CH2NH] reduced amide isosteres
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Synthesis and biological evaluation of novel C (7) modified chrysin analogues as antibacterial agents
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Synthesis and monoamine transporter affinity of new 2β-carbomethoxy-3β-[aryl or heteroaryl]phenyltropanes
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Modular polyketide synthases: Investigating intermodular communication using 6 deoxyerythronolide B synthase module 2
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Optimization of CCR4 antagonists: Side-chain exploration
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Identification and initial evaluation of 4-N-aryl-[1,4]diazepane ureas as potent CXCR3 antagonists
Fulltext Access 4 Pages 2006
Synthesis and preliminary biological evaluation of (2S,1′R,2′S)- and (2S,1′S,2′R)-2-(2′-phosphonocyclopropyl)glycines, two novel conformationally constrained l-AP4 analogues
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New 7,8-ethylenedioxy-2,3-benzodiazepines as noncompetitive AMPA receptor antagonists
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Affinity identification of δ-opioid receptors using latex nanoparticles
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Synthesis, structure analysis, and antitumor activity of 3,6-disubstituted-1,4-dihydro-1,2,4,5-tetrazine derivatives
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3-Arylpiperazinylethyl-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione derivatives as novel, high-affinity and selective α1-adrenoceptor ligands
Fulltext Access 4 Pages 2006
4-Phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives, a novel class of selective δ-opioid agonists
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The structure–activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs
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New metabolically stable fatty acid amide ligands of cannabinoid receptors: Synthesis and receptor affinity studies
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Design and synthesis of downsized metastin (45–54) analogs with maintenance of high GPR54 agonistic activity
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The design, synthesis, and evaluation of two universal doxorubicin-linkers: Preparation of conjugates that retain topoisomerase II activity
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Tetrahydrobenzothiophene inhibitors of hepatitis C virus NS5B polymerase
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Scaffold oriented synthesis. Part 1: Design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitors
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NBD-labeled derivatives of the immunomodulatory drug FTY720 as tools for metabolism and mode of action studies
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Pyrazole CCK1 receptor antagonists. Part 2: SAR studies by solid-phase library synthesis and determination of Free-Wilson additivity
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Crystal structure of human ERK2 complexed with a pyrazolo[3,4-c]pyridazine derivative
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Design, synthesis and evaluation of novel uracil amino acid conjugates for the inhibition of Trypanosoma cruzi dUTPase
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Aryloxyethylamines: Binding at α7 nicotinic acetylcholine receptors
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Mapping the bound conformation and protein interactions of microtubule destabilizing peptides by STD–NMR spectroscopy
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Bicyclo[3.1.0]hexyl urea melanin concentrating hormone (MCH) receptor-1 antagonists: Impacting hERG liability via aryl modifications
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Synthesis and evaluation of novel 1-(2-acylhydrazinocarbonyl)-cycloalkyl carboxamides as interleukin-1β converting enzyme (ICE) inhibitors
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Lactones from a brown alga endophytic fungus (No. ZZF36) from the South China Sea and their antimicrobial activities
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Synthesis and biological evaluations of sulfanyltriazoles as novel HIV-1 non-nucleoside reverse transcriptase inhibitors
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Crystal structure, spectroscopic, and biological study of the copper(II) complex with third-generation quinolone antibiotic sparfloxacin
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Neurotrophic peptide aldehydes: Solid phase synthesis of fellutamide B and a simplified analog
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Privileged structure based ligands for melanocortin receptors—4,4-Disubstituted piperidine derivatives
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3-Substituted gem-cyclohexane sulfone based γ-secretase inhibitors for Alzheimer’s disease: Conformational analysis and biological activity
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Efforts toward oral bioavailability in factor VIIa inhibitors
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Novel γ-secretase inhibitors discovered by library screening of in-house synthetic natural product intermediates
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Peptide inhibitors of dengue virus NS3 protease. Part 2: SAR study of tetrapeptide aldehyde inhibitors
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Nanomolar inhibition of the enterobactin biosynthesis enzyme, EntE: Synthesis, substituent effects, and additivity
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Binding of methoxy-substituted N1-benzenesulfonylindole analogs at human 5-HT6 serotonin receptors
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3-Benzimidazol-2-yl-1H-indazoles as potent c-ABL inhibitors
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Bivalent inhibitors of glutathione S-transferase: The effect of spacer length on isozyme selectivity
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Synthesis of a potential photoactivatable anandamide analog
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Evaluations of substrate specificity and inhibition at PR/p3 cleavage site of HTLV-1 protease
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Identification of potent 5-pyrimidinyl-2-aminothiazole CDK4, 6 inhibitors with significant selectivity over CDK1, 2, 5, 7, and 9
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Radical scavenging activities of α-alanine C60 adduct
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Novel class of cyclophosphamide prodrug: Cyclophosphamide spiropiperaziniums (CPSP)
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Design of cyclic peptides with agonist activity at melanocortin receptor-4
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Inactivation of GABA transaminase by 4-acryloylphenol
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4-Hydroxyisoleucine an unusual amino acid as antidyslipidemic and antihyperglycemic agent
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Synthesis and interactions of 7-deoxy-, 10-deacetoxy, and 10-deacetoxy-7-deoxypaclitaxel with NCI/ADR-RES cancer cells and bovine brain microvessel endothelial cells
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Stereoselective synthesis and glycosidase inhibitory activity of 3,4-dihydroxy-pyrrolidin-2-one, 3,4-dihydroxy-piperidin-2-one and 1,2-dihydroxy-pyrrolizidin-3-one
Fulltext Access 4 Pages 2006
Synthesis and antibacterial activity of substituted 1,2,3,4-tetrahydropyrazino [1,2-a] indoles
Fulltext Access 4 Pages 2006
1-[4-(1H-Benzoimidazol-2-yl)-phenyl]-3-[4-(1H-benzoimidazol-2-yl)-phenyl]-urea derivatives as small molecule heparanase inhibitors
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Synthesis and antibacterial activity of 9-substituted minocycline derivatives
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Macrolactonization to 10-deoxymethynolide catalyzed by the recombinant thioesterase of the picromycin/methymycin polyketide synthase
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Synthesis of N-benzylated-2-aminoquinolines as ligands for the Tec SH3 domain
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The identification of potent and selective imidazole-based inhibitors of B-Raf kinase
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Biomimetic synthesis and ultrastructural characterization of a zerovalent gold–hydroxyapatite composite
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Discovery of N-(2-hydroxy-2-aryl-cyclohexyl) substituted spiropiperidines as GlyT1 antagonists with improved pharmacological profile
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Leptostatin: A synthetic hybrid of the cytotoxic polyketides callystatin A and leptomycin B
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A new chemical tool for exploring the physiological function of the PDE2 isozyme
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Design of novel hexahydropyrazinoquinolines as potent and selective dopamine D3 receptor ligands with improved solubility
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Biphenyl-4-ylcarbamoyl thiophene carboxylic acids as potent DHODH inhibitors
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Non-covalent modification of the heme-pocket of apomyoglobin by a 1,10-phenanthroline derivative
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Inhibitory activity of cyclohexenyl chalcone derivatives and flavonoids of fingerroot, Boesenbergia rotunda (L.), towards dengue-2 virus NS3 protease
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An improved synthesis of psammaplin A
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Structure–activity relationship studies on UK-2A, a novel antifungal antibiotic from Streptomyces sp. 517-02. Part 5: Roles of the 9-membered dilactone-ring moiety in respiratory inhibition
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Design, synthesis, and evaluation of novel kazusamycin A derivatives as potent antitumor agents
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Design and synthesis of a biotin-tagged photoaffinity probe of paeoniflorin
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A new non-azole inhibitor of ABA 8′-hydroxylase: Effect of the hydroxyl group substituted for geminal methyl groups in the six-membered ring
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1,1′-Xylyl bis-1,4,8,11-tetraaza cyclotetradecane: A new potential copper chelator agent for neuroprotection in Alzheimer’s disease. Its comparative effects with clioquinol on rat brain copper distribution
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Protein tyrosine phosphatase 1B inhibitory activity of triterpenes isolated from Astilbe koreana
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Synthesis of 2-alkoxy-8-hydroxyadenylpeptides: Towards synthetic epitope-based vaccines
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Potent 4-amino-5-azaindole factor VIIa inhibitors
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Peptide inhibitors of dengue virus NS3 protease. Part 1: Warhead
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High affinity inhibitors of the dopamine transporter (DAT): Novel biotinylated ligands for conjugation to quantum dots
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Identification of small-molecule inhibitors of the Aβ–ABAD interaction
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The synthesis and nicotinic binding activity of (±)-epiquinamide and (±)-C(1)-epiepiquinamide
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Synthesis and anticonvulsant activity of new N-1′,N-3′-disubstituted-2′H,3H,5′H-spiro-(2-benzofuran-1,4′-imidazolidine)-2′,3,5′-triones
Fulltext Access 4 Pages 2006
Synthesis and evaluation of (2-phenethyl-2H-1,2,3-triazol-4-yl)(phenyl)methanones as Kv1.5 channel blockers for the treatment of atrial fibrillation
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3-Aryl-4-hydroxyquinolin-2(1H)-one derivatives as type I fatty acid synthase inhibitors
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Synthesis and molecular modeling of a lisinopril–tryptophan analogue inhibitor of angiotensin I-converting enzyme
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Synthesis of novel keto-ACE analogues as domain-selective angiotensin I-converting enzyme inhibitors
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Synthesis and anti-angiogenesis activity of coumarin derivatives
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A practical and green approach toward synthesis of N3-substituted dihydropyrimidinones: Using Aza-Michael addition reaction catalyzed by KF/Al2O3
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Synthesis and evaluation of phenoxy acetic acid derivatives as anti-mycobacterial agents
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Stilbene-based anticancer agents: Resveratrol analogues active toward HL60 leukemic cells with a non-specific phase mechanism
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N-Tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1
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Synthesis, biochemical evaluation and rationalisation of the inhibitory activity of a series of 4-hydroxyphenyl ketones as potential inhibitors of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3)
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Synthesis of a red-shifted fluorescence polarization probe for Hsp90
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Fluorogenic ester substrates to assess proteolytic activity
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An efficient one-pot synthesis of octahydroquinazolinone derivatives using catalytic amount of H2SO4 in water
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Metabolism investigation leading to novel drug design 2: Orally active prostacyclin mimetics. Part 5
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Structure of a new cyclic nonapeptide, segetalin F, and vasorelaxant activity of segetalins from Vaccaria segetalis
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Selective COX-2 inhibitors. Part 1: Synthesis and biological evaluation of phenylazobenzenesulfonamides
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Acryloylamino-salicylanilides as EGFR PTK inhibitors
Fulltext Access 4 Pages 2006
Design and synthesis of 3,4-dihydro-1H-[1]-benzothieno[2,3-c]pyran and 3,4-dihydro-1H-pyrano[3,4-b]benzofuran derivatives as non-nucleoside inhibitors of HCV NS5B RNA dependent RNA polymerase
Fulltext Access 4 Pages 2006
Development of chemically stable solid phases for the target isolation with reduced nonspecific binding proteins
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