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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Carbonic anhydrase inhibitors: Interactions of phenols with the 12 catalytically active mammalian isoforms (CA I–XIV)
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2-Aminotetralones: Novel inhibitors of MurA and MurZ
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Arylsulfonamide CB2 receptor agonists: SAR and optimization of CB2 selectivity
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An efficient route into synthetically challenging bridged achiral 1,2,4,5-tetraoxanes with antimalarial activity
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Synthesis and antioxidant activities of 3,5-dialkoxy-4-hydroxycinnamamides
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Novel non-peptidic and small-sized BACE1 inhibitors
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BACE1 inhibitors: Optimization by replacing the P1′ residue with non-acidic moiety
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Synthesis of hybrid acetogenins, α,β-unsaturated-γ-lactone-free nitrogen-containing heterocyclic analogues, and their cytotoxicity against human cancer cell lines
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A cell-penetrating peptidic GRP78 ligand for tumor cell-specific prodrug therapy
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Aurora kinase A inhibitors: Identification, SAR exploration and molecular modeling of 6,7-dihydro-4H-pyrazolo-[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione scaffold
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Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists
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Design, synthesis, and evaluation of novel ethambutol analogues
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Use of the X-ray structure of the Beta2-adrenergic receptor for drug discovery
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Synthesis and biological evaluation of trimethyl-substituted cap analogs
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Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase
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Substrate specificity and screening of the integral membrane protease Pla
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Discovery of an orally efficaceous 4-phenoxypyrrolidine-based BACE-1 inhibitor
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1-Hydroxy-2-pyridinone-based MMP inhibitors: Synthesis and biological evaluation for the treatment of ischemic stroke
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Design, synthesis, and studies of small molecule STAT3 inhibitors
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Identification of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted kinase inhibitors
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Sulfonamide derivatives of bridgehead substituted bicyclo[4.2.1]nonanes as γ-secretase inhibitors
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Truncation and non-natural amino acid substitution studies on HTLV-I protease hexapeptidic inhibitors
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In vitro SAR of pyrrolidine-containing histamine H3 receptor antagonists: Trends across multiple chemical series
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Uncovering false positives on a virtual screening search for cruzain inhibitors
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Biphenyl amide p38 kinase inhibitors 2: Optimisation and SAR
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Synthetic study of VLA-4/VCAM-1 inhibitors: Synthesis and structure-activity relationship of piperazinylphenylalanine derivatives
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Synthesis and biological evaluation of bengacarboline derivatives
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Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents
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N-(3-(Phenylcarbamoyl)arylpyrimidine)-5-carboxamides as potent and selective inhibitors of Lck: Structure, synthesis and SAR
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Synthesis and antimicrobial activity of novel C-linked imidazole glycoconjugates
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Synthesis and antispasmodic activity of lidocaine derivatives endowed with reduced local anesthetic action
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Pyrazolopyridines with potent activity against herpesviruses: Effects of C5 substituents on antiviral activity
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Discovery of novel orally active ureido NPY Y5 receptor antagonists
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β-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: Part 1. Design, synthesis, and lead identification
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Synthesis and characterization of 8-ethynyl-1,3-dihydro-benzo[b][1,4]diazepin-2-one derivatives: Part 2. New potent non-competitive metabotropic glutamate receptor 2/3 antagonists
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Chemical resolution of (±)-calanolide A, (±)-cordatolide A and their 11-demethyl analogues
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Design and synthesis of 4-[(s-triazin-2-ylamino)methyl]-N-(2-aminophenyl)-benzamides and their analogues as a novel class of histone deacetylase inhibitors
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Targeting ACE and ECE with dual acting inhibitors
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pH sensing in living cells using fluorescent microspheres
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Discovery of potent LPA2 (EDG4) antagonists as potential anticancer agents
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BACE-1 inhibitors part 3: Identification of hydroxy ethylamines (HEAs) with nanomolar potency in cells
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BACE-1 inhibitors part 2: Identification of hydroxy ethylamines (HEAs) with reduced peptidic character
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Identifying the important structural elements of brominated furanones for inhibiting biofilm formation by Escherichia coli
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Potent heteroarylpiperidine and carboxyphenylpiperidine 1-alkyl-cyclopentane carboxamide CCR2 antagonists
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Design, synthesis, and in vitro antitumor activity of new 1,4-diarylimidazole-2-ones and their 2-thione analogues
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Hybrid angiogenesis inhibitors: Synthesis and biological evaluation of bifunctional compounds based on 1-deoxynojirimycin and aryl-1,2,3-triazoles
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Synthesis and structure–activity relationships of soluble 8-substituted 4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as inhibitors of the Wee1 and Chk1 checkpoint kinases
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Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents
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Lysinyl macrocyclic hexaoxazoles: Synthesis and selective G-quadruplex stabilizing properties
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New fused benzazepine as selective D3 receptor antagonists. Synthesis and biological evaluation. Part 2: [g]-Fused and hetero-fused systems
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Synthesis and antimicrobial activity of β-lactam–bile acid conjugates linked via triazole
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Synthesis and biological activity of quinolinone and dihydroquinolinone p38 MAP kinase inhibitors
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Synthesis, in vitro and in vivo activity of thiamine antagonist transketolase inhibitors
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Novel CADD-based peptidyl vinyl ester derivatives as potential proteasome inhibitors
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Tritium radiolabelling of PB28, a potent sigma-2 receptor ligand: pharmacokinetic and pharmacodynamic characterization
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Adenosine analogues as inhibitors of P2Y12 receptor mediated platelet aggregation
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Discovery and SAR of hydrazide antagonists of the pituitary adenylate cyclase-activating polypeptide (PACAP) receptor type 1 (PAC1-R)
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Fluorescent 7-diethylaminocoumarin pyrrolobenzodiazepine conjugates: Synthesis, DNA interaction, cytotoxicity and differential cellular localization
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Discovery of a novel class of 1,3-dioxane-2-carboxylic acid derivatives as subtype-selective peroxisome proliferator-activated receptor α (PPARα) agonists
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Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH)
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Synthesis and biological properties of β-turned Aβ31–35 constrained analogues
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An asymmetric C8/C8′-tripyrrole-linked sequence-selective pyrrolo[2,1-c][1,4]benzodiazepine (PBD) dimer DNA interstrand cross-linking agent spanning 11 DNA base pairs
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Structure-based design of novel groups for use in the P1 position of thrombin inhibitor scaffolds. Part 2: N-acetamidoimidazoles
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Structure and property based design of factor Xa inhibitors: Pyrrolidin-2-ones with biaryl P4 motifs
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Capillary zone electrophoresis for separation and analysis of four diarylheptanoids and an α-tetralone derivative in the green walnut husks (Juglans regia L.)
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The impact of primary packaging on the quality of parenteral products
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Chromatographic behavior of zwitterionic enalapril—Exploring the conditions for lipophilicity assessment
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Utility of cyclodextrins in the formulation of genistein: Part 1. Preparation and physicochemical properties of genistein complexes with native cyclodextrins
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Validated HPTLC methods for the determination of salicin in Salix sp. and of harpagoside in Harpogophytum procumbens
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Investigation of mass-balance issue in e-beam sterilized paclitaxel eluting coronary stents by SPME/GC-MS
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Pharmacokinetics of amoxicillin in human urine using online coupled capillary electrophoresis with electrogenerated chemiluminescence detection
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Liquid chromatographic–tandem mass spectrometric method for the simultaneous quantitation of telmisartan and hydrochlorothiazide in human plasma
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Bioequivalence study of bromhexine by liquid chromatography–electrospray ionization-mass spectrometry after oral administration of bromhexine hydrochloride tablets
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High-performance liquid chromatographic and pharmacokinetic analyses of an intravenous submicron emulsion of perillyl alcohol in rats
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Quantitative determination of spinosin in rat plasma by liquid chromatography-tandem mass spectrometry method
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Design and identification of selective HER-2 sheddase inhibitors via P1′ manipulation and unconventional P2′ perturbations to induce a molecular metamorphosis
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Substituted 2-oxo-azepane derivatives are potent, orally active γ-secretase inhibitors
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Design, synthesis, and in vitro photodynamic activities of benzochloroporphyrin derivatives as tumor photosensitizers
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Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: Optimising brain penetration
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Azaterphenyl diamidines as antileishmanial agents
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Development of dimeric modulators for anti-apoptotic Bcl-2 proteins
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Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists
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Discovery of amide and heteroaryl isosteres as carbamate replacements in a series of orally active γ-secretase inhibitors
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Identification and synthesis of a unique thiocarbazate cathepsin L inhibitor
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Design and synthesis of 4-quinolinone 2-carboxamides as calpain inhibitors
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Low-density lipoprotein (LDL)-antioxidant lignans from Myristica fragrans seeds
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Imidazolyl benzimidazoles and imidazo[4,5-b]pyridines as potent p38α MAP kinase inhibitors with excellent in vivo antiinflammatory properties
Fulltext Access 5 Pages 2008
Trisubstituted 1,2,4-triazoles as ligands for the ghrelin receptor: On the significance of the orientation and substitution at position 3
Fulltext Access 5 Pages 2008
Extraction and determination of 2-pyrazoline derivatives using liquid phase microextraction based on solidification of floating organic drop
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Development of CXCR3 antagonists. Part 3: Tropenyl and homotropenyl-piperidine urea derivatives
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Diastereoselective synthesis of (R)-(alkyl)-β-d-galactopyranoside by using β-galactosidase (Aspergillus oryzae) in low-water media
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Efficient enhancement of DNA cleavage activity by introducing guanidinium groups into diiron(III) complex
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Antimicrobial activities of the bromophenols from the red alga Odonthalia corymbifera and some synthetic derivatives
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Synthesis and anti-inflammation evaluation of new C60 fulleropyrrolidines bearing biologically active xanthine
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The discovery of GSK221149A: A potent and selective oxytocin antagonist
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1-Toluene-sulfonyl-3-[(3′-hydroxy-5′-substituted)-γ-butyrolactone]-indoles: Synthesis, COX-2 inhibition and anti-cancer activities
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Development of potent, allosteric dual Akt1 and Akt2 inhibitors with improved physical properties and cell activity
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Novel thiol-based TACE inhibitors. Part 2: Rational design, synthesis, and SAR of thiol-containing aryl sulfones
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Synthesis and biological activity of piperazine and diazepane amides that are histamine H3 antagonists and serotonin reuptake inhibitors
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Amino acid derivatives as histone deacetylase inhibitors
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