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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Probing structure/affinity relationships for the Plasmodium falciparum hexose transporter with glucose derivatives
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CDK2/cyclinA inhibitors: Targeting the cyclinA recruitment site with small molecules derived from peptide leads
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Hetaryl imidazoles: A novel dual inhibitors of VEGF receptors I and II
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Design and synthesis of 3-substituted benzamide derivatives as Bcr-Abl kinase inhibitors
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In silico fragment-based discovery of DPP-IV S1 pocket binders
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Design and synthesis of 2′-anilino-4,4′-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3
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New Gly-Pro-Glu (GPE) analogues: Expedite solid-phase synthesis and biological activity
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Design, synthesis, and evaluation of novel 6-chloro-/fluorochromone derivatives as potential topoisomerase inhibitor anticancer agents
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Triazolo[1,5-a]pyrimidines as novel CDK2 inhibitors: Protein structure-guided design and SAR
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Chemiluminescent acridinium-9-carboxamide boronic acid probes: Application to a homogeneous glycated hemoglobin assay
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Triaminotriazine DNA helicase inhibitors with antibacterial activity
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Biological evaluation of isothiazoloquinolones containing aromatic heterocycles at the 7-position: In vitro activity of a series of potent antibacterial agents that are effective against methicillin-resistant Staphylococcus aureus
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Isothiazoloquinolones containing functionalized aromatic hydrocarbons at the 7-position: Synthesis and in vitro activity of a series of potent antibacterial agents with diminished cytotoxicity in human cells
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Synthesis of Tic-d-Phe Ψ[CH2–CH2] isostere and its use in the development of melanocortin receptor agonists
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Thyroid receptor ligands. Part 5: Novel bicyclic agonist ligands selective for the thyroid hormone receptor β
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(+)-12α-Hydroxysophocarpine, a new quinolizidine alkaloid and related anti-HBV alkaloids from Sophora flavescens
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New benzimidazoles as thrombopoietin receptor agonists
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Synthesis and biological evaluation of novel hexahydro-pyrido[3′,2′:4,5]pyrrolo[1,2-a]pyrazines as potent and selective 5-HT2C receptor agonists
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5-Heteroatom-substituted pyrazoles as canine COX-2 inhibitors: Part 2. Structure–activity relationship studies of 5-alkylethers and 5-thioethers
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Novel lactam NK1 antagonists with anti-emetic activity
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Stimulation on DNA triplet repeat strand slippage synthesis by the designed spirocycles
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Imidazo[1,2-a]pyrimidines as functionally selective GABAA ligands
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Synthesis and structure–activity relationships of novel pyrrolocarbazole lactam analogs as potent and cell-permeable inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)
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Potent 2-[(pyrimidin-4-yl)amine}-1,3-thiazole-5-carbonitrile-based inhibitors of VEGFR-2 (KDR) kinase
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Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers
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Design, synthesis, and evaluation of 2-alkoxydihydrocinnamates as PPAR agonists
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Cyclic urea derivatives as potent NK1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions
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The discovery of fluoropyridine-based inhibitors of the factor VIIa/TF complex—Part 2
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A novel nicotinic acetylcholine receptor antagonist radioligand for PET studies
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Phthalazinones 2: Optimisation and synthesis of novel potent inhibitors of poly(ADP-ribose)polymerase
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Phenolic P2/P3 core motif as thrombin inhibitors-Design, synthesis, and X-ray co-crystal structure
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Intermolecular interactions in the crystal structures of potential HIV-1 integrase inhibitors
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Enhanced FTase activity achieved via piperazine interaction with catalytic zinc
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Analysis of anti-PDE3 activity of 2-morpholinochromone derivatives reveals multiple mechanisms of anti-platelet activity
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The discovery of a potent and selective lethal factor inhibitor for adjunct therapy of anthrax infection
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Isolation, structure elucidation, antioxidative and immunomodulatory properties of two novel dihydrocoumarins from Aloe vera
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Synthesis and structure–activity relationships of novel poly(ADP-ribose) polymerase-1 inhibitors
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Inhibition of DNA helicases with DNA-competitive inhibitors
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New, potent P1/P2-morpholinone-based HIV-protease inhibitors
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Discovery of a potent phenolic N1-benzylidene–pyridinecarboxamidrazone selective against Gram-positive bacteria
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Synthesis and structure–activity relationships of a new series of 2α-substituted trans-4,5-dimethyl-4-(3-hydroxyphenyl)piperidine as μ-selective opioid antagonists
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Design, synthesis, and biological evaluation of monopyrrolinone-based HIV-1 protease inhibitors possessing augmented P2′ side chains
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Substituted 4-hydroxyphenyl sulfonamides as pathway-selective estrogen receptor ligands
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Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties
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Androstenediol analogs as ER-β-selective SERMs
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Synthesis and pharmacochemical study of novel polyfunctional molecules combining anti-inflammatory, antioxidant, and hypocholesterolemic properties
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Structure–activity relationship study of 1,4-dihydropyridine derivatives blocking N-type calcium channels
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The reversed binding of β-phenethylamine inhibitors of DPP-IV: X-ray structures and properties of novel fragment and elaborated inhibitors
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Novel, potent P2–P3 pyrrolidine derivatives of ketoamide-based cathepsin K inhibitors
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2-((1H-Azol-1-yl)methyl)-N-arylbenzamides: Novel dual inhibitors of VEGFR-1/2 kinases
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3-(Indol-2-yl)indazoles as Chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6
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Potent, selective pyrimidinetrione-based inhibitors of MMP-13
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p38 MAP kinase inhibitors. Part 6: 2-Arylpyridazin-3-ones as templates for inhibitor design
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A novel 99mTc-labeled testosterone derivative as a potential agent for targeting androgen receptors
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Solid-phase combinatorial approach for the optimization of soluble epoxide hydrolase inhibitors
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N′,2-Diphenylquinoline-4-carbohydrazide based NK3 receptor antagonists II
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Arylsulfonamides: A study of the relationship between activity and conformational preferences for a series of factor Xa inhibitors
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Synthesis and antiviral activity against tobacco mosaic virus and 3D-QSAR of α-substituted-1,2,3-thiadiazoleacetamides
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Inhibitors of unactivated p38 MAP kinase
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Synthesis and evaluation of some lipidic aminoalcohols and diamines as immunomodulators
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Synthesis and activity of novel bile-acid conjugated glucocorticoid receptor antagonists
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Genotoxic activity of halogenated phenylglycine derivatives
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Identification and optimisation of 5-amino-7-aryldihydro-1,4-diazepines as 5-HT2A ligands
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Fluorinated and hemifluorinated surfactants derived from maltose: Synthesis and application to handling membrane proteins in aqueous solution
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Synthesis, aerobic cytotoxicity, and radiosensitizing activity of novel 2,4-dinitrophenylamine tethered 5-fluorouracil and hydroxyurea
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Synthesis and study of anti-inflammatory activity of some novel cyclophane amides
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Synthesis and biological evaluation of 5-arylamino-6-chloro-1H-indazole-4,7-diones as inhibitors of protein kinase B/Akt
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Identification of non-furan containing A2A antagonists using database mining and molecular similarity approaches
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Synthesis and anti-HIV properties of new hydroxyquinoline–polyamine conjugates on cells infected by HIV-1 LAV and HIV-1 BaL viral strains
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The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck)
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Synthesis and SAR of GlyT1 inhibitors derived from a series of N-((4-(morpholine-4-carbonyl)-1-(propylsulfonyl)piperidin-4-yl)methyl)benzamides
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Identification of a novel boron-containing antibacterial agent (AN0128) with anti-inflammatory activity, for the potential treatment of cutaneous diseases
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Adamantane 11-β-HSD-1 inhibitors: Application of an isocyanide multicomponent reaction
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Structure- and property-based design of factor Xa inhibitors: Pyrrolidin-2-ones with acyclic alanyl amides as P4 motifs
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A series of novel, potent, and selective histone deacetylase inhibitors
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A novel class of AMPA receptor allosteric modulators. Part 1: Design, synthesis, and SAR of 3-aryl-4-cyano-5-substituted-heteroaryl-2-carboxylic acid derivatives
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From arylureas to biarylamides to aminoquinazolines: Discovery of a novel, potent TRPV1 antagonist
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Synthesis and SAR of conformationally restricted inhibitors of soluble epoxide hydrolase
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Design and synthesis of substituted quinolines as novel and selective melanin concentrating hormone antagonists as anti-obesity agents
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Kinase-mediated trapping of bi-functional conjugates of paclitaxel or vinblastine with thymidine in cancer cells
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Conjugated indole-imidazole derivatives displaying cytotoxicity against multidrug resistant cancer cell lines
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Carbonic anhydrase activators: The first X-ray crystallographic study of an adduct of isoform I
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Synthesis and biological evaluation of benzamides and benzamidines as selective inhibitors of VEGFR tyrosine kinases
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Structure-based drug design of a highly potent CDK1,2,4,6 inhibitor with novel macrocyclic quinoxalin-2-one structure
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Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors
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Novel tricyclic azepine derivatives: Biological evaluation of pyrimido[4,5-b]-1,4-benzoxazepines, thiazepines, and diazepines as inhibitors of the epidermal growth factor receptor tyrosine kinase
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Synthesis of 3H-spiro[benzofuran-2,1′-cyclohexane] derivatives from naturally occurring filifolinol and their classical complement pathway inhibitory activity
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Peptidomimetic C5a receptor antagonists with hydrophobic substitutions at the C-terminus: Increased receptor specificity and in vivo activity
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Polyoxometalates—a new class of potent ecto-nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitors
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Benzodiazepine calcitonin gene-related peptide (CGRP) receptor antagonists: Optimization of the 4-substituted piperidine
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Structurally diverse 5-substituted pyrimidine nucleosides as inhibitors of Leishmania donovani promastigotes in vitro
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Synthesis, structure, and bioactivity of N′-substituted benzylidene-3,4,5-trimethoxybenzohydrazide and 3-acetyl-2-substituted phenyl-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazole derivatives
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Syntheses of triazole-modified zanamivir analogues via click chemistry and anti-AIV activities
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Discovery of potent inhibitors of pseudomonal quorum sensing via pharmacophore modeling and in silico screening
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Potent antagonists of the Kv1.5 potassium channel: Synthesis and evaluation of analogous N,N-diisopropyl-2-(pyridine-3-yl)acetamides
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Synthesis and structure-activity relationships of 3-phenyl-2-propenamides as inhibitors of glycogen phosphorylase a
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Naphtho[2,3-b][1,4]-thiazine-5,10-diones and 3-substituted-1,4-dioxo-1,4-dihydronaphthalen-2-yl-thioalkanoate derivatives: Synthesis and biological evaluation as potential antibacterial and antifungal agents
Fulltext Access 5 Pages 2006
Discovery of small molecule inhibitors of integrin αvβ3 through structure-based virtual screening
Fulltext Access 5 Pages 2006
Discovery and synthesis of tetrahydroindolone derived semicarbazones as selective Kv1.5 blockers
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Effects of α-substitutions on structure and biological activity of anticancer chalcones
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