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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Synthesis and evaluation of diverse thio avarol derivatives as potential UVB photoprotective candidates
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β-Secretase (BACE-1) inhibitors: Accounting for 10s loop flexibility using rigid active sites
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Human ACAT inhibitory effects of shikonin derivatives from Lithospermum erythrorhizon
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Intestinal permeability of antivirus constituents from the fruits of Eucalyptus globulus Labill. in Caco-2 Cell Model
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Design and synthesis of a novel class of furan-based molecules as potential 20S proteasome inhibitors
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Synthesis and in vitro photodynamic activity of mono-substituted amphiphilic zinc(II) phthalocyanines
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Design and synthesis of furoxan-based nitric oxide-releasing glucocorticoid derivatives with potent anti-inflammatory activity and improved safety
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Novel tetrahydroisoquinolines are histamine H3 antagonists and serotonin reuptake inhibitors
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Further studies of tyrosine surrogates in opioid receptor peptide ligands
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Epoxygenase eicosanoids: Synthesis of tetrahydrofuran-diol metabolites and their vasoactivity
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4-N-Methyl-N′-(2-dihydroxyboryl-benzyl)amino benzonitrile and its boronate analogue sensing saccharides and fluoride ion
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Pyrrolidino-tetrahydroisoquinolines as potent dual H3 antagonist and serotonin transporter inhibitors
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Synthesis and inhibition of cancer cell proliferation of (1,3′)-bis-tetrahydroisoquinolines and piperazine systems
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Structure–activity relationships of some taxoids as multidrug resistance modulator
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Non-covalent complexes between bis-β-carbolines and double-stranded DNA: A study by electrospray ionization FT-ICR mass spectrometry (I)
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Novel 2-aminobenzothiazoles as selective neuronal nitric oxide synthase inhibitors
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Thienopyrimidinone bis-aminopyrrolidine ureas as potent melanin-concentrating hormone receptor-1 (MCH-R1) antagonists
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Synthesis of new sugar derivatives from Stachys sieboldi Miq and antibacterial evaluation against Mycobacterium tuberculosis, Mycobacterium avium, and Staphylococcus aureus
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Identification of a novel class of succinyl-nitrile-based Cathepsin S inhibitors
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Synthesis and biological evaluation of novel analogues of dictyostatin
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Synthesis and biological evaluation of pyrido[3′,2′:4,5]furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110α inhibitors
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Synthesis and in vivo antihyperglycemic activity of nature-mimicking furanyl-2-pyranones in STZ-S model
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Synthesis of marine alkaloid: 8,9-Dihydrocoscinamide B and its analogues as Novel class of antileishmanial agents
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Synthesis and biological activity of enantiomeric pairs of 5-vinylthiolactomycin congeners
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Design, synthesis, and SAR of macrocyclic tertiary carbinamine BACE-1 inhibitors
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Thiosialoside clusters using carbosilane dendrimer core scaffolds as a new class of influenza neuraminidase inhibitors
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The discovery of a new class of large-conductance Ca2+-activated K+ channel opener targeted for overactive bladder: synthesis and structure–activity relationships of 2-amino-4-azaindoles
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Synthesis of thiazolone-based sulfonamides as inhibitors of HCV NS5B polymerase
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Solid phase-assisted synthesis and screening of a small library of N-(4-hydroxyphenyl)retinamide (4-HPR) analogs
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Evaluating scoring functions for docking and designing β-secretase inhibitors
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Aminomethyl tetrahydronaphthalene biphenyl carboxamide MCH-R1 antagonists—Increasing selectivity over hERG
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Synthesis and SAR of potent and selective androgen receptor antagonists: 5,6-Dichloro-benzimidazole derivatives
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Dopamine-selective potentiometric responses by new ditopic sensory elements based on a hexahomotrioxacalix[3]arene
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Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinaseγ
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Analogues of the dopamine D2 receptor antagonist L741,626: Binding, function, and SAR
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Benzothiazole benzimidazole (S)-isothiazolidinone derivatives as protein tyrosine phosphatase-1B inhibitors
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Spirodiketopiperazine-based CCR5 antagonists: Lead optimization from biologically active metabolite
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Pharmacophore identification of KSP inhibitors
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Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 antagonists
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Structure–activity relationship in the 3-iodo-4-phenoxypyridinone (IOPY) series: The nature of the C-3 substituent on anti-HIV activity
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Design, synthesis, and evaluation of efflux substrate–metal chelator conjugates as potential antimicrobial agents
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Dual serotonin transporter/histamine H3 ligands: Optimization of the H3 pharmacophore
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Identification and structure–activity relationships of 1-aryl-3-piperidin-4-yl-urea derivatives as CXCR3 receptor antagonists
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Influence of an additional 2-amino substituent of the 1-aminoethyl pharmacophore group on the potency of rimantadine against influenza virus A
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Synthesis and biological activities of novel dexibuprofen tetraacetylriboflavin conjugates
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Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies
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Novel pyrazolopiperazinone- and pyrrolopiperazinone-based MCH-R1 antagonists
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Design of cell-permeable, fluorescent activity-based probes for the lysosomal cysteine protease asparaginyl endopeptidase (AEP)/legumain
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Synthesis of pyochelin–norfloxacin conjugates
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Highly constrained bicyclic VLA-4 antagonists
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Mutation and inhibition studies of mevalonate 5-diphosphate decarboxylase
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New biologically active epidioxysterols from Stereum hirsutum
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Novel heparin/heparan sulfate mimics as inhibitors of HGF/SF-induced MET activation
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Conformationally restricted macrocyclic analogues of combretastatins
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A novel flavonoid from Lespedeza virgata (Thunb.) DC.: Structural elucidation and antioxidative activity
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Discovery of 2,4,6-trisubstituted N-arylsulfonyl piperidines as γ-secretase inhibitors
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ω-Alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: A study of chain-length and stereochemical dependence
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Unique spirocyclopiperazinium salt III: Further investigation of monospirocyclopiperazinium (MSPZ) salts as potential analgesics
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Modification of cap group in δ-lactam-based histone deacetylase (HDAC) inhibitors
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Convenient method for the addition of disulfides to alkenes
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Peptidomimetic inhibitors of farnesyltransferase with high in vitro activity and significant cellular potency
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New 1,2,3,4-tetrahydropyrrolo[3,4-b]indole derivatives as selective CB2 receptor agonists
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Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: Peptidomimetic replacement of the P2 amino acid by 2-aminoaryl acids and other non-natural amino acids
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Enhanced efficacy of 7-hydroxy-3-methoxycadalene via glycosylation in in vivo xenograft study
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Substituted 2-pyrrolinone inhibitors of HIV-1 integrase
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Antiproliferative activities of a library of hybrids between indanones and HDAC inhibitor SAHA and MS-275 analogues
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Flavin-sensitized photoreduction of thymidine glycol
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Synthetic studies of neoclerodane diterpenes from Salvia divinorum: Exploration of the 1-position
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Novel scaffold for cathepsin K inhibitors
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Synthesis and biological evaluation of novel cytotoxic azanaphthoquinone annelated pyrrolo oximes
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Synthesis and evaluation of a 99mTc-BAT-phenylbenzothiazole conjugate as a potential in vivo tracer for visualization of amyloid β
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Potent 2′-aminoanilide inhibitors of cFMS as potential anti-inflammatory agents
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Cyathane diterpenes from Sarcodon cyrneus and evaluation of their activities of neuritegenesis and nerve growth factor production
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Synthesis of xanthone derivatives with extended π-systems as α-glucosidase inhibitors: Insight into the probable binding mode
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9-Nitroanthracene derivative as a precursor of anthraquinone for photodynamic therapy
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Antiproliferative and apoptosis inducing properties of pyrano[3,2-c]pyridones accessible by a one-step multicomponent synthesis
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Synthesis and radiopharmacological characterization of [11C]AL-438 as a nonsteroidal ligand for imaging brain glucocorticoid receptors
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2-Arylimino-5,6-dihydro-4H-1,3-thiazines as a new class of cannabinoid receptor agonists. Part 1: Discovery of CB2 receptor selective compounds
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Synthesis and preliminary evaluation of mono-[123I]iodohypericin monocarboxylic acid as a necrosis avid imaging agent
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Novel heterocyclic thyromimetics. Part 2
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Identification and SAR of potent and selective non-peptide obeline somatostatin sst1 receptor antagonists
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Discovery of pyrazine carboxamide CB1 antagonists: The introduction of a hydroxyl group improves the pharmaceutical properties and in vivo efficacy of the series
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Liver X receptor antagonists with a phthalimide skeleton derived from thalidomide-related glucosidase inhibitors
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(Phenylpiperidinyl)cyclohexylsulfonamides: Development of α1a/1d-selective adrenergic receptor antagonists for the treatment of benign prostatic hyperplasia/lower urinary tract symptoms (BPH/LUTS)
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2-Arylimino-5,6-dihydro-4H-1,3-thiazines as a new class of cannabinoid receptor agonists. Part 2: Orally bioavailable compounds
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Co-crystal structure guided array synthesis of PPARγ inverse agonists
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Discovery of novel dialkyl substituted thiophene inhibitors of HCV by in silico screening of the NS5B RdRp
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Synthesis and antibacterial activity of 3-keto-6-O-carbamoyl-11,12-cyclic thiocarbamate erythromycin A derivatives
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The isolation of secondary metabolites and in vitro potent anti-cancer activity of clerodermic acid from Enicosanthum membranifolium
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Discovery of para-alkylthiophenoxyacetic acids as a novel series of potent and selective PPARδ agonists
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7-Oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamides: Synthesis and biological activity of a new class of highly potent inhibitors of human cytomegalovirus DNA polymerase
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C-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase
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Novel linear polymers bearing thiosialosides as pendant-type epitopes for influenza neuraminidase inhibitors
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Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 1: Design, synthesis and biological activity
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Facile one-pot synthesis of thio and selenourea derivatives: A new class of potent urease inhibitors
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3,5-Disubstituted quinolines as novel c-Jun N-terminal kinase inhibitors
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Synthesis and biological evaluation of substituted 6-alkynyl-4-anilinoquinazoline derivatives as potent EGFR inhibitors
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Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen
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A novel class of Hsp90 inhibitors isolated by structure-based virtual screening
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Design and synthesis via click chemistry of 8,9-anhydroerythromycin A 6,9-hemiketal analogues with anti-MRSA and -VRE activity
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