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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Mechanism based protein crosslinking of domains from the 6-deoxyerythronolide B synthase
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Design and campaign synthesis of piperidine- and thiazole-based histone deacetylase inhibitors
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Design and synthesis of morpholine derivatives. SAR for dual serotonin & noradrenaline reuptake inhibition
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Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists
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Design and campaign synthesis of pyridine-based histone deacetylase inhibitors
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An efficient one-pot synthesis of tethered cyclohexadiene enaminonitriles from methyl-ketones: An effective route to quinazolines
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Synthetic libraries of tyrosine-derived bacterial metabolites
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Functionalization of the 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) core
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Top-down mass spectrometry on low-resolution instruments: Characterization of phosphopantetheinylated carrier domains in polyketide and non-ribosomal biosynthetic pathways
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Synthesis and analysis of a fluorinated product analogue as an inhibitor for 1-deoxy-d-xylulose 5-phosphate reductoisomerase
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A set of phosphatase-inert “molecular rulers” to probe for bivalent mannose 6-phosphate ligand–receptor interactions
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Possible chemical mechanisms underlying the antitumor activity of S-deoxyleinamycin
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Facile synthesis of substituted trans-2-arylcyclopropylamine inhibitors of the human histone demethylase LSD1 and monoamine oxidases A and B
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Synthesis and antimicrobial properties of Monensin A esters
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Synthesis and in vitro antimycobacterial activity of B-ring modified diaryl ether InhA inhibitors
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Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety
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Dopamine/serotonin receptor ligands. Part 17: A cross-target SAR approach: Affinities of azecine-styled ligands for 5-HT2A versus D1 and D2 receptors
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Preliminary in vivo evaluation of a novel 99mTc-Labeled HYNIC-cys-annexin A5 as an apoptosis imaging agent
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Design, synthesis, and structure–activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethyl spiropiperidine
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Pyrrolo[2,1-c][1,4]benzodiazepine-β-glucuronide prodrugs with a potential for selective therapy of solid tumors by PMT and ADEPT strategies
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2-Aminopropane-1,2,3-tricarboxylic acid: Synthesis and co-crystallization with the class A β-lactamase BS3 of Bacillus licheniformis
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Synthesis and biological activities of reveromycin A and spirofungin A derivatives
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Discovery and biological evaluation of novel α-glucosidase inhibitors with in vivo antidiabetic effect
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Discovery of new binding elements in DPP-4 inhibition and their applications in novel DPP-4 inhibitor design
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Discovery of potent, orally active benzimidazole glucagon receptor antagonists
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Synthesis and characterization of 1,3-dihydro-benzo[b][1,4]diazepin-2-one derivatives: Part 3. New potent non-competitive metabotropic glutamate receptor 2/3 antagonists
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4-Amino-2-cyanopyrimidines: Novel scaffold for nonpeptidic cathepsin S inhibitors
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A novel peptide from α5 helix of Asterina pectinifera cyclin B conjugated to HIV-Tat49-57 with cytotoxic and apoptotic effects against human cancer cells
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4-(1,1-Dioxo-1,4-dihydro-1λ6-benzo[1,4]thiazin-3-yl)-5-hydroxy-2H-pyridazin-3-ones as potent inhibitors of HCV NS5B polymerase
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4-Amino-6-arylamino-pyrimidine-5-carbaldehyde hydrazones as potent ErbB-2/EGFR dual kinase inhibitors
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Knowledge-based design of 7-azaindoles as selective B-Raf inhibitors
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Synthesis and anti-inflammatory activity of 2-aryloxy methyl oxazolines
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Aminoquinazolines as TRPV1 antagonists: Modulation of drug-like properties through the exploration of 2-position substitution
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Factor VIIa inhibitors: Target hopping in the serine protease family using X-ray structure determination
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Zwitterionic uracil derivatives as potent GnRH receptor antagonists with improved pharmaceutical properties
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2-Arylpyrimidines: Novel CRF-1 receptor antagonists
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Discovery of dihydroquinoxalinone acetamides containing bicyclic amines as potent Bradykinin B1 receptor antagonists
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N-Pyridin-3-yl- and N-quinolin-3-yl-benzamides: Modulators of Human Vanilloid Receptor 1 (TRPV1)
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Studies on the structure–activity relationship of bicifadine analogs as monoamine transporter inhibitors
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Pyrano-[2,3b]-pyridines as potassium channel antagonists
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Development of 2-tbutyl-N-methyl pyrimidones as potent inhibitors of HIV integrase
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Identification of prostaglandin D2 receptor antagonists based on a tetrahydropyridoindole scaffold
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Scaffold oriented synthesis. Part 2: Design, synthesis and biological evaluation of pyrimido-diazepines as receptor tyrosine kinase inhibitors
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A novel bifunctional maleimido CHX-A″ chelator for conjugation to thiol-containing biomolecules
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2-Arylbenzoxazoles as novel cholesteryl ester transfer protein inhibitors: Optimization via array synthesis
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Synthesis of small molecule inhibitors of the orphan nuclear receptor steroidogenic factor-1 (NR5A1) based on isoquinolinone scaffolds
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Hypoxia-inducible factor-1 and nuclear factor-κB inhibitory meroterpene analogues of bakuchiol, a constituent of the seeds of Psoralea corylifolia
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4′-Methyl-4,5′-bithiazole-based correctors of defective ΔF508-CFTR cellular processing
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New chemotypes for cathepsin K inhibitors
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Synthesis of new benzimidazole linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates with efficient DNA-binding affinity and potent cytotoxicity
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Antioxidant capacity of human blood plasma and human urine: Simultaneous evaluation of the ORAC index and ascorbic acid concentration employing pyrogallol red as probe
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Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonates using NMR spectroscopy
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Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones
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Halicyclamine A, a marine spongean alkaloid as a lead for anti-tuberculosis agent
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2-N-Methyl modifications and SAR studies of manzamine A
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Thiahomoisocitrate: A highly potent inhibitor of homoisocitrate dehydrogenase involved in the α-aminoadipate pathway
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Targeted inhibition of hedgehog signaling by cyclopamine prodrugs for advanced prostate cancer
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Chemical synthesis of scyllo-inosamine and catabolism studies in Sinorhizobium meliloti
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Kinetic parameters and recognition of thymidine analogues with varying functional groups by thymidine phosphorylase
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Ratiometric multimodal chemosensors based on cubic silsesquioxanes for monitoring solvent polarity
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Petiolins A–C, phloroglucinol derivatives from Hypericum pseudopetiolatum var. kiusianum
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Evaluation of ligand-binding affinity using polynomial empirical scoring functions
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Synthesis and biological evaluation of immunosuppressive agent DZ2002 and its stereoisomers
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Identification of neomycin B-binding site in T box antiterminator model RNA
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In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II
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Axial chirality and affinity at the GABAA receptor of pyrimido[1,2-a][1,4]benzodiazepines and related compounds
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Hedgehog/GLI-mediated transcriptional inhibitors from Zizyphus cambodiana
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Lycoparins A-C, new alkaloids from Lycopodium casuarinoides inhibiting acetylcholinesterase
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Hybrids of 1-deoxynojirimycin and aryl-1,2,3-triazoles and biological studies related to angiogenesis
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Graphical contents list
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Synthesis and antimicrobial activity of dermaseptin S1 analogues
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Cyclic voltammetric analysis of 2-styrylchromones: Relationship with the antioxidant activity
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Synthesis and bio-evaluation of a new fatty acid derivative for myocardial imaging
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Salicylanilides: Selective inhibitors of interleukin-12p40 production
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Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis
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Cytotoxic bromotyrosine derivatives from a two-sponge association of Jaspis sp. and Poecillastra sp.
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Synthesis and structure–activity relationship of benzetimide derivatives as human CXCR3 antagonists
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Piperidine dispiro-1,2,4-trioxane analogues
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Synthesis and biological evaluation of the Zn (II)-IDB complexes appended with oligopolyamide as potent artificial nuclease
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Synthesis and evaluation of pyrazolo[1,5-b]pyridazines as selective cyclin dependent kinase inhibitors
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Tetrakis-azaaromatic quaternary ammonium salts: Novel subtype-selective antagonists at neuronal nicotinic receptors that mediate nicotine-evoked dopamine release
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New classes of Gram-positive selective antibacterials: Inhibitors of MRSA and surrogates of the causative agents of anthrax and tuberculosis
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N-Glycine-sulfonamides as potent dual orexin 1/orexin 2 receptor antagonists
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Inhibitors of the tyrosine kinase EphB4. Part 2: Structure-based discovery and optimisation of 3,5-bis substituted anilinopyrimidines
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Peptide deformylase inhibitors of Mycobacterium tuberculosis: Synthesis, structural investigations, and biological results
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Synthesis of trans-caffeate analogues and their bioactivities against HIV-1 integrase and cancer cell lines
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Synthesis and biological evaluation of homopiperazine derivatives with β-aminoacyl group as dipeptidyl peptidase IV inhibitors
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Modulation of PPAR receptor subtype selectivity of the ligands: Aliphatic chain vs aromatic ring as a spacer between pharmacophore and the lipophilic moiety
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Screening of herbal constituents for aromatase inhibitory activity
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Dihydropyrazolopyrimidine Inhibitors of KV1.5 (IKur)
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The discovery of AZD5597, a potent imidazole pyrimidine amide CDK inhibitor suitable for intravenous dosing
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Discovery of diacylphloroglucinols as a new class of GPR40 (FFAR1) agonists
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Identification and optimization of N3,N6-diaryl-1H-pyrazolo[3,4-d]pyrimidine-3,6-diamines as a novel class of ACK1 inhibitors
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Carbonic anhydrase inhibitors. Inhibition of the β-class enzyme from the yeast Saccharomyces cerevisiae with anions
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Synthesis, SAR, and antibacterial activity of novel oxazolidinone analogues possessing urea functionality
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Antitumor effects of curcumin and structurally β-diketone modified analogs on multidrug resistant cancer cells
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Chemotherapeutic bone-targeted bisphosphonate prodrugs with hydrolytic mode of activation
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Design of a pyrene-containing fluorescence probe for labeling of RNA poly(A) tracts
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The influence of esters and carboxylic acids as the N-substituent of opioids. Part 1: Benzomorphans
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Inhibition of 15-lipoxygenase-catalysed oxygenation of arachidonic acid by substituted benzoic acids
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