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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Site-specific immobilization of proteins in a microarray using intein-mediated protein splicing
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5-Lipoxygenase inhibitors: convenient synthesis of 4-[3-(4-heterocyclylphenylthio)phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxamide analogues
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Synthesis and evaluation of 3D templates based on a taxane skeleton to circumvent P-glycoprotein-associated multidrug resistance of cancer
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Macrolactonization catalyzed by the terminal thioesterase domain of the nonribosomal peptide synthetase responsible for lichenysin biosynthesis
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Discovery of 4-(dimethylamino)quinazolines as potent and selective antagonists for the melanin-concentrating hormone receptor 1
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Structure–activity relationships of arylbenzofuran H3 receptor antagonists
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3,3-Bisaryloxindoles as mineralocorticoid receptor antagonists
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Redefining the structure–activity relationships of 2,6-methano-3-benzazocines. Part 3: 8-Thiocarboxamido and 8-thioformamido derivatives of cyclazocine
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4-Alkyl and 4,4′-dialkyl 1,2-bis(4-chlorophenyl)pyrazolidine-3,5-dione derivatives as new inhibitors of bacterial cell wall biosynthesis
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In vitro advanced antimycobacterial screening of isoniazid-related hydrazones, hydrazides and cyanoboranes: Part 14
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Structure-based design of protein tyrosine phosphatase-1B inhibitors
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Synthesis and biological evaluation of new biphalin analogues with non-hydrazine linkers
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Discovery of novel conformationally constrained tropane-based biaryl and arylacetylene ligands as potent and selective norepinephrine transporter inhibitors and potential antidepressants
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Geometry, topology, and atom-weights assembly descriptors to predicting A1 adenosine receptors agonists
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1-((S)-γ-Substituted prolyl)-(S)-2-cyanopyrrolidine as a novel series of highly potent DPP-IV inhibitors
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Structure–activity relationship of a series of cyclohexylpiperidines bearing an amide side chain as antagonists of the human melanocortin-4 receptor
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Identification of aminopiperidine benzamides as MCHr1 antagonists
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(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: Further optimisation as highly potent and selective MSK-1-inhibitors
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(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors
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Deoxyribosyl analogues of methionyl and isoleucyl sulfamate adenylates as inhibitors of methionyl-tRNA and isoleucyl-tRNA synthetases
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Synthesis and biological evaluation of quinoxaline-5,8-diones that inhibit vascular smooth muscle cell proliferation
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Syntheses of NAMDA derivatives inhibiting NO production in BV-2 cells stimulated with lipopolysaccharide
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Active site binding modes of curcumin in HIV-1 protease and integrase
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6-Aryl-4-methylsulfanyl-2H-pyran-2-one-3-carbonitriles as PPAR-γ activators
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(2R)-2-Methylchromane-2-carboxylic acids: Discovery of selective PPARα agonists as hypolipidemic agents
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Novel 3,4-diarylpyrazolines as potent cannabinoid CB1 receptor antagonists with lower lipophilicity
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Novel, selective indole-based ECE inhibitors: Lead optimization via solid-phase and classical synthesis
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Correlation of cytotoxic activity of betulinines and their hydroxy analogues
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Hepatitis C virus NS3-4A serine protease inhibitors: SAR of P2′ moiety with improved potency
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Synthesis and in vitro pharmacological studies of C(4) modified salvinorin A analogues
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Carbonic anhydrase inhibitors: Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with benzo[b]thiophene 1,1-dioxide sulfonamides
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Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists
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Carbonic anhydrase inhibitors: Inhibition of the tumor-associated isozymes IX and XII with a library of aromatic and heteroaromatic sulfonamides
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Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 1
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Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 2
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Synthesis and evaluation of 18F-labeled dopamine D3 receptor ligands as potential PET imaging agents
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Activity and QSAR study of baogongteng A and its derivatives as muscarinic agonists
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Synthesis of [1,2,4]triazolo[1,5-a]pyrazines as adenosine A2A receptor antagonists
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Synthesis of cationic β-vinyl substituted meso-tetraphenylporphyrins and their in vitro activity against herpes simplex virus type 1
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The discovery of fluoropyridine-based inhibitors of the Factor VIIa/TF complex
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Total and semisynthesis and in vitro studies of both enantiomers of 20-fluorocamptothecin
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Parallel synthesis and biological evaluation of 5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidin-4(3H)-one cytotoxic agents selective for p21-deficient cells
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Novel C2–C3′ N-peptide linked macrocyclic taxoids. Part 1: Synthesis and biological activities of docetaxel analogues with a peptide side chain at C3′
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An efficient synthesis of argifin: A natural product chitinase inhibitor with chemotherapeutic potential
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Identification of a potent and selective 5-HT1B receptor antagonist
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Diamino-C,N-diarylpyridine positional isomers as inhibitors of lysophosphatidic acid acyltransferase-β
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Bioisosteric phentolamine analogs as potent α-adrenergic antagonists
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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold
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Neamine dimers targeting the HIV-1 TAR RNA
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Selective interaction between tylophorine B and bulged DNA
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Induction of apoptosis by a novel indirubin-5-nitro-3′-monoxime, a CDK inhibitor, in human lung cancer cells
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Discovery and optimisation of potent, selective, ethanolamine inhibitors of bacterial phenylalanyl tRNA synthetase
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Furanyl-1,3-thiazol-2-yl and benzoxazol-5-yl acetic acid derivatives: novel classes of heparanase inhibitor
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The development of monocyclic pyrazolone based cytokine synthesis inhibitors
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Analogues of the neuroprotective tripeptide Gly-Pro-Glu (GPE): synthesis and structure–activity relationships
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Benzimidazoles as non-peptide luteinizing hormone-releasing hormone (LHRH) antagonists. Part 3: Discovery of 1-(1H-benzimidazol-5-yl)-3-tert-butylurea derivatives
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Novel approach to pro-drugs of lactones: water soluble imidate and ortho-ester derivatives of a furanone-based COX-2 selective inhibitor
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Design, synthesis and biological evaluation of novel, simplified analogues of laulimalide: modification of the side chain
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Studies on the reactivity of CDDO, a promising new chemopreventive and chemotherapeutic agent: implications for a molecular mechanism of action
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A structural screening approach to ketoamide-based inhibitors of cathepsin K
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Novel 4-amino-furo[2,3-d]pyrimidines as Tie-2 and VEGFR2 dual inhibitors
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Effects of linking 15-zinc finger domains on DNA binding specificity and multiple DNA binding modes
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Structure–activity relationships of 1-alkyl-5-(3,4-dichlorophenyl)-5-{2-[3-(substituted)-1-azetidinyl]-ethyl}-2-piperidones. Part 2: Improving oral absorption
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Solid-phase synthesis and antibacterial evaluations of N-demethylvancomycin derivatives
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Bradykinin B1 antagonists: SAR studies in the 2,3-diaminopyridine series
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Estrogen receptor ligands. Part 13: Dihydrobenzoxathiin SERAMs with an optimized antagonist side chain
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Ketoheterocycle-based inhibitors of cathepsin K: A novel entry into the synthesis of peptidic ketoheterocycles
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Lipophilic versus hydrogen-bonding effect in P3 on potency and selectivity of valine aspartyl ketones as caspase 3 inhibitors
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2-Aminoquinazoline inhibitors of cyclin-dependent kinases
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Radiosynthesis of carbon-11-labeled camptothecin derivatives as potential positron emission tomography tracers for imaging of topoisomerase I in cancers
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Synthesis of an N-acyl sulfamate analog of luciferyl-AMP: A stable and potent inhibitor of firefly luciferase
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SAR and biological evaluation of novel trans-3,4-dimethyl-4-arylpiperidine derivatives as opioid antagonists
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A 3D-QSAR model for CYP2D6 inhibition in the aryloxypropanolamine series
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Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3
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Synthesis of doxorubicin–peptide conjugate with multidrug resistant tumor cell killing activity
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Antibiotics GE23077, novel inhibitors of bacterial RNA polymerase. Part 3: Chemical derivatization
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Synthesis and biological evaluation of benzothiazole derivatives as potent antitumor agents
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Novel heterocyclic glucocorticoids: in vitro profile and in vivo efficacy
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Nanodroplet profiling of enzymatic activities in a microarray
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Discovery of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid diamides that increase CFTR mediated chloride transport
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Design, synthesis and ribosome binding of chloramphenicol nucleotide and intercalator conjugates
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2-(Arylmethyl)-3-substituted quinuclidines as selective α7 nicotinic receptor ligands
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2-Ethoxybenzoxazole as a bioisosteric replacement of an ethyl benzoate group in a human rhinovirus (HRV) capsid binder
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Kinesin spindle protein (KSP) inhibitors. Part 1: The discovery of 3,5-diaryl-4,5-dihydropyrazoles as potent and selective inhibitors of the mitotic kinesin KSP
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Synthesis and antibacterial activity of alkyl derivatives of the glycopeptide antibiotic A40926 and their amides
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Synthesis of novel curcumin mimics with asymmetrical units and their anti-angiogenic activity
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Chemical modification of the naphthoyl 3-position of JWH-015: In search of a fluorescent probe to the cannabinoid CB2 receptor
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Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands
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Synthesis and antidepressant activity of some 1,3,5-triphenyl-2-pyrazolines and 3-(2″-hydroxy naphthalen-1″-yl)-1,5-diphenyl-2-pyrazolines
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Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives
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Functionalized head-to-head hairpin polyamides: Synthesis, double-stranded DNA-binding activity and affinity
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Discovery and SAR of 4-amino-2-biarylbutylurea MCH 1 receptor antagonists through solid-phase parallel synthesis
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2-(2-Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: Highly potent, orally active, adenosine A2A antagonists. Part 1
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4-Fluorosulfonylpiperidines: Selective 5-HT2A ligands for the treatment of insomnia
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Synthesis and bioactivities of two multiple antigen peptides as potential vaccine against schistosoma
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Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase
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The development of new isoxazolone based inhibitors of tumor necrosis factor-alpha (TNF-α) production
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3-(2-Ethoxy-4-{4-[3-hydroxy-2-methyl-4-(3-methylbutanoyl)phenoxy]butoxy}phenyl)propanoic acid: a brain penetrant allosteric potentiator at the metabotropic glutamate receptor 2 (mGluR2)
Fulltext Access 5 Pages 2005
Synthesis and anthelmintic activity of 7-substituted 3,4a-dimethyl-4a,5a,8a,8b-tetrahydro-6H-pyrrolo[3′,4′:4,5]furo[3,2-b]pyridine-6,8(7H)-diones
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Optimization of purine based PDE1/PDE5 inhibitors to a potent and selective PDE5 inhibitor for the treatment of male ED
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