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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Stereoselective synthesis of a novel 2-aza-7-oxabicyclo[3.3.0]octane as neurokinin-1 receptor antagonist
Fulltext Access 4 Pages 2007
Antitrypanosomal activity of quaternary naphthalimide derivatives
Fulltext Access 4 Pages 2007
Synthesis and evaluation of prodrugs for anti-angiogenic pyrrolylmethylidenyl oxindoles
Fulltext Access 4 Pages 2007
Identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitor
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Antibody catalyzed hydrolysis of a quorum sensing signal found in Gram-negative bacteria
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Discovery of an androgen receptor modulator pharmacophore based on 2-quinolinones
Fulltext Access 4 Pages 2007
Novel hydroxamic acid-related phosphinates: Inhibition of neutral aminopeptidase N (APN)
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Probing binding requirements of NAD kinase with modified substrate (NAD) analogues
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High-affinity carbamate analogues of morphinan at opioid receptors
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The role of fluorine substitution in the structure–activity relationships (SAR) of classical cannabinoids
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Investigation of the terminal P4 domain in a series of d-phenylglycinamide-based factor Xa inhibitors
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Synthesis and biological evaluation of N-(aryl)-2-thiophen-2-ylacetamides series as a new class of antitubercular agents
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Synthesis of andrographolide derivatives and their TNF-α and IL-6 expression inhibitory activities
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Efficient synthesis and biological evaluation of ω-oxygenated analogues of vitamin K2: Study of modification and structure–activity relationship of vitamin K2 metabolites
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Novel sequence-responding fluorescent oligoDNA probe bearing a silylated pyrene molecule
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A polyacetylene compound from herbal medicine regulates genes associated with thrombosis in endothelial cells
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Spermatinamine, the first natural product inhibitor of isoprenylcysteine carboxyl methyltransferase, a new cancer target
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Synthesis and in vivo activity of MK2 and MK2 substrate-selective p38αMAPK inhibitors in Werner syndrome cells
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Novel substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(±)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents
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Syntheses of novel myxopyronin B analogs as potential inhibitors of bacterial RNA polymerase
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A novel series of highly selective inhibitors of MMP-3
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Dipeptidyl-α,β-epoxyesters as potent irreversible inhibitors of the cysteine proteases cruzain and rhodesain
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Highly regioselective enzymatic synthesis of polymerizable derivatives of methyl shikimate
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New antioxidant polyphenols from the medicinal mushroom Inonotus obliquus
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Nitrogen-containing flavonoids as CDK1/Cyclin B inhibitors: Design, synthesis, and biological evaluation
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Design, synthesis, and biological evaluation of novel analogues of archazolid: A highly potent simplified V-ATPase inhibitor
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Aminocarbonylation route to tolvaptan
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Enantioselective synthesis and vanilloid activity evaluation of 1-β-(p-methoxycinnamoyl)polygodial, an antinociceptive compound from Drymis winteri barks
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Synthesis, in vitro inhibitory activity towards COX-2 and haemolytic activity of derivatives of Esculentoside A
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Xanthones from Cudrania Tricuspidata displaying potent α-glucosidase inhibition
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Stereoselective synthesis and cytotoxicity of a cancer chemopreventive naphthoquinone from Tabebuia avellanedae
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Antihyperglycemic and antidyslipidemic agent from Aegle marmelos
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Synthesis of novel diaryl ethers and their evaluation as antimitotic agents
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Synthesis of potent and tissue-selective androgen receptor modulators (SARMs): 2-(2,2,2)-Trifluoroethyl-benzimidazole scaffold
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Specific stabilization of DNA triple helices by indolo[2,1-b]quinazolin-6,12-dione derivatives
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Discovery of non-covalent dipeptidyl peptidase IV inhibitors which induce a conformational change in the active site
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N-Caffeoylphenalkylamide derivatives as bacterial efflux pump inhibitors
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Butyl 2-(4-[1.1′-biphenyl]-4-yl-1H-imidazol-2-yl)ethylcarbamate, a potent sodium channel blocker for the treatment of neuropathic pain
Fulltext Access 4 Pages 2007
New antifungal flavonoid glycoside from Vitex negundo
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Oxazolidinones as novel human CCR8 antagonists
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Discovery of tetralin ureas as potent melanin concentrating hormone 1 receptor antagonists
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A spectroscopic and molecular modeling study of sinomenine binding to transferrin
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Further studies on the binding of N1-substituted tryptamines at h5-HT6 receptors
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A novel, non-substrate-based series of glycine type 1 transporter inhibitors derived from high-throughput screening
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Solid-phase analogue synthesis of caspase-3 inhibitors via palladium-catalyzed amination of 3-bromopyrazinones
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Inhibition of the mitochondrial F1F0-ATPase by ligands of the peripheral benzodiazepine receptor
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Structure–activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors
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3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonists
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Synthesis and evaluation of 4-O-alkylated 2-deoxy-2,3-didehydro-N-acetylneuraminic acid derivatives as inhibitors of human parainfluenza virus type-3 sialidase activity
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Structural modifications of (1S,3S)-3-amino-4-difluoromethylenecyclopentanecarboxylic acid, a potent irreversible inhibitor of GABA aminotransferase
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In vitro biotransformations of the prostaglandin D2 (DP) antagonist MK-0524 and synthesis of metabolites
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A novel butyrolactone derivative inhibited apoptosis and depressed integrin β4 expression in vascular endothelial cells
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Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase
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Design and synthesis of substrate-mimic inhibitors of mycothiol-S-conjugate amidase from Mycobacterium tuberculosis
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5-HT2C antagonists based on fused heterotricyclic templates: Design, synthesis and biological evaluation
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New competitive inhibitors of cytosolic (NADH-dependent) rabbit muscle glycerophosphate dehydrogenase
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Kynurenic acid amides as novel NR2B selective NMDA receptor antagonists
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Antiviral 2,5-disubstituted imidazo[4,5-c]pyridines: From anti-pestivirus to anti-hepatitis C virus activity
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Trimethylsilylpyrazoles as novel inhibitors of p38 MAP kinase: A new use of silicon bioisosteres in medicinal chemistry
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From dihydroxypyrimidine carboxylic acids to carboxamide HIV-1 integrase inhibitors: SAR around the amide moiety
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Antitumor activity of the marine natural product dibromophakellstatin in vitro
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New carbon-linked azole oxazolidinones with improved potency and pharmacokinetics
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Synthesis and evaluation of peptidic maleimides as transglutaminase inhibitors
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Constrained azacyclic analogues of the immunomodulatory agent FTY720 as molecular probes for sphingosine 1-phosphate receptors
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Potent and selective xanthine-based inhibitors of phosphodiesterase 5
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Newer tetracycline derivatives: Synthesis, anti-HIV, antimycobacterial activities and inhibition of HIV-1 integrase
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Application of the Suzuki–Miyaura cross-coupling to increase antimicrobial potency generates promising novel antibacterials
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Fluorinated NSC as a Cdc25 inhibitor
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Preparation of novel antibacterial agents. Replacement of the central aromatic ring with heterocycles
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Evaluation of fluorescently labeled xylopyranosides as probes for proteoglycan biosynthesis
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Design of antimicrobial compounds based on peptide structures
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Inhibitors of HCV NS5B polymerase: Synthesis and structure–activity relationships of unsymmetrical 1-hydroxy-4,4-dialkyl-3-oxo-3,4-dihydronaphthalene benzothiadiazine derivatives
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An analogue of AICAR with dual inhibitory activity against WNV and HCV NTPase/helicase: Synthesis and in vitro screening of 4-carbamoyl-5-(4,6-diamino-2,5-dihydro-1,3,5-triazin-2-yl)imidazole-1-β-d-ribofuranoside
Fulltext Access 4 Pages 2007
Synthesis and structure–activity relationships of N-substituted spiropiperidines as nociceptin receptor ligands
Fulltext Access 4 Pages 2007
Synthesis and evaluation of galactofuranosyl N,N-dialkyl sulfenamides and sulfonamides as antimycobacterial agents
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Structure–activity delineation of quinones related to the biologically active Calothrixin B
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Glucose-specific poly(allylamine) hydrogels—A reassessment
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CCR5 receptor antagonists: Discovery and SAR study of guanylhydrazone derivatives
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Identification of a series of highly potent activators of the Nurr1 signaling pathway
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SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[d][1,3]oxazin-2-ones as progesterone receptor antagonists
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Identification of novel, selective and potent Chk2 inhibitors
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Mono, di and tri-mannopyranosyl phosphates as mannose-1-phosphate prodrugs for potential CDG-Ia therapy
Fulltext Access 4 Pages 2007
Structure–activity relationships of the ultrapotent vanilloid resiniferatoxin (RTX): The homovanillyl moiety
Fulltext Access 4 Pages 2007
The discovery of a potent orally efficacious indole androgen receptor antagonist through in vivo screening
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Ponapensin, a cyclopenta[bc]benzopyran with potent NF-κB inhibitory activity from Aglaia ponapensis
Fulltext Access 4 Pages 2007
Intermediate analogue inhibitors of mandelate racemase: N-Hydroxyformanilide and cupferron
Fulltext Access 4 Pages 2007
Ezetimibe analogs with a reorganized azetidinone ring: Design, synthesis, and evaluation of cholesterol absorption inhibitions
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Synthesis and structure–activity studies of antofine analogues as potential anticancer agents
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Novel thiol-based TACE inhibitors: Rational design, synthesis, and SAR of thiol-containing aryl sulfonamides
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Design of potent inhibitors of human β-secretase. Part 2
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Antibiotic-conjugated polyacrylate nanoparticles: New opportunities for development of anti-MRSA agents
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(3R)-4-[(3R)-3-Amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one, a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
Fulltext Access 4 Pages 2007
Kojic acid and its manganese and zinc complexes as potential radioprotective agents
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Samarium(II) promoted stereoselective synthesis of antiproliferative cis-β-alkoxy-γ-alkyl-γ-lactones
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Novel nucleotide triphosphates as potent P2Y2 agonists
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Novel nucleotide triphosphates as potent P2Y2 agonists with enhanced stability over UTP
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Rational design of a nonpeptide general chemical scaffold for reversible inhibition of PDZ domain interactions
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Novel poly(ADP-ribose) polymerase-1 inhibitors
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Identification of selective neuropeptide Y2 peptide agonists
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Synthesis and activity of a potent, specific azabicyclo[3.3.0]-octane-based DPP II inhibitor
Fulltext Access 4 Pages 2007
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