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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Pyrazole inhibitors of coactivator associated arginine methyltransferase 1 (CARM1)
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Synthesis and DNA binding ability of cyclam–amino acid conjugates
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Tubulysin analogs incorporating desmethyl and dimethyl tubuphenylalanine derivatives
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Design, synthesis and evaluation of 2-phenyl-1H-benzo[d]imidazole-4,7-diones as vascular smooth muscle cell proliferation inhibitors
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N-Acetylhexosaminidase inhibitory properties of C-1 homologated GlcNAc- and GalNAc-thiazolines
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Discovery of amino-acetonitrile derivatives, a new class of synthetic anthelmintic compounds
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Antagonists of the human adenosine A2A receptor. Part 2: Design and synthesis of 4-arylthieno[3,2-d]pyrimidine derivatives
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Antagonists of the human adenosine A2A receptor. Part 1: Discovery and synthesis of thieno[3,2-d]pyrimidine-4-methanone derivatives
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Pyridyl-phenyl ether monoamine reuptake inhibitors: Impact of lipophilicity on dual SNRI pharmacology and off-target promiscuity
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Synthesis and PKCθ inhibitory activity of a series of 4-(indol-5-ylamino)thieno[2,3-b]pyridine-5-carbonitriles
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The isolation, structure determination and cytotoxicity of the new fungal metabolite, trichodermamide C
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Development of a fluorescence polarization based assay for histone deacetylase ligand discovery
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Synthesis and evaluation of sulfamide-type indolizidines as glycosidase inhibitors
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Design and synthesis of 6-amino-1,4-oxazepane-3,5-dione derivatives as novel broad spectrum anticonvulsants
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Synthesis and evaluation of α,α′-disubstituted phenylacetate derivatives for T-type calcium channel blockers
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2-Alkenylthieno[2,3-b]pyridine-5-carbonitriles: Potent and selective inhibitors of PKCθ
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Synthesis of some novel imidazole-based dicationic carbazolophanes as potential antibacterials
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Synthesis and anti-inflammatory activity of 2-(2-aroylaroxy)-4,6-dimethoxy pyrimidines
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Sialyl α(2 → 3) lactose clusters using carbosilane dendrimer core scaffolds as influenza hemagglutinin blockers
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Benzodiazepine ligands can act as allosteric modulators of the Type 1 cholecystokinin receptor
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Synthesis and biological evaluation of a focused library of beauveriolides
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Discovery of imidazole carboxamides as potent and selective CCK1R agonists
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The identification of potent, selective and CNS penetrant furan-based inhibitors of B-Raf kinase
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Successful kinase bypass with new acyclovir phosphoramidate prodrugs
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Pyrrolidinyl pyridone and pyrazinone analogues as potent inhibitors of prolyl oligopeptidase (POP)
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Efficient synthesis and evaluation of bimodal ligand NETA
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Synthesis and in vitro activity of 1-(2,3-dichlorophenyl)-N-(pyridin-3-ylmethyl)-1H-1,2,4-triazol-5-amine and 4-(2,3-dichlorophenyl)-N-(pyridin-3-ylmethyl)-4H-1,2,4-triazol-3-amine P2X7 antagonists
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Synthesis and biological evaluation of PEG-tirofiban conjugates
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N-Alkyl-4-piperidinyl-2,3-diarylpyrrole derivatives with heterocyclic substitutions as potent and broad spectrum anticoccidial agents
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Glycosidase profiling with immobilised glycosidase-inhibiting iminoalditols—A proof-of-concept study
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Synthesis and evaluation of 3- and 7-substituted geranylgeranyl pyrophosphate analogs
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Induction of apoptosis of human tumor cells by hybrid liposomes including docosahexaenoic acid
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Synthesis and pharmacological evaluation of a new targeted drug carrier system: β-Cyclodextrin coupled to oxytocin
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N-Methylpyridoxamine: Novel canine vitamin B6 urine metabolite
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Synthesis of all stereoisomers of 3-hydroxypipecolic acid and 3-hydroxy-4,5-dehydropipecolic acid and their evaluation as glycosidase inhibitors
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[4-(Phenoxy)pyridin-3-yl]methylamines: A new class of selective noradrenaline reuptake inhibitors
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Indole- and indolizine-glyoxylamides displaying cytotoxicity against multidrug resistant cancer cell lines
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Electrophilic α-thiocyanation of chiral and achiral N-acyl imides. A convenient route to 5-substituted and 5,5-disubstituted 2,4-thiazolidinediones
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Discovery of triazolinone non-nucleoside inhibitors of HIV reverse transcriptase
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Design and synthesis of hydroxy-alkynoic acids and their methyl esters as novel activators of BK channels
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New anti-inflammatory ergostane-type ecdysteroids from the sclerotium of Polyporus umbellatus
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Designing better coumarin-based fluorogenic substrates for PTP1B
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Design and synthesis of N-alkyl oxindolylidene acetic acids as a new class of potent Cdc25A inhibitors
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Synthesis of 2-[3-(7-Chloro-quinolin-4-ylamino)-alkyl]-1-(substituted phenyl)-2,3,4,9-tetrahydro-1H-β-carbolines as a new class of antimalarial agents
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Novel ORL1-selective antagonists with oral bioavailability and brain penetrability
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Identification of novel benzimidazole series of potent and selective ORL1 antagonists
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Improved synthesis of antibacterial 3-substituted 6-anilinouracils
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IRAK-4 inhibitors. Part 1: A series of amides
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Design and synthesis of releasable folate–drug conjugates using a novel heterobifunctional disulfide-containing linker
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New PPARγ ligands based on 2-hydroxy-1,4-naphthoquinone: Computer-aided design, synthesis, and receptor-binding studies
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Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human β3-adrenergic receptor agonists: Part IV
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Design, synthesis, biochemical, and biological evaluation of nitrogen-containing trifluoro structural modifications of combretastatin A-4
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7-[1H-Indol-2-yl]-2,3-dihydro-isoindol-1-ones as dual Aurora-A/VEGF-R2 kinase inhibitors: Design, synthesis, and biological activity
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Identification of ring-fused pyrazolo pyridin-2-ones as novel poly(ADP-ribose)polymerase-1 inhibitors
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Novel hypoglycemic dihydropyridones serendipitously discovered from O- versus C-alkylation in the synthesis of VMAT2 antagonists
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Bradykinin B1 receptor antagonists: An α-hydroxy amide with an improved metabolism profile
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Design, synthesis, and bioactivity of putative tubulin ligands with adamantane core
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Synthesis and antibacterial activity of the C-7 side chain of 3-aminoquinazolinediones
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Discovery and optimization of (R)-prolinol-derived agonists of the Growth Hormone Secretagogue receptor (GHSR)
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Design, synthesis and preliminary biological evaluation of new hydroxamate histone deacetylase inhibitors as potential antileukemic agents
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PNA/DNA interstrand cross-links from a modified PNA base upon photolysis or oxidative conditions
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Promising core structure for nuclear receptor ligands: Design and synthesis of novel estrogen receptor ligands based on diphenylamine skeleton
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Impacts of baicalein analogs with modification of the 6th position of A ring on the activity toward NF-κB-, AP-1-, or CREB-mediated transcription
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1-[4-(2-Aminoethoxy)phenylcarbonyl]-3,5-bis-(benzylidene)-4-oxopiperidines: A novel series of highly potent revertants of P-glycoprotein associated multidrug resistance
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Structure-guided design of substituted aza-benzimidazoles as potent hypoxia inducible factor-1α prolyl hydroxylase-2 inhibitors
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ortho-Dihydroxyisoflavone derivatives from aged Doenjang (Korean fermented soypaste) and its radical scavenging activity
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Hexahydro-pyrrolo- and hexahydro-1H-pyrido[1,2-b]pyridazin-2-ones as potent inhibitors of HCV NS5B polymerase
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Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARα/γ dual agonists
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Synthesis of N-isobutylnoroxymorphone from naltrexone by a selective cyclopropane ring opening reaction
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Synthesis of a 200-member library of squaric acid N-hydroxylamide amides
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New PPARγ ligands based on barbituric acid: Virtual screening, synthesis and receptor binding studies
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Discovery of thieno[2,3-c]pyridines as potent COT inhibitors
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Discovery of pyrazolopyrimidines as the first class of allosteric agonists for the high affinity nicotinic acid receptor GPR109A
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Design and synthesis of fluorescent SGLT2 inhibitors
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New iodoreboxetine analogues for SPECT imaging of the noradrenaline transporter
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Design and synthesis of novel furoquinoline based inhibitors of multiple targets in the PI3K/Akt-mTOR pathway
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Synthesis and evaluation of heteroaryl-ketone derivatives as a novel class of VEGFR-2 inhibitors
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Synthesis of hydantoin analogues of (2S,3R,4S)-4-hydroxyisoleucine with insulinotropic properties
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N-(thiazol-2-yl)-2-thiophene carboxamide derivatives as Abl inhibitors identified by a pharmacophore-based database screening of commercially available compounds
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N-Acyl-3-amino-5H-furanone derivatives as new inhibitors of LuxR-dependent quorum sensing: Synthesis, biological evaluation and binding mode study
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Molecular modeling of a PAMAM-CGS21680 dendrimer bound to an A2A adenosine receptor homodimer
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N-Benzyl-N-(pyrrolidin-3-yl)carboxamides as a new class of selective dual serotonin/noradrenaline reuptake inhibitors
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Structure–activity relationships of 2-aryl-1H-indole inhibitors of the NorA efflux pump in Staphylococcus aureus
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Structure–activity relationship studies on vitamin D lactam derivatives as vitamin D receptor antagonist
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Design and optimization of potent, selective antagonists of Oxytocin
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Design and synthesis of tetrahydroisoquinoline derivatives as potential multidrug resistance reversal agents in cancer
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Design, synthesis and evaluation of potent thymidylate synthase X inhibitors
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Analogues of N-hydroxy-N′-phenylthiourea and N-hydroxy-N′-phenylurea as inhibitors of tyrosinase and melanin formation
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N-Alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists
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Carbonic anhydrase inhibitors: Inhibition of the new membrane-associated isoform XV with phenols
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Monoglycerides from the brown alga Sargassum sagamianum: Isolation, synthesis, and biological activity
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Oligonucleotide microarrays with stem–loop probes: Enhancing the hybridization of nucleic acids for sensitive analysis
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2,5-Diaminopyrimidines and 3,5-disubstituted azapurines as inhibitors of glycogen synthase kinase-3 (GSK-3)
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4,5-Disubstituted oxazolidinones: High affinity molecular effectors of RNA function
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Synthesis of BC-ring model of globostellatic acid X methyl ester, an anti-angiogenic substance from marine sponge
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Synthesis of diketopiperazine-based carboline homodimers and in vitro growth inhibition of human carcinomas
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Discovery and Initial SAR of Arylsulfonylpiperazine Inhibitors of 11β-Hydroxysteroid Dehydrogenase Type 1 (11β-HSD1)
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The effect of different electrostatic potentials on docking accuracy: A case study using DOCK5.4
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Development of potent and selective small-molecule human Urotensin-II antagonists
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Binding properties of positively charged deoxynucleic guanidine (DNG), AgTgAgTgAgT and DNG/DNA chimeras to DNA
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