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Daneshyari Pharmaceutical Science Journas Latest Articles

Pharmaceutical Science Research Articles

Antiproliferative activity of 4-chloro-5,6-dihydro-2H-pyrans. Part 2: Enhancement of drug cytotoxicity
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Synthesis of new plant growth regulator: N-(Fatty acid) O-aryloxyacetyl ethanolamine
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Evaluation of nitrate-substituted pseudocholine esters of aspirin as potential nitro-aspirins
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2-Hydroxy-N-arylbenzenesulfonamides as ATP-citrate lyase inhibitors
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Synthesis, biological evaluations, and tubulin binding poses of C-2α sulfur linked taxol analogues
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Formation of an enolate intermediate is required for the reaction catalyzed by 3-hydroxyacyl-CoA dehydrogenase
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4-Substituted indazoles as new inhibitors of neuronal nitric oxide synthase
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Methylenebis(sulfonamide) linked nicotinamide adenine dinucleotide analogue as an inosine monophosphate dehydrogenase inhibitor
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Preparation of novel anthranilic acids as antibacterial agents: Extensive evaluation of structural and physical properties on antibacterial activity and human serum albumin affinity
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Piperazinyl CCR1 antagonists—optimization of human liver microsome stability
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Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on melanin synthesis
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Concise synthesis of dideoxy-epigallocatechin gallate (DO-EGCG) and evaluation of its anti-influenza virus activity
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Glaziovianin A, a new isoflavone, from the leaves of Ateleia glazioviana and its cytotoxic activity against human cancer cells
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Antiproliferative activity of 2-alkyl-4-halopiperidines and 2-alkyl-4-halo-1,2,5,6-tetrahydropyridines in solid tumor cell lines
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Dual M3 antagonists-PDE4 inhibitors. Part 2: Synthesis and SAR of 3-substituted azetidinyl derivatives
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Synthesis and biological evaluation of 2β,3α-(substituted phenyl)nortropanes as potential norepinephrine transporter imaging agents
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The thioesterase domain from the pimaricin and erythromycin biosynthetic pathways can catalyze hydrolysis of simple thioester substrates
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Synthesis and antitubercular activity of phenothiazines with reduced binding to dopamine and serotonin receptors
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Design, synthesis, and evaluation of tetrahydroquinoline and pyrrolidine sulfonamide carbamates as γ-secretase inhibitors
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Potent bradykinin B1 receptor antagonists: 4-Substituted phenyl cyclohexanes
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Design, synthesis, and antitumor activity of bile acid–polyamine–nucleoside conjugates
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Synthesis and biological evaluation of nitric oxide-releasing derivatives of oleanolic acid as inhibitors of HepG2 cell apoptosis
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A tetra(l-lysine)-grafted poly(organophosphazene) for gene delivery
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Amyloid-forming propensity of the hydrophobic non-natural amino acid on the fibril-forming core peptide of human tau
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Ortho-azo substituted phenylboronic acids for colorimetric sugar sensors
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Synthesis of fluorescent-labeled aeruginosin derivatives for high-throughput fluorescence correlation spectroscopy assays
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A glycosylated complex of gadolinium, a new potential contrast agent for magnetic resonance angiography?
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Synthesis and biological evaluation of two glycerolipidic prodrugs of didanosine for direct lymphatic delivery against HIV
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Synthesis and antimicrobial activity of some novel phenyl and benzimidazole substituted benzyl ethers
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Convenient synthesis and in vitro pharmacological activity of 2-thioanalogs of salvinorins A and B
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Structure-activity relationship studies on anti-HCV activity of ring-expanded ('fat') nucleobase analogues containing the imidazo[4,5-e][1,3]diazepine-4,8-dione ring system
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Structural requirements of HDAC inhibitors: SAHA analogs functionalized adjacent to the hydroxamic acid
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Synthesis and bioactivity of 4-alkyl(aryl)thioquinazoline derivatives
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Substituted acyclic sulfonamides as human cannabinoid-1 receptor inverse agonists
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Synthesis and in vitro cytotoxicity of novel lipophilic (diamine)platinum(II) complexes of salicylate derivatives
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Novel 3-galloylamido-N′-substituted-2,6-piperidinedione-N-acetamide peptidomimetics as metalloproteinase inhibitors
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Sulfonamide-related conformational effects and their importance in structure-based design
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Selective and dual action orally active inhibitors of thrombin and factor Xa
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The crystal structures of copper(II), manganese(II), and nickel(II) complexes of a (Z)-2-hydroxy-N′-(2-oxoindolin-3-ylidene) benzohydrazide—potential antitumor agents
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Analogs of the marine alkaloid makaluvamines: Synthesis, topoisomerase II inhibition, and anticancer activity
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Synthesis, structural analysis, and SAR studies of triazine derivatives as potent, selective Tie-2 inhibitors
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Syntheses and antiproliferative evaluation of oxyphenisatin derivatives
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Synthesis of enantiomerically pure milnacipran analogs and inhibition of dopamine, serotonin, and norepinephrine transporters
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Small molecule inhibitors of E. coli primase, a novel bacterial target
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Synthesis and biological evaluation of 12 allenic aromatic ethers
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Minimum structure requirement of immunomodulatory glycolipids for predominant Th2 cytokine induction and the discovery of non-linear phytosphingosine analogs
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Probing length effects and mechanism of cell penetrating agents mounted on a polyproline helix scaffold
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Cobaltpolyoxometalate-catalyzed cyclization of glucal with aryl amines: Synthesis of 2,4-disubstituted tetrahydroquinolines
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DNA cleavage promoted by 2,9-dimethyl-4,7-diazadecane-2,9-dithiol (DDD) derivatives
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SAR studies on thiazolo[4,5-d]pyrimidine based CXCR2 antagonists involving a novel tandem displacement reaction
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Sulfenamides as prodrugs of NH-acidic compounds: A new prodrug option for the amide bond
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Pyrazolone methylamino piperidine derivatives as novel CCR3 antagonists
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Potent macrocyclic antagonists to the motilin receptor presenting novel unnatural amino acids
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Synthesis and in vitro protozoocidal activity of diazabicyclic benzotropolone derivatives
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Design, synthesis, and biological activity of novel triazole amino acids used to probe binding interactions between ligand and neutral amino acid transport protein SN1
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Praziquantel derivatives I: Modification of the aromatic ring
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A novel arginine methyltransferase inhibitor with cellular activity
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(2R,3S)-(+)- and (2S,3R)-(−)-Halofuginone lactate: Synthesis, absolute configuration, and activity against Cryptosporidium parvum
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Thyroid receptor ligands. Part 8: Thyromimetics derived from N-acylated-α-amino acid derivatives displaying modulated pharmacological selectivity compared with KB-141
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Discovery of 5-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-7-phenyl-(E)-2,3,6,7-tetrahydro-1,4-thiazepines as a new series of apoptosis inducers using a cell- and caspase-based HTS assay
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Synthesis and evaluation of a phosphonate analogue of the soluble guanylate cyclase activator YC-1
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Interaction of O-(undec-10-en)-yl-d-glucose derivatives with the Plasmodium falciparum hexose transporter (PfHT)
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Synthesis and evaluation of α,β-unsaturated α-aryl-substituted fosmidomycin analogues as DXR inhibitors
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Synthesis, determination of stereochemistry, and evaluation of new bisindole alkaloids from the myxomycete Arcyria ferruginea: An approach for Wnt signal inhibitor
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New triterpene glucosides, oligoporins A–C, from Oligoporus tephroleucus protect DNA from Fenton reaction
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A relationship between amide hydrogen bond strength and quinone reduction potential: Implications for photosystem I and bacterial reaction center quinone function
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Quinazoline derivatives as MC-I inhibitors: Evaluation of myocardial uptake using Positron Emission Tomography in rat and non-human primate
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Metabolically labile cannabinoid esters: A ‘soft drug’ approach for the development of cannabinoid-based therapeutic drugs
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Synthesis and anti-influenza activities of carboxyl alkoxyalkyl esters of 4-guanidino-Neu5Ac2en (zanamivir)
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α,α-Cyclic aminoacids as useful scaffolds for the preparation of hNK2 receptor antagonists
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Oxazolones as potent inhibitors of 11β-hydroxysteroid dehydrogenase type 1
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Synthesis and structure–activity relationship of RXR antagonists based on the diazepinylbenzoic acid structure
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Synthesis and structure–activity relationship of novel RXR antagonists: Orally active anti-diabetic and anti-obesity agents
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Caprolactams as potent CGRP receptor antagonists for the treatment of migraine
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[1,2,3]Triazolo[4,5-h]quinolones. A new class of potent antitubercular agents against multidrug resistant Mycobacterium tuberculosis strains
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Synthesis and SAR studies of potent imidazopyridine anticoccidial agents
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Derivatives of oxoisoaporphine alkaloids: A novel class of selective acetylcholinesterase inhibitors
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Phosphonic acid analogs of GABA through reductive dealkylation of phosphonic diesters with lithium trialkylborohydrides
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Synthesis and biological evaluation of analogues of the anti-tumor alkaloid naamidine A
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Structure–activity relationship, kinetic mechanism, and selectivity for a new class of ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitors
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Synthesis and anticonvulsant activity of 4-(2-(2,6-dimethylphenylamino)-2-oxoethylamino)-N-(substituted)butanamides: A pharmacophoric hybrid approach
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Antitumor anthraquinones from an endophytic actinomycete Micromonospora lupini sp. nov.
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Synthesis and antifungal activities of new fluconazole analogues with azaheterocycle moiety
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Improvement of base selectivity and binding affinity by controlling hydrogen bonding motifs between nucleobases and isoxanthopterin: Application to the detection of T/C mutation
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Design, synthesis, and anti-HIV activity of 2′,3′-didehydro-2′,3′-dideoxyuridine (d4U), 2′,3′-dideoxyuridine (ddU) phosphoramidate ‘ProTide’ derivatives
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A novel artemisinin–quinine hybrid with potent antimalarial activity
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Design, synthesis, and structure–activity relationship of carbamate-tethered aryl propanoic acids as novel PPARα/γ dual agonists
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Radioiodinated aza-diphenylacetylenes as potential SPECT imaging agents for β-amyloid plaque detection
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Mycophenolic acid as a latent agonist of PPARγ
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Synthesis and antibacterial activity of 5-deoxy-5-episubstituted arbekacin derivatives
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Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors
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SAR of a novel 'Anthranilamide Like' series of VEGFR-2, multi protein kinase inhibitors for the treatment of cancer
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Pyrrolidino-tetrahydroisoquinolines bearing pendant heterocycles as potent dual H3 antagonist and serotonin transporter inhibitors
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2-Cycloalkyl phenoxyacetic acid CRTh2 receptor antagonists
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Antimicrobial activity of rationally designed amino terminal modified peptides
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Anti-AIDS agents 72. Bioisosteres (7-carbon-DCKs) of the potent anti-HIV lead DCK
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Positional linker effects in haptens for cocaine immunopharmacotherapy
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3D-QSAR studies on sildenafil analogues, selective phosphodiesterase 5 inhibitors
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Aqua mediated synthesis of substituted 2-amino-4H-chromenes catalyzed by green and reusable Preyssler heteropolyacid
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The role of molecular size in ligand efficiency
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