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Daneshyari Molecular Biology Journas Latest Articles

Molecular Biology Research Articles

The discovery of a selective, high affinity A2B adenosine receptor antagonist for the potential treatment of asthma
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1-(Phenyl)isoquinoline carboxamides: a novel class of subtype selective inhibitors of thyrotropin-releasing hormone (TRH) receptors
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Active site directed inhibitors of replication-specific bacterial DNA polymerases
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Estrogen receptor ligands. Part 11: Synthesis and activity of isochromans and isothiochromans
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Pyrenyldiazomethane, a versatile reagent for nucleotide phosphate alkylation
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Synthesis and antifungal activity of noble 5-arylamino- and 6-arylthio-4,7-dioxobenzoselenazoles
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Parallel synthesis of pteridine derivatives as potent inhibitors for hepatitis C virus NS5B RNA-dependent RNA polymerase
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Cleavage at 5-methylcytosine in DNA by photosensitized oxidation with 2-methyl-1,4-naphthoquinone tethered oligodeoxynucleotides
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Truncated azinomycin analogues intercalate into DNA
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Inhibitors of type I MetAPs containing pyridine-2-carboxylic acid thiazol-2-ylamide. Part 1: SAR studies on the determination of the key scaffold
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Biarylcarboxybenzamide derivatives as potent vanilloid receptor (VR1) antagonistic ligands
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Design and synthesis of a peptide-PEG transporter tool for carrying adenovirus vector into cells
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Acyl sulfonamide anti-proliferatives. Part 2: Activity of heterocyclic sulfonamide derivatives
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Design and synthesis of macrocycles active against vancomycin-resistant enterococci (VRE): the interplay between d-Ala-d-Lac binding and hydrophobic effect
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Studies on the structure-activity relationship of 2′,6′-dimethyl-l-tyrosine (Dmt) derivatives: bioactivity profile of H-Dmt-NH-CH3
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Generation of a new class of hNK2 receptor ligands using the 'fragment approach'
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Synthesis of modified proanthocyanidins: easy and general introduction of a hydroxy group at C-6 of catechin; efficient synthesis of elephantorrhizol
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Synthesis of modified proanthocyanidins: introduction of acyl substituents at C-8 of catechin. Selective synthesis of a C-4 → O → C-3 ether-linked procyanidin-like dimer
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Structure-activity relationship studies on ortho-substituted cinnamic acids, a new class of selective EP3 antagonists
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Synthesis and acetylcholinesterase inhibition of derivatives of huperzine B
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Enantiomerical excess determination, purification and biological evaluation of (3S) and (3R) α,β-butenolide analogues of isobenzofuranone
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2-Mercaptoimidazoles, a new class of potent CCR2 antagonists
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Instructions to contributors
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In vivo incorporation of an alkyne into proteins in Escherichia coli
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Glucokinase-activating ureas
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Synthesis of cyclic peptidosulfonamides as scaffolds for MC4 pharmacophoric groups
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Instructions to Authors
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Design and synthesis of (E)-1,1,2-triarylethenes: novel inhibitors of the cyclooxygenase-2 (COX-2) isozyme
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Synthesis and SAR of novel 4,5-diarylimidazolines as potent P2X7 receptor antagonists
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Optimization of CRF1R binding affinity of 2-(2,4,6-trichlorophenyl)-4-trifluoromethyl-5-aminomethylthiazoles through rapid and selective parallel synthesis
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Pyrimidine containing RSV fusion inhibitors
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IKCa-channel blockers. Part 2: Discovery of cyclohexadienes
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Saucerneol B derivatives as human acyl-CoA: cholesterol acyltransferase inhibitors
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(S,E)-N-[1-(3-Heteroarylphenyl)ethyl]-3-(2-fluorophenyl)acrylamides: synthesis and KCNQ2 potassium channel opener activity
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Isoterreulactone A, a novel meroterpenoid with anti-acetylcholinesterase activity produced by Aspergillus terreus
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Potent 4-aminopiperidine based antimalarial agents
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Schizophyllan-folate conjugate as a new non-cytotoxic and cancer-targeted antisense carrier
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Structure-antioxidant activity relationships of flavonoids isolated from the resinous exudate of Heliotropium sinuatum
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Structure-activity relationships of dimeric PPAR agonists
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Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers
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A new ligand binding to G-G mismatch having improved thermal and alkaline stability
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Discovery of a novel, potent and selective human β3-adrenergic receptor agonist
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Instructions to contributors
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Crystallographic determination of stereochemistry of biologically active 2″,3″-dibromo-7-epi-10-deacetylcephalomannine
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DNA topoisomerase I inhibitors from Rinorea anguifera
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1-Hydroxyalkyl-3-phenylthioureas as novel HDL-elevating agents
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Triaryl bis-sulfones as a new class of cannabinoid CB2 receptor inhibitors: identification of a lead and initial SAR studies
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Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors
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Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure-activity relationships
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Novel 3-aminochromans as potential pharmacological tools for the serotonin 5-HT7 receptor
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Optimization of pyrrolidinone based HIV protease inhibitors
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2,3-Diphenylpropionic acids as potent VLA-4 antagonists
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Himeic acid A: a new ubiquitin-activating enzyme inhibitor isolated from a marine-derived fungus, Aspergillus sp.
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Design, synthesis, and biological evaluation of achiral analogs of duocarmycin SA
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Efficient cleavage of RNA, enhanced cellular uptake, and controlled intracellular localization of conjugate DNAzymes
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Cytotoxic neolignans: an SAR study
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Synthesis of digalactosyl diacylglycerols and their structure-inhibitory activity on human lanosterol synthase
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Synthesis and activity of 8-substituted benzo[c]quinolizin-3-ones as dual inhibitors of human 5α-reductases 1 and 2
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New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties
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Design, synthesis, and structural analysis of inhibitors of influenza neuraminidase containing a 2,3-disubstituted tetrahydrofuran-5-carboxylic acid core
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Heterocyclic sulfoxide and sulfone inhibitors of fatty acid amide hydrolase
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Amide derivatives of 9,11-seco-estra-1,3,5(10)-trien-11-oic acid as modified orally active estrogen agonists with moderate antagonistic activity
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Characterization of l-glutamine:2-deoxy-scyllo-inosose aminotransferase (tbmB) from Streptomyces tenebrarius
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A new class of androgen receptor antagonists bearing carborane in place of a steroidal skeleton
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Design, synthesis and evaluation of 5-substituted amino-2,4-diamino-8-chloropyrimido-[4,5-b]quinolines as novel antimalarials
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2,3-Ethylene- and 2,3-trimethylene-bridged analogues of the group III metabotropic glutamate receptor ligand 2-amino-4-phosphonobutanoic acid
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Syntheses of 2,4,6-trisubstituted pyrimidine derivatives as a new class of antifilarial topoisomerase II inhibitors
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Modulators of the human CCR5 receptor. Part 1: Discovery and initial SAR of 1-(3,3-diphenylpropyl)-piperidinyl amides and ureas
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A new strategy to combat Alzheimer's disease. Combining radical-scavenging potential with metal-protein-attenuating ability in one molecule
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Instructions to contributors
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From a total synthesis of cepabactin and its 3:1 ferric complex to the isolation of a 1:1:1 mixed complex between iron (III), cepabactin and pyochelin
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Identification of a 5-HT4 receptor antagonist clinical candidate through side-chain modification
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Glycosylation of allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-d-glucopyranoside with bulky substituted glycosyl donors
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Synthesis of the β anomer of the spacer-equipped tetrasaccharide side chain of the major glycoprotein of the Bacillus anthracis exosporium
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Synthesis of benzylidenated hexopyranosides in ionic liquids
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Interaction of dopamine and acetylcholine with an amphiphilic resorcinarene receptor in aqueous micelle system
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Synthesis and evaluation of diverse analogs of amygdalin as potential peptidomimetics of peptide T
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Aglycon specificity profiling of α-glucosidases using synthetic probes
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2-Substituted-4-aryl-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,5]oxazocin-5-one as a structurally new NK1 antagonist
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Crystal structures of human HSP90α-complexed with dihydroxyphenylpyrazoles
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Electronic structure calculations on the thiazole-containing antibiotic thiostrepton: molecular mechanics, semi-empirical and ab initio analyses
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Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity
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Structure-activity relationships and sub-type selectivity in an oxabicyclic estrogen receptor α/β agonist scaffold
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Protein microarray using α-amino acids as metal tags on chips
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4-(2-Aminoethoxy)-N-(phenylsulfonyl)indoles as novel 5-HT6 receptor ligands
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Chemistry and biology of mercaptoacetamides as novel histone deacetylase inhibitors
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Utilization of a nitrobenzoxadiazole (NBD) fluorophore in the design of a Grb2 SH2 domain-binding peptide mimetic
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The synthesis of substituted bipiperidine amide compounds as CCR3 antagonists
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A short synthesis of d-glycero-d-manno-heptose 7-phosphate
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Ab initio studies of the properties of intracellular thiols ergothioneine and ovothiol
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Biaryls and heterobiaryls as α-glucosidase and protein tyrosine phosphatase inhibitors
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Synthesis and evaluation of pyrazolidine derivatives as dipeptidyl peptidase IV (DP-IV) inhibitors
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The discovery and synthesis of novel adenosine receptor (A2A) antagonists
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Synthesis and biological activity of new 5-O-sugar modified ketolide and 2-fluoro-ketolide antibiotics
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Synthesis and radiopharmacological evaluation of 2′-(4-fluorophenyl)-21-[18F]fluoro-20-oxo-11β,17α-dihydroxy-pregn-4-eno[3,2-c]pyrazole as potential glucocorticoid receptor ligand for positron emission tomography (PET)
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Functionalized dendrimers as endotoxin sponges
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Amino acid conjugates as κ opioid receptor agonists
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Instructions to Authors
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Antitumor agents. Part 236: Synthesis of water-soluble colchicine derivatives
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Novel 1β-methylcarbapenems with isoxazoloethenyl moieties containing carboxylic acid sodium salt
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