About: http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/w

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/w Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/m/print http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/m/web
Date Copyrighted	2006
Rights	Copyright © 2006 American Chemical Society
issue	18
Rights Holder	American Chemical Society
is Is Part Of of	Stereochemical Diversity-Oriented Conformational Restriction Strategy. Development of PotentHistamine H3 and/or H4 Receptor Antagonists with an Imidazolylcyclopropane Structure Highly Potent and Selective Phenylmorphan-Based Inverse Agonists of the Opioid δ Receptor Structure−Activity Relationships of Uridine 5‘-Diphosphate Analogues at the Human P2Y6Receptor 3-[5-(4,5-Dihydro-1H-imidazol-2-yl)-furan-2-yl]phenylamine (Amifuraline), a PromisingReversible and Selective Peripheral MAO-A Inhibitor Synthesis, Characterization, and BiologicalEvaluation of M(I)(CO)3(NNO) Complexes (M =Re, 99mTc) Conjugated to2-(4-Aminophenyl)benzothiazole as PotentialBreast Cancer Radiopharmaceuticals Molecular Toxicology. Second Edition By P. David Josephyand Bengt Mannervik. Oxford University Press, New York.2006. xviii + 589 pp. 19 × 26 cm. ISBN 0-19-517620-0.$144.50. Preparation and Biological Evaluation of 10B-Enriched3-[5-{2-(2,3-Dihydroxyprop-1-yl)-o-carboran-1-yl}pentan-1-yl]thymidine (N5-2OH),a New Boron Delivery Agent for Boron Neutron Capture Therapy of Brain Tumors Dissecting the Determinants of Cyclin-Dependent Kinase 2 and Cyclin-Dependent Kinase 4Inhibitor Selectivity Novel Potent Anticonvulsant Agent Containing a Tetrahydroisoquinoline Skeleton Homobivalent Quinazolinimines as NovelNanomolar Inhibitors of Cholinesterases withDirigible Selectivity toward Butyrylcholinesterase Carbonic Anhydrase Inhibitors: Hypoxia-Activatable Sulfonamides Incorporating DisulfideBonds that Target the Tumor-Associated Isoform IX 3-Demethoxy-3-glycosylaminothiocolchicines: Synthesis of a New Class of Putative MuscleRelaxant Compounds Uncompetitive Antagonism of AMPA Receptors: Mechanistic Insights from Studies ofPolyamine Toxin Derivatives Anti-AIDS Agents 69. Moronic Acid and Other Triterpene Derivatives asNovel Potent Anti-HIV Agents Redefining the Structure−Activity Relationships of 2,6-Methano-3-benzazocines. 4. OpioidReceptor Binding Properties of 8-[N-(4‘-phenyl)-phenethyl)carboxamido] Analogues ofCyclazocine and Ethylketocycalzocine Comparison of the Binding of 3-Fluoromethyl-7-sulfonyl-1,2,3,4-tetrahydroisoquinolines withTheir Isosteric Sulfonamides to the Active Site of Phenylethanolamine N-Methyltransferase Synthesis and Cytotoxicity of Leinamycin Antibiotic Analogues A Novel Computational Analysis of Ligand-Induced Conformational Changes in the ATPBinding Sites of Cyclin Dependent Kinases Antitumor Agents. 254. Synthesis and Biological Evaluation of Novel Neo-tanshinlactoneAnalogues as Potent Anti-Breast Cancer Agents Binding of Aminoglycosidic Antibiotics to the Oligonucleotide A-Site Model and 30S RibosomalSubunit: Poisson−Boltzmann Model, Thermal Denaturation, and Fluorescence Studies Thrombin Receptor (Protease Activated Receptor-1) Antagonists as Potent AntithromboticAgents with Strong Antiplatelet Effects New Opioid Designed Multiple Ligand from Dmt-Tic and Morphinan Pharmacophores Complexes of Alkylene-Linked Tacrine Dimers with Torpedo californica Acetylcholinesterase: Binding of Bis(5)-tacrine Produces a Dramatic Rearrangement in the Active-Site Gorge Design, Synthesis, and Biophysical and Biological Evaluation of a Series ofPyrrolobenzodiazepine−Poly(N-methylpyrrole) Conjugates Effect of Lysine at C-Terminus of the Dmt-Tic Opioid Pharmacophore Structural and Solution Chemistry, Antiproliferative Effects, and DNA and Protein BindingProperties of a Series of Dinuclear Gold(III) Compounds with Bipyridyl Ligands A Chloroquine-like Molecule Designed to Reverse Resistance in Plasmodium falciparum 5‘-O-Tritylinosine and Analogues as Allosteric Inhibitors of Human Thymidine Phosphorylase Synthesis and Agonist Activity of Cyclic ADP-Ribose Analogues with Substitution of theNorthern Ribose by Ether or Alkane Chains Synthesis, Characterization, and in Vitro Evaluation of Novel Ruthenium(II) η6-AreneImidazole Complexes A Structure-Guided Approach to an OrthogonalEstrogen-Receptor-Based Gene Switch Activatedby Ligands Suitable for in Vivo Studies

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata