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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_26/m/print http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_26/m/web
Date Copyrighted	2006
Rights	Copyright © 2006 American Chemical Society
issue	26
Rights Holder	American Chemical Society
is Is Part Of of	Insights on Resistance to Reverse Transcriptase: The Different Patterns of Interaction of theNucleoside Reverse Transcriptase Inhibitors in the Deoxyribonucleotide Triphosphate BindingSite Relative to the Normal Substrate Scaffold of the Cyclooxygenase-2 (COX-2)Inhibitor Carprofen Provides Alzheimerγ-Secretase Modulators Computer Applications in Pharmaceutical Research andDevelopment Edited by Sean Ekins. John Wiley & Sons, Inc.,Hoboken, NJ. 2006. xix + 805 pp. 16 × 24 cm. ISBN 0-471-73779-8. $125.00. Discovery of Potent, Orally-Active, andMuscle-Selective Androgen Receptor ModulatorsBased on an N-Aryl-hydroxybicyclohydantoinScaffold Antitubercular Nucleosides That Inhibit Siderophore Biosynthesis: SAR of theGlycosyl Domain Synthesis of 2-Methyl-3-indolylacetic Derivatives as Anti-Inflammatory Agents That InhibitPreferentially Cyclooxygenase 1 without Gastric Damage N-Substituted Thymine Derivatives as Mitochondrial Thymidine Kinase (TK-2) Inhibitors Biological Mechanisms of Action of Novel C-10 Non-Acetal Trioxane Dimers in Prostate CancerCell Lines Combinatorial Chemistry: From Theory to Application.Second Revised Edition Edited by Willi Bannwarth andBerthold Hinzen. Wiley/VCH, Weinheim, Germany. 2006.xxii+ 629 pp. 15.5 × 24.5 cm. ISBN 3527306935. $205.00 Discovery of N-[(1S,2S)-3-(4-Chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]-2-methyl-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanamide(MK-0364), a Novel, Acyclic Cannabinoid-1Receptor Inverse Agonist for the Treatment ofObesity Synthesis of Novel Caspase Inhibitors for Characterization of the Active Caspase Proteome inVitro and in Vivo Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Novel α-Borano-NucleotideAnalogues of 9-[2-(Phosphonomethoxy)ethyl]adenine and(R)-9-[2-(Phosphonomethoxy)propyl]adenine Arylpiperazinylalkylpyridazinones and Analogues as Potent and Orally Active AntinociceptiveAgents: Synthesis and Studies on Mechanism of Action Synthesis and Structure−Activity Relationships of 3,8-Diazabicyclo[4.2.0]octane Ligands, PotentNicotinic Acetylcholine Receptor Agonists A Systematic Study of Nitrated Indenoisoquinolines Reveals a Potent Topoisomerase I Inhibitor Topomimetics of Amphipathic β-Sheet and Helix-Forming Bactericidal Peptides NeutralizeLipopolysaccharide Endotoxins Microwave Assisted Organic Synthesis Edited by Jason P.Tierney and Pelle Lidstrom. Blackwell Publishing, Oxford, U.K.2005. xi + 280 pp. 18 × 21 cm. ISBN 0-8493-2371-1. £89.50. A Comparative Molecular Field Analysis (CoMFA) and Comparative Molecular SimilarityIndices Analysis (CoMSIA) of Anthranilamide Derivatives That Are Multidrug ResistanceModulators Synthesis and Evaluation of Multisubstrate Bicyclic Pyrimidine Nucleoside Inhibitors of HumanThymidine Phosphorylase Synthesis and Characterization of a Novel Liver-Targeted Prodrug ofCytosine-1-β-d-arabinofuranoside Monophosphate for the Treatment of HepatocellularCarcinoma Synthesis of Low-Hemolytic AntimicrobialDehydropeptides Based on Gramicidin S Synthesis and Antitumor Activity of Guanylhydrazones from6-(2,4-Dichloro-5-nitrophenyl)imidazo[2,1-b]thiazoles and 6-Pyridylimidazo[2,1-b]thiazoles Synthesis, Antifungal Activity, and Structure−Activity Relationships of Coruscanone AAnalogues Organic Synthesis. State of the Art 2003−2005 By DouglasF. Taber. John Wiley and Sons, Inc., Hoboken, New Jersey.2006. ix + 216 pp. 16 × 24.5 cm. ISBN 0-470-05331-3. $99.95. Design, Synthesis, Potency, and Cytoselectivity of Anticancer Agents Derived by ParallelSynthesis from α-Aminosuberic Acid Binding Properties of Aromatic Carbon-Bound Fluorine 9-Benzylidene-naphtho[2,3-b]thiophen-4-ones as Novel Antimicrotubule AgentsSynthesis,Antiproliferative Activity, and Inhibition of Tubulin Polymerization Synthesis and Anti-Human Immunodeficiency Virus Activity of 4‘-Branched(±)-4‘-Thiostavudines Novel Multipotent Tacrine−DihydropyridineHybrids with Improved AcetylcholinesteraseInhibitory and Neuroprotective Activities asPotential Drugs for the Treatment of Alzheimer'sDisease Transplatin Is Cytotoxic When Photoactivated: Enhanced Formation of DNA Cross-Links Synthesis and Antituberculosis Activity of a Novel Series of Optically Active6-Nitro-2,3-dihydroimidazo[2,1-b]oxazoles Design, Synthesis, and Evaluation of a Potent, Cell-Permeable, Conformationally ConstrainedSecond Mitochondria Derived Activator of Caspase (Smac) Mimetic New Benzopyran-Based Openers of theMitochondrial ATP-Sensitive Potassium Channelwith Potent Anti-Ischemic Properties N,N‘-Bisbenzylidenebenzene-1,4-diamines and N,N‘-Bisbenzylidenenaphthalene-1,4-diamines asSirtuin Type 2 (SIRT2) Inhibitors Discovery of2-Hydroxy-N,N-dimethyl-3-{2-[[(R)-1-(5-methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobut-1-enylamino}benzamide (SCH 527123): A Potent, Orally Bioavailable CXCR2/CXCR1Receptor Antagonist Design, Synthesis, and Biological Evaluation of Peptidomimetic Inhibitors of Factor XIa asNovel Anticoagulants Design, Synthesis, and Biological Evaluation of Phenylamino-Substituted6,11-Dihydro-dibenzo[b,e]oxepin-11-ones and Dibenzo[a,d]cycloheptan-5-ones: Novel p38 MAPKinase Inhibitors Quinol-4-ones as Steroid A-Ring Mimetics in Nonsteroidal Dissociated Glucocorticoid Agonists Structure−Brain Exposure Relationships Modeling Subtype-Selective Agonists Binding with α4β2 and α7 Nicotinic AcetylcholineReceptors: Effects of Local Binding and Long-Range Electrostatic Interactions 2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents: Synthesis, In VitroSAR, Protein Crystallography, and In Vivo Activity Rapid Discovery and Structure−Activity Profiling of Novel Inhibitors of HumanImmunodeficiency Virus Type 1 Protease Enabled by the Copper(I)-Catalyzed Synthesis of1,2,3-Triazoles and Their Further Functionalization Small-Molecule Targeting of Heat Shock Protein 90 Chaperone Function: RationalIdentification of a New Anticancer Lead Structure−Activity Relationship Studies of Ethyl2-Amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (HA 14-1), anAntagonist for Antiapoptotic Bcl-2 Proteins To Overcome Drug Resistance in Cancer Synthesis and Src Kinase Inhibitory Activity of a Series of4-[(2,4-Dichloro-5-methoxyphenyl)amino]-7-furyl-3-quinolinecarbonitriles Fundamentals of Early Clinical Drug Development. FromSynthesis Design to Formulation Edited by A. F. Abdel-Magid and Stéphane Caron. John Wiley & Sons, New York.2006. xv + 323 pp. 16 × 24 cm. ISBN 0-471-69278-6. $99.95.

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