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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_17/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_17/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	17
Rights Holder	American Chemical Society
is Is Part Of of	The First Potent and Selective Inhibitorsof the Glycine Transporter Type 2 Discovery of Estrogen SulfotransferaseInhibitors from a Purine Library Screen Synthesis, Mechanism of Action, and Antiviral Activity of a New Series ofCovalent Mechanism-Based Inhibitors of S-Adenosyl-l-Homocysteine Hydrolase Methylated Analogues of Methyl (R)-4-(3,4-Dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate (GR-89,696)as Highly Potent κ-Receptor Agonists: Stereoselective Synthesis,Opioid-Receptor Affinity, Receptor Selectivity, and Functional Studies Design, Synthesis, and Structure−Activity Relationships of a Series of3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives asAcetylcholinesterase Inhibitors 3-Phenyl-5-acyloxymethyl-2H,5H-furan-2-ones: Synthesis and Biological Activityof a Novel Group of Potential Antifungal Drugs Photochemical Synthesis of N-Arylbenzophenanthridine Selective EstrogenReceptor Modulators (SERMs) Sorbitol Dehydrogenase Inhibitors (SDIs): A New Potent, Enantiomeric SDI,4-[2-1R-Hydroxy-ethyl)-pyrimidin-4-yl]-piperazine-1-sulfonic AcidDimethylamide Human Thioredoxin Reductase Is Efficiently Inhibited by(2,2‘:6‘,2‘ ‘-Terpyridine)platinum(II) Complexes. Possible Implications for a NovelAntitumor Strategy Prediction of the Aroma Quality and the Threshold Values of Some PyrazinesUsing Artificial Neural Networks Synthesis and Evaluation of4-Fluoro-8-substituted-2,3,4,5-tetrahydro-1H-2-benzazapines as SelectiveInhibitors of Phenylethanolamine N-Methyltransferase versus theα2-Adrenoceptor Synthesis and in Vitro and in Vivo Antimalarial Activity of New4-Anilinoquinolines 6-Substituted-4-(3-bromophenylamino)quinazolines as Putative IrreversibleInhibitors of the Epidermal Growth Factor Receptor (EGFR) and HumanEpidermal Growth Factor Receptor (HER-2) Tyrosine Kinases with EnhancedAntitumor Activity Adaptive Neuro-Fuzzy Inference System: An Instant and Architecture-FreePredictor for Improved QSAR Studies Rationally Based Efficacy Tuning ofSelective Dopamine D4 Receptor LigandsLeading to the Complete Antagonist2-[4-(4-Chlorophenyl)piperazin-1-ylmethyl]pyrazolo[1,5-a]pyridine(FAUC 213) Development of Serine Protease Inhibitors Displaying a Multicentered Short(<2.3 Å) Hydrogen Bond Binding Mode: Inhibitors of Urokinase-TypePlasminogen Activator and Factor Xa Synthesis of and a Comparative Study on the Inhibition of Muscle and LiverGlycogen Phosphorylases by Epimeric Pairs of d-Gluco- andd-Xylopyranosylidene-spiro-(thio)hydantoins and N-(d-Glucopyranosyl) Amides Identification of the First trans-(3R,4R)-Dimethyl-4-(3-hydroxyphenyl)piperidineDerivative To Possess Highly Potent andSelective Opioid κ Receptor AntagonistActivity Toward the Design of Chemical Libraries for Mass Screening Biased againstMutagenic Compounds Selective Activation of Mitomycin A by Thiols To Form DNA Cross-links andMonoadducts: Biochemical Basis for the Modulation of Mitomycin Cytotoxicityby the Quinone Redox Potential Fluorosulfonyl- and Bis-(β-chloroethyl)amino-phenylamino FunctionalizedPyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives: IrreversibleAntagonists at the Human A3 Adenosine Receptor and Molecular ModelingStudies

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