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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_6/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_6/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	6
Rights Holder	American Chemical Society
is Is Part Of of	Carbonic Anhydrase and Matrix Metalloproteinase Inhibitors: Sulfonylated Amino Acid Hydroxamates withMMP Inhibitory Properties Act as Efficient Inhibitorsof CA Isozymes I, II, and IV, and N-Hydroxysulfonamides Inhibit Both These Zinc Enzymes Solid-Phase Synthesis and Inhibitory Effects of Some Pyrido[1,2-c]pyrimidineDerivatives on Leukocyte Functions and Experimental Inflammation New Synthesis of Benzo-δ-carbolines, Cryptolepines, and Their Salts: In VitroCytotoxic, Antiplasmodial, and Antitrypanosomal Activities of δ-Carbolines,Benzo-δ-carbolines, and Cryptolepines Structure−Activity Relationship Studies of4-[2-(Diphenylmethoxy)ethyl]-1-benzylpiperidine Derivatives and TheirN-Analogues: Evaluation of Behavioral Activity of O- and N-Analogues andTheir Binding to Monoamine Transporters Enantiospecific Synthesis and Pharmacological Evaluation of a Series ofSuper-Potent, Conformationally Restricted 5-HT2A/2C Receptor Agonists High-Throughput Permeability pH Profile and High-Throughput Alkane/Waterlog P with Artificial Membranes Inhibition of Heme Detoxification Processes Underlies the Antimalarial Activityof Terpene Isonitrile Compounds from Marine Sponges Bisphosphonates Inhibit the Growth of Trypanosoma brucei, Trypanosomacruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: A Potential Route to Chemotherapy Discovery of Inhibitors of Cell Adhesion Molecule Expression in HumanEndothelial Cells. 1. Selective Inhibition of ICAM-1 and E-Selectin Expression Pharmacophore Analysis of the Nuclear Oxysterol Receptor LXRα Solid-Phase Synthesis and Combinatorial Technologies By Pierfausto Seneci. Wiley-Interscience,New York. 2000. xii + 637 pp. 16 × 24 cm. ISBN0471331953. $109.95. A Potent, Nonpeptidyl 1H-Quinolone Antagonist for theGonadotropin-Releasing Hormone Receptor α2 Adrenoceptor Agonists as Potential Analgesic Agents. 3.Imidazolylmethylthiophenes Investigation of the Selectivity of Oxymorphone- and Naltrexone-DerivedLigands via Site-Directed Mutagenesis of Opioid Receptors: Exploring the‘Address' Recognition Locus Molecular Modeling Studies of the Akt PH Domain and Its Interaction withPhosphoinositides A Novel Series of Highly Potent Benzimidazole-Based Microsomal TriglycerideTransfer Protein Inhibitors Factors Influencing Agonist Potency and Selectivity for the Opioid δ ReceptorAre Revealed in Structure−Activity Relationship Studies of the4-[(N-Substituted-4-piperidinyl)arylamino]-N,N-diethylbenzamides Synthesis of 2-Amino-5-sulfanyl-1,3,4-thiadiazole Derivatives and Evaluation ofTheir Antidepressant and Anxiolytic Activity Pyrido[2,3-d]pyrimidin-7-one Inhi-bitors of Cyclin-Dependent Kinases. Comparative Binding Energy (COMBINE) Analysis of InfluenzaNeuraminidase−Inhibitor Complexes

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