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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_10/m/print http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_10/m/web
Date Copyrighted	1997
Rights	Copyright © 1997 American Chemical Society
issue	10
Rights Holder	American Chemical Society
is Is Part Of of	Dihydro(alkylthio)(naphthylmethyl)oxopyrimidines: Novel Non-NucleosideReverse Transcriptase Inhibitors of the S-DABO Series Folate-Based Inhibitors of Thymidylate Synthase: Synthesis and AntitumorActivity of γ-Linked Sterically Hindered Dipeptide Analogues of2-Desamino-2-methyl-N10-propargyl-5,8-dideazafolic Acid (ICI 198583) Enantiomers of Diastereoisomeric cis-N-[1-(2-Hydroxy-2-phenylethyl)-3-methyl-4-piperidyl]-N-phenylpropanamides: Synthesis, X-ray Analysis, and Biological Activities Conformationally Constrained Analogues of Diacylglycerol. 13.1Protein Kinase C Ligands Based on Templates Derivedfrom 2,3-Dideoxy-l-erythro(threo)-hexono-1,4-lactone and2-Deoxyapiolactone Inhibition of Thyroid Hormone Uptake by Calcium Antagonists of theDihydropyridine Class Discovery and Synthesis of [6-Hydroxy-3-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-(4-hydroxyphenyl)]benzo[b]thiophene: A Novel, Highly Potent, SelectiveEstrogen Receptor Modulator Tyrosine Kinase Inhibitors. 11. Soluble Analogues of Pyrrolo- andPyrazoloquinazolines as Epidermal Growth Factor Receptor Inhibitors: Synthesis, Biological Evaluation, and Modeling of the Mode of Binding Novel Heterocyclic-Fused Pyridazinones as Potent and SelectivePhosphodiesterase IV Inhibitors Binding Affinities for Sulfonamide Inhibitors with Human Thrombin UsingMonte Carlo Simulations with a Linear Response Method Chemistry and Toxicology of Diverse Classes ofAlkaloids Edited by Murray S. Blum. Alaken, Inc.,Fort Collins, Co. 1996. 386 pp. 16 × 23.5 cm. ISBN1-880293-04-8. $99.50. Smart Region Definition: A New Way To Improve the Predictive Ability andInterpretability of Three-Dimensional Quantitative Structure−ActivityRelationships Synthesis, Antiviral Activity, and Biological Properties of VinylacetyleneAnalogs of Enviroxime Improved P1/P1‘ Substituents for Cyclic Urea Based HIV-1 Protease Inhibitors: Synthesis, Structure−Activity Relationship, and X-ray Crystal StructureAnalysis Conformationally Constrained [p-(ω-Aminoalkyl)phenacetyl]-l-seryl-l-lysylDipeptide Amides as Potent Peptidomimetic Inhibitors of Candida albicansand Human Myristoyl-CoA:Protein N-Myristoyl Transferase Selection, Preparation and Pharmacological Evaluation of Plant Material By Elizabeth M. Williamson,David T. Okpako, and Fred J. Evans. John Wiley &Sons, Chichester, U.K. 1996. ix + 228 pp. 15.5 × 23.5cm. ISBN 0-471-94217-0. $39.95 (pbk). A Comparison of Structure−Activity Relationships between Spermidine andSpermine Analogue Antineoplastics Preparation and Anti-HIV Activity of N-3-Substituted Thymidine NucleosideAnalogs Synthesis and Structure−Activity Relationships of 17β-Substituted14β-Hydroxysteroid 3-(α-l-Rhamnopyranoside)s: Steroids That Bind to theDigitalis Receptor

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