Journal of Medicinal Chemistry
Volume 39, Issue 23 (November 8, 1996)
Copyright © 1996
American Chemical Society
4527-4530 | Potent and Selective Thrombin Inhibitors Incorporating the Constrained Arginine Mimic L-3-Piperidyl(N-guanidino)alanine at P1
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4531-4536 | Design, Synthesis, and Evolution of a Novel, Selective, and Orally Bioavailable Class of Thrombin Inhibitors: P1-Argininal Derivatives Incorporating P3-P4 Lactam Sulfonamide Moieties
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4537-4539 | Synthesis of Novel trans-4-(Substituted-benzamido)-3,4-dihydro-2H-benzo[b]pyran-3-ol Derivatives as Potential Anticonvulsant Agents with a Distinctive Binding Profile
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4540-4546 | High-Resolution Crystal Structures of Human Cyclin-Dependent Kinase 2 with and without ATP: Bound Waters and Natural Ligand as Guides for Inhibitor Design
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4547-4553 | Studies on Selectin Blocker. 3. Investigation of the Carbohydrate Ligand Sialyl Lewis X Recognition Site of P-Selectin
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4554-4562 | Targeting the Minor Groove of DNA: Crystal Structures of Two Complexes between Furan Derivatives of Berenil and the DNA Dodecamer d(CGCGAATTCGCG)2
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4563-4568 | 2-Amino-4-oxo-5-substituted-pyrrolo[2,3-d]pyrimidines as Nonclassical Antifolate Inhibitors of Thymidylate Synthase1a,b
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4569-4575 | Synthesis and Biological Activity of Aromatic Amino Acid Phosphoramidates of 5-Fluoro-2'-deoxyuridine and 1--Arabinofuranosylcytosine: Evidence of Phosphoramidase Activity
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4576-4582 | Synthesis, Biological Evaluation, Calcium Channel Antagonist Activity, and Anticonvulsant Activity of Felodipine Coupled to a Dihydropyridine-Pyridinium Salt Redox Chemical Delivery System
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4583-4591 | Non-Peptide Glycoprotein IIb/IIIa Antagonists. 11. Design and in Vivo Evaluation of 3,4-Dihydro-1(1H)-isoquinolinone-Based Antagonists and Ethyl Ester Prodrugs
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4592-4601 | N-Aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: KATP Potassium Channel Openers. Modifications on the Western Region
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4602-4607 | Synthesis and Biological Profile of the Enantiomers of [4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)-cis-octahydroquinoxalin-1-yl]furan- 2-ylmethanone (Cyclazosin), a Potent Competitive 1B-Adrenoceptor Antagonist
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4608-4621 | Synthesis, Structure-Activity Relationships, and Pharmacokinetic Properties of Dihydroorotate Dehydrogenase Inhibitors: 2-Cyano-3-cyclopropyl-3-hydroxy- N-[3'-methyl-4'-(trifluoromethyl)phenyl]propenamide and Related Compounds
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4622-4629 | Molecular Electronic Properties of a Series of 4-Quinolinecarbinolamines Define Antimalarial Activity Profile
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4630-4642 | Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors
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4643-4653 | Analogs of 3-Hydroxy-1H-1-benzazepine-2,5-dione: Structure-Activity Relationship at N-Methyl-D-aspartate Receptor Glycine Sites
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4654-4666 | High-Affinity -Aminobutyric Acid A/Benzodiazepine Ligands: Synthesis and Structure-Activity Relationship Studies of a New Series of Tetracyclic Imidazoquinoxalines
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4667-4675 | 6-Phenyl-1,4-dihydropyridine Derivatives as Potent and Selective A3 Adenosine Receptor Antagonists
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4676-4681 | In Vitro and in Vivo Evaluation of 6-Azido-2',3'-dideoxy-2'-fluoro--D-arabinofuranosylpurine and N6-Methyl-2',3'-dideoxy-2'-fluoro--D-arabinofuranosyladenine as Prodrugs of the Anti-HIV Nucleosides 2'-F-ara-ddA and 2'-F-ara-ddI
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4682-4686 | Structure-Activity Relationships of 4-Hydroxy-3-nitroquinolin-2(1H)-ones as Novel Antagonists at the Glycine Site of N-Methyl-D-aspartate Receptors
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4687-4687 | Biotechnology Intelligence Unit. Structure-Property Correlations in Drug Development Edited by Han van de Waterbeemd. Academic Press, Inc., San Diego, CA. Academic Press Ltd., London, United Kingdom. R. G. Landes Co., Georgetown, TX. 1996. 210 pp. 18.5 × 26 cm. ISBN 0-12-711650-8. $69.95.
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4687-4687 | The Practice of Medicinal Chemistry Edited by Camille G. Wermuth. Academic Press, London. 1996. xvii + 968 pp. 17 × 25 cm. ISBN 0-12-744640-0. $89.00.
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4687-4688 | Bioorganic Chemistry. A Chemical Approach to Enzyme Action. Third Edition Hermann Dugas. Springer-Verlag, New York. 1996. xvii + 700 pp. 16 × 24 cm. ISBN 0-387-94494-X. $49.95.
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4688-4688 | Books of Interest [Full Article - PDF] |