Journal of Medicinal Chemistry
Volume 39, Issue 5 (March 1, 1996)
Copyright © 1996
American Chemical Society
1013-1015 | N-Terminus Urea-Substituted Chemotactic Peptides: New Potent Agonists and Antagonists toward the Neutrophil fMLF Receptor
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1016-1017 | Betulinic Acid and Dihydrobetulinic Acid Derivatives as Potent Anti-HIV Agents
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1018-1020 | Carbohydrates in an Acidic Multivalent Assembly: Nanomolar P-Selectin Inhibitors
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1021-1027 | 4'-O-[2-(2-Fluoromalonyl)]-L-tyrosine: A Phosphotyrosyl Mimic for the Preparation of Signal Transduction Inhibitory Peptides
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1028-1032 | Structure-Activity Relationship for Antineoplastic Imidazoacridinones: Synthesis and Antileukemic Activity in Vivo
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1033-1038 | Time-Dependent Inactivation of Aromatase by 6-Alkylandrosta-1,4-diene-3,17-diones. Effects of Length and Configuration of the 6-Alkyl Group
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1039-1048 | 2,4-Diarylpyrrolidine-3-carboxylic Acids-Potent ETA Selective Endothelin Receptor Antagonists. 1. Discovery of A-127722
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1049-1055 | Bisindolylmaleimides Linked to DNA Minor Groove Binding Lexitropsins: Synthesis, Inhibitory Activity against Topoisomerase I, and Biological Evaluation
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1056-1068 | Betulinic Acid Derivatives: A New Class of Human Immunodeficiency Virus Type 1 Specific Inhibitors with a New Mode of Action
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1069-1083 | Betulinic Acid Derivatives: A New Class of Specific Inhibitors of Human Immunodeficiency Virus Type 1 Entry
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1084-1094 | Hypoxia-Selective Antitumor Agents. 12. Nitrobenzyl Quaternary Salts as Bioreductive Prodrugs of the Alkylating Agent Mechlorethamine
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1095-1099 | Toward a Novel Metal-Based Chemotherapy against Tropical Diseases. 2. Synthesis and Antimalarial Activity in Vitro and in Vivo of New Ruthenium- and Rhodium-Chloroquine Complexes
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1100-1105 | New Mustard Prodrugs for Antibody-Directed Enzyme Prodrug Therapy: Alternatives to the Amide Link
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1106-1111 | Studies on the Mechanism of Phosphatidylinositol 3-Kinase Inhibition by Wortmannin and Related Analogs
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1112-1124 | Nonpeptidic Inhibitors of Human Neutrophil Elastase. 7. Design, Synthesis, and in Vitro Activity of a Series of Pyridopyrimidine Trifluoromethyl Ketones
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1125-1129 | 8-[4-[2-(1,2,3,4-Tetrahydroisoquinolinyl)]butyl]-8-azaspiro[4.5]decane-7,9-dione: A New 5-HT1A Receptor Ligand with the Same Activity Profile as Buspirone
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1130-1135 | Synthesis and Biological Evaluation of 1',2'-Seconucleo-5'-phosphonates
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1136-1141 | Design, Synthesis, and Biological Activities of Cyclic Lactam Peptide Analogues of Dynorphin A(1-11)-NH2
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1142-1147 | Antagonistic Properties of Centrally Truncated Analogs of [D-Trp32]NPY
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1148-1156 | Nitric Oxide-Releasing Polymers Containing the [N(O)NO]- Group
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1157-1163 | Novel Carbamates as Potent Histamine H3 Receptor Antagonists with High in Vitro and Oral in Vivo Activity
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1164-1171 | Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives: Potent and Selective A2A Adenosine Antagonists
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1172-1188 | Structure-Activity Relationships of a Series of Substituted Benzamides: Potent D2/5-HT2 Antagonists and 5-HT1a Agonists as Neuroleptic Agents
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1189-1189 | Peptide-Based Drug Design: Controlling Transport and Metabolism Editors: Michael D. Taylor and Gordon L. Amidon. American Chemical Society, Washington, D.C. 1995. xviii + 567 pp. 18.5 × 26 cm. ISBN 0-8412-3058-7. $99.95.
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1189-1190 | Exploring QSAR: Hydrophobic, Electronic, and Steric Constants C. Hansch, A. Leo, and D. Hoekman. American Chemical Society, Washington, DC. 1995. Xix + 348 pp. 22 × 28.5 cm. Exploring QSAR: Fundamentals and Applications in Chemistry and Biology. C. Hansch and A. Leo. American Chemical Society, Washington, DC. 1995. Xvii + 557 pp. 18.5 × 26 cm. ISBN 0-8412-2993-7 (set). $99.95 (set).
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1190-1190 | Heterocyclic Compounds. Isoquinolines. Volume 38. Part 3 Edited by Gary M. Coppola and Herbert F. Schuster. John Wiley & Sons, Inc., New York. 1995. xi + 552 pp. 16 × 24 cm. ISBN 0-471-62853-7. $225.00.
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1190-1191 | Angiotensin II Receptors Volume 1. Molecular Biology, Biochemistry, and Clinical Perspectives Edited by Robert R. Ruffolo, Jr. CRC Press, Boca Raton, FL. 1994. 170 pp. 16 × 24 cm. ISBN 0-8493-8380-3. $99.50; Volume 2. Medicinal Chemistry. 1994. 225 pp. 16 × 24 cm. ISBN 0-8493-8545-3. $99.50.
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1191-1191 | Books of Interest [Full Article - PDF] |
1191-1191 | [Full Article - PDF] |
1192-1192 | 4-Aza-3-oxo-5-androst-1-ene-17-N-arylcarboxamides as Dual Inhibitors of Human Type 1 and Type 2 Steroid 5-Reductases. Dramatic Effect of N-Aryl Substituents on Type 1 and Type 2 5-Reductase Inhibitory Potency
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