Journal of Medicinal Chemistry
Volume 39, Issue 2 (January 19, 1996)
Copyright © 1996
American Chemical Society
343-346 | Substituted 1,2-Dihydrophthalazines: Potent, Selective, and Noncompetitive Inhibitors of the AMPA Receptor
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347-349 | (2S,3S,5R)-2-(3,5-Difluorophenyl)-3,5- dimethyl-2-morpholinol: A Novel Antidepressant Agent and Selective Inhibitor of Norepinephrine Uptake
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350-352 | Two New Criteria for Choosing Sample Size in Combinatorial Chemistry
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353-358 | Potent, Cell Active, Non-Thiol Tetrapeptide Inhibitors of Farnesyltransferase
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359-370 | Synthesis and Quantitative Structure-Activity Relationship of a Novel Series of Small Conductance Ca2+-Activated K+ Channel Blockers Related to Dequalinium
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371-379 | 2-Carbomethoxy-3-(diarylmethoxy)-1H,5H-tropane Analogs: Synthesis and Inhibition of Binding at the Dopamine Transporter and Comparison with Piperazines of the GBR Series
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380-387 | A Comparative Molecular Field Analysis Study of N-Benzylpiperidines as Acetylcholinesterase Inhibitors
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388-391 | A Study of the Active Site of Influenza Virus Sialidase: An Approach to the Rational Design of Novel Anti-influenza Drugs
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392-397 | A Novel, Picomolar Inhibitor of Human Immunodeficiency Virus Type 1 Protease
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398-406 | Tetrahydrobenzothiophenone Derivatives as a Novel Class of Adenosine Receptor Antagonists
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407-423 | Syntheses and Conformational Analyses of Glutamate Analogs: 2-(2-Carboxy-3-substituted-cyclopropyl)glycines as Useful Probes for Excitatory Amino Acid Receptors
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424-431 | Drug Delivery Systems: Water Soluble Taxol 2'-Poly(ethylene glycol) Ester Prodrugs-Design and in Vivo Effectiveness
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432-435 | Characterizations of the Unusual Dissociation Properties of Melanotropin Peptides from the Melanocortin Receptor, hMC1R
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436-445 | Studies on 6-Aminoquinolones: Synthesis and Antibacterial Evaluation of 6-Amino-8-methylquinolones
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446-457 | The Chemistry of Pseudomonic Acid. Synthesis and Antibacterial Activity of a Series of 5-Alkyl, 5-Alkenyl, and 5-Heterosubstituted Oxazoles
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458-470 | Indium(III) and Gallium(III) Complexes of Bis(aminoethanethiol) Ligands with Different Denticities: Stabilities, Molecular Modeling, and in Vivo Behavior
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471-479 | Structure-Activity Analysis of Anandamide Analogs: Relationship to a Cannabinoid Pharmacophore
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480-486 | Investigation of (Oxodioxolenyl)methyl Carbamates as Nonchiral Bioreversible Prodrug Moieties for Chiral Amines
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487-493 | Design, Synthesis, and Structure-Activity Relationship Studies of Novel 1-[(1-Acyl-4-piperidyl)methyl]-1H-2-methylimidazo[4,5-c]pyridine Derivatives as Potent, Orally Active Platelet-Activating Factor Antagonists
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494-502 | Dual Metalloprotease Inhibitors. 6. Incorporation of Bicyclic and Substituted Monocyclic Azepinones as Dipeptide Surrogates in Angiotensin-Converting Enzyme/Neutral Endopeptidase Inhibitors
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503-507 | Metal-Chelating Inhibitors of a Zinc Finger Protein HIV-EP1. Remarkable Potentiation of Inhibitory Activity by Introduction of SH Groups
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508-514 | Correlation of Anti-HIV Potency with Lipophilicity in a Series of Cosalane Analogs Having Normal Alkenyl and Phosphodiester Chains as Cholestane Replacements
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515-521 | Neuroactive Polyamine Wasp Toxins: Nuclear Magnetic Resonance Spectroscopic Analysis of the Protolytic Properties of Philanthotoxin-343
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522-530 | 2-Sulfonyl-4-chloroanilino Moiety: A Potent Pharmacophore for the Anti-Human Immunodeficiency Virus Type 1 Activity of Pyrrolyl Aryl Sulfones
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531-537 | Cross-Linking and Sequence Specific Alkylation of DNA by Aziridinylquinones. 1. Quinone Methides
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538-542 | Synthesis and Antiviral Activity of 2'-Deoxy-4'-thio Purine Nucleosides
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543-548 | N-Substituted Analogs of 2-Carbomethoxy-3-(4'-iodophenyl)tropane (-CIT) with Selective Affinity to Dopamine or Serotonin Transporters in Rat Forebrain
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549-555 | 8,9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: A Potent Full Dopamine D1 Agonist Containing a Rigid -Phenyldopamine Pharmacophore
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556-561 | Approaches to Short-Acting Neuromuscular Blocking Agents: Nonsymmetrical Bis-tetrahydroisoquinolinium Mono- and Diesters
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562-569 | Discovery of 1,5-Benzodiazepines with Peripheral Cholecystokinin (CCK-A) Receptor Agonist Activity. 1. Optimization of the Agonist "Trigger"
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570-581 | Synthesis and Structure-Activity Relationships of N-Propyl-N-(4-pyridinyl)-1H-indol-1-amine (Besipirdine) and Related Analogs as Potential Therapeutic Agents for Alzheimer's Disease
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582-587 | Substituted (Pyrroloamino)pyridines: Potential Agents for the Treatment of Alzheimer's Disease
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588-595 | Ionophore Properties of Monensin Derivatives Studied on Human Erythrocytes by 23Na NMR and K+ and H+ Potentiometry: Relationship with Antimicrobial and Antimalarial Activities
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596-604 | 2-[(2-Aminobenzyl)sulfinyl]-1-(2-pyridyl)-1,4,5,6-tetrahydrocyclopent[d]imidazoles as a Novel Class of Gastric H+/K+-ATPase Inhibitors
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605-608 | Antitumor Activity of the R- and S-Enantiomers of RS-2-[[Hydroxy[[2-[(octadecyloxy)methyl]tetrahydrofuran-2-yl]methoxy]phosphinyl]oxy]-N,N,N-trimethylethylaminium Hydroxide Inner Salt
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609-613 | Aminoacetyl Moiety as a Potential Surrogate for Diacylhydrazine Group of SC-51089, a Potent PGE2 Antagonist, and Its Analogs
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614-618 | Analogues of 10-Deazaaminopterin and 5-Alkyl-5,10-dideazaaminopterin with the 4-Substituted 1-Naphthoyl Group in the Place of 4-Substituted Benzoyl
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619-622 | Design, Synthesis, and Biological Activity of a Potent Inhibitor of the Neuropeptidase N-Acetylated -Linked Acidic Dipeptidase
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623-623 | Ketenes Thomas T. Tidwell. John Wiley & Sons, Inc., New York. 1995. xv + 665 pp. 16.5 × 24.5 cm. ISBN 0-471-57580-1. $69.95.
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623-623 | Books of Interest [Full Article - PDF] |
623-623 | [Full Article - PDF] |
624-624 |
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