| 101 |
|
2-Substituted Piperazines as Constrained Amino Acids. Application to theSynthesis of Potent, Non Carboxylic Acid Inhibitors of Farnesyltransferase
|
Williams, T. M
|
American Chemical Society
|
1980
|
|
|
|
| 102 |
|
2-Substitution of Adenine Nucleotide Analogues Containing a Bicyclo[3.1.0]hexane Ring System Locked in a Northern Conformation: Enhanced Potency as P2Y~1 Receptor Antagonists/
|
Kim, H. S
|
American Chemical Society
|
2003
|
|
|
|
| 103 |
|
2-Sulfonyl-4-chloroanilino Moiety: A Potent Pharmacophore for the Anti-Human Immunodeficiency Virus Type 1 Activity of Pyrrolyl Aryl Sulfones
|
Artico, M
|
American Chemical Society
|
1980
|
|
|
|
| 104 |
|
[3+2] versus [2+2] Addition of Metal Oxides Across C═C Bonds. Reconciliation of Experiment and Theory/
|
Deubel, D. V
|
American Chemical Society
|
2003
|
|
|
|
| 105 |
|
3-1[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1-yl]methyl-1H-pyrrol[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the HumanDopamine D~4 Receptor
|
Kulagowski, J. J
|
American Chemical Society
|
1980
|
|
|
|
| 106 |
|
3-(1H-Indazol-3ylmethyl)-1,5-benzodiazepines: CCK-A Agonists That Demonstrate Oral Activity as Satiety Agents
|
Henke, B. R
|
American Chemical Society
|
1980
|
|
|
|
| 107 |
|
3-(2-Benzofuranyl)quinuclidin-2-ene Derivatives: Novel Muscarinic Antagonists
|
Nordvall, G
|
American Chemical Society
|
1980
|
|
|
|
| 108 |
|
3-[2-(N-Phehylacetamide)]-1,5-benzodiazepines: Orally Active, Binding Selective CCK-A Agonists
|
Willson, T. M
|
American Chemical Society
|
1980
|
|
|
|
| 109 |
|
3-[2-(Pyrrolidin-1-yl)ethyl]indoles and 3-[3-(Piperidin-1-yl)propyl]indoles: Agonists for the h5-HT~1~D Receptor with High Selectivity over the h5-HT~1~B Subtype
|
Castro, J. L
|
American Chemical Society
|
1980
|
|
|
|
| 110 |
|
3-(3,5-Dimethoxyphenyl)-1,6-naphthyridine-2,7-diamines and Related 2-Urea Derivatives Are Potent and Selective Inhibitors of the FGF Receptor-1 Tyrosine Kinase/
|
Thompson, Andrew M
|
American Chemical Society
|
2000
|
|
|
|
| 111 |
|
3,3-Dialkyl- and 3-Alkyl-3-Benzyl-Substituted 2-Pyrrolidinones: A New Class of Anticonvulsant Agents
|
Reddy, P. A
|
American Chemical Society
|
1980
|
|
|
|
| 112 |
|
3,3'-Dichlorobenzidine Transformation Processes in Natural Sediments
|
Nyman, M. C
|
American Chemical Society
|
1980
|
|
|
|
| 113 |
|
3-[[(4-Aryl- 1-piperazinyl)alkyl] cyclohexyl]- 1H-indoles as Dopamine D2Partial Agonists and Autoreceptor Agonists
|
Wustrow, D. J
|
American Chemical Society
|
1980
|
|
|
|
| 114 |
|
3-(4-{[Benzyl(methyl)amino]methyl}phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) Inhibits Both Acetylcholinesterase and Acetylcholinesterase-Induced beta-Amyloid Aggregation: A Dual Function Lead for Alzheimer's Disease Therapy/
|
Piazzi, L
|
American Chemical Society
|
2003
|
|
|
|
| 115 |
|
^3^6Cl and ^1^2^9I in the Yenisei, Kolyma, and Mackenzie Rivers
|
Beasley, T. M
|
American Chemical Society
|
1980
|
|
|
|
| 116 |
|
3,6-Dibromocarbazole Piperazine Derivatives of 2-Propanol as First Inhibitors of Cytochrome c Release via Bax Channel Modulation/
|
Bombrun, A
|
American Chemical Society
|
2003
|
|
|
|
| 117 |
|
3-Amino-3,4-dihydro-2H-1-benzopyran Derivatives as 5-HT~1~A Receptor Ligands and Potential Anxiolytic Agents. 2. Synthesis and Quantitative Structure-Activity Relationship Studies of Spiro[pyrrolidine- and piperidine-2,3'(2'H)-benzopyrans]
|
Comoy, C
|
American Chemical Society
|
1980
|
|
|
|
| 118 |
|
3- and 4-Pyridylalkyl Adamantanecarboxylates: Inhibitors of Human Cytochrome P450~1~7~�(17�Hydroxylase/C~1~7~,~2~0-Lyase). Potential Nonsteroidal Agents for the Treatment of Prostatic Cancer
|
Chan, F. C. Y
|
American Chemical Society
|
1980
|
|
|
|
| 119 |
|
3- and 4-Substituted 4H-Pyrido[4,3-e]-1,2,4-thiadiazine 1,1-Dioxides as Potassium Channel Openers: Synthesis, Pharmacological Evaluation, and Structure-Activity Relationships
|
De Tullio, P
|
American Chemical Society
|
1980
|
|
|
|
| 120 |
|
3-Aryl-1,2-diacetamidopropane Derivatives as Novel and Potent NK-1 Receptor Antagonists
|
Hipskind, P. A
|
American Chemical Society
|
1980
|
|
|
|