| 141 |
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Design and Synthesis of 4,5-Diphenyl-4-isoxazolines: Novel Inhibitors of Cyclooxygenase-2 with Analgesic and Antiinflammatory Activity/
|
Habeeb, A G
|
American Chemical Society
|
2001
|
|
|
|
| 142 |
|
Design and Synthesis of 4,6-Di-tert-butyl-2,3-dihydro-5-benzofuranols as a Novel Series of Antiatherogenic Antioxidants/
|
Tamura, K
|
American Chemical Society
|
2003
|
|
|
|
| 143 |
|
Design and Synthesis of 4-Azaindoles as Inhibitors of p38 MAP Kinase/
|
Trejo, A
|
American Chemical Society
|
2003
|
|
|
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| 144 |
|
Design and Synthesis of 4-Substituted Benzamides as Potent, Selective, and Orally Bioavailable IKs Blockers/
|
Lloyd, J
|
American Chemical Society
|
2001
|
|
|
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| 145 |
|
Design and Synthesis of a Potent and Selective Triazolone-Based Peroxisome Proliferator-Activated Receptor alpha Agonist/
|
Xu, Y
|
American Chemical Society
|
2003
|
|
|
|
| 146 |
|
Design and Synthesis of a Series of Non-Peptide High-Affinity Human Corticotropin-Releasing Factor Receptor Antagonists
|
Chen, C
|
American Chemical Society
|
1980
|
|
|
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| 147 |
|
Design and Synthesis of Bipyridyl-Containing Conjugated Polymers: Effects of Polymer Rigidity on Metal Ion Sensing/
|
Liu, B
|
American Chemical Society
|
2001
|
|
|
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| 148 |
|
Design and Synthesis of Celecoxib and Rofecoxib Analogues as Selective Cyclooxygenase-2 (COX-2) Inhibitors: Replacement of Sulfonamide and Methylsulfonyl Pharmacophores by an Azido Bioisostere/
|
Habeeb, A G
|
American Chemical Society
|
2001
|
|
|
|
| 149 |
|
Design and Synthesis of Highly Potent Benzodiazepine gamma-Secretase Inhibitors: Preparation of (2S,3R)-3-(3,4-Difluorophenyl)-2-(4-fluorophenyl)-4-hydroxy-N-((3S)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]-diazepin-3-yl)butyramide by Use of an/
|
Churcher, I
|
American Chemical Society
|
2003
|
|
|
|
| 150 |
|
Design and Synthesis of Histidine Analogues of Folic Acid and Methotrexate as Potential Folylpolyglutamate Synthetase Inhibitors
|
Mao, Z
|
American Chemical Society
|
1980
|
|
|
|
| 151 |
|
Design and Synthesis of Low Cost, Sustainable CO2-philes/
|
Sarbu, Traian
|
American Chemical Society
|
2000
|
|
|
|
| 152 |
|
Design and Synthesis of Matrix Metalloproteinase Inhibitors Guided by Molecular Modeling. Picking the S1 Pocket Using Conformationally Constrained Inhibitors/
|
Hanessian, S
|
American Chemical Society
|
2001
|
|
|
|
| 153 |
|
Design and Synthesis of New Linear and Cyclic Bradykinin Antagonists
|
Thurieau, C
|
American Chemical Society
|
1980
|
|
|
|
| 154 |
|
Design and Synthesis of Non-Peptide Ras CAAX Mimetics as Potent Farnesyltransferase Inhibitors
|
Qian, Y
|
American Chemical Society
|
1980
|
|
|
|
| 155 |
|
Design and Synthesis of Non-peptidic Inhibitors for the Syk C-Terminal SH2 Domain Based on Structure-Based In-Silico Screening/
|
Niimi, T
|
American Chemical Society
|
2001
|
|
|
|
| 156 |
|
Design and Synthesis of Novel Dimeric Morphinan Ligands for kappa and mu Opioid Receptors/
|
Neumeyer, J. L
|
American Chemical Society
|
2003
|
|
|
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| 157 |
|
Design and Synthesis of Novel Imidazole-Substituted Dipeptide Amides as Potent and Selective Inhibitors of Candida albicans MyristoylCoA:Protein N-Myristoyltransferase and Identification of Related Tripeptide Inhibitors with Mechanism-Based Antifungal Activity
|
Devadas, B
|
American Chemical Society
|
1980
|
|
|
|
| 158 |
|
Design and Synthesis of Poly ADP-ribose Polymerase-1 Inhibitors. 2. Biological Evaluation of Aza-5[H]-phenanthridin-6-ones as Potent, Aqueous-Soluble Compounds for the Treatment of Ischemic Injuries/
|
Ferraris, D
|
American Chemical Society
|
2003
|
|
|
|
| 159 |
|
Design and Synthesis of Potent Antitumor 5,4'-Diaminoflavone DerivativesBased on Metabolic Considerations
|
Akama, T
|
American Chemical Society
|
1980
|
|
|
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| 160 |
|
Design and Synthesis of Potent C2-Symmetric Diol-Based HIV-1 Protease Inhibitors: Effects of Fluoro Substitution/
|
Pyring, D
|
American Chemical Society
|
2001
|
|
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