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Results: 1-7 |
Results: 7
Synthesis and antiviral activities of the major metabolites of the HIV protease inhibitor ABT-378 (Lopinavir)
Authors: Sham, HL Betebenner, DA Herrin, T Kumar, G Saldivar, A Vasavanonda, S Molla, A Kempf, DJ Plattner, JJ Norbeck, DW
Citation: Hl. Sham et al., Synthesis and antiviral activities of the major metabolites of the HIV protease inhibitor ABT-378 (Lopinavir), BIOORG MED, 11(11), 2001, pp. 1351-1353
Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens
Authors: Ma, ZK Clark, RF Brazzale, A Wang, SY Rupp, MJ Li, LP Griesgraber, G Zhang, SM Yong, H Phan, LT Nemoto, PA Chu, DTW Plattner, JJ Zhang, XL Zhong, P Cao, ZS Nilius, AM Shortridge, VD Flamm, R Mitten, M Meulbroek, J Ewing, P Alder, J Or, YS
Citation: Zk. Ma et al., Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens, J MED CHEM, 44(24), 2001, pp. 4137-4156
Total synthesis and antifungal evaluation of cyclic aminohexapeptides
Authors: Klein, LL Li, LP Chen, HJ Curty, CB DeGoey, DA Grampovnik, DJ Leone, CL Thomas, SA Yeung, CM Funk, KW Kishore, V Lundell, EO Wodka, D Meulbroek, JA Alder, JD Nilius, AM Lartey, PA Plattner, JJ
Citation: Ll. Klein et al., Total synthesis and antifungal evaluation of cyclic aminohexapeptides, BIO MED CH, 8(7), 2000, pp. 1677-1696
Antifungal rapamycin analogues with reduced immunosuppressive activity
Authors: Dickman, DA Ding, H Li, Q Nilius, AM Balli, DJ Ballaron, SJ Trevillyan, JM Smith, ML Seif, LS Kim, K Sarthy, A Goldman, RC Plattner, JJ Bennani, YL
Citation: Da. Dickman et al., Antifungal rapamycin analogues with reduced immunosuppressive activity, BIOORG MED, 10(13), 2000, pp. 1405-1408
Synthesis and structure-activity relationships of 2-pyridones. Part 2: 8-(Fluoro-substituted pyrrolidinyl)-2-pyridones as antibacterial agents (vol 8, pg 1953, 1998)
Authors: Li, Q Wang, W Berst, KB Claiborne, A Hasvold, L Raye, K Tufano, M Nilius, A Shen, LL Flamm, R Alder, J Marsh, K Crowell, D Chu, DTW Plattner, JJ
Citation: Q. Li et al., Synthesis and structure-activity relationships of 2-pyridones. Part 2: 8-(Fluoro-substituted pyrrolidinyl)-2-pyridones as antibacterial agents (vol 8, pg 1953, 1998), BIOORG MED, 9(7), 1999, pp. 1067-1067
Practical synthesis of 2-pyridone core: Ethyl 8-chloro-1-cyclopropyl-7-fluoro-9-methyl-4-oxo-4H-quinolizinone-3-carboxylate
Authors: Li, Q Sowin, T Claiborne, A Lijewski, L Zhang, XL Raye, K Mazdiyasni, H Arnold, W Melcher, LM Wang, WB Hasvold, L Fung, A Chu, DTW Plattner, JJ
Citation: Q. Li et al., Practical synthesis of 2-pyridone core: Ethyl 8-chloro-1-cyclopropyl-7-fluoro-9-methyl-4-oxo-4H-quinolizinone-3-carboxylate, HETEROCYCLE, 51(6), 1999, pp. 1345
ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease
Authors: Sham, HL Kempf, DJ Molla, A Marsh, KC Kumar, GN Chen, CM Kati, W Stewart, K Lal, R Hsu, A Betebenner, D Korneyeva, M Vasavanonda, S McDonald, E Saldivar, A Wideburg, N Chen, XQ Niu, P Park, C Jayanti, V Grabowski, B Granneman, GR Sun, E Japour, AJ Leonard, JM Plattner, JJ Norbeck, DW
Citation: Hl. Sham et al., ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease, ANTIM AG CH, 42(12), 1998, pp. 3218-3224
Risultati: 1-7 |