AAAAAA

   
Results: 1-8 |
Results: 8
STRUCTURE-BASED DESIGN OF NOVEL CALCINEURIN (PP2B) INHIBITORS
Authors: TATLOCK JH LINTON MA HOU XJ KISSINGER CR PELLETIER LA SHOWALTER RE TEMPCZYK A VILLAFRANCA JE
Citation: Jh. Tatlock et al., STRUCTURE-BASED DESIGN OF NOVEL CALCINEURIN (PP2B) INHIBITORS, Bioorganic & medicinal chemistry letters, 7(8), 1997, pp. 1007-1012
VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE
Authors: KALDOR SW KALISH VJ DAVIES JF SHETTY BV FRITZ JE APPELT K BURGESS JA CAMPANALE KM CHIRGADZE NY CLAWSON DK DRESSMAN BA HATCH SD KHALIL DA KOSA MB LUBBEHUSEN PP MUESING MA PATICK AK REICH SH SU KS TATLOCK JH
Citation: Sw. Kaldor et al., VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE, Journal of medicinal chemistry, 40(24), 1997, pp. 3979-3985
DESIGN, SYNTHESIS AND X-RAY CRYSTALLOGRAPHIC STUDIES OF [7.3.1]MACROCYCLIC AND [8.3.1]MACROCYCLIC FKBP-12 LIGANDS
Authors: BABINE RE BLECKMAN TM LITTLEFIELD ES PARGE HE PELLETIER LAK LEWIS CT FRENCH JV IMBACUAN M KATOH S TATLOCK JH SHOWALTER RE ERNEST J
Citation: Re. Babine et al., DESIGN, SYNTHESIS AND X-RAY CRYSTALLOGRAPHIC STUDIES OF [7.3.1]MACROCYCLIC AND [8.3.1]MACROCYCLIC FKBP-12 LIGANDS, Bioorganic & medicinal chemistry letters, 6(4), 1996, pp. 385-390
STRUCTURE-BASED DESIGN OF NOVEL, UREA-CONTAINING FKBP12 INHIBITORS
Authors: DRAGOVICH PS BARKER JE FRENCH J IMBACUAN M KALISH VJ KISSINGER CR KNIGHTON DR LEWIS CT MOOMAW EW PARGE HE PELLETIER LAK PRINS TJ SHOWALTER RE TATLOCK JH TUCKER KD VILLAFRANCA JE
Citation: Ps. Dragovich et al., STRUCTURE-BASED DESIGN OF NOVEL, UREA-CONTAINING FKBP12 INHIBITORS, Journal of medicinal chemistry, 39(9), 1996, pp. 1872-1884
STRUCTURE-BASED DRUG DESIGN OF NONPEPTIDIC P-2 SUBSTITUENTS FOR HIV-1PROTEASE INHIBITORS
Authors: KALISH VJ TATLOCK JH DAVIES JF KALDOR SW DRESSMAN BA REICH S PINO M NYUGEN D APPELT K MUSICK L WU BW
Citation: Vj. Kalish et al., STRUCTURE-BASED DRUG DESIGN OF NONPEPTIDIC P-2 SUBSTITUENTS FOR HIV-1PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 727-732
HIGH-AFFINITY FKBP-12 LIGANDS DERIVED FROM (R)-(-)-CARVONE - SYNTHESIS AND EVALUATION OF PK506 PYRANOSE RING REPLACEMENTS
Authors: TATLOCK JH KALISH VJ PARGE HE KNIGHTON DR SHOWALTER RE LEWIS CT FRENCH JV VILLAFRANCA JE
Citation: Jh. Tatlock et al., HIGH-AFFINITY FKBP-12 LIGANDS DERIVED FROM (R)-(-)-CARVONE - SYNTHESIS AND EVALUATION OF PK506 PYRANOSE RING REPLACEMENTS, Bioorganic & medicinal chemistry letters, 5(21), 1995, pp. 2489-2494
OXIDATION OF ALKYNYL ETHERS WITH POTASSIUM-PERMANGANATE - A NEW ACYL ANION EQUIVALENT FOR THE PREPARATION OF ALPHA-KETO ESTERS
Authors: TATLOCK JH
Citation: Jh. Tatlock, OXIDATION OF ALKYNYL ETHERS WITH POTASSIUM-PERMANGANATE - A NEW ACYL ANION EQUIVALENT FOR THE PREPARATION OF ALPHA-KETO ESTERS, Journal of organic chemistry, 60(19), 1995, pp. 6221-6223
4,5-DIHYDRO-1-PHENYL-1H-2,4-BENZODIAZEPINES - NOVEL ANTIARRHYTHMIC AGENTS
Authors: JOHNSON RE BAIZMAN ER BECKER C BOHNET EA BELL RH BIRSNER NC BUSACCA CA CARABATEAS PM CHADWICK CC GRUETT MD HANE JT HERRMANN JL JOSEF KA KRAFTE DS KULLNIG RK MICHNE WF PAREENE PA PERNI RB OCONNOR B SALVADOR UJ SANNER MA SCHLEGEL DC SILVER PJ SWESTOCK J STANKUS GP TATLOCK JH VOLBERG WA WEIGELT CC ERZIN AM
Citation: Re. Johnson et al., 4,5-DIHYDRO-1-PHENYL-1H-2,4-BENZODIAZEPINES - NOVEL ANTIARRHYTHMIC AGENTS, Journal of medicinal chemistry, 36(22), 1993, pp. 3361-3370
Risultati: 1-8 |