Authors:
SANDERSON PEJ
CUTRONA KJ
DORSEY BD
DYER DL
MCDONOUGH CM
NAYLOROLSEN AM
CHEN IW
CHEN ZG
COOK JJ
GARDELL SJ
KRUEGER JA
LEWIS SD
LIN JH
LUCAS BJ
LYLE EA
LYNCH JJ
STRANIERI MT
VASTAG K
SHAFER JA
VACCA JP
Citation: Pej. Sanderson et al., L-374,087, AN EFFICACIOUS, ORALLY BIOAVAILABLE, PYRIDINONE ACETAMIDE THROMBIN INHIBITOR, Bioorganic & medicinal chemistry letters, 8(7), 1998, pp. 817-822
Authors:
ISAACS RCA
CUTRONA KJ
NEWTON CL
SANDERSON PEJ
SOLINSKY MG
BASKIN EP
CHEN IW
COOPER CM
COOK JJ
GARDELL SJ
LEWIS SD
LUCAS RJ
LYLE EA
LYNCH JJ
NAYLOROLSEN AM
STRANIERI MT
VASTAG K
VACCA JP
Citation: Rca. Isaacs et al., C6 MODIFICATION OF THE PYRIDINONE CORE OF THROMBIN INHIBITOR L-374,087 AS A MEANS OF ENHANCING ITS ORAL ABSORPTION, Bioorganic & medicinal chemistry letters, 8(13), 1998, pp. 1719-1724
Authors:
BRADY SF
STAUFFER KJ
LUMMA WC
SMITH GM
RAMJIT HG
LEWIS SD
LUCAS BJ
GARDELL SJ
LYLE EA
APPLEBY SD
COOK JJ
HOLAHAN MA
STRANIERI MT
LYNCH JJ
LIN JH
CHEN IW
VASTAG K
NAYLOROLSEN AM
VACCA JP
Citation: Sf. Brady et al., DISCOVERY AND DEVELOPMENT OF THE NOVEL POTENT ORALLY-ACTIVE THROMBIN INHIBITOR N-(9-HYDROXY-9-FLUORENECARBOXY)PROLYL TRANS-4-AMINOCYCLOHEXYLMETHYL AMIDE (L-372,460) - COAPPLICATION OF STRUCTURE-BASED DESIGN AND RAPID MULTIPLE ANALOG SYNTHESIS ON SOLID SUPPORT, Journal of medicinal chemistry, 41(3), 1998, pp. 401-406
Authors:
SANDERSON PEJ
LYLE TA
CUTRONA KJ
DYER DL
DORSEY BD
MCDONOUGH CM
NAYLOROLSEN AM
CHEN IW
CHEN ZG
COOK JJ
COOPER CM
GARDELL SJ
HARE TR
KRUEGER JA
LEWIS SD
LIN JH
LUCAS BJ
LYLE EA
LYNCH JJ
STRANIERI MT
VASTAG K
YAN YW
SHAFER JA
VACCA JP
Citation: Pej. Sanderson et al., EFFICACIOUS, ORALLY BIOAVAILABLE THROMBIN INHIBITORS BASED ON 3-AMINOPYRIDINONE OR 3-AMINOPYRAZINONE ACETAMIDE PEPTIDOMIMETIC TEMPLATES, Journal of medicinal chemistry, 41(23), 1998, pp. 4466-4474
Authors:
KIM BM
GUARE JP
VACCA JP
MICHELSON SR
DARKE PL
ZUGAY JA
EMINI EA
SCHLEIF W
LIN JH
CHEN IW
VASTAG K
ANDERSON PS
HUFF JR
Citation: Bm. Kim et al., THIOPHENE DERIVATIVES AS EXTREMELY HIGH-AFFINITY P-3' LIGANDS FOR THEHYDROXYETHYLPIPERAZINE CLASS OF HIV-1 PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 5(2), 1995, pp. 185-190
Authors:
KIM BM
HANIFIN CM
ZARTMAN CB
VACCA JP
MICHELSON SR
LIN JH
CHEN IW
VASTAG K
DARKE PL
ZUGAY JA
EMINI EA
SCHLEIF W
ANDERSON PS
HUFF JR
Citation: Bm. Kim et al., SUBSTITUTED ALKYLPYRIDINES AS P-3' LIGANDS FOR THE HYDROXYETHYLPIPERAZINE CLASS OF HIV-1 PROTEASE INHIBITORS - IMPROVED PHARMACOKINETIC PROFILES, Bioorganic & medicinal chemistry letters, 5(19), 1995, pp. 2239-2244
Authors:
KIM BM
VACCA JP
GUARE JP
HANIFIN CM
MICHELSON SR
DARKE PL
ZUGAY JA
EMINI EA
SCHLEIF W
LIN JH
CHEN IW
VASTAG K
OSTOVIC D
ANDERSON PS
HUFF JR
Citation: Bm. Kim et al., A NEW HYDROXYETHYLAMINE CLASS OF HIV-1 PROTEASE INHIBITORS WITH HIGH ANTIVIRAL POTENCY AND ORAL BIOAVAILABILITY, Bioorganic & medicinal chemistry letters, 4(19), 1994, pp. 2273-2278
Authors:
VACCA JP
DORSEY BD
SCHLEIF WA
LEVIN RB
MCDANIEL SL
DARKE PL
ZUGAY J
QUINTERO JC
BLAHY OM
ROTH E
SARDANA VV
SCHLABACH AJ
GRAHAM PI
CONDRA JH
GOTLIB L
HOLLOWAY MK
LIN J
CHEN IW
VASTAG K
OSTOVIC D
ANDERSON PS
EMINI EA
HUFF JR
Citation: Jp. Vacca et al., L-735,524 - AN ORALLY BIOAVAILABLE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE INHIBITOR, Proceedings of the National Academy of Sciences of the United Statesof America, 91(9), 1994, pp. 4096-4100