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Results: 1-7 |
Results: 7
DISCOVERY OF RITONAVIR, A POTENT INHIBITOR OF HIV PROTEASE WITH HIGH ORAL BIOAVAILABILITY AND CLINICAL EFFICACY
Authors: KEMPF DJ SHAM HL MARSH KC FLENTGE CA BETEBENNER D GREEN BE MCDONALD E VASAVANONDA S SALDIVAR A WIDEBURG NE KATI WM RUIZ L ZHAO C FINO LM PATTERSON J MOLLA A PLATTNER JJ NORBECK DW
Citation: Dj. Kempf et al., DISCOVERY OF RITONAVIR, A POTENT INHIBITOR OF HIV PROTEASE WITH HIGH ORAL BIOAVAILABILITY AND CLINICAL EFFICACY, Journal of medicinal chemistry, 41(4), 1998, pp. 602-617
GS4071 IS A SLOW-BINDING INHIBITOR OF INFLUENZA NEURAMINIDASE FROM BOTH A-STRAINS AND B-STRAINS
Authors: KATI WM SALDIVAR AS MOHAMADI F SHAM HL LAVER WG KOHLBRENNER WE
Citation: Wm. Kati et al., GS4071 IS A SLOW-BINDING INHIBITOR OF INFLUENZA NEURAMINIDASE FROM BOTH A-STRAINS AND B-STRAINS, Biochemical and biophysical research communications, 244(2), 1998, pp. 408-413
LACK OF STEREOSPECIFICITY IN THE BINDING OF THE P2 AMINO-ACID OF RITONAVIR TO HIV PROTEASE
Authors: KEMPF DJ MOLLA A MARSH KC PARK C RODRIGUES AD KORNEYEVA M VASAVANONDA S MCDONALD E FLENTGE CA MUCHMORE S WIDEBURG NE SALDIVAR A COOPER A KATI WM STEWART KD NORBECK DW
Citation: Dj. Kempf et al., LACK OF STEREOSPECIFICITY IN THE BINDING OF THE P2 AMINO-ACID OF RITONAVIR TO HIV PROTEASE, Bioorganic & medicinal chemistry letters, 7(6), 1997, pp. 699-704
NOVEL TRITERPENE SULFATES FROM FUSARIUM-COMPACTUM USING A RHINOVIRUS-3C PROTEASE INHIBITOR SCREEN
Authors: BRILL GM KATI WM MONTGOMERY D KARWOWSKI JP HUMPHREY PE JACKSON M CLEMENT JJ KADAM S CHEN RH MCALPINE JB
Citation: Gm. Brill et al., NOVEL TRITERPENE SULFATES FROM FUSARIUM-COMPACTUM USING A RHINOVIRUS-3C PROTEASE INHIBITOR SCREEN, Journal of antibiotics, 49(6), 1996, pp. 541-546
MECHANISM OF INHIBITION OF HIV-1 REVERSE-TRANSCRIPTASE BY NONNUCLEOSIDE INHIBITORS
Authors: SPENCE RA KATI WM ANDERSON KS JOHNSON KA
Citation: Ra. Spence et al., MECHANISM OF INHIBITION OF HIV-1 REVERSE-TRANSCRIPTASE BY NONNUCLEOSIDE INHIBITORS, Science, 267(5200), 1995, pp. 988-993
ABT-538 IS A POTENT INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE AND HAS HIGH ORAL BIOAVAILABILITY IN HUMANS
Authors: KEMPF DJ MARSH KC DENISSEN JF MCDONALD E VASAVANONDA S FLENTGE CA GREEN BE FINO L PARK CH KONG XP WIDEBURG NE SALDIVAR A RUIZ L KATI WM SHAM HL ROBINS T STEWART KD HSU A PLATTNER JJ LEONARD JM NORBECK DW
Citation: Dj. Kempf et al., ABT-538 IS A POTENT INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE AND HAS HIGH ORAL BIOAVAILABILITY IN HUMANS, Proceedings of the National Academy of Sciences of the United Statesof America, 92(7), 1995, pp. 2484-2488
INHIBITION PATTERN OF REVERSE-TRANSCRIPTASE BY NONNUCLEOSIDE INHIBITORS
Authors: SPENCE RA KATI WM JOHNSON KA
Citation: Ra. Spence et al., INHIBITION PATTERN OF REVERSE-TRANSCRIPTASE BY NONNUCLEOSIDE INHIBITORS, Biophysical journal, 66(2), 1994, pp. 10000369-10000369
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