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Results: 1-12 |
Results: 12
SYNTHESIS AND BIOACTIVITY OF NOVEL BIS (HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS AND INCREASED METABOLIC STABILITY OF NOVEL SUBSTITUTED PYRIDINE ANALOGS
Authors: GENIN MJ POEL TJ YAGI Y BILES C ALTHAUS I KEISER BJ KOPTA LA FRIIS JM REUSSER F ADAMS WJ OLMSTED RA VOORMAN RL THOMAS RC ROMERO DL
Citation: Mj. Genin et al., SYNTHESIS AND BIOACTIVITY OF NOVEL BIS (HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS AND INCREASED METABOLIC STABILITY OF NOVEL SUBSTITUTED PYRIDINE ANALOGS, Journal of medicinal chemistry, 39(26), 1996, pp. 5267-5275
THE AMPHIPHILIC PROPERTIES OF NOVENAMINES DETERMINE THEIR ACTIVITY ASINHIBITORS OF HIV-1 RNASE-H
Authors: ALTHAUS IW FRANKS KM LANGLEY KB KEZDY FJ PETERSON T BUXSER SE DECKER DE DOLAK LA ULRICH RG REUSSER F
Citation: Iw. Althaus et al., THE AMPHIPHILIC PROPERTIES OF NOVENAMINES DETERMINE THEIR ACTIVITY ASINHIBITORS OF HIV-1 RNASE-H, Experientia, 52(4), 1996, pp. 329-335
THE BENZYLTHIO-PYRIMIDINE U-31,355, A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE
Authors: ALTHAUS IW CHOU KC LEMAY RJ FRANKS KM DEIBEL MR KEZDY FJ RESNICK L BUSSO ME SO AG DOWNEY KM ROMERO DL THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., THE BENZYLTHIO-PYRIMIDINE U-31,355, A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE, Biochemical pharmacology, 51(6), 1996, pp. 743-750
NOVENAMINES AS INHIBITORS OF 2 INDEPENDENT ENZYMES DURING DNA-REPLICATION IN A TOLUENIZED ESCHERICHIA-COLI CELL SYSTEM
Authors: ALTHAUS IW KEZDY FJ PETERSON T SPILMAN CH REUSSER F
Citation: Iw. Althaus et al., NOVENAMINES AS INHIBITORS OF 2 INDEPENDENT ENZYMES DURING DNA-REPLICATION IN A TOLUENIZED ESCHERICHIA-COLI CELL SYSTEM, Biochemical pharmacology, 51(10), 1996, pp. 1373-1378
DISCOVERY, SYNTHESIS, AND BIOACTIVITY OF BIS(HETEROARYL)PIPERAZINES .1. A NOVEL CLASS OF NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS
Authors: ROMERO DL MORGE RA BILES C BERRIOSPENA TN MAY PD PALMER JR JOHNSON PD SMITH HW BUSSO M TAN CK VOORMAN RL REUSSER F ALTHAUS IW DOWNEY KM SO AG RESNICK L TARPLEY WG ARISTOFF PA
Citation: Dl. Romero et al., DISCOVERY, SYNTHESIS, AND BIOACTIVITY OF BIS(HETEROARYL)PIPERAZINES .1. A NOVEL CLASS OF NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS, Journal of medicinal chemistry, 37(7), 1994, pp. 999-1014
STEADY-STATE KINETIC-STUDIES WITH THE POLYSULFONATE U-9843, AN HIV REVERSE-TRANSCRIPTASE INHIBITOR
Authors: ALTHAUS IW CHOU JJ GONZALES AJ LEMAY RJ DEIBEL MR CHOU KC KEZDY FJ ROMERO DL THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., STEADY-STATE KINETIC-STUDIES WITH THE POLYSULFONATE U-9843, AN HIV REVERSE-TRANSCRIPTASE INHIBITOR, Experientia, 50(1), 1994, pp. 23-28
KINETIC-STUDIES WITH THE NONNUCLEOSIDE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INHIBITOR U-90152E
Authors: ALTHAUS IW CHOU JJ GONZALES AJ DEIBEL MR CHOU KC KEZDY FJ ROMERO DL THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., KINETIC-STUDIES WITH THE NONNUCLEOSIDE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INHIBITOR U-90152E, Biochemical pharmacology, 47(11), 1994, pp. 2017-2028
KINETICS OF PROCESSIVE NUCLEIC-ACID POLYMERASES AND NUCLEASES
Authors: CHOU KC KEZDY FJ REUSSER F
Citation: Kc. Chou et al., KINETICS OF PROCESSIVE NUCLEIC-ACID POLYMERASES AND NUCLEASES, Analytical biochemistry, 221(2), 1994, pp. 217-230
U-90152, A POTENT INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION
Authors: DUEWEKE TJ POPPE SM ROMERO DL SWANEY SM SO AG DOWNEY KM ALTHAUS IW REUSSER F BUSSO M RESNICK L MAYERS DI LANE J ARISTOFF PA THOMAS RC TARPLEY WG
Citation: Tj. Dueweke et al., U-90152, A POTENT INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION, Antimicrobial agents and chemotherapy, 37(5), 1993, pp. 1127-1131
BIS(HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL SUBSTITUTED INDOLE ANALOGS AND THE IDENTIFICATION OF ]-4-[3-[(1-METHYLETHYL)AMINO]-PYRIDINYL]PIPERAZINE MONOMETHANESULFONATE (U-90152S), A 2ND-GENERATION CLINICAL CANDIDATE
Authors: ROMERO DL MORGE RA GENIN MJ BILES C BUSSO M RESNICK L ALTHAUS IW REUSSER F THOMAS RC TARPLEY WG
Citation: Dl. Romero et al., BIS(HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL SUBSTITUTED INDOLE ANALOGS AND THE IDENTIFICATION OF ]-4-[3-[(1-METHYLETHYL)AMINO]-PYRIDINYL]PIPERAZINE MONOMETHANESULFONATE (U-90152S), A 2ND-GENERATION CLINICAL CANDIDATE, Journal of medicinal chemistry, 36(10), 1993, pp. 1505-1508
THE QUINOLINE U-78036 IS A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE
Authors: ALTHAUS IW GONZALES AJ CHOU JJ ROMERO DL DEIBEL MR CHOU KC KEZDY FJ RESNICK L BUSSO ME SO AG DOWNEY KM THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., THE QUINOLINE U-78036 IS A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE, The Journal of biological chemistry, 268(20), 1993, pp. 4875-4880
KINETIC-STUDIES WITH THE NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITOR-U-88204E
Authors: ALTHAUS IW CHOU JJ GONZALES AJ DEIBEL MR CHOU KC KEZDY FJ ROMERO DL PALMER JR THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., KINETIC-STUDIES WITH THE NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITOR-U-88204E, Biochemistry, 32(26), 1993, pp. 6548-6554
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