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Novel 1,5-Diphenylpyrazole Nonnucleoside HIV-1 Reverse Transcriptase Inhibitors with Enhanced Activity versus the Delavirdine-Resistant P236L Mutant: Lead Identification and SAR of 3- and 4-Substituted Derivatives

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.1034-1040

2000

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Human T Cells Are Highly Sensitive to Suppression of Mitogenesis by Polycyclic Aromatic Hydrocarbons and This Effect Is Differentially Reversed by α-Naphthoflavone

Toxicology and applied pharmacology, 1996-08, Vol.139 (2), p.333-341

1996

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Nonnucleoside Reverse Transcriptase Inhibitors that Potently and Specifically Block Human Immunodeficiency Virus Type 1 Replication

Proceedings of the National Academy of Sciences - PNAS, 1991-10, Vol.88 (19), p.8806-8810

1991

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The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

The Journal of biological chemistry, 1993-07, Vol.268 (20), p.14875-14880

1993

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U-90152, a potent inhibitor of human immunodeficiency virus type 1 replication

Antimicrobial Agents and Chemotherapy, 1993-05, Vol.37 (5), p.1127-1131

1993

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The solid phase synthesis of tetrahydroisoquinolines having cdc25B inhibitory activity

Bioorganic & medicinal chemistry letters, 2000-04, Vol.10 (7), p.649-652

2000

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Depletion of Glutathione by Benzo(a)pyrene Metabolites, Ionomycin, Thapsigargin, and Phorbol Myristate in Human Peripheral Blood Mononuclear Cells

Toxicology and applied pharmacology, 1997-05, Vol.144 (1), p.62-69

1997

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The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

Biochemical pharmacology, 1996-03, Vol.51 (6), p.743-750

1996

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Prevention of the spread of HIV-1 infection with nonnucleoside reverse transcriptase inhibitors

Virology (New York, N.Y.), 1992-09, Vol.190 (1), p.269-277

1992

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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, 1996-12, Vol.39 (26), p.5267-5275

1996

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Synthesis and Structure−Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4140-4149

1999

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Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

The Journal of biological chemistry, 1993-03, Vol.268 (9), p.6119-6124

1993

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Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Biochemistry (Easton), 1993-07, Vol.32 (26), p.6548-6554

1993

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Synthesis and characterization of TiO2 doping with rare earths by sol–gel method: photocatalytic activity for phenol degradation

Journal of sol-gel science and technology, 2010-12, Vol.56 (3), p.219-226

2010

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Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Journal of medicinal chemistry, 1996-11, Vol.39 (23), p.4630-4642

1996

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Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3769-3789

1996

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Bis(heteroaryl)piperazine (BHAP) reverse transcriptase inhibitors: structure-activity relationships of novel substituted indole analogues and the identification of 1-[(5-methanesulfonamido-1H-indol-2-yl)-carbonyl]-4-[3- [(1-methylethyl)amino]-pyridinyl]piperazine monomethanesulfonate (U-90152S), a second-generation clinical candidate

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1505-1508

1993

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Local coherence and the temporal development of second harmonic emission

Journal of physics. B, Atomic, molecular, and optical physics, 2001-06, Vol.34 (11), p.2177-2187

2001

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Metformin inhibits ovarian cancer growth and increases sensitivity to paclitaxel in mouse models

American journal of obstetrics and gynecology, 2015-04, Vol.212 (4), p.479.e1-479.e10

2015

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Steady-state kinetic studies with the polysulfonate U-9843, and HIV reverse transcriptase inhibitor

Experientia, 1994-01, Vol.50 (1), p.23-28

1994

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P-253 Clinical efficacy of PGT-A according to maternal age and embryo quality in blastocyst stage

Human reproduction (Oxford), 2023-06, Vol.38 (Supplement_1)

2023

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Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

Biochemical pharmacology, 1994-06, Vol.47 (11), p.2017-2028

1994

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(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

Journal of Virology, 1996-06, Vol.70 (6), p.3698-3705

1996

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Resistance mapping and mode of action of a novel class of antibacterial anthranilic acids: evidence for disruption of cell wall biosynthesis

Journal of antimicrobial chemotherapy, 2008-10, Vol.62 (4), p.720-729

2008

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Sequential decoding of non-binary LDPC codes on graphics processing units

2012 Conference Record of the Forty Sixth Asilomar Conference on Signals, Systems and Computers (ASILOMAR), 2012, p.1267-1271

2012

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Novel 1,5-Diphenylpyrazole Nonnucleoside HIV-1 Reverse Transcriptase Inhibitors with Enhanced Activity versus the Delavirdine-Resistant P236L Mutant: Lead Identification and SAR of 3- and 4-Substituted Derivatives

Human T Cells Are Highly Sensitive to Suppression of Mitogenesis by Polycyclic Aromatic Hydrocarbons and This Effect Is Differentially Reversed by α-Naphthoflavone

Nonnucleoside Reverse Transcriptase Inhibitors that Potently and Specifically Block Human Immunodeficiency Virus Type 1 Replication

The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

U-90152, a potent inhibitor of human immunodeficiency virus type 1 replication

The solid phase synthesis of tetrahydroisoquinolines having cdc25B inhibitory activity

Depletion of Glutathione by Benzo(a)pyrene Metabolites, Ionomycin, Thapsigargin, and Phorbol Myristate in Human Peripheral Blood Mononuclear Cells

The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

Prevention of the spread of HIV-1 infection with nonnucleoside reverse transcriptase inhibitors

Synthesis and Bioactivity of Novel Bis(heteroaryl)piperazine (BHAP) Reverse Transcriptase Inhibitors: Structure−Activity Relationships and Increased Metabolic Stability of Novel Substituted Pyridine Analogs

Synthesis and Structure−Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution

Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Synthesis and characterization of TiO2 doping with rare earths by sol–gel method: photocatalytic activity for phenol degradation

Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

Local coherence and the temporal development of second harmonic emission

Metformin inhibits ovarian cancer growth and increases sensitivity to paclitaxel in mouse models

Steady-state kinetic studies with the polysulfonate U-9843, and HIV reverse transcriptase inhibitor

P-253 Clinical efficacy of PGT-A according to maternal age and embryo quality in blastocyst stage

Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

Resistance mapping and mode of action of a novel class of antibacterial anthranilic acids: evidence for disruption of cell wall biosynthesis

Sequential decoding of non-binary LDPC codes on graphics processing units

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