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Novel Non-Nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 6. 2-Indol-3-yl- and 2-Azaindol-3-yl- dipyridodiazepinones

Journal of medicinal chemistry, 1997-07, Vol.40 (15), p.2430-2433

1997

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Characterization of a receptor for human monocyte-derived neutrophil chemotactic factor/interleukin-8

The Journal of biological chemistry, 1990-05, Vol.265 (14), p.8311-8316

1990

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Effect of Structural Modification of Enol−Carboxamide-Type Nonsteroidal Antiinflammatory Drugs on COX-2/COX-1 Selectivity

Journal of medicinal chemistry, 1997-03, Vol.40 (6), p.980-989

1997

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Novel Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase. 7. 8-Arylethyldipyridodiazepinones as Potent Broad-Spectrum Inhibitors of Wild-Type and Mutant Enzymes

Journal of medicinal chemistry, 1998-07, Vol.41 (16), p.2960-2971

1998

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Novel Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase. 8. 8-Aryloxymethyl- and 8-Arylthiomethyldipyridodiazepinones

Journal of medicinal chemistry, 1998-07, Vol.41 (16), p.2972-2984

1998

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Characterization of the human melanoma nerve growth factor receptor

The Journal of biological chemistry, 1985-07, Vol.260 (13), p.8044-8049

1985

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Characterization of the binding site for nevirapine (BI-RG-587), a nonnucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase

The Journal of biological chemistry, 1991-08, Vol.266 (22), p.14670-14674

1991

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Nonnucleoside inhibitors of HIV-1 reverse transcriptase : nevirapine as prototype drug

AIDS research and human retroviruses, 1992-02, Vol.8 (2), p.145-152

1992

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Affinity Labeling and Partial Purification of Nerve Growth Factor Receptors from Rat Pheochromocytoma and Human Melanoma Cells

Proceedings of the National Academy of Sciences - PNAS, 1983-11, Vol.80 (22), p.6819-6823

1983

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Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site

Nature structural & molecular biology, 2002-04, Vol.9 (4), p.268-272

2002

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A novel, dipyridodiazepinone inhibitor of HIV-1 reverse transcriptase acts through a nonsubstrate binding site

Biochemistry (Easton), 1991-02, Vol.30 (8), p.2022-2026

1991

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Modification of nerve growth factor receptor properties by wheat germ agglutinin

The Journal of biological chemistry, 1983-12, Vol.258 (23), p.14136-14143

1983

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Selective inhibition of human cyclo-oxygenase-2 by meloxicam

Inflammopharmacology, 1996-06, Vol.4 (2), p.125-135

1996

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Prophylaxis against HIV-1 infection in chimpanzees by nevirapine, a nonnucleoside inhibitor of reverse transcriptase

Nature medicine, 1997-06, Vol.3 (6), p.665-670

1997

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Steady state kinetics and inhibition of HIV-1 reverse transcriptase by a non-nucleoside dipyridodiazepinone, BI-RG-587, using a heteropolymeric template

Nucleic acids research, 1991-06, Vol.19 (11), p.3035-3039

1991

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Copper Chelate Affinity Chromatography of Human Fibroblast and Leucocyte Interferons

Journal of general virology, 1979-06, Vol.43 (3), p.701-706

1979

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Glycosylation of human leukocyte interferon: effects of tunicamycin

Archives of virology, 1980-01, Vol.64 (2), p.109-117

1980

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Novel Non-nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 5. 4-Substituted and 2,4-Disubstituted Analogs of Nevirapine

Journal of medicinal chemistry, 1995-11, Vol.38 (24), p.4839-4847

1995

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Separation of human leukocyte interferon components by concanavalin A-agarose affinity chromatography and their characterization

Biochemistry (Easton), 1979-12, Vol.18 (26), p.5782-5786

1979

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Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site

Acta crystallographica. Section A, Foundations of crystallography, 2002-08, Vol.58 (s1), p.c231-c231

2002

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Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. V: 4-Substituted and 2,4-disubstituted analogs of nevirapine

Journal of medicinal chemistry, 1995, Vol.38 (24), p.4839-4847

1995

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Affinity of human leukocyte interferon for polyribonucleotides

Cell biology international reports, 1979-11, Vol.3 (8), p.663-669

1979

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High-performance liquid chromatography and photoaffinity crosslinking to explore the binding environment of nevirapine to reverse transcriptase of human immunodeficiency virus

Journal of chromatography. A, 1994-07, Vol.676 (1), p.99-112

1994

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Inactivation of cell surface receptors by pheophorbide a, a green pigment isolated from Psychotria acuminata

Photochemistry and photobiology, 1995-07, Vol.62 (1), p.144-150

1995

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Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. IV: 2-substituted dipyridodiazepinones as potent inhibitors of both wild-type and cysteine-181 HIV-1 reverse transcriptase enzymes

Journal of medicinal chemistry, 1995, Vol.38 (24), p.4830-4838

1995

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Novel Non-Nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 6. 2-Indol-3-yl- and 2-Azaindol-3-yl- dipyridodiazepinones

Characterization of a receptor for human monocyte-derived neutrophil chemotactic factor/interleukin-8

Effect of Structural Modification of Enol−Carboxamide-Type Nonsteroidal Antiinflammatory Drugs on COX-2/COX-1 Selectivity

Novel Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase. 7. 8-Arylethyldipyridodiazepinones as Potent Broad-Spectrum Inhibitors of Wild-Type and Mutant Enzymes

Novel Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase. 8. 8-Aryloxymethyl- and 8-Arylthiomethyldipyridodiazepinones

Characterization of the human melanoma nerve growth factor receptor

Characterization of the binding site for nevirapine (BI-RG-587), a nonnucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase

Nonnucleoside inhibitors of HIV-1 reverse transcriptase : nevirapine as prototype drug

Affinity Labeling and Partial Purification of Nerve Growth Factor Receptors from Rat Pheochromocytoma and Human Melanoma Cells

Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site

A novel, dipyridodiazepinone inhibitor of HIV-1 reverse transcriptase acts through a nonsubstrate binding site

Modification of nerve growth factor receptor properties by wheat germ agglutinin

Selective inhibition of human cyclo-oxygenase-2 by meloxicam

Prophylaxis against HIV-1 infection in chimpanzees by nevirapine, a nonnucleoside inhibitor of reverse transcriptase

Steady state kinetics and inhibition of HIV-1 reverse transcriptase by a non-nucleoside dipyridodiazepinone, BI-RG-587, using a heteropolymeric template

Copper Chelate Affinity Chromatography of Human Fibroblast and Leucocyte Interferons

Glycosylation of human leukocyte interferon: effects of tunicamycin

Novel Non-nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 5. 4-Substituted and 2,4-Disubstituted Analogs of Nevirapine

Separation of human leukocyte interferon components by concanavalin A-agarose affinity chromatography and their characterization

Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. V: 4-Substituted and 2,4-disubstituted analogs of nevirapine

Affinity of human leukocyte interferon for polyribonucleotides

High-performance liquid chromatography and photoaffinity crosslinking to explore the binding environment of nevirapine to reverse transcriptase of human immunodeficiency virus

Inactivation of cell surface receptors by pheophorbide a, a green pigment isolated from Psychotria acuminata

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. IV: 2-substituted dipyridodiazepinones as potent inhibitors of both wild-type and cysteine-181 HIV-1 reverse transcriptase enzymes

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