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Characterization of BMS-911543, a functionally selective small-molecule inhibitor of JAK2

Leukemia, 2012-02, Vol.26 (2), p.280-288

2012

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Cyclin-Dependent Kinase Inhibitors: Useful Targets in Cell Cycle Regulation

Journal of medicinal chemistry, 2000-01, Vol.43 (1), p.1-18

2000

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Expanded-Spectrum Nonnucleoside Reverse Transcriptase Inhibitors Inhibit Clinically Relevant Mutant Variants of Human Immunodeficiency Virus Type 1

Antimicrobial Agents and Chemotherapy, 1999-12, Vol.43 (12), p.2893-2897

1999

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Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1729-1731

2000

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Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVA TM)

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (22), p.3221-3224

1999

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Synthesis and evaluation of analogs of Efavirenz (SUSTIVA TM) as HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 1999-10, Vol.9 (19), p.2805-2810

1999

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Inhibition of Clinically Relevant Mutant Variants of HIV-1 by Quinazolinone Non-Nucleoside Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 2000-05, Vol.43 (10), p.2019-2030

2000

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Selective inhibition of bacterial dihydroorotate dehydrogenases by thiadiazolidinediones

Biochemical pharmacology, 2000-08, Vol.60 (3), p.339-342

2000

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A System for Rapid DNA Sequencing with Fluorescent Chain-Terminating Dideoxynucleotides

Science (American Association for the Advancement of Science), 1987-10, Vol.238 (4825), p.336-341

1987

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MEK inhibitors: The chemistry and biological activity of U0126, its analogs, and cyclization products

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (20), p.2839-2844

1998

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Nonsymmetric P2/P2‘ Cyclic Urea HIV Protease Inhibitors. Structure−Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues

Journal of medicinal chemistry, 1998-06, Vol.41 (13), p.2411-2423

1998

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Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (7), p.967-972

1999

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Thiazolo[4,5-d]pyrimidine thiones and -ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1185-1188

1999

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Parallel Synthesis of Potent, Pyrazole-Based Inhibitors of Helicobacter pylori Dihydroorotate Dehydrogenase

Journal of medicinal chemistry, 2002-10, Vol.45 (21), p.4669-4678

2002

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Quinazolines as cyclin dependent kinase inhibitors

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1157-1160

2001

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Synthesis and Evaluation of Efavirenz (Sustiva TM) Analogues as HIV-1 Reverse Transcriptase Inhibitors: Replacement of the Cyclopropylacetylene Side Chain

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1177-1179

2001

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The importance of plasma protein binding in drug discovery

Expert opinion on drug discovery, 2007-01, Vol.2 (1), p.51-64

Trainor, George L

2007

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DNA recognition of base analogue and chemically modified substrates by the TaqI restriction endonuclease

The Journal of biological chemistry, 1992-04, Vol.267 (12), p.8106-8116

1992

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DNA sequencing, automation, and the human genome

Analytical chemistry (Washington), 1990-03, Vol.62 (5), p.418-426

Trainor, George L

1990

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Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries

Nucleic acids research, 1996-05, Vol.24 (10), p.1901-1907

1996

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Helicobacter pylori-selective Antibacterials Based on Inhibition of Pyrimidine Biosynthesis

The Journal of biological chemistry, 2000-10, Vol.275 (43), p.33373-33378

2000

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Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms

Nucleic acids research, 1994-10, Vol.22 (20), p.4167-4175

1994

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Identification of selective inhibitors of cyclin dependent kinase 4

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (16), p.2209-2211

2001

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Regulated Expression of the Escherichia coli lepB Gene as a Tool for Cellular Testing of Antimicrobial Compounds That Inhibit Signal Peptidase I In Vitro

Antimicrobial Agents and Chemotherapy, 2002-11, Vol.46 (11), p.3549-3554

2002

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Biodistribution and metabolism of internally 3H-labeled oligonucleotides. I. Comparison of a phosphodiester and a phosphorothioate

Molecular pharmacology, 1994-05, Vol.45 (5), p.932-943

1994

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Characterization of BMS-911543, a functionally selective small-molecule inhibitor of JAK2

Cyclin-Dependent Kinase Inhibitors: Useful Targets in Cell Cycle Regulation

Expanded-Spectrum Nonnucleoside Reverse Transcriptase Inhibitors Inhibit Clinically Relevant Mutant Variants of Human Immunodeficiency Virus Type 1

Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors

Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVA TM)

Synthesis and evaluation of analogs of Efavirenz (SUSTIVA TM) as HIV-1 reverse transcriptase inhibitors

Inhibition of Clinically Relevant Mutant Variants of HIV-1 by Quinazolinone Non-Nucleoside Reverse Transcriptase Inhibitors

Selective inhibition of bacterial dihydroorotate dehydrogenases by thiadiazolidinediones

A System for Rapid DNA Sequencing with Fluorescent Chain-Terminating Dideoxynucleotides

MEK inhibitors: The chemistry and biological activity of U0126, its analogs, and cyclization products

Nonsymmetric P2/P2‘ Cyclic Urea HIV Protease Inhibitors. Structure−Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues

Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists

Thiazolo[4,5-d]pyrimidine thiones and -ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists

Parallel Synthesis of Potent, Pyrazole-Based Inhibitors of Helicobacter pylori Dihydroorotate Dehydrogenase

Quinazolines as cyclin dependent kinase inhibitors

Synthesis and Evaluation of Efavirenz (Sustiva TM) Analogues as HIV-1 Reverse Transcriptase Inhibitors: Replacement of the Cyclopropylacetylene Side Chain

The importance of plasma protein binding in drug discovery

DNA recognition of base analogue and chemically modified substrates by the TaqI restriction endonuclease

DNA sequencing, automation, and the human genome

Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries

Helicobacter pylori-selective Antibacterials Based on Inhibition of Pyrimidine Biosynthesis

Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms

Identification of selective inhibitors of cyclin dependent kinase 4

Regulated Expression of the Escherichia coli lepB Gene as a Tool for Cellular Testing of Antimicrobial Compounds That Inhibit Signal Peptidase I In Vitro

Biodistribution and metabolism of internally 3H-labeled oligonucleotides. I. Comparison of a phosphodiester and a phosphorothioate

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