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Jared Bruce John Milbank

Pfizer

13

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228

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The discovery of potent nonstructural protein 5A (NS5A) inhibitors with a unique resistance profile-Part 2.

2014 ChemMedChem
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Inhibiteurs du virus de l'hépatite c

2011
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Synthesis and Evaluation of Stable Bidentate Transition Metal Complexes of 1-(Chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1H-pyrrolo[3,2-f]quinoline (seco-6-azaCBI-TMI) as Hypoxia Selective Cytotoxins

2009 Journal of Medicinal Chemistry
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Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists

2007 Bioorganic & Medicinal Chemistry Letters
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Rational design of 7-arylquinolines as non-competitive metabotropic glutamate receptor subtype 5 antagonists

2007 Bioorganic & Medicinal Chemistry Letters
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4-Anilino-5-carboxamido-2-pyridone Derivatives as Noncompetitive Inhibitors of Mitogen-Activated Protein Kinase Kinase

2007 Journal of Medicinal Chemistry
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Benzimidazole derivatives as inhibitors mek

2004
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Benzimidazoles n-methyle-substitues

2004
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Cytotoxicity and DNA Interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)-carbonyl]indoline (amino-seco-CI-TMI)

1999 Chemical Research in Toxicology
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1-acryloylindolin derivatives and their use as prodrugs of anticancer agent

1997
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