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Cost Allocation in Manufacturing-Remanufacturing Operations

Production and operations management, 2011-11, Vol.20 (6), p.841-847

2011

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Discovery of Pyrrolopyridine−Pyridone Based Inhibitors of Met Kinase: Synthesis, X-ray Crystallographic Analysis, and Biological Activities

Journal of medicinal chemistry, 2008-09, Vol.51 (17), p.5330-5341

2008

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Macrocyclic pyrrolobenzodiazepine dimers as antibody-drug conjugate payloads

Bioorganic & medicinal chemistry letters, 2017-12, Vol.27 (23), p.5267-5271

2017

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Discovery of Potent Heterodimeric Antagonists of Inhibitor of Apoptosis Proteins (IAPs) with Sustained Antitumor Activity

Journal of medicinal chemistry, 2015-02, Vol.58 (3), p.1556-1562

2015

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Identification of a phenylacylsulfonamide series of dual Bcl-2/Bcl-xL antagonists

Bioorganic & medicinal chemistry letters, 2012-06, Vol.22 (12), p.3946-3950

2012

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Pyrazole and pyrimidine phenylacylsulfonamides as dual Bcl-2/Bcl-xL antagonists

Bioorganic & medicinal chemistry letters, 2012-06, Vol.22 (12), p.3951-3956

2012

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Discovery of orally active pyrrolopyridine- and aminopyridine-based Met kinase inhibitors

Bioorganic & medicinal chemistry, 2008-06, Vol.18 (11), p.3224-3229

2008

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Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer

ACS medicinal chemistry letters, 2015-07, Vol.6 (7), p.770-775

2015

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Synthesis, SAR, and Evaluation of 4-[2,4-Difluoro-5-(cyclopropylcarbamoyl)phenylamino]pyrrolo[2,1- f][1,2,4]triazine-based VEGFR-2 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2008-02, Vol.18 (4), p.1354-1358

2008

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Structure based approach to the design of bicyclic-1H-isoindole-1,3(2H)-dione based androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (2), p.271-276

2005

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Metabolism of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): identification of an unusual N-acetylglucosamine conjugate in the cynomolgus monkey

Drug metabolism and disposition, 2008-12, Vol.36 (12), p.2475-2483

2008

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The synthesis and evaluation of [2.2.1]-bicycloazahydantoins as androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.6107-6111

2004

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Identification of a novel class of androgen receptor antagonists based on the bicyclic-1H-isoindole-1,3(2H)-dione nucleus

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (2), p.389-393

2005

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Polymeric Gadolinium Chelate Magnetic Resonance Imaging Contrast Agents: Design, Synthesis, and Properties

Bioconjugate chemistry, 1999-05, Vol.10 (3), p.361-370

1999

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Pyrrolopyridazine MEK inhibitors

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (3), p.628-632

2006

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Discovery of Non-Nucleotide Small-Molecule STING Agonists via Chemotype Hybridization

Journal of medicinal chemistry, 2022-02, Vol.65 (4), p.3518-3538

2022

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Substituted diaryl ether compounds as retinoic acid-related orphan Receptor-γt (RORγt) agonists

Bioorganic & medicinal chemistry letters, 2021-03, Vol.35, p.127778-127778, Article 127778

2021

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Diagnostic Microbiology of the Immunocompromised Host

2nd edition., 2016

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Oxo-piperazine Derivatives of N-Arylpiperazinones as Inhibitors of Farnesyltransferase

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (4), p.537-540

2001

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Inter-Departmental Cost Allocation and Investment Incentives

Review of accounting studies, 2004-03, Vol.9 (1), p.97-116

Wei, Donna

2004

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Identification of pyrrolo[2,1- f][1,2,4]triazine-based inhibitors of Met kinase

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (6), p.1945-1951

2008

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Discovery and preclinical studies of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)- N-(2-methyl-1 H-pyrrolo[2,3- b]pyridin-5-yl)pyrrolo[2,1- f][1,2,4]triazin-4-amine (BMS-645737), an in vivo active potent VEGFR-2 inhibitor

Bioorganic & medicinal chemistry letters, 2008-05, Vol.18 (9), p.2985-2989

2008

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Cost Allocation in Manufacturing-Remanufacturing Operations

Discovery of Brivanib Alaninate ((S)-((R)-1-(4-(4-Fluoro-2-methyl-1H-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan-2-yl)2-aminopropanoate), A Novel Prodrug of Dual Vascular Endothelial Growth Factor Receptor-2 and Fibroblast Growth Factor Receptor-1 Kinase Inhibitor (BMS-540215)

Discovery of Pyrrolopyridine−Pyridone Based Inhibitors of Met Kinase: Synthesis, X-ray Crystallographic Analysis, and Biological Activities

Macrocyclic pyrrolobenzodiazepine dimers as antibody-drug conjugate payloads

Discovery of Potent Heterodimeric Antagonists of Inhibitor of Apoptosis Proteins (IAPs) with Sustained Antitumor Activity

Identification of a phenylacylsulfonamide series of dual Bcl-2/Bcl-xL antagonists

Pyrazole and pyrimidine phenylacylsulfonamides as dual Bcl-2/Bcl-xL antagonists

Discovery of orally active pyrrolopyridine- and aminopyridine-based Met kinase inhibitors

Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer

Synthesis, SAR, and Evaluation of 4-[2,4-Difluoro-5-(cyclopropylcarbamoyl)phenylamino]pyrrolo[2,1- f][1,2,4]triazine-based VEGFR-2 kinase inhibitors

Structure based approach to the design of bicyclic-1H-isoindole-1,3(2H)-dione based androgen receptor antagonists

Metabolism of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): identification of an unusual N-acetylglucosamine conjugate in the cynomolgus monkey

The synthesis and evaluation of [2.2.1]-bicycloazahydantoins as androgen receptor antagonists

Identification of a novel class of androgen receptor antagonists based on the bicyclic-1H-isoindole-1,3(2H)-dione nucleus

Discovery of N-(4-(2-Amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide (BMS-777607), a Selective and Orally Efficacious Inhibitor of the Met Kinase Superfamily

Polymeric Gadolinium Chelate Magnetic Resonance Imaging Contrast Agents: Design, Synthesis, and Properties

Pyrrolopyridazine MEK inhibitors

Discovery of Non-Nucleotide Small-Molecule STING Agonists via Chemotype Hybridization

Substituted diaryl ether compounds as retinoic acid-related orphan Receptor-γt (RORγt) agonists

Discovery and Preclinical Studies of (R)-1-(4-(4-Fluoro-2-methyl-1H-indol-5-yloxy)-5- methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan- 2-ol (BMS-540215), an In Vivo Active Potent VEGFR-2 Inhibitor

Diagnostic Microbiology of the Immunocompromised Host

Oxo-piperazine Derivatives of N-Arylpiperazinones as Inhibitors of Farnesyltransferase

Inter-Departmental Cost Allocation and Investment Incentives

Identification of pyrrolo[2,1- f][1,2,4]triazine-based inhibitors of Met kinase

Discovery and preclinical studies of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)- N-(2-methyl-1 H-pyrrolo[2,3- b]pyridin-5-yl)pyrrolo[2,1- f][1,2,4]triazin-4-amine (BMS-645737), an in vivo active potent VEGFR-2 inhibitor

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