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Nucleophilic (Radio)Fluorination of Redox-Active Esters via Radical-Polar Crossover Enabled by Photoredox Catalysis

Journal of the American Chemical Society, 2020-05, Vol.142 (20), p.9493-9500

2020

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The discovery and evaluation of [18F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement

European journal of nuclear medicine and molecular imaging, 2024-03, Vol.51 (4), p.978-990

2024

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Synthesis of stable‐isotope‐labeled N‐(3‐dimethylaminopropyl)‐N′‐ethylcarbodiimide and N‐(3‐dimethylaminopropyl)‐N′‐ethylurea

Journal of labelled compounds & radiopharmaceuticals, 2020-11, Vol.63 (13), p.526-530

2020

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Synthesis and Preclinical Evaluation of a 68Ga-Labeled Adnectin, 68Ga-BMS-986192, as a PET Agent for Imaging PD-L1 Expression

The Journal of nuclear medicine (1978), 2021-09, Vol.62 (9), p.1228-1234

2021

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Distinguishing a phosphate ester prodrug from its isobaric sulfate metabolite by mass spectrometry without the metabolite standard

Rapid communications in mass spectrometry, 2009-10, Vol.23 (19), p.3107-3113

2009

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Synthesis and Preclinical Evaluation of a 68 Ga-Labeled Adnectin, 68 Ga-BMS-986192, as a PET Agent for Imaging PD-L1 Expression

Journal of Nuclear Medicine, 2021-09, Vol.62 (9), p.1228-1234

2021

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Development, Characterization, and Radiation Dosimetry Studies of 18F-BMS-986229, a 18F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

Molecular imaging and biology, 2024-04, Vol.26 (2), p.301-309

2024

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LC-MS/MS bioanalysis of plasma 1, 14-tetradecanedioic acid and 1, 16-hexadecanedioic acid as candidate biomarkers for organic anion-transporting polypeptide mediated drug-drug interactions

Bioanalysis, 2018-09, Vol.10 (18), p.1473-1485

2018

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Synthesis of [D4]- and [D7]-4β-hydroxycholesterols for use in a novel drug-drug interaction assay

Journal of labelled compounds & radiopharmaceuticals, 2012-02, Vol.55 (2), p.61-65

2012

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Synthesis and Biologic Evaluation of a Novel 18 F-Labeled Adnectin as a PET Radioligand for Imaging PD-L1 Expression

Journal of Nuclear Medicine, 2018-03, Vol.59 (3), p.529-535

2018

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The synthesis of 14C-labeled N-succinimidyl-3-maleimidopropionate, a linker molecule for PEGylated biologics

Journal of labelled compounds & radiopharmaceuticals, 2014-10, Vol.57 (12), p.667-669

2014

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The synthesis of 14C-labeled, 13CD2-labeled saxagliptin, and its 13CD2-labeled 5-hydroxy metabolite

Journal of labelled compounds & radiopharmaceuticals, 2014-03, Vol.57 (3), p.136-140

2014

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Synthesis of 14C-labeled and 13C-,15N-labeled dasatinib and its piperazine N-dealkyl metabolite

Journal of labelled compounds & radiopharmaceuticals, 2008-01, Vol.51 (1), p.41-47

2008

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Synthesis of an adenine N-3 substituted CBI adduct by alkylation of adenine with a 1-iodomethylindoline seco-CBI precursor

Tetrahedron, 2018-11, Vol.74 (46), p.6680-6688

2018

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A facile and efficient synthesis of d3-labelled Reyataz

Journal of labelled compounds & radiopharmaceuticals, 2005-12, Vol.48 (14), p.1041-1047

2005

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Synthesis of tritium labeled 30-KDa PEG and conjugation to form 3 HPegbelfermin

Journal of labelled compounds & radiopharmaceuticals, 2021-10, Vol.64 (12), p.477

2021

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The 14C, 13C, and 15N syntheses of a potent VEGFR-2 kinase inhibitor, Brivanib, and its prodrug, Brivanib Alaninate

Journal of labelled compounds & radiopharmaceuticals, 2011-05, Vol.54 (6), p.324-331

2011

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Synthesis of isotopically labeled daclatasvir for use in human clinical studies: J. Easter et al

Journal of labelled compounds & radiopharmaceuticals, 2016-04, Vol.59 (4), p.164-170

2016

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Abstract 2479: Preclinical assessment of imaging agents for identification of fucosyl-GM1 expression in vivo

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.2479-2479

2022

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Abstract 871: [18F]BMS-986192 as a novel PET imaging agent for assessment of PD-L1 expression in vivo

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.871-871

2017

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Whole body PD-L1 PET in patients with NSCLC and melanoma

Journal of clinical oncology, 2018-02, Vol.36 (5_suppl), p.139-139

2018

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Synthesis and Biologic Evaluation of a Novel ^sup 18^F-Labeled Adnectin as a PET Radioligand for Imaging PD-L1 Expression

The Journal of nuclear medicine (1978), 2018-03, Vol.59 (3), p.529

2018

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Whole body PD-1 and PD-L1 PET with 89 Zr-nivolumab and 18 F- BMS-986192 in pts with NSCLC

Journal of clinical oncology, 2017-05, Vol.35 (15_suppl), p.e20047-e20047

2017

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Stereochemistry of the Thermal Isomerizations of trans-1-Ethenyl-2-phenylcyclopropane to 4-Phenylcyclopentene

Journal of the American Chemical Society, 1996-09, Vol.118 (35), p.8258-8265

1996

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The synthesis of 14 C‐labeled N ‐succinimidyl‐3‐maleimidopropionate, a linker molecule for PEGylated biologics

Journal of labelled compounds & radiopharmaceuticals, 2014-10, Vol.57 (12), p.667-669

2014

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Nucleophilic (Radio)Fluorination of Redox-Active Esters via Radical-Polar Crossover Enabled by Photoredox Catalysis

The discovery and evaluation of [18F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement

Synthesis of stable‐isotope‐labeled N‐(3‐dimethylaminopropyl)‐N′‐ethylcarbodiimide and N‐(3‐dimethylaminopropyl)‐N′‐ethylurea

Synthesis and Preclinical Evaluation of a 68Ga-Labeled Adnectin, 68Ga-BMS-986192, as a PET Agent for Imaging PD-L1 Expression

Distinguishing a phosphate ester prodrug from its isobaric sulfate metabolite by mass spectrometry without the metabolite standard

Synthesis and Preclinical Evaluation of a 68 Ga-Labeled Adnectin, 68 Ga-BMS-986192, as a PET Agent for Imaging PD-L1 Expression

Development, Characterization, and Radiation Dosimetry Studies of 18F-BMS-986229, a 18F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

LC-MS/MS bioanalysis of plasma 1, 14-tetradecanedioic acid and 1, 16-hexadecanedioic acid as candidate biomarkers for organic anion-transporting polypeptide mediated drug-drug interactions

Synthesis of [D4]- and [D7]-4β-hydroxycholesterols for use in a novel drug-drug interaction assay

Synthesis and Biologic Evaluation of a Novel 18 F-Labeled Adnectin as a PET Radioligand for Imaging PD-L1 Expression

The synthesis of 14C-labeled N-succinimidyl-3-maleimidopropionate, a linker molecule for PEGylated biologics

The synthesis of 14C-labeled, 13CD2-labeled saxagliptin, and its 13CD2-labeled 5-hydroxy metabolite

Synthesis of 14C-labeled and 13C-,15N-labeled dasatinib and its piperazine N-dealkyl metabolite

Synthesis of an adenine N-3 substituted CBI adduct by alkylation of adenine with a 1-iodomethylindoline seco-CBI precursor

A facile and efficient synthesis of d3-labelled Reyataz

Synthesis of tritium labeled 30-KDa PEG and conjugation to form 3 HPegbelfermin

The 14C, 13C, and 15N syntheses of a potent VEGFR-2 kinase inhibitor, Brivanib, and its prodrug, Brivanib Alaninate

Synthesis of isotopically labeled daclatasvir for use in human clinical studies: J. Easter et al

Abstract 2479: Preclinical assessment of imaging agents for identification of fucosyl-GM1 expression in vivo

Abstract 871: [18F]BMS-986192 as a novel PET imaging agent for assessment of PD-L1 expression in vivo

Whole body PD-L1 PET in patients with NSCLC and melanoma

Synthesis and Biologic Evaluation of a Novel ^sup 18^F-Labeled Adnectin as a PET Radioligand for Imaging PD-L1 Expression

Whole body PD-1 and PD-L1 PET with 89 Zr-nivolumab and 18 F- BMS-986192 in pts with NSCLC

Stereochemistry of the Thermal Isomerizations of trans-1-Ethenyl-2-phenylcyclopropane to 4-Phenylcyclopentene

The synthesis of 14 C‐labeled N ‐succinimidyl‐3‐maleimidopropionate, a linker molecule for PEGylated biologics

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