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

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

2024

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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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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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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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Synthesis of a dual carbon‐14‐labeled calcitonin gene‐related peptide receptor antagonist for use in a human absorption–distribution–metabolism–elimination study

Journal of labelled compounds & radiopharmaceuticals, 2022-05, Vol.65 (5), p.126-139

2022

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Synthesis of carbon‐14 and stable isotope labeled Censavudine

Journal of labelled compounds & radiopharmaceuticals, 2022-04, Vol.65 (4), p.112-122

2022

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Synthesis of tritium labeled 30‐KDa PEG and conjugation to form [3H]Pegbelfermin

Journal of labelled compounds & radiopharmaceuticals, 2021-10, Vol.64 (12), p.477-481

2021

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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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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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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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Chemoselective Methionine Bioconjugation: Site-Selective Fluorine-18 Labeling of Proteins and Peptides

Bioconjugate chemistry, 2020-08, Vol.31 (8), p.1908-1916

2020

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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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Direct Carbon Isotope Exchange through Decarboxylative Carboxylation

Journal of the American Chemical Society, 2019-01, Vol.141 (2), p.774-779

2019

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

The Journal of nuclear medicine (1978), 2018-03, Vol.59 (3), p.529-535

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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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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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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Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand ^sup 11^C-BMT-136088 for Lung Imaging in Rhesus Monkeys

The Journal of nuclear medicine (1978), 2018-02, Vol.59 (2), p.327

2018

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Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand 11C-BMT-136088 for Lung Imaging in Rhesus Monkeys

The Journal of nuclear medicine (1978), 2018-02, Vol.59 (2), p.327-333

2018

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Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand 11 C-BMT-136088 for Lung Imaging in Rhesus Monkeys

Journal of Nuclear Medicine, 2018-02, Vol.59 (2), p.327-333

2018

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Radiosynthesis and preclinical PET evaluation of 89 Zr-nivolumab (BMS-936558) in healthy non-human primates

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (20), p.5407

2017

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Radiosynthesis and preclinical PET evaluation of 89Zr-nivolumab (BMS-936558) in healthy non-human primates

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (20), p.5407-5414

2017

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

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

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

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

Synthesis of a dual carbon‐14‐labeled calcitonin gene‐related peptide receptor antagonist for use in a human absorption–distribution–metabolism–elimination study

Synthesis of carbon‐14 and stable isotope labeled Censavudine

Synthesis of tritium labeled 30‐KDa PEG and conjugation to form [3H]Pegbelfermin

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

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

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

Chemoselective Methionine Bioconjugation: Site-Selective Fluorine-18 Labeling of Proteins and Peptides

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

Direct Carbon Isotope Exchange through Decarboxylative Carboxylation

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

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

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

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

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

Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand ^sup 11^C-BMT-136088 for Lung Imaging in Rhesus Monkeys

Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand 11C-BMT-136088 for Lung Imaging in Rhesus Monkeys

Evaluation of the Lysophosphatidic Acid Receptor Type 1 Radioligand 11 C-BMT-136088 for Lung Imaging in Rhesus Monkeys

Radiosynthesis and preclinical PET evaluation of 89 Zr-nivolumab (BMS-936558) in healthy non-human primates

Radiosynthesis and preclinical PET evaluation of 89Zr-nivolumab (BMS-936558) in healthy non-human primates

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

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