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Published in 2025 at "Molecular Cancer Therapeutics"
DOI: 10.1158/1535-7163.targ-25-c088
Abstract: We present an integrated hit discovery platform for radiopharmaceutical drug conjugates (RDCs) that synergizes high-throughput biophysical screening (SPR, MST) with phage display technology to rapidly identify and optimize high-affinity cyclic peptide binders against oncology targets.…
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Keywords:
methodology;
discovery platform;
hit discovery;
cyclic peptide ... See more keywords
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Published in 2025 at "Clinical Cancer Research"
DOI: 10.1158/1557-3265.aimachine-a013
Abstract: Efficient hit discovery is a critical step in drug development, traditionally achieved through high-throughput screening (HTS). Newer methods such as DNA-Encoded Libraries (DEL) and Affinity Selection Mass Spectrometry (ASMS) offer large-scale, cost-effective alternatives. However, they…
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Keywords:
chemistry;
discovery;
hit discovery;
platform ... See more keywords