Development of Ligand-Drug Conjugates Targeting Melanoma through the Overexpressed Melanocortin 1 Receptor
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona 85721, United States
Funder
University of Arizona
National Institute of Diabetes and Digestive and Kidney Diseases
Center for Scientific Review
Publisher
American Chemical Society (ACS)
Subject
Pharmacology (medical),Pharmacology
Link
https://pubs.acs.org/doi/pdf/10.1021/acsptsci.0c00072
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1. Recommended Tool Compounds for the Melanocortin Receptor (MCR) G Protein-Coupled Receptors (GPCRs);ACS Pharmacology & Translational Science;2024-08-26
2. Targeting the Melanocortin 1 Receptor in Melanoma: Biological Activity of α-MSH–Peptide Conjugates;International Journal of Molecular Sciences;2024-01-16
3. Melanocortin 1 Receptor (MC1R): Pharmacological and Therapeutic Aspects;International Journal of Molecular Sciences;2023-07-29
4. Late-Stage Functionalization with Cysteine Staples Generates Potent and Selective Melanocortin Receptor-1 Agonists;J MED CHEM;2022
5. Late-Stage Functionalization with Cysteine Staples Generates Potent and Selective Melanocortin Receptor-1 Agonists;Journal of Medicinal Chemistry;2022-09-27
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