Summary for 9J0K
| Entry DOI | 10.2210/pdb9j0k/pdb |
| Related | 9IX5 |
| Descriptor | Thyroid hormone receptor beta, Nuclear receptor coactivator 2, 2-[[7-[3-(aminomethyl)phenoxy]-1-methoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid, ... (4 entities in total) |
| Functional Keywords | thyroid hormone receptor b, agonist, resistance, transcription |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 4 |
| Total formula weight | 62546.08 |
| Authors | |
| Primary citation | Li, Q.,Yao, B.,Zhao, S.,Lu, Z.,Wu, X.,Lu, Z.,Wu, T.,Li, J.,Chen, X.,Chen, Z.,Zhang, C.,Wu, D.,Zhang, Y.,Xiang, Q.,Li, Y.,Xu, Y. Discovery of a Potent, Selective, and Multiple His435 Mutation-Sensitive Thyroid Hormone Receptor beta Agonist. J.Med.Chem., 68:13471-13490, 2025 Cited by PubMed Abstract: Beyond selectivity concerns for thyroid hormone receptor β (THR-β) agonists, intolerance to the His435 mutation remains a challenge. Following our previous study, we performed detailed modifications on the 7-position of isoquinoline, specifically targeting the hydrophobic region of the THR-β ligand-binding pocket (LBP). This led to the identification of compound , which showed potent THR-β agonistic activity (EC: 3.2 nM), moderately selectivity (∼10-fold), and good activation of multiple His435 mutants (EC: 134.2 nM to 515.5 nM). Co-crystal structures revealed that the introduction of small-volume groups into the hydrophobic pocket of THR-β almost did not significantly displace helix 11 or helix 3, explaining why can activate multiple His435 mutants simultaneously. Multiple experiments confirmed that exhibits excellent lipid metabolism, safety, and pharmacokinetic properties. Together, emerges as a potent, selective, and His435 mutation-sensitive THR-β agonist, offering potential for treating dyslipidemia, metabolic dysfunction-associated steatohepatitis (MASH), or resistance to thyroid hormone (RTH). PubMed: 40539969DOI: 10.1021/acs.jmedchem.5c00164 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.698 Å) |
Structure validation
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