6H6R

Fragment Derived XIAP inhibitor

Summary for 6H6R

• Entry DOI: 10.2210/pdb6h6r/pdb
• Descriptor: E3 ubiquitin-protein ligase XIAP, ZINC ION, SODIUM ION, ... (5 entities in total)
• Functional Keywords: inhibitor of apoptosis, caspase inhibitor zinc binding domain, apoptosis
• Biological source: Homo sapiens (Human)
• Total number of polymer chains: 1
• Total formula weight: 15205.36

Authors

Williams, P.A. (deposition date: 2018-07-30, release date: 2018-08-22, Last modification date: 2024-05-15)

Primary citation

Johnson, C.N.,Ahn, J.S.,Buck, I.M.,Chiarparin, E.,Day, J.E.H.,Hopkins, A.,Howard, S.,Lewis, E.J.,Martins, V.,Millemaggi, A.,Munck, J.M.,Page, L.W.,Peakman, T.,Reader, M.,Rich, S.J.,Saxty, G.,Smyth, T.,Thompson, N.T.,Ward, G.A.,Williams, P.A.,Wilsher, N.E.,Chessari, G.
A Fragment-Derived Clinical Candidate for Antagonism of X-Linked and Cellular Inhibitor of Apoptosis Proteins: 1-(6-[(4-Fluorophenyl)methyl]-5-(hydroxymethyl)-3,3-dimethyl-1 H,2 H,3 H-pyrrolo[3,2- b]pyridin-1-yl)-2-[(2 R,5 R)-5-methyl-2-([(3R)-3-methylmorpholin-4-yl]methyl)piperazin-1-yl]ethan-1-one (ASTX660).
J. Med. Chem., 61:7314-7329, 2018

PubMed Abstract: Inhibitor of apoptosis proteins (IAPs) are promising anticancer targets, given their roles in the evasion of apoptosis. Several peptidomimetic IAP antagonists, with inherent selectivity for cellular IAP (cIAP) over X-linked IAP (XIAP), have been tested in the clinic. A fragment screening approach followed by structure-based optimization has previously been reported that resulted in a low-nanomolar cIAP1 and XIAP antagonist lead molecule with a more balanced cIAP-XIAP profile. We now report the further structure-guided optimization of the lead, with a view to improving the metabolic stability and cardiac safety profile, to give the nonpeptidomimetic antagonist clinical candidate 27 (ASTX660), currently being tested in a phase 1/2 clinical trial (NCT02503423).

PubMed: 30091600
DOI: 10.1021/acs.jmedchem.8b00900

Experimental method

X-RAY DIFFRACTION (2.03 Å)