8X71

Crystal structure of Peroxiredoxin I in complex with compound 19-064

Summary for 8X71

• Entry DOI: 10.2210/pdb8x71/pdb
• Descriptor: Peroxiredoxin-1, methyl 3-[[(2~{R},4~{a}~{S},6~{a}~{R},6~{a}~{S},14~{a}~{S},14~{b}~{R})-2,4~{a},6~{a},6~{a},9,14~{a}-hexamethyl-10-oxidanyl-11-oxidanylidene-1,3,4,5,6,13,14,14~{b}-octahydropicen-2-yl]carbamoylamino]oxetane-3-carboxylate (3 entities in total)
• Functional Keywords: oxidoreductase-inhibitor complex, oxidoreductase/inhibitor
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 39831.61

Authors

Zhang, H.,Luo, C. (deposition date: 2023-11-22, release date: 2024-06-19)

Primary citation

Wang, J.,Rong, Q.,Ye, L.,Fang, B.,Zhao, Y.,Sun, Y.,Zhou, H.,Wang, D.,He, J.,Cui, Z.,Zhang, Q.,Kang, D.,Hu, L.
Discovery of a Novel Orally Bioavailable FLT3-PROTAC Degrader for Efficient Treatment of Acute Myeloid Leukemia and Overcoming Resistance of FLT3 Inhibitors.
J.Med.Chem., 67:7197-7223, 2024

PubMed Abstract: Fms-like tyrosine receptor kinase 3 (FLT3) proteolysis-targeting chimeras (PROTACs) represent a promising approach to eliminate the resistance of FLT3 inhibitors. However, due to the poor druggability of PROTACs, the development of orally bioavailable FLT3-PROTACs faces great challenges. Herein, a novel orally bioavailable FLT3-ITD degrader with excellent pharmacokinetic properties was discovered through reasonable design. selectively inhibited the proliferation of FLT3-ITD mutant acute myeloid leukemia (AML) cells and potently induced FLT3-ITD degradation through the ubiquitin-proteasome system. Notably, oral administration of resulted in complete tumor regression on subcutaneous AML xenograft models. Furthermore, on systemic AML xenograft models, could completely eliminate the CD45CD33 human leukemic cells in murine and significantly prolonged the survival time of mice. Most importantly, exerted significantly improved antiproliferative activity against drug-resistant AML cells compared to existing FLT3 inhibitors. These findings suggested that could serve as a promising drug candidate for relapsed or refractory AML.

PubMed: 38655686
DOI: 10.1021/acs.jmedchem.4c00051

Experimental method

X-RAY DIFFRACTION (1.58 Å)