| Literature DB >> 34011155 |
Dongfeng Zhang1, Peng Li1, Yongxin Gao1, Yaoyao Song2, Yaqin Zhu2, Hong Su2, Beibei Yang1, Li Li1, Gang Li1, Ningbo Gong3, Yang Lu3, Huanjie Shao2, Chunrong Yu4, Haihong Huang1.
Abstract
BCR-ABL kinase inhibition is an effective strategy for the treatment of chronic myeloid leukemia (CML). Herein, we report compound 3a-P1, bearing a difluoro-indene scaffold, as a novel potent pan-inhibitor against BCR-ABL mutants, including the most refractory T315I mutant. As the privileged (S)-isomer compared to its (R)-isomer 3a-P2, 3a-P1 exhibited potent antiproliferative activities against K562 and Ku812 CML cells and BCR-ABL and BCR-ABLT315I BaF3 cells, with IC50 values of 0.4, 0.1, 2.1, and 4.7 nM, respectively. 3a-P1 displayed a good safety profile in a battery of assays, including single-dose toxicity, hERG K+, and genotoxicity. It also showed favorable mice pharmacokinetic properties with a good oral bioavailability (32%), a reasonable half-life (4.61 h), and a high exposure (1386 h·ng/mL). Importantly, 3a-P1 demonstrated a higher potency than ponatinib in a mice xenograft model of BaF3 harboring BCR-ABLT315I. Overall, the results indicate that 3a-P1 is a promising drug candidate for the treatment of CML to overcome the imatinib-resistant T315I BCR-ABL mutation.Entities:
Year: 2021 PMID: 34011155 DOI: 10.1021/acs.jmedchem.1c00082
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446