| Literature DB >> 24900352 |
Julie L Lukkarila1, Sara R da Silva1, Mohsin Ali2, Vijay M Shahani1, G Wei Xu2, Judd Berman3, Andrew Roughton3, Sirano Dhe-Paganon4, Aaron D Schimmer2, Patrick T Gunning1.
Abstract
MLN4924 is a selective inhibitor of the NEDD8-activating enzyme (NAE) and has advanced into clinical trials for the treatment of both solid and hematological malignancies. In contrast, the structurally similar compound 1 (developed by Millennium: The Takeda Oncology Company) is a pan inhibitor of the E1 enzymes NAE, ubiquitin activating enzyme (UAE), and SUMO-activating enzyme (SAE) and is currently viewed as unsuitable for clinical use given its broad spectrum of E1 inhibition. Here, we sought to understand the determinants of NAE selectivity. A series of compound 1 analogues were synthesized through iterative functionalization of the purine C6 position and evaluated for NAE specificity. Optimal NAE specificity was achieved through substitution with primary N-alkyl groups, while bulky or secondary N-alkyl substituents were poorly tolerated. When assessed in vitro, inhibitors reduced the growth and viability of malignant K562 leukemia cells. Through this study, we have successfully identified a series of sub-10 nM NAE-specific inhibitors and thereby highlighted the functionalities that promote NAE selectivity.Entities:
Keywords: NAE inhibitors; anticancer drugs; leukemia; proteasomal inhibitors
Year: 2011 PMID: 24900352 PMCID: PMC4018054 DOI: 10.1021/ml2000615
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345