An N,N-Bis(benzimidazolylpicolinoyl)piperazine (BT-11): A Novel Lanthionine Synthetase C-Like 2-Based Therapeutic for Inflammatory Bowel Disease

被引:31
作者
Carbo, Adria [1 ]
Gandour, Richard D. [1 ]
Hontecillas, Raquel [1 ]
Philipson, Noah [1 ]
Uren, Aykut [2 ]
Bassaganya-Riera, Josep [1 ]
机构
[1] Biotherapeutics Inc, 1800 Kraft Dr,Suite 200, Blacksburg, VA 24060 USA
[2] Georgetown Univ, Med Ctr, Washington, DC 20057 USA
关键词
NECROSIS-FACTOR-ALPHA; HUMAN MONONUCLEAR-CELLS; ABSCISIC-ACID; SUPPRESSION; DESIGN; TARGET; AGENTS;
D O I
10.1021/acs.jmedchem.6b00412
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Lanthionine synthetase C-like 2 (LANCL2), a novel therapeutic target for inflammatory and autoimmune diseases and diabetes, exerts anti-inflammatory and insulin-sensitizing effects. This study reports the first LANCL2-based therapeutics for inflammatory bowel disease (IBD). Analogues of 1 (ABA) and 2 (NSC61610) were screened by molecular docking, then synthesized and analyzed for binding to LANCL2 by surface plasmon resonance. Piperazine-1,4-diylbis(6-benzo[d]imidazole-2-yl)pyridine-2-yl(methanone, 7, was identified as the lead LANCL2-binding compound for treating IBD. The oral treatment with 7 (8 mg/kg/d) in a mouse model of IBD resulted in lowering the disease activity index, decreasing colonic inflammatory lesions by 4-fold, and suppressing inflammatory markers (e.g., TNF-alpha, and interferon-gamma) in the gut. Furthermore, studies in LANCL2-/- mice demonstrated that loss of LANCL2 abrogated beneficial actions of 7, suggesting high selectivity for the target. In conclusion, 7 merits continued development as a LANCL2-based, first-in-class orally active therapeutic for IBD.
引用
收藏
页码:10113 / 10126
页数:14
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