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首页> 外文期刊>Journal of Medicinal Chemistry >An N,N-Bis(benzimidazolylpicolinoyl)piperazine (BT-11): A Novel Lanthionine Synthetase C-Like 2-Based Therapeutic for Inflammatory Bowel Disease
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An N,N-Bis(benzimidazolylpicolinoyl)piperazine (BT-11): A Novel Lanthionine Synthetase C-Like 2-Based Therapeutic for Inflammatory Bowel Disease

机译:N,N-双(苯并咪唑基吡啶啉基)哌嗪(BT-11):一种新型的基于L-硫氨酸合成酶C样2的炎症性肠病治疗方法

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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.
机译:羊毛硫氨酸合成酶C样2(LANCL2)是炎症和自身免疫性疾病及糖尿病的新型治疗靶标,具有抗炎和胰岛素敏感的作用。这项研究报告了第一个基于LANCL2的炎症性肠病(IBD)治疗药物。通过分子对接筛选1(ABA)和2(NSC61610)的类似物,然后合成并通过表面等离振子共振分析其与LANCL2的结合。哌嗪-1,4-二基双(6-苯并[d]咪唑-2-基)吡啶-2-基(甲酮,7,被确定为治疗IBD的主要LANCL2结合化合物。口服治疗7(8毫克/千克/天)在IBD小鼠模型中可导致疾病活动指数降低,结肠炎性病变减少4倍,并抑制肠道中的炎性标志物(例如TNF-α和干扰素-γ)。 ,在LANCL2-/-小鼠中的研究表明,LANCL2的丧失废除了7的有益作用,表明对靶标具有高度选择性,总之,7具有作为基于LANCL2的IBD一流口服活性治疗剂的优势。

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