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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and discovery of new compounds bearing coumarin scaffold for the treatment of pulmonary fibrosis
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Synthesis and discovery of new compounds bearing coumarin scaffold for the treatment of pulmonary fibrosis

机译:轴承香豆素支架治疗肺纤维化的新化合物的合成与发现

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摘要

Idiopathic pulmonary fibrosis, characterized by excess accumulation of extracellular matrix, involved in many chronic diseases or injuries, threatens human health greatly. We have reported a series of compounds bearing coumarin scaffold which potently inhibited TGF-beta-induced total collagen accumulation in NRK-49F cell line and migration of macrophages. Compound 9d also suppressed the TGF-beta-induced protein expression of COL1A1, alpha-SMA, and p-Smad3 in vitro. Meanwhile, 9d at a dose of 100 mg/kg/day through oral administrations for 4 weeks effectively alleviated infiltration of inflammatory cells in lung tissue and fibrotic degree in bleomycin-induced pulmonary fibrosis model, which may related to its inhibition of TGF-beta/Smad3 pathway and anti-inflammation efficacy. In addition, 9d demonstrated decent bioavailability (T-1/2 = 39.88%) and suitable eliminated half-life time alp =13.09 h), suggesting that 9d could be a potential drug candidate for the treatment of fibrotic diseases. (C) 2019 Published by Elsevier Masson SAS.
机译:特征性肺纤维化,其特征在于细胞外基质的过度积累,涉及许多慢性疾病或伤害,大大威胁人类健康。我们报道了一系列轴承香豆素支架的化合物,其在NRK-49F细胞系和巨噬细胞的迁移中具有高效地抑制TGF-β诱导的总胶原积累。化合物9d还抑制了体外Col1a1,α-sma和p-smad3的Tgf-beta诱导的蛋白表达。同时,通过口服施用100mg / kg /天的剂量为100mg / kg /天,有效地减轻了肺组织中肺组织和抗血症诱导的肺纤维化模型中的炎性细胞的浸润,这可能与其对TGF-β的抑制相关/ Smad3途径和抗炎效果。此外,9D证明了体面的生物利用度(T-1/2 = 39.88%)和合适的消除半衰期ALP = 13.09h),表明9D可以是治疗纤维化疾病的潜在药物候选者。 (c)2019年由Elsevier Masson SA发布。

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