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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis of benzofuran derivatives as selective inhibitors of tissue-nonspecific alkaline phosphatase: effects on cell toxicity and osteoblast-induced mineralization
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Synthesis of benzofuran derivatives as selective inhibitors of tissue-nonspecific alkaline phosphatase: effects on cell toxicity and osteoblast-induced mineralization

机译:苯并呋喃衍生物作为组织非特异性碱性磷酸酶的选择性抑制剂的合成:对细胞毒性和成骨细胞诱导矿化的影响

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摘要

Tissue-nonspecific alkaline phosphatase (TNAP) by hydrolyzing pyrophosphate, an inhibitor of apatite formation, promotes extracellular matrix calcification during bone formation and growth, as well as during ectopic calcification under pathological conditions. TNAP is a target for the treatment of soft tissue pathological ossification. We synthesized a series of benzofuran derivatives. Among these, SMA14, displayed TNAP activity better than levamisole. SMA14 was found to be not toxic at doses of up to 40 mu M in osteoblast-like Saos-2 cells and primary osteoblasts. As probed by Alizarin Red staining, this compound inhibited mineral formation in murine primary osteoblast and in osteoblast-like Saos-2 cells. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过水解焦磷灰石(磷灰石形成的抑制剂)的组织非特异性碱性磷酸酶(TNAP),可在骨骼形成和生长以及病理条件下的异位钙化过程中促进细胞外基质钙化。 TNAP是治疗软组织病理性骨化的目标。我们合成了一系列苯并呋喃衍生物。其中,SMA14的TNAP活性优于左旋咪唑。发现SMA14在成骨细胞样Saos-2细胞和原代成骨细胞中的剂量高达40μM时无毒。如茜素红染色所探测,该化合物抑制鼠原代成骨细胞和成骨细胞样Saos-2细胞中矿物质的形成。 (C)2016 Elsevier Ltd.保留所有权利。

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