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首页> 外文期刊>Bio/Technology >Remodeling MMPIs -- Matrix metalloproteinase inhibitors will be approved as drugs, probably this year, but questions remain concerning their specificity, bioavailability, and potential long-term toxicity
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Remodeling MMPIs -- Matrix metalloproteinase inhibitors will be approved as drugs, probably this year, but questions remain concerning their specificity, bioavailability, and potential long-term toxicity

机译:重塑MMPI-基质金属蛋白酶抑制剂可能会在今年获得批准,但其特异性,生物利用度和潜在的长期毒性仍存在疑问

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Matrix metaiioproteinases (MMPs) are ubiquitous in human disease and development. That much is increasingly ciear In 1994, researchers at Glaxo (Research Triangle Park, NC) and British Bio-Technology (Oxford, U.K.) independently showed that metalioproteinases were involved in the conversion of inactive tumor .necrosis factor (TNF) precursor into active TNF. Since TNF is implicated in rheumatoid arthritis, Crohn'sdisease, multiple sclerosis, and cachexia (and sepsis, too, if anyone has the energy or inclination), this discovery added many new diseases to the !ist of those that might be treatable using MMP inhibitors (MMPIs) Many industry analysts feel that the questions surrounding MMPIs as potential drugs (in cancer, at least) are no longer "if" and "whether" but "when" and "which compounds."
机译:基质金属蛋白酶(MMPs)在人类疾病和发展中普遍存在。 1994年,葛兰素史克公司(北卡罗莱纳州三角公园)和英国生物技术公司(英国牛津)的研究人员独立地表明,金属蛋白酶参与了将非活性肿瘤坏死因子(TNF)前体转化为活性TNF的过程。 。由于TNF涉及类风湿性关节炎,克罗恩病,多发性硬化症和恶病质(以及败血症,如果有人有精力或倾向也是如此),因此这一发现为那些使用MMP可以治疗的疾病增加了许多新疾病!抑制剂(MMPI)许多行业分析家认为,围绕MMPIs作为潜在药物(至少在癌症中)的问题不再是“如果”和“是否”,而是“何时”和“哪些化合物”。

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