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Complementary Approaches to Existing Target Based Drug Discovery for Identifying Novel Drug Targets

机译:现有的基于靶标的药物发现新药物靶标的补充方法

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In the past decade, it was observed that the relationship between the emerging New Molecular Entities and the quantum of R&D investment has not been favorable. There might be numerous reasons but few studies stress the introduction of target based drug discovery approach as one of the factors. Although a number of drugs have been developed with an emphasis on a single protein target, yet identification of valid target is complex. The approach focuses on an in vitro single target, which overlooks the complexity of cell and makes process of validation drug targets uncertain. Thus, it is imperative to search for alternatives rather than looking at success stories of target-based drug discovery. It would be beneficial if the drugs were developed to target multiple components. New approaches like reverse engineering and translational research need to take into account both system and target-based approach. This review evaluates the strengths and limitations of known drug discovery approaches and proposes alternative approaches for increasing efficiency against treatment.
机译:在过去的十年中,观察到新兴的新分子实体与R&D投资额之间的关系并不理想。可能有很多原因,但是很少有研究强调将基于靶标的药物发现方法作为因素之一。尽管已经开发了多种药物,重点是单一蛋白质靶标,但是有效靶标的鉴定却很复杂。该方法侧重于体外单个靶标,该靶标忽略了细胞的复杂性并使验证药物靶标的过程不确定。因此,必须寻找替代方法,而不是寻找基于靶标的药物发现的成功案例。如果将药物开发为靶向多种成分,将是有益的。逆向工程和转换研究等新方法需要同时考虑系统方法和基于目标的方法。这篇综述评估了已知药物发现方法的优势和局限性,并提出了提高治疗效率的替代方法。

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