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首页> 外文期刊>Current topics in medicinal chemistry >Small Molecule p38 Inhibitors: Novel Structural Features and Advances from 2002-2005.
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Small Molecule p38 Inhibitors: Novel Structural Features and Advances from 2002-2005.

机译:小分子p38抑制剂:2002-2005年的新型结构特征和研究进展。

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摘要

The discovery and development of selective, efficacious, and safe small molecule p38 mitogen-activated protein kinase inhibitors for the treatment of inflammatory diseases remains the focus of many pharmaceutical research programs. Advances in small molecule p38 inhibitor design in potency and oral efficacy have been accelerated with the large number of available inhibitor-enzyme x-ray structures. These advances have allowed for the discovery of diverse sets of inhibitors with the opportunity to map inhibitor interactions and design selective inhibitors. This review covers recent compound disclosures in the patent and published literature over the last three years. Many disclosures represent new chemotypes as well as creative modifications of known structures.
机译:选择性,有效和安全的小分子p38丝裂原活化蛋白激酶抑制剂在炎性疾病治疗中的发现和开发仍然是许多药物研究计划的重点。小分子p38抑制剂设计在功效和口服功效方面的进展已通过大量可用的抑制剂-酶X射线结构得到了加速。这些进展允许发现各种抑制剂,并有机会绘制抑制剂相互作用图谱并设计选择性抑制剂。这篇综述涵盖了过去三年来专利和公开文献中最新的化合物公开内容。许多公开内容代表新的化学型以及对已知结构的创造性修饰。

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