摘要
Originally thought to be nondruggable, kinases represent attractive drug targets for pharmaceutical companies and academia. To date, there are over 40 kinase inhibitors approved by the US FDA, with 32 of these being small molecules, in addition to the three mammalian target of rapamycin inhibitor macrolides (sirolimus, temsirolimus and everolimus). Despite the rapid development of kinase inhibitors for cancer, presently none of these agents are approved for CNS indications. This mini perspective highlights selected kinase targets for CNS disorders, of which brain-permeable small-molecule inhibitors are reported, with demonstrated preclinical proof-of-concept efficacy. This is followed by a brief discussion on the key challenges of blood-brain barrier penetration and selectivity profiles in developing kinase inhibitors for CNS disorders.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 303-314 |
| 页数 | 12 |
| 期刊 | Future Medicinal Chemistry |
| 卷 | 9 |
| 期 | 3 |
| DOI | |
| 出版状态 | 已出版 - 3月 2017 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
学术指纹
探究 'Kinase targets in CNS drug discovery' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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