西罗莫司
替西罗莫司
依维莫司
FKBP公司
PI3K/AKT/mTOR通路
药理学
雷帕霉素的作用靶点
mTOR抑制剂的发现与发展
激酶
药品
生物利用度
医学
化学
信号转导
内科学
生物化学
作者
Ajla Hodzic Kuerec,Andrea B. Maier
出处
期刊:Gerontology
[S. Karger AG]
日期:2023-01-01
卷期号:69 (6): 657-659
被引量:5
摘要
Rapamycin (sirolimus) is an immunosuppressive drug approved by the Food and Drug Administration (FDA). It is also a leading candidate for targeting aging. Rapamycin and its analogs (everolimus, temsirolimus, ridaforolimus) inhibit the mammalian target of rapamycin (mTOR) kinase by binding to FK506-binding proteins (FKBP) and have a similar chemical structure that only differs in the functional group present at carbon-40. Analogs of rapamycin were developed to improve its pharmacological properties, such as low oral bioavailability and a long half-life. The analogs of rapamycin are referred to as “rapalogs.” Rapamycin is the parent compound and should therewith not be called a “rapalog.”
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