运输机
肌酸
化学
生物化学
羧酸
立体化学
药理学
医学
基因
作者
Clemens V. Farr,Yi Xiao,Ali El‐Kasaby,Manuel Schupp,Matej Hoťka,Giovanni Di Mauro,Amy Clarke,Miryam Pastor Fernandez,Walter Sandtner,Thomas Stockner,Christoph Klade,Nuno Maulide,Michael Freissmuth
出处
期刊:Molecular Pharmacology
[American Society for Pharmacology and Experimental Therapeutics]
日期:2024-09-25
卷期号:106 (6): 319-333
标识
DOI:10.1124/molpharm.124.000995
摘要
The creatine transporter-1 (CRT-1/SLC6A8) maintains the uphill transport of creatine into cells against a steep concentration gradient. Cellular creatine accumulation is required to support the ATP-buffering by phosphocreatine. More than 60 compounds have been explored in the past for their ability to inhibit cellular creatine uptake, but the number of active compounds is very limited. Here, we show that all currently known inhibitors are full alternative substrates. We analyzed their structure-activity relationship for inhibition of CRT-1 to guide a rational approach to the synthesis of novel creatine transporter ligands. Measurements of both inhibition of [
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