The present invention includes novel molecules and methods of using an amphiphilic kanamycin molecule having substitutions at the O-4", 0-6", or O-4" and 0-6" positions having reduced antimicrobial activity for targeting Connexin Hemichannels.
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机译:本发明包括新颖的分子和使用在 O I> -4”,0-6”或 O I> -4”和0-处具有取代基的两亲卡那霉素分子的方法。具有降低的针对连接蛋白半通道的抗菌活性的6英寸位置。
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