不
孤菲肽受体
止痛药
兴奋剂
类阿片
医学
药理学
麻醉
受体
阿片肽
内科学
作者
Stefan Schunk,Klaus Linz,Claudia Hinze,Sven Frormann,Stefan Oberbörsch,Bernd Sundermann,Saskia Zemolka,Werner Englberger,Tieno Germann,Thomas Christoph,Babette-Y. Kögel,Wolfgang Schröder,Stephanie Harlfinger,Derek Saunders,Achim Kless,Hans Schick,Helmut Sonnenschein
摘要
In a previous communication, our efforts leading from 1 to the identification of spiro[cyclohexane-dihydropyrano[3,4-b]indole]-amine 2a as analgesic NOP and opioid receptor agonist were disclosed and their favorable in vitro and in vivo pharmacological properties revealed. We herein report our efforts to further optimize lead 2a, toward trans-6′-fluoro-4′,9′-dihydro-N,N-dimethyl-4-phenyl-spiro[cyclohexane-1,1′(3′H)-pyrano[3,4-b]indol]-4-amine (cebranopadol, 3a), which is currently in clinical development for the treatment of severe chronic nociceptive and neuropathic pain.
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