化学
去甲肾上腺素转运体
血清素转运体
西酞普兰
再摄取抑制剂
运输机
药理学
血清素
去甲肾上腺素
生物化学
内科学
多巴胺
受体
医学
基因
作者
Jonas N. N. Eildal,Jacob Andersen,Anders S. Kristensen,Anne Marie Jørgensen,Benny Bang‐Andersen,Morten Egevang Jørgensen,Kristian Strømgaard
摘要
Citalopram and talopram are structurally closely related, but they have very distinct pharmacological profiles as selective inhibitors of the serotonin and norepinephrine transporters, respectively. A systematic structure-activity relationship study was performed, in which each of the four positions distinguishing the two compounds were varied. The inhibitory potencies of the resulting 16 compounds were tested at both serotonin and norepinephrine transporters. This showed that particularly two of the four positions are determinants for the biological activity.
科研通智能强力驱动
Strongly Powered by AbleSci AI