化学
兴奋剂
药理学
立体化学
受体
生物化学
医学
作者
Víctor Hernández‐Olmos,Jan Heering,Beatrice Marinescu,Tina Schermeng,Vladimir V. Ivanov,Yurii S. Moroz,Sheila Nevermann,Marius Mathes,Johanna H. M. Ehrler,Mohamad Wessam Alnouri,Markus Wolf,Alicia S. Haydo,Tessa Schmachtel,Andrea Zaliani,Georg Höfner,Astrid Kaiser,Manfred Schubert‐Zsilavecz,Annette G. Beck‐Sickinger,Stefan Offermanns,Philipp Gribbon
标识
DOI：10.1021/acs.jmedchem.3c02164
摘要
-phenylalanine (T-10418) exhibiting higher potency than the reference and natural ligand 9-HODE and high selectivity among G protein-coupled receptors. With its favorable activity, a clean selectivity profile, excellent solubility, and high metabolic stability, T-10418 qualifies as a pharmacological tool to investigate the effects of G2A activation.
科研通智能强力驱动
Strongly Powered by AbleSci AI
PDF的下载单位、IP信息已删除
(2025-6-4)
Nole
秋风
无极微光
DW
Enigma_GEB
xing_xing
老的火龙果
cdercder
拆迁办禁言
科研狗
热切菩萨
aajhajkahna
牧青
GingerF
369ninja
OK
悦耳的怀寒
Gauss
殷勤的紫槐
我能私信骂你吗
皖公网安备34019202002308
