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WFRF:(Zhang Zhen Yu)
 

Sökning: WFRF:(Zhang Zhen Yu) > (2015-2019) > Design, Synthesis, ...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003755naa a2200697 4500
001oai:DiVA.org:umu-158574
003SwePub
008190527s2019 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1585742 URI
024a https://doi.org/10.1021/acs.jmedchem.8b017782 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Chen, Zhen4 aut
2451 0a Design, Synthesis, and Evaluation of Reversible and Irreversible Monoacylglycerol Lipase Positron Emission Tomography (PET) Tracers Using a "Tail Switching" Strategy on a Piperazinyl Azetidine Skeleton
264 c 2019-03-04
264 1b American Chemical Society (ACS),c 2019
338 a print2 rdacarrier
520 a Monoacylglycerol lipase (MAGL) is a senile hydrolase that degrades 2-arachidonoylglycerol (2-AG) in the endocannabinoid system (eCB). Selective inhibition of MAGL has emerged as a potential therapeutic approach for the treatment of diverse pathological conditions, including chronic pain, inflammation, cancer, and neurodegeneration. Herein, we disclose a novel array of reversible and irreversible MAGL inhibitors by means of "tail switching" on a piperazinyl azetidine scaffold. We developed a lead irreversible-binding MAGL inhibitor 8 and reversible-binding compounds 17 and 37, which are amenable for radiolabeling with C-11 or F-18. [C-11]8 ([C-11]MAGL-2-11) exhibited high brain uptake and excellent binding specificity in the brain toward MAGL. Reversible radioligands [C-11]17 ([C-11]PAD) and [F-18]37 ([F-18]MAGL-4-11) also demonstrated excellent in vivo binding specificity toward MAGL in peripheral organs. This work may pave the way for the development of MAGL-targeted positron emission tomography tracers with tunability in reversible and irreversible binding mechanisms.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinsk bioteknologix Medicinsk bioteknologi0 (SwePub)304012 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Medical Biotechnologyx Medical Biotechnology0 (SwePub)304012 hsv//eng
700a Mori, Wakana4 aut
700a Deng, Xiaoyun4 aut
700a Cheng, Ran4 aut
700a Ogasawara, Daisuke4 aut
700a Zhang, Genwei4 aut
700a Schafroth, Michael A.4 aut
700a Dahl, Kenneth4 aut
700a Fu, Hualong4 aut
700a Hatori, Akiko4 aut
700a Shao, Tuo4 aut
700a Zhang, Yiding4 aut
700a Yamasaki, Tomoteru4 aut
700a Zhang, Xiaofei4 aut
700a Rong, Jian4 aut
700a Yu, Qngzhen4 aut
700a Hu, Kuan4 aut
700a Fujinaga, Masayuki4 aut
700a Xie, Lin4 aut
700a Kumata, Katsushi4 aut
700a Gou, Yuancheng4 aut
700a Chen, Jingjin4 aut
700a Gu, Shuyin4 aut
700a Bao, Liang4 aut
700a Wang, Lu4 aut
700a Collier, Thomas Lee4 aut
700a Vasdev, Neil4 aut
700a Shao, Yihan4 aut
700a Ma, Jun-An4 aut
700a Cravatt, Benjamin F.4 aut
700a Fowler, Christopheru Umeå universitet,Farmakologi4 aut0 (Swepub:umu)chfo0001
700a Josephson, Lee4 aut
700a Zhang, Ming-Rong4 aut
700a Liang, Steven H.4 aut
710a Umeå universitetb Farmakologi4 org
773t Journal of Medicinal Chemistryd : American Chemical Society (ACS)g 62:7, s. 3336-3353q 62:7<3336-3353x 0022-2623x 1520-4804
856u https://europepmc.org/articles/pmc6581563?pdf=render
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-158574
8564 8u https://doi.org/10.1021/acs.jmedchem.8b01778

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