7p0k: Difference between revisions

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== Function ==
== Function ==
[https://www.uniprot.org/uniprot/ENPP2_RAT ENPP2_RAT]  
[https://www.uniprot.org/uniprot/ENPP2_RAT ENPP2_RAT]  
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== Publication Abstract from PubMed ==
Autotaxin (ATX) is a secreted phosphodiesterase that has been implicated in a remarkably wide array of pathologies, especially in fibrosis and cancer. While ATX inhibitors have entered the clinical arena, a validated probe for positron emission tomography (PET) is currently lacking. With the aim to develop a suitable ATX-targeted PET radioligand, we have synthesized a focused library of fluorinated imidazo[1,2-a]pyridine derivatives, determined their inhibition constants, and confirmed their binding mode by crystallographic analysis. Based on their promising in vitro properties, compounds 9c, 9f, 9h, and 9j were radiofluorinated. Also, a deuterated analog of [(18)F]9j, designated as [(18)F]ATX-1905 ([(18)F]20), was designed and proved to be highly stable against in vivo radiodefluorination compared with [(18)F]9c, [(18)F]9f, [(18)F]9h, and [(18)F]9j. These results along with in vitro and in vivo studies toward ATX in a mouse model of LPS-induced liver injury suggest that [(18)F]ATX-1905 is a suitable PET probe for the non-invasive quantification of ATX.
Imaging Autotaxin In Vivo with (18)F-Labeled Positron Emission Tomography Ligands.,Deng X, Salgado-Polo F, Shao T, Xiao Z, Van R, Chen J, Rong J, Haider A, Shao Y, Josephson L, Perrakis A, Liang SH J Med Chem. 2021 Oct 28;64(20):15053-15068. doi: 10.1021/acs.jmedchem.1c00913. , Epub 2021 Oct 18. PMID:34662125<ref>PMID:34662125</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
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</StructureSection>
</StructureSection>

Latest revision as of 09:03, 17 October 2024

Crystal structure of Autotaxin (ENPP2) with 18F-labeled positron emission tomography ligand

7p0k, resolution 2.20Å

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