Positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4). Part II: Challenges in hit-to-lead

The synthesis and SAR of two mGluR4 positive allosteric modulator leads 6 and 7 is described. VU001171 ( 6) represents the most potent (EC 50 = 650 nM), efficacious (141% Glu Max) and largest fold shift (36-fold) of any mGluR4 PAM ever described. However, this work highlights the challenges in hit-t...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2009-02, Vol.19 (3), p.962-966
Hauptverfasser: Williams, Richard, Niswender, Colleen M., Luo, Qingwei, Le, Uyen, Conn, P. Jeffrey, Lindsley, Craig W.
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Sprache:eng
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Zusammenfassung:The synthesis and SAR of two mGluR4 positive allosteric modulator leads 6 and 7 is described. VU001171 ( 6) represents the most potent (EC 50 = 650 nM), efficacious (141% Glu Max) and largest fold shift (36-fold) of any mGluR4 PAM ever described. However, this work highlights the challenges in hit-to-lead for mGluR4 PAMs, with multiple confirmed HTS hits displaying little or no tractable SAR. This Letter describes the synthesis and SAR of two mGluR4 positive allosteric modulator leads, 6 and 7. VU001171 ( 6) represents the most potent (EC 50 = 650 nM), efficacious (141% Glu Max) and largest fold shift (36-fold) of any mGluR4 PAM reported to date. However, this work highlights the challenges in hit-to-lead for mGluR4 PAMs, with multiple confirmed HTS hits displaying little or no tractable SAR.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2008.11.104