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 |
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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. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2008.11.104 |