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- W2091296205 abstract "A series of PPARγ agonists were synthesized from l-tyrosine that incorporated low molecular weight N-substituents. The most potent analogue, pyrrole (Scheme 1, Scheme 2), demonstrated a Ki of 6.9 nM and an EC50 of 4.7 nM in PPARγ binding and functional assays, respectively. Pyrrole (Scheme 1, Scheme 2), which is readily synthesized from l-tyrosine methyl ester in four steps, also demonstrated in vivo activity in a rodent model of Type 2 diabetes." @default.
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- W2091296205 date "2001-12-01" @default.
- W2091296205 modified "2023-09-29" @default.
- W2091296205 title "Synthesis and biological activity of l-tyrosine-based PPARγ agonists with reduced molecular weight" @default.
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- W2091296205 doi "https://doi.org/10.1016/s0960-894x(01)00649-7" @default.
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