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- W1981668790 abstract "We discovered that the introduction of a methyl group to the benzylic position of the N-benzyl group in lead compound 1a has a dramatic effect on improving the binding selectivity of this ligand for the prostanoid receptors DP1 (receptor for prostaglandin D2) as compared to TP (receptor for thromboxane A2). Based on this discovery, we have synthesized a series of potent and highly selective DP1 antagonists. Among them, compound 1h was identified as a highly selective DP1 antagonist with excellent overall properties. It has a Ki of 0.43 nM to DP1 in binding assay and an IC50 of 2.5 nM in the DP1 functional assay. Its selectivity for DP1 over TP (the most potent receptor after DP1) exceeds 750-fold based on both binding and functional assays. These properties make 1h a very potent and highly selective DP1 receptor antagonist suitable for investigating the biological functions of DP1 in normal physiology and models of disease" @default.
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- W1981668790 date "2010-12-01" @default.
- W1981668790 modified "2023-10-16" @default.
- W1981668790 title "Potent and highly selective DP1 antagonists with 2,3,4,9-tetrahydro-1H-carbazole as pharmacophore" @default.
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- W1981668790 doi "https://doi.org/10.1016/j.bmcl.2010.10.018" @default.
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