Chemical Structure : GSK1820795A
Catalog No.: PC-27046Not For Human Use, Lab Use Only.
GSK1820795A is a potent, specific antagonist of G-protein-coupled receptor GPR132 (G2A), blocks agonist-induced association of hGPR132 with β-arrestin with pIC50 of 7.8, also is a dual angiotensin AT1 antagonist and PPARγ modulator.
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GSK1820795A is a potent, specific antagonist of G-protein-coupled receptor GPR132 (G2A), blocks agonist-induced association of hGPR132 with β-arrestin with pIC50 of 7.8, also is a dual angiotensin AT1 antagonist and PPARγ modulator.
GSK1820795A does not antagonize free fatty acid receptor FFA2.
GSK1820795A blocks rGPR132.
GSK1820795A blocks activation of yeast cells expressing hGPR132a by N‐acylamides.
| M.Wt | 566.71 | |
| Formula | C35H34N8 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Foster JR, et al. Pharmacol Res Perspect. 2019;7(6):e00542.
2. James R Foster, et al. Pharmacol Res Perspect. 2019 Nov 21;7(6):e00542.
3. Lamotte Y, F, et al. Bioorg Med Chem Lett. 2014;24(4):1098-1103.

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