SC 51089
Chemical Name: 8-Chlorodibenz(Z)[b,f][1,4]oxazepine-10(11H)-carboxylic acid 2-[1-oxo-3-(4-pyridinyl)propyl]hydrazide hydrochloride
Purity: ≥99%
Biological Activity
SC 51089 is a selective EP1 prostanoid receptor antagonist (Ki values are 1.3, 11.2, 17.5, 61.1, > 100, > 100, > 100, >100 and > 100 μM for EP1, TP, EP3, EP2, EP4, FP and DP receptors respectively). Attenuates PGE2-induced neuronal cell death in vitro and slows tumor growth in vivo.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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The utilization of recombinant prostanoid receptors determine the affinities and selectivities of prostaglandins and related analogs.
Abramovitz et al.
Biochim.Biophys.Acta, 2000;1483:285 -
Effect of EP1 receptor on cerebral blood flow in the middle cerebral artery occlusion model of stroke in mice.
Saleem et al.
J.Neurosci.Res., 2007;85:2433
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Citation for SC 51089
The citations listed below are publications that use Tocris products. Selected citations for SC 51089 include:
1 Citation: Showing 1 - 1
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Rat prostaglandin EP3 receptor is highly promiscuous and is the sole prostanoid receptor family member that regulates INS-1 (832/3) cell glucose-stimulated insulin secretion.
Authors: Sarah E Et al.
Pharmacol Res Perspect 2021;9:e00736
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