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Biological Activity for EMD 66684
EMD 66684 is a highly potent and very selective non-peptide angiotensin AT1 receptor antagonist (IC50 values are 0.7 and > 10000 nM for AT1 and AT2 receptors respectively). Potently inhibits angiotensin II-induced contractions in isolated rabbit aorta (IC50 = 0.2 nM) and reduces blood pressure in hypertensive rats.
Compound Libraries for EMD 66684
Technical Data for EMD 66684
|Storage||Desiccate at +4°C|
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.
Solubility Data for EMD 66684
|Solvent||Max Conc. mg/mL||Max Conc. mM|
Preparing Stock Solutions for EMD 66684
The following data is based on the product molecular weight 547.05. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|0.5 mM||3.66 mL||18.28 mL||36.56 mL|
|2.5 mM||0.73 mL||3.66 mL||7.31 mL|
|5 mM||0.37 mL||1.83 mL||3.66 mL|
|25 mM||0.07 mL||0.37 mL||0.73 mL|
References for EMD 66684
References are publications that support the biological activity of the product.
Mederski et al (1994) Non-peptide angiotensin II receptor antagonists: synthesis and biological activity of a series of novel 4,5-dihydro-4-oxo-3H-imidazo[4,5-c]pyridine derivatives. J.Med.Chem. 37 1632 PMID: 8201597
Mederski et al (1995) 4,5-Dihydro-4-oxo-3H-imidazo[4,5-c]pyridines: potent arylacetic acid-derived AT1 antagonists with improved affinity for the AT2 receptor. Bioorg.Med.Chem.Lett. 5 2665
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Keywords: EMD 66684, EMD 66684 supplier, Potent, selective, non-peptide, AT1, antagonists, Receptors, Angiotensin, EMD66684, 1849, Tocris Bioscience
Citations for EMD 66684
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Literature in this Area
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