Name | Xamoterol |
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Synonyms |
XAMOTEROL FUMARATE
N-(2-((2-hydroxy-3-(4-hydroxyphenoxy)propyl)amino)ethyl)-4-morpholinecarboxamide |
Description | Xamoterol is a selective and potent agonist of beta1-adrenergic receptor. Xamoterol has the potential for the research of arrhythmogenesis. Xamoterol has the potential for the investigating the relationship between β1-adrenergic stimulation and IKr[1]. |
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Related Catalog | |
References |
Density | 1.265g/cm3 |
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Boiling Point | 651.4ºC at 760 mmHg |
Molecular Formula | C20H29N3O9 |
Molecular Weight | 455.45900 |
Flash Point | 347.7ºC |
Exact Mass | 455.19000 |
PSA | 177.89000 |
LogP | 0.19480 |
Appearance | solid | white |
Index of Refraction | 1.571 |
Water Solubility | H2O: 10 mg/mL at 60 °C, soluble |
Safety Phrases | 22-24/25 |
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WGK Germany | 3 |
~% 81801-12-9 |
Literature: Barlow; Main; Snow Journal of Medicinal Chemistry, 1981 , vol. 24, # 3 p. 315 - 322 |
~% 81801-12-9 |
Literature: Barlow; Main; Snow Journal of Medicinal Chemistry, 1981 , vol. 24, # 3 p. 315 - 322 |
~% 81801-12-9 |
Literature: Barlow; Main; Snow Journal of Medicinal Chemistry, 1981 , vol. 24, # 3 p. 315 - 322 |
Precursor 2 | |
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DownStream 0 |