Ro 363 hydrochloride, an effective inotropic stimulant, is a potent and highly selective β1-adrenoceptor agonist. Ro 363 hydrochloride is a cardiovascular modulator that reduces diastolic blood pressure and pronounces increases in myocardial contractility . In Vitro Isolated perfused heart preparations from guinea-pigs developed arrhythmic contractions following the administration of Ro 363 in doses producing 70-100% of its maximal chronotropic responses. In spontaneously contracted tracheal preparations from the guinea-pig, RO 363 is a full agonist and is approximately half as potent as (-)-Isoprenaline. These effects of RO 363 are due to the activation of a population of β1-receptors in the tissue since RO 363 and (-)-Isoprenaline have the same relative potencies in trachea, cardiac and ileal preparations. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo In chloralose-anaesthetized cats, Ro 363, when compared to epinephrine (adrenaline), is essentially devoid of arrhythmogenic activity in animals in which cardiac sensitization is induced by U-0882 or halothane . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid
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Ro 363 hydrochloride
CAS number:250580-70-2 molecular formula:C19H26ClNO6
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| Chinese alias | Ro363盐酸盐 | ||
| English alias | - | ||
| CAS number | 250580-70-2 | molecular formula | C19H26ClNO6 |
| molecular weight | 399.87 g/mol | Exact mass | ≥95% |
| PSA | - | logp | - |
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