Xamoterol hemifumarate [73210-73-8]

AdipoGen Life Sciences

Xamoterol hemifumarate [73210-73-8]

10

73210-73-8

Research Use Only

>98%

Warning

C16H25N3O5 1/2C4H4O4

339.4 . 58.0

A phenoxypropanolamine derivative that is a selective partial agonist of beta1-adrenergic receptors (beta1-ARs) (pA2 values are 7.4 - 7.8 and 5.2 - 6.2 at beta1- and beta2-adrenoceptors, respectively), and has shown to improve systolic and diastolic function in studies with heart failure patients. It modulates the sympathetic control of the heart but has no agonist action on beta2-adrenoceptors. Xamoterol has an EC50 value of 80nM for the generation of cyclic AMP (cAMP) in neonatal rat cardiomyocyte cultures. It increases spontaneous contraction of isolated rat right atria (EC50 = 4.67nM). In vivo, xamoterol increases heart rate, an effect that is reversed by the selective beta1-AR antagonist betaxolol but not the selective beta2-AR antagonist ICI 118551. - Chemical. CAS: 73210-73-8. Formula: C16H25N3O5 1/2C4H4O4. MW: 339.4 . 58.0. Soluble in water (20mg/ml) or DMSO (40mg/ml). A phenoxypropanolamine derivative that is a selective partial agonist of beta1-adrenergic receptors (beta1-ARs) (pA2 values are 7.4 - 7.8 and 5.2 - 6.2 at beta1- and beta2-adrenoceptors, respectively), and has shown to improve systolic and diastolic function in studies with heart failure patients. It modulates the sympathetic control of the heart but has no agonist action on beta2-adrenoceptors. Xamoterol has an EC50 value of 80nM for the generation of cyclic AMP (cAMP) in neonatal rat cardiomyocyte cultures. It increases spontaneous contraction of isolated rat right atria (EC50 = 4.67nM). In vivo, xamoterol increases heart rate, an effect that is reversed by the selective beta1-AR antagonist betaxolol but not the selective beta2-AR antagonist ICI 118551.

O=C(NCC[NH2+]CC(O)COC1=CC=C(O)C=C1)N2CCOCC2.[O-]C(/C=C/C(O)=O)=O

-20°C,2°C to 8°C

12352200