| Name | N-[5-(4,5-dihydro-1H-imidazol-2-yl)-2-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl]methanesulfonamide,hydrobromide |
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| Description | A-61603 is a selective α1A-adrenergic receptor agonist[1]. A-61603 increases the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro[2]. |
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| Related Catalog | |
| Target |
α1A-adrenergic receptor |
| References |
| Boiling Point | 548.4ºC at 760mmHg |
|---|---|
| Molecular Formula | C14H19N3O3S |
| Molecular Weight | 309.38400 |
| Flash Point | 285.5ºC |
| Exact Mass | 309.11500 |
| PSA | 99.17000 |
| LogP | 2.10350 |
| Vapour Pressure | 1.23E-12mmHg at 25°C |