ADRA1D receptor antagonist 1 is a potent, selective and orally active α 1D adrenoceptor antagonist, with a K i of 1.6 nM In Vitro ADRA1D receptor antagonist 1 shows low hERG inhibition. ADRA1D receptor antagonist 1 exhibits higher selectivity for α1D-AR over α1A- and α1B-ARs. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo ADRA1D receptor antagonist 1 (4.4 µg/kg; i.v.) dose-dependently decreases the non-voiding bladder contractions during the urinary storage phase in rats with BOO . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Rat with bladder outlet obstruction (BOO) Dosage: 4.4 µg/kg Administration: Intravenous injection Result: Dose-dependently decreased the non-voiding bladder contractions during urinary storage phase in rats with BOO. IC50& Target:Ki: 1.6 nM (α 1D adrenoceptor)
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ADRA1D receptor antagonist 1
CAS number:1191908-14-1(DMSO) molecular formula:C15H14Cl2N4O
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| Chinese alias | ADRA1D 受体拮抗剂 1 | ||
| English alias | - | ||
| CAS number | 1191908-14-1(DMSO) | molecular formula | C15H14Cl2N4O |
| molecular weight | 337.20 g/mol | Exact mass | 10mM in DMSO |
| PSA | - | logp | - |
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