| Identification | Back Directory | [Name]
6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide | [CAS]
67287-54-1 | [Synonyms]
SKF 82526 HydrobroMide
FenoldopaM HydrobroMide
(±)-SKF 82526 HydrobroMide
FENOLDOPAM MONOHYDROBROMIDE
6-Chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol HydrobroMide
6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide
6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1h-3-benzazepine-7,8-diol monohydrobromide | [EINECS(EC#)]
266-634-7 | [Molecular Formula]
C16H16ClNO3.BrH | [MDL Number]
MFCD27977921 | [MOL File]
67287-54-1.mol | [Molecular Weight]
386.67 |
| Hazard Information | Back Directory | [Uses]
Dopamine D1-receptor agonist. Antihypertensive. | [Biochem/physiol Actions]
Fenoldopam is a selective dopamine agonist that is being considered for the parenteral treatment of systemic hypertension. In both an oral and parenteral form, fenoldopam causes peripheral vasodilation by stimulating dopamine-1 adrenergic receptors. Intravenous fenoldopam may provide advantages over sodium nitroprusside because it can induce both a diuresis and natriuresis, is not light sensitive, and is not associated with cyanide toxicity. There is no evidence for rebound hypertension after discontinuation of fenoldopam infusion. |
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