Fenoldopam: Difference between revisions
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Revision as of 02:39, 9 August 2012
Clinical data | |
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[[Regulation of therapeutic goods |Template:Engvar data]] |
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Pregnancy category |
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Routes of administration | Intravenous |
ATC code | |
Pharmacokinetic data | |
Bioavailability | n/a |
Metabolism | Hepatic (CYP not involved) |
Elimination half-life | 5 minutes |
Excretion | Renal (90%) and fecal (10%) |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C16H16ClNO3 |
Molar mass | 305.756 g/mol |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Fenoldopam is a synthetic compound that acts as a selective peripheral dopamine D1A receptor agonist. Fenoldopam is used as an antihypertensive agent. It lowers blood pressure through arteriolar vasodilation, decreasing afterload and also through specific dopamine receptors along the nephron promoting sodium excretion.
Template:Dopamine agonists Template:Adrenergic and dopaminergic agents
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