Human Pharmacology of Urapidil

Research output: Contribution to journalArticlepeer-review

7 Scopus citations


Urapidil is a phenylpiperazine-substituted uracil derivative used in hypertension. It is rapidly absorbed when given by mouth. Peak blood concentrations of the slow release capsule occur 4 to 6 hours after administration. Oral bioavailability is 78% (range 72 to 84%) and distribution half-life and terminal half-life are about 35 minutes and 3 hours, respectively. Plasma clearance is 12 L/h and renal clearance 1.8 L/h. Seventeen percent appears in urine as the parent compound within 24 hours of dosing. There is extensive hepatic metabolism to the parahydroxylated(34% in urine), N-demethylated (4% in urine) and O-demethylated (3% in urine) products. Elimination is not saturable at usual clinical doses. The major action of urapidil is post-synaptic α1adrenergic blockade, with a minor degree of β1-adrenergic blockade and a centrally mediated reduction in sympathetic outflow which has an as yet unidentified basis.

Original languageEnglish (US)
Pages (from-to)34-39
Number of pages6
Issue number6
StatePublished - Jun 1988

ASJC Scopus subject areas

  • Pharmacology (medical)


Dive into the research topics of 'Human Pharmacology of Urapidil'. Together they form a unique fingerprint.

Cite this