Urapidil
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| AHFS/Drugs.com | International Drug Names | 
| Routes of administration  | Oral | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.047.377 | 
| Chemical and physical data | |
| Formula | C20H29N5O3 | 
| Molar mass | 387.484 g·mol−1 | 
| 3D model (JSmol) | |
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Urapidil is a sympatholytic antihypertensive drug. It acts as an α1-adrenoceptor antagonist and as an 5-HT1A receptor agonist. Although an initial report suggested that urapidil was also an α2-adrenoceptor agonist, this was not substantiated in later studies that demonstrated it was devoid of agonist actions in the dog saphenous vein and the guinea-pig ileum. Unlike some other α1-adrenoceptor antagonists, urapidil does not elicit reflex tachycardia, and this may be related to its weak β1-adrenoceptor antagonist activity, as well as its effect on cardiac vagal drive. Urapidil is currently not approved by the U.S. Food and Drug Administration, but it is available in Europe.