What alprostadil is
Synthetic form of prostaglandin E1 (PGE1). While technically a prostaglandin rather than a peptide, included due to clinical relevance alongside peptide therapies. FDA-approved for ED as Caverject (injection, 1995) and MUSE (urethral pellet, 1997). Also approved for neonatal cardiac defects.
Mechanism, in plain English
Binds EP2 and EP4 receptors on penile smooth muscle cells, activating adenylate cyclase and increasing cAMP. This relaxes smooth muscle, dilates arteries, and produces erection. Direct-acting, works regardless of sexual arousal or nerve function. PDE5 inhibitors require intact nerve signaling; alprostadil bypasses that entirely.
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Caverject: 70-80% success rate, including in men who failed PDE5 inhibitors. Erection in 5-20 minutes, lasting 30-60 minutes. MUSE: 43-65% success but non-injectable. Works in neurogenic ED (spinal cord injury, post-prostatectomy). Combination with PDE5 inhibitors shows synergy.
FDA status
FDA-approved. Caverject (1995), MUSE (1997), Prostin VR (neonatal).
Common synonyms
Alprostadil, prostaglandin E1, PGE1, Caverject, MUSE, Edex
Safety and adverse-event landscape
Penile pain (37% injection), prolonged erection/priapism (1-4%, seek medical attention if >4 hours), urethral burning with MUSE. Injection site fibrosis with long-term use.
Frequently asked questions
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