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Acetildenafil

Acetildenafil (a.k.a. Hongdenafil) is an unapproved research chemical often detected as an undeclared adulterant in "herbal" sexual-enhancement supplements. Pharmacologically it shows sub-micromolar PDE-5 inhibition comparable to sildenafil (IC50 ≈ 7.6 nM), with a slightly longer half-life (≈ 3–5 hours) and anecdotal reports of milder facial flushing. Because it is metabolised mainly via CYP3A4, potent inhibitors can greatly increase its plasma concentration. Users report effective erectile support at 10–40 mg; however, some counterfeit tablets contain 80–120 mg, raising the risk of priapism, headache, and hypotension.

Acetildenafil molecular structure
Acetildenafil molecular structure diagram from the DrugsPRO substance library.

Also known as: Hongdenafil

Classification

  • Chemical: Medicine
  • Tag: Not psychoactive
  • Tag: PDE-5-inhibitor
  • Tag: Pyrazolopyrimidinone
  • Tag: Research-Chemical
  • Tag: Supplement

Effects

  • Improved Ability To Achievemaintain Erection
  • Increased Penile Firmness
  • Facialupperbody Flushing
  • Mild Nasal Congestion
  • Headachepressure Behind Eyes
  • Dyspepsia
  • Warmth In Extremities
  • Open Eye Visuals

Routes of Administration

Oral

Dosage

  • Threshold: 5 mg
  • Light: 5 – 15 mg
  • Common: 15 – 40 mg
  • Strong: 40 – 60 mg
  • Heavy: 60 mg +

Duration

  • Onset: 0.5-1 h
  • Peak: 1-2 h
  • Offset: 3-5 h
  • After Effects: 0.1-0.4 h

Sublingual

Dosage

  • Threshold: 2 mg
  • Light: 3 – 10 mg
  • Common: 10 – 25 mg
  • Strong: 25 – 40 mg
  • Heavy: 40 mg +

Duration

  • Onset: 0.17-0.75 h
  • Peak: 1-2 h
  • Offset: 3-5 h
  • After Effects: 0.1-0.4 h

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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Acetildenafil - DrugsPRO anyag útmutató

Acetildenafil: Acetildenafil (a.k.a. Hongdenafil) is an unapproved research chemical often detected as an undeclared adulterant in "herbal" sexual-enhancement supplements. Pharmacologically it shows sub-micromolar PDE-5 inhibition comparable to sildenafil (IC50 ≈ 7.6 nM), with a slightly longer half

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