library.onepin.app/yohimbine-hcl Peptide Education Library
Education only, not medical advice 21+ Every dose is an example to finalize with a licensed provider

OnePin Peptide Library · Metabolic

Metabolic Alpha-2 Adrenergic Antagonist Controlled substance Prescription drug

Yohimbine HCl

Yohimbine Hydrochloride · Yohimbe

Alpha-2 Adrenergic AntagonistIndole AlkaloidHistorical ED treatment (FDA)Dietary supplement (US)

Yohimbine is an indole alkaloid isolated from the bark of the Pausinystalia yohimbe tree (native to central and western Africa), and also found in several other plants including Rauwolfia species. The hydrochloride salt (yohimbine HCl) is the pharmaceutical-grade form used in research and in products positioned for sexual health and stubborn-fat-loss applications. It is a selective alpha-2 adrenergic receptor antagonist.

Quick Start
Route
Oral
Start low
5mg
Frequency
1-2x daily
Timing
Take fasted for regional fat-loss effect

Standard protocol is 0.1-0.2 mg/kg body weight taken 30-45 minutes before fasted morning cardio. A 70 kg user starts at 5-7 mg, works up to 10-14 mg if tolerated. Do not take with food if the goal is regional fat loss - insulin suppresses the lipolytic effect. Avoid evening dosing; the short half-life is convenient but the CNS stimulation disrupts sleep.

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Quick Start
Conservative start
5mg · Oral · 1-2x daily
Lowest starting point. Hold about a week to assess tolerance before stepping up.
5mg
1-2x daily
Intermediate
Fasted Stubborn Fat Mobilization
5-10 mg · Oral · Daily
human clinical trial · Ostojic 2006 (Res Sports Med)
5-10 mg
Daily
01

How it works

Yohimbine is a selective competitive antagonist at alpha-2 adrenergic receptors (both pre- and postsynaptic). In adipose tissue, alpha-2 receptors are inhibitory autoreceptors - when noradrenaline binds them, lipolysis is dampened. Regional fat depots with high alpha-2-to-beta-receptor ratios (for example the lower abdomen and lower back in men, hips and thighs in women) are relatively resistant to lipolysis because alpha-2 signaling out-competes beta signaling locally. Blocking alpha-2 with yohimbine removes this brake and allows beta-adrenergic lipolysis (endogenous or stimulated by exercise / fasted state) to act on these regional depots.

Yohimbine is a selective competitive antagonist at alpha-2 adrenergic receptors (both pre- and postsynaptic). In adipose tissue, alpha-2 receptors are inhibitory autoreceptors - when noradrenaline binds them, lipolysis is dampened. Regional fat depots with high alpha-2-to-beta-receptor ratios (for example the lower abdomen and lower back in men, hips and thighs in women) are relatively resistant to lipolysis because alpha-2 signaling out-competes beta signaling locally. Blocking alpha-2 with yohimbine removes this brake and allows beta-adrenergic lipolysis (endogenous or stimulated by exercise / fasted state) to act on these regional depots.

At the central nervous system level, alpha-2 antagonism increases noradrenergic tone by disinhibiting presynaptic noradrenaline release - this drives the characteristic anxiety, tachycardia, and elevated blood pressure seen at higher doses. Insulin concurrently suppresses lipolysis (insulin-stimulated adipose tissue has little noradrenergic traffic for yohimbine to augment), which is why fasted-state dosing is standard for fat-loss use.

Yohimbine has a notably short half-life (around 36 minutes to 2 hours depending on individual CYP2D6 metabolism), so effects rise and fall quickly. It also has mild 5-HT and alpha-1 activity at higher concentrations.

02

What to expect

Early
Days 1–7

First dose: CNS activation within 20-45 minutes - alertness, mild anxiety, warmth, slight tremor. Effects peak at 1-2 hours and fade by 3-4 hours in most users.

Mid
Weeks 2–4

Week 1-2: regional fat-loss effect becomes measurable when combined with fasted cardio and caloric deficit. Users often report improved skin tightness in traditionally resistant areas.

Later
Weeks 4–12

Weeks 3-6: continued regional fat loss. Because yohimbine removes a local brake rather than driving lipolysis directly, it works best as an adjunct to an established caloric deficit and exercise plan, not as a standalone fat-loss agent.

03

Evidence

HumanPresent
AnimalPresent
In-vitroPresent
1998Yohimbine for erectile dysfunction: a systematic review and meta-analysis of randomized clinical trials · Ernst E, Pittler MH, Journal of Urology ↗review
1997Double-blind, placebo-controlled safety and efficacy trial with yohimbine hydrochloride in the treatment of nonorganic erectile dysfunction · Vogt HJ, Brandl P, Kockott G, et al, International Journal of Impotence Research ↗peer reviewed
2001Yohimbine in erectile dysfunction: the facts · Tam SW, Worcel M, Wyllie M, International Journal of Impotence Research ↗review
1987Is yohimbine effective in the treatment of organic impotence? Results of a controlled trial · Morales A, Condra M, Owen JA, Surridge DH, Fenemore J, Harris C, Journal of Urology ↗peer reviewed
04

Interactions & stacking

What's safe to combine, and what belongs in a separate pin.

Keep separate

05

Side effects & safety

Commonly reported

  • Anxiety, jitteriness, feeling 'wired'
  • Increased heart rate
  • Sweating
  • Mild hypertension
  • GI upset (nausea, abdominal discomfort)
  • Urinary urgency or frequency
  • Sleep disturbance if dosed later in the day

Less common & notes

  • Panic attacks (especially in susceptible individuals), severe hypertension, chest pain, palpitations, arrhythmia, tremor severe enough to interfere with fine motor tasks, headache, dizziness.
  • Rare but serious: hypertensive crisis (particularly if combined with MAOIs, SSRIs, or other sympathomimetics), myocardial infarction at very high doses or in users with underlying cardiac disease, psychiatric destabilization in bipolar or panic-disorder patients.
  • Priapism has been reported rarely.
06

Pharmacokinetics

Illustrative plasma concentration · 24 h
Half-life
~36 minutes to 2 hours (highly variable by CYP2D6 metabolizer phenotype)
Peak · Tmax
45-60 minutes
Elimination
6-12 hours
Activity
2-4 hours per dose - supports pre-cardio or pre-training use

Storage. Store at controlled room temperature (20-25°C / 68-77°F). Protect from light and moisture. Keep in original container. Shelf life typically 2-3 years from manufacture date. Keep out of reach of children - overdose can produce severe hypertension and anxiety.

07

Regulatory status

Yohimbine HCl historically FDA-approved as Yocon (Palisades Pharmaceuticals) for erectile dysfunction; the brand is largely absent from the US market today. Prescription yohimbine HCl remains available through compounding pharmacies. Yohimbine is also sold as a dietary supplement in the United States at lower potencies. Not a controlled substance. Not prohibited by WADA, though monitored. Banned for sale in some jurisdictions (Canada, Australia) outside of prescription.

Put it to work

Calculate, log & track

Open Yohimbine HCl straight into OnePin with your vial and dose pre-filled, then let it handle the syringe math and remind you before the vial runs out.

Open Yohimbine HCl in the app →

Go deeper

The guide & community

The complete Yohimbine HCl walkthrough, real protocol discussion and coaching live inside the BlessUp community on Skool.

Join the community ↗
Open in app Community