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Comparison

AOD-9604 vs Bromantane

Side-by-side of AOD-9604 and Bromantane. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

AOD-9604

  • Modified 16-amino-acid synthetic fragment of human growth hormone (residues 176-191)
  • Preclinical models show lipolytic activity in adipose tissue without GH-axis growth effects
  • Phase 2 obesity trial (Heffernan 2001) showed no significant weight-loss difference versus placebo
  • Anecdotal protocols use 250 to 500 mcg subcutaneously daily on an empty stomach
  • No FDA approval; the obesity drug development program was discontinued in 2007
  • Granted GRAS status in some jurisdictions for compounded use; not validated for fat loss in humans

Bromantane

  • Russian RCT base (Voznesenskaya 2010, n=728) supports 50 mg daily for asthenia and fatigue over 4 weeks
  • Atypical actogenic mechanism: induces tyrosine hydroxylase rather than direct monoamine release
  • Subjective profile is anxiolytic plus mildly motivating, distinct from classical stimulants
  • Long half-life of around 11 hours supports once-daily morning dosing
  • WADA-banned since 1996; relevant for tested athletes
  • Western evidence base is thin; most published trials are Russian-language and not independently replicated

Side-by-side

Attribute AOD-9604 Bromantane
Category peptide nootropic
Also known as hGH fragment 176-191, Human Growth Hormone Fragment 176-191 Ladasten, ADK-709, N-(4-bromophenyl)adamantan-2-amine
Half-life (hr) 0.5 11
Typical dose (mg) 0.3 75
Dosing frequency daily daily, morning
Routes subcutaneous oral
Onset (hr) 1 3
Peak (hr) 2 168
Molecular weight 1815.17 280.21
Molecular formula C78H125N23O23S2 C16H20BrN
Mechanism Modified C-terminal fragment of human growth hormone proposed to stimulate beta-3 adrenergic receptor signaling in adipocytes, increasing lipolysis and fatty-acid oxidation without engaging the GH receptor or activating IGF-1. Indirect dopaminergic and serotonergic actogenic activity via induction of tyrosine hydroxylase and selective increases in serotonin synthesis in hippocampus and hypothalamus.
Legal status Not FDA approved; research-use-only grey market in most jurisdictions Approved in Russia (Ladasten); unscheduled and unapproved in US, EU, UK
WADA status unknown banned
DEA / Rx Not FDA approved; not scheduled; research-chemical status Not scheduled in the US
Pregnancy Insufficient data; not recommended Not recommended
CAS 221231-10-3 87913-26-6
PubChem CID 71300630 9576456
Wikidata Q4654106 Q4093816

Safety profile

AOD-9604

Common side effects

  • injection-site reactions
  • transient mild headache (anecdotal)
  • minimal in clinical trials

Contraindications

  • pregnancy
  • lactation
  • no established human safety profile for chronic use

Interactions

  • beta-blockers: theoretical antagonism of beta-3 adrenergic lipolytic signaling(minor)

Bromantane

Common side effects

  • mild GI upset
  • headache
  • skin rash
  • occasional insomnia at higher doses

Contraindications

  • pregnancy
  • lactation
  • severe hepatic impairment
  • severe renal impairment
  • pediatric use

Interactions

  • MAOIs: theoretical additive dopaminergic and serotonergic activity(major)
  • levodopa and dopamine agonists: additive dopaminergic activity(moderate)
  • SSRIs and other serotonergic drugs: theoretical serotonergic additivity(moderate)
  • classical stimulants: theoretical additive activity, undocumented(moderate)

Which Should You Take?

Bromantane comes out ahead for most readers on the criteria we weight: 3 catalogued goals, controlled substance, oral dosing, with a Tier-C outcome catalogued. AOD-9604 is the right call when one of the conditionals below applies.

  • If your priority is fat loss, pick AOD-9604.
  • If your priority is body composition, pick AOD-9604.
  • If your priority is focus or working memory, pick Bromantane.
  • If your priority is fatigue resistance, pick Bromantane.

Edge case: If you cannot self-administer injections, Bromantane is the only oral option in this pair.

Default choice: Bromantane. Wider use case, and broader goal coverage. Reach for AOD-9604 only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between AOD-9604 and Bromantane?

AOD-9604 and Bromantane differ in category (peptide vs nootropic), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, AOD-9604 or Bromantane?

AOD-9604 half-life is 0.5 hours; Bromantane half-life is 11 hours.

Can you stack AOD-9604 with Bromantane?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

Go deeper