COMPOUNDS / NOOTROPIC / LADASTEN
NOOTROPIC

LADASTEN

LOW RISK
BEST FOR:Energy●●●●●●●○○○7/10
LADASTEN · BROMANTANE · BROMANTAN · ADK-709 · N-(2-ADAMANTYL)-N-(PARA-BROMOPHENYL)-AMINE · LAVADASTEN
NootropicStimulantAnxiolyticSoviet / RussianAdamantaneAnti-asthenic

Russian adamantane-derived atypical stimulant with anxiolytic properties, used for asthenic disorders and neurasthenia.

ROUTE / DOSAGE
LOW10-50mg
STANDARD50-100mg
HIGH100-200mg
Note: Take in the morning to avoid insomnia; bioavailability ~42%
CYCLE
Daily use acceptable for therapeutic courses of 2-4 weeks no standard cycling protocol
BIOAVAILABILITY
~42% oral
ACTIVE DURATION
8-12h (subjective)
STORAGE
Room temperature dry away from light
DURATION BREAKDOWN
Total8-12 hours
Onset30-60 min
Come up1-2 hours
Peak2-4 hours
Offset3-5 hours
After effects4-8 hours
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Increased energy and alertness
Reduced anxiety
Improved motivation
Enhanced cognitive performance
Mild mood elevation
Reduced fatigue
Anti-inflammatory action
§ 02 — RISKS
Insomnia if taken late in the day
Potential overstimulation at high doses
Limited long-term safety data outside Russian clinical use
WADA-prohibited substance in competitive sports
Unknown safety in pregnancy and lactation
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Ladasten was developed in Russia as an antiasthenic drug combining psychostimulant and anxiolytic effects, an unusual profile for a stimulant. A pilot clinical trial demonstrated efficacy in patients with psychogenic asthenic disorder, with predominant stimulant action and good tolerability. Animal studies show it differentially regulates tyrosine hydroxylase and dopamine content across brain regions and reinforces hippocampal long-term potentiation. It also shows anti-inflammatory effects superior to imipramine in reducing TNF-α and IL-6 in an LPS-induced depression model. However, clinical evidence is limited primarily to Russian trials, and no large-scale Western randomized controlled trials have been published.

§ 06 — SOURCES
[1]
PubMed PMID 17854844 - Effects of ladasten on dopaminergic neurotransmission and hippocampal synaptic plasticity
pubmed.ncbi.nlm.nih.gov ↗
[2]
PubMed PMID 16995430 - Pilot clinical trial of ladasten
pubmed.ncbi.nlm.nih.gov ↗
[3]
PubMed PMID 22803040 - Effect of ladasten on cytokine markers and behavior in depression-like syndrome
pubmed.ncbi.nlm.nih.gov ↗
[4]
PubMed PMID 24771370 - Correcting effect of ladasten on T lymphocyte subpopulations
pubmed.ncbi.nlm.nih.gov ↗
[5]
PubMed PMID 22834121 - Ladasten versus placebo in neurasthenia patients with different EEG types
pubmed.ncbi.nlm.nih.gov ↗
[6]
PubMed PMID 15999825 - Effect of ladasten on gene expression in rat brain
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 16027847 - Psychotropic effects of sidnocarb and ladasten in mice
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 21165444 - Proteomic analysis of ladasten target proteins in rat brain
pubmed.ncbi.nlm.nih.gov ↗
[9]
PsychonautWiki - Bromantane
psychonautwiki.org ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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