Bromantane

Bromantane

Bromantane

Bromantane

Bromantane (Ladasten / ADK-709 / N-(4-bromophenyl)adamantan-2-amine) is a synthetic polyhedral adamantane derivative classified in Russian literature as an atypical actoprotector and anxiolytic reference standard. Operating through genomic and enzymatic upregulation, Bromantane stimulates the transcriptional expression of Tyrosine Hydroxylase (TH) and aromatic L-amino acid decarboxylase (AAAD), accelerating de novo dopamine and catecholamine biosynthesis in hypothalamic neuronal assays.

$49.00

Quantity Discounted Price
4 - 6 $47.04
7 - 9 $46.06
10 + $45.08

What is Bromantane (Ladasten)?

Bromantane (known chemically as Ladasten, ADK-709, or N-(4-bromophenyl)adamantan-2-amine) is a synthetic adamantane derivative classified as an actoprotector—a unique category of non-depleting metabolic adaptogens engineered to sustain physical and cognitive capacity without increasing oxygen consumption or provoking hyperstimulation.

Unlike conventional central nervous system psychostimulants that function by forcing reverse-transporter monoamine release or competitive reuptake transporter blockade, Bromantane operates through an indirect genomic mechanism. In cellular and neurochemical models, it upregulates the gene transcription and protein expression of Tyrosine Hydroxylase (TH) and aromatic L-amino acid decarboxylase (AAAD) across the striatum, hypothalamus, and ventral tegmental area. Because Tyrosine Hydroxylase represents the rate-limiting enzyme in catecholamine biosynthesis, this transcriptional drive accelerates de novo dopamine and norepinephrine generation while preserving intracellular vesicular stores.

Simultaneously, Bromantane exhibits a distinct anxiolytic profile mediated by the facilitation of central GABAergic transmission and the suppression of GABA transporter clearance mechanisms. This dual catecholaminergic-GABAergic mechanism produces alertness and endurance while maintaining resistance against excitotoxic stress and hyperactive adrenergic cascades.

Batch-verified for high analytical purity and mass calibration at Modern Aminos, Bromantane is offered in two standardized laboratory configurations: pre-measured **25MG dry-fill solid capsules (60 units per bottle)** and a stable **50MG/ML analytical liquid solution (30ML bottle)**. Researchers evaluating catecholaminergic enzyme kinetics, actoprotective bioenergetics, and synaptic neuroplasticity study Bromantane alongside complementary reference standards available on the site, such as Phenylpiracetam Hydrazide, Noopept, Sunifiram, and L-THP.

Chemical and Molecular Data

Compound Name Bromantane (Ladasten / ADK-709)
Available Formats 25MG Dry-Fill Solid Capsules (60 Count) & 50MG/ML Liquid Solution (30ML)
Biological Target Central Nervous System / Tyrosine Hydroxylase (TH) Transcription & GABAergic Modulatory Networks
Chemical Classification Synthetic Adamantane Derivative / Polyhedral Actoprotector
Synonyms / Alt Names Bromantan, Ladasten, ADK-709, N-(2-Adamantyl)-N-(4-bromophenyl)amine, 2-(4-bromoanilino)adamantane
CAS Number 87913-26-6
Chemical Formula C16H20BrN
Molecular Weight 306.24 g/mol
IUPAC Name N-(4-bromophenyl)adamantan-2-amine
InChIKey InChIKey=LWJALJDRFBXHKX-UHFFFAOYSA-N
SMILES Code C1C2CC3CC1CC(C2)C3NC4=CC=C(C=C4)Br

What are the Mechanisms of Action?

The biochemical pathways and cellular targets of Bromantane (Ladasten) in laboratory research include:

  • Tyrosine Hydroxylase (TH) Genomic Transcription: Bromantane induces rapid, long-lasting transcriptional upregulation of the TH and AAAD genes within dopaminergic neurons in the striatum, substantia nigra, and ventral tegmental area. By stimulating the synthesis of the rate-limiting enzyme in catecholamine production, Bromantane accelerates de novo dopamine synthesis without relying on the depletion of pre-existing vesicular stores.
  • Non-Depleting Dopaminergic Neurotransmission: Because it elevates the biosynthetic machinery rather than forcing non-vesicular release or blocking transporter complexes, extracellular dopamine increases in a physiological, stimulus-dependent manner. This avoids dopamine receptor downregulation, tachyphylaxis, and post-stimulatory exhaustion in neuronal culture models.
  • GABAergic Synaptic Facilitation: Bromantane enhances central GABAergic inhibition by strengthening GABA-receptor complex mediation and downregulating GABA transporter activity. This mechanism limits excessive cortical excitation, providing intrinsic anxiolytic and neuroprotective properties alongside catecholaminergic stimulation.
  • Neurotrophin & Anti-Inflammatory Signaling: Preclinical evaluations demonstrate that Bromantane stimulates the expression of neurotrophic factors, including Brain-Derived Neurotrophic Factor (BDNF) and Nerve Growth Factor (NGF), while suppressing pro-inflammatory cytokine expression (IL-6, IL-17, IL-4) in stressed neurocellular environments.

What do Preclinical & Academic Studies Show for Bromantane?

When evaluating published scientific literature and neurochemical monographs for Bromantane (Ladasten):

  • Tyrosine Hydroxylase Upregulation & Dopamine Synthesis (PubMed): Foundational neuropharmacological studies published on PubMed (PMID: 17854844) demonstrate that a single administration of Bromantane produces a significant increase in Tyrosine Hydroxylase mRNA and protein expression across five major brain regions, establishing its genomic mode of action.
  • Actoprotector Pharmacology & Work Capacity (PMC): Comprehensive biomedical reviews archived in PMC (PMC3762282) document the pharmacology of actoprotectors, detailing Bromantane’s unique capacity to enhance physical stamina, cellular bioenergetics, and mental focus without increasing core temperature or oxygen debt.
  • Chemical Profiling & Molecular Verification (PubChem): Official structural characterization maintained on PubChem verifies the molecular mass (306.24 g/mol), polyhedral adamantane core, and analytical identification benchmarks of CAS 87913-26-6.

How does Bromantane compare to other nootropic and neurochemical standards?

In neurochemical, cognitive, and psychostimulatory research, compounds differ substantially in their molecular targets, receptor kinetics, and metabolic outcomes:

Bromantane vs. Phenylpiracetam Hydrazide vs. Noopept vs. Sunifiram

  • Bromantane: Polyhedral adamantane actoprotector. Acts upstream at the genomic level to upregulate Tyrosine Hydroxylase (TH) and catecholamine biosynthesis, paired with GABAergic facilitation for non-depleting endurance and anxiolysis.
  • Phenylpiracetam Hydrazide: Phenylated pyrrolidone hydrazide derivative. Functions as a positive allosteric modulator of AMPA glutamatergic receptors and enhances high-affinity choline uptake (HACU), providing rapid synaptic transmission enhancement.
  • Noopept (GVS-111): Proline-containing dipeptide ester. Operates by modulating central AMPA and NMDA receptor affinities while upregulating hippocampal NGF and BDNF expression to drive long-term neuroplasticity.
  • Sunifiram (DM-235): Piperazine-derived ampakine. Acts as an ultra-potent positive allosteric modulator of AMPA receptors and stimulates glycine-dependent NMDA signaling, activating CaMKII and PKCα phosphorylation cascades at nanomolar concentrations.
Compound / Reference Chemical Structure & Class Primary Mechanistic Target Primary Research Focus
Bromantane Synthetic Adamantane Derivative Upregulates Tyrosine Hydroxylase (TH) transcription & GABA facilitation De novo dopamine synthesis, non-depleting actoprotection, and anxiolytic resilience
Phenylpiracetam Hydrazide Phenylated Pyrrolidone Hydrazide AMPA positive allosteric modulation & high-affinity choline uptake Rapid membrane diffusion, glutamatergic synaptic plasticity, and cholinergic kinetics
Noopept Cycloprolylglycine Dipeptide Ester AMPA/NMDA receptor modulation & hippocampal BDNF/NGF upregulation Synaptogenesis, neurotrophin expression, and memory consolidation modeling
Sunifiram Piperazine Ampakine Derivative AMPA allosteric activation & CaMKII / PKCα phosphorylation Ultra-high-potency glutamatergic long-term potentiation (LTP) and acetylcholine release

Frequently Asked Questions (FAQs)

1. Is Modern Aminos a reliable place to buy Bromantane?

Yes, Modern Aminos is a highly trusted vendor for analytical research chemicals and neurochemical standards. Every batch undergoes strict third-party analytical verification (including HPLC and High-Resolution Mass Spectrometry) to confirm minimum 98%+ active chemical purity, verified molecular weight (306.24 g/mol), exact volumetric or gravimetric fill calibration, and the complete absence of heavy metals or synthesis impurities.

2. What is Bromantane and how is it classified chemically?

Bromantane (Ladasten / ADK-709) is a synthetic adamantane derivative chemically designated as N-(4-bromophenyl)adamantan-2-amine. It belongs to the actoprotector class of compounds, designed to support physical and mental work capacity through genomic and metabolic adaptation.

3. What is the mechanism of action of Bromantane on Tyrosine Hydroxylase?

Bromantane stimulates the gene transcription and protein expression of Tyrosine Hydroxylase (TH), the rate-limiting enzyme in catecholamine synthesis. This genomic upregulation increases cellular L-DOPA and dopamine production without triggering rapid intracellular neurotransmitter depletion.

4. How does Bromantane produce an anxiolytic effect alongside stimulation?

Bromantane facilitates central GABAergic neurotransmission and suppresses GABA transporter expression, strengthening inhibitory tone. This unique dual mechanism offsets dopamine-induced hyperstimulation, providing focused vigilance without anxiety, tremor, or restlessness.

5. What formats does Modern Aminos offer for Bromantane?

Modern Aminos offers Bromantane in two calibrated formats: pre-measured 25MG dry-fill solid capsules (60 count bottle) for gravimetric precision, and a stabilized 50MG/ML analytical liquid solution (30ML bottle) for precise volumetric liquid handling in laboratory assays.

6. How does Bromantane differ from Phenylpiracetam Hydrazide and Noopept?

The research suggests that:

  • Bromantane works upstream on dopamine synthesis via Tyrosine Hydroxylase gene upregulation.
  • Phenylpiracetam Hydrazide acts as an allosteric modulator of AMPA receptors and enhances choline uptake.
  • Noopept stimulates neurotrophin expression (BDNF/NGF) and peptide-mediated synaptic plasticity.

7. How does Modern Aminos verify the chemical purity and concentration of Bromantane?

Modern Aminos utilizes High-Performance Liquid Chromatography (HPLC) to verify active compound purity exceeding 98% and High-Resolution Mass Spectrometry (HRMS) to confirm the exact molecular weight (306.24 g/mol) and adamantane fragmentation pattern prior to batch release.

8. What are the recommended storage parameters for Bromantane products?

Both Bromantane capsule bottles and liquid solution bottles should be stored tightly sealed in a cool, dry environment (15°C to 25°C) protected from direct sunlight, thermal extremes, and atmospheric moisture to preserve solid-phase and carrier solution stability.

Disclaimer: All compounds and research materials provided by Modern Aminos are strictly for laboratory and research professional use only. They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA). These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

The products offered by Modern Aminos are intended strictly for laboratory research purposes only and are sold exclusively to qualified professionals, institutions, and entities. These products are not for human consumption, veterinary use, or any other application involving living organisms, including but not limited to diagnostic, therapeutic, or recreational purposes.

By purchasing this product, you confirm that:

  • You are a qualified professional or entity with the necessary knowledge, training, and facilities to handle chemical reagents safely and appropriately.
  • You will use this product in full compliance with all applicable local, state, and federal laws and regulations.

Prohibited Uses

  • This product is not to be used as an active pharmaceutical ingredient (API) in compounding or manufacturing drugs for human or veterinary use.
  • It is strictly prohibited to use this product for administration to humans or animals under any circumstances.
  • Modern Aminos does not condone or permit the use of its products for the development, testing, or production of illegal substances.

Regulatory Compliance

Modern Aminos does not claim that this product is approved by the U.S. Food and Drug Administration (FDA) for any purpose. The statements regarding this product have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease.

Liability Statement

The buyer assumes full responsibility for ensuring the safe handling, storage, and use of this product. Modern Aminos is not liable for any damages, direct or indirect, resulting from improper handling, storage, or unauthorized use of this product. Furthermore, Modern Aminos reserves the right to refuse sales to any individual or entity suspected of misusing its products.

If you have questions about the safe and lawful use of this product, consult a qualified professional with expertise in laboratory research. By proceeding with this purchase, you agree to these terms and conditions.

0