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Adamax

peptide · headlineResearch use only

Upregulates BDNF (brain-derived neurotrophic factor) expression in hippocampus and cortex

Overview

Adamax is a next-generation nootropic peptide and enhanced Semax analog featuring N-terminal acetylation and C-terminal adamantane modification for superior stability and blood-brain barrier penetration. It upregulates BDNF, enhances TrkB receptor sensitivity, modulates monoamines, and provides neuroprotection against oxidative stress and excitotoxicity.

How it works

  • Upregulates BDNF (brain-derived neurotrophic factor) expression in hippocampus and cortex
  • Enhances TrkB receptor sensitivity for improved neurotrophin signaling
  • Modulates monoamine neurotransmitter levels (dopamine, norepinephrine, serotonin)
  • Activates neuroprotective pathways reducing oxidative stress
  • Stabilizes microtubules through ADNP-derived mechanisms
  • Reduces excitotoxicity through neuromodulation

Dosing

Standard dose: 300-1000 mcg daily via intranasal spray or injection, administered daily with gradual titration.

Intranasal Spray500 mcg standardrange 3001000 mcg· daily
Subcutaneous Injection300 mcg standardrange 100500 mcg· daily

Caution: Start with the lowest recommended dose (300 mcg) to assess individual tolerance. Adamax can cause insomnia and anxiety in sensitive individuals; avoid dosing after 2 PM. Do not exceed 1000 mcg daily without medical supervision. Limited long-term human safety data exists.

Cycling

  • Can be used daily without cycling; however, some users rotate 5 days on / 2 days off to prevent tolerance development. Nasal mucosa health should be monitored during extended use.
  • Daily administration recommended without cycling for cognitive support. Some protocols suggest 3 weeks on / 1 week off for tolerance management.

Side effects

Common
  • Nasal irritation or congestion (intranasal administration)
  • Mild headache (usually transient)
  • Slight insomnia if dosed late in the day
Warnings
  • May cause anxiety or overstimulation at high doses
  • Risk of sleep disruption if taken in evening
  • Limited long-term human safety data available
Long Term
  • Long-term safety profile unknown in humans
  • Extrapolated from Semax clinical experience only

Stacking & combinations

With

Semax

Benefit

Additive BDNF and neuroprotective effects; Adamax potentially superior bioavailability

With

P21

Benefit

Combined cognitive enhancement and neuroprotection; complementary mechanisms of action

With

BPC-157

Benefit

Synergistic neuroprotection and tissue repair; enhanced recovery from neurological stress

Lifestyle support

Diet

Nutrient-dense diet rich in antioxidants. Adequate hydration.

Sleep

Adequate sleep (7–9 hours). Stable circadian rhythm. Stress management supports neuroprotective benefits.

Timing

Avoid late-day dosing to prevent sleep disruption.

Exercise

Regular aerobic exercise.

Reconstitution calculator

Subcutaneous Injection
Draw to6 units

= 0.06 mL on a U-100 insulin syringe

Concentration5 mg/mL
Doses / vial33

Assumes a U-100 insulin syringe (100 units = 1 mL). This is a preparation aid, not a protocol — dose and route are the prescriber's decision. Refrigerate at 2-8°C (35.6-46.4°F) after reconstitution with bacteriostatic water. Use within 2-4 weeks. Discard if solution becomes discolored.

Chemistry & PK

Sequence
Ac-SEMAX-Adamantyl
Half Life
2-4 hours (intranasal); 6-8 hours (subcutaneous)
Degradation
Enzymatic degradation by serum proteases; slower degradation than native Semax due to adamantane modification.
Molecular Weight
1568
Molecular Formula
C72H111N21O13
Tissue Specificity
CNS-specific distribution with high hippocampal, cortical, and striatal accumulation.

Bioavailability

Oral
Not available orally - peptide degradation in GI tract prevents absorption.
Subq
High bioavailability via subcutaneous injection, bypasses first-pass metabolism and blood-brain barrier restrictions via receptor-mediated transport.

Storage & handling

Lyophilized

Store at -20°C (-4°F) in a cool, dark place away from light and moisture. Stability of 2+ years when properly stored.

Reconstituted

Refrigerate at 2-8°C (35.6-46.4°F) after reconstitution with bacteriostatic water. Use within 2-4 weeks. Discard if solution becomes discolored.

Used for

No condition evidence rows yet.

Legal / compounding

Research use only
EU
Not Approved - Research Chemical
FDA
Not Approved - Research Chemical
Canada
Not Approved - Research Chemical
Australia
Not Approved - Research Chemical

Legal status is a hard gate: non-compoundable or delisted agents cannot be filled and are blocked from protocol export. Keep 503A status current.