Skip to content
Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

AdamaxvsChonluten

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AAnimal-StrongHUMAN-REVIEWED20/47 cited
BAnimal-MechanisticHUMAN-REVIEWED8/38 cited
Adamax
ACTH(4-10) Analogue · Russian Nootropic
1.4×BDNF protein ↑Dolotov 2006
BDNF mRNA (exon III)Dolotov 2006
1.6×trkB phosphorylationDolotov 2006
Intranasal · Research Use Only
Chonluten
Khavinson Bioregulator · Bronchial Mucosa
BronchialTarget tissue
In vitroEvidence tierAvolio 2022
THP-1Model systemAvolio 2022
Oral · Sublingual · Per Protocol

01Mechanism of Action

Parameter
Adamax
Chonluten
Primary target
Melanocortin receptors (MC-Rs) in hippocampus and cortex
Bronchial epithelial cells and respiratory mucosa tissue complexes
Pathway
ACTH(4-10) fragment → MC-R binding → BDNF/trkB upregulation → neurotrophic signaling
Bioregulatory peptide interaction → modulation of proliferative and inflammatory pathways in monocyte/macrophage populationsAvolio 2022
Downstream effect
Increased hippocampal BDNF expression, trkB tyrosine phosphorylation, enhanced conditioned avoidance learning, circadian rhythm normalizationDolotov 2006Arushanian 2008
Regulation of proliferative activity and inflammatory mediator production in respiratory-associated immune cellsAvolio 2022
Feedback intact?
Non-endocrine — devoid of adrenal axis effectsvan 1978
Origin
ACTH(4-10) fragment with modified amino acid sequence at positions 8, 9, 10Teter 2001
Khavinson bioregulator peptide complex derived from bronchial mucosa tissue extract methodology
Antibody development

02Dosage Protocols

Parameter
Adamax
Chonluten
Animal dose (rat)
50 mcg/kg body weightDolotov 2006
Single intranasal application; produced maximal BDNF response.
Route
Oral (capsule) or sublingual
Sublingual claimed for enhanced bioavailability; not validated.
Frequency
Single-dose or chronic administration protocols
Chronic dosing normalized circadian rhythms; single-dose produced acute BDNF elevation.
Once or twice daily
Human dose (exploratory)
Not established — limited human data
ACTH(4-10) and analogs dosed 30–60 mcg intranasally in early human studies.
Evidence basis
Animal (rodent, rabbit) studies; minimal human RCT data
In vitro mechanistic
Timing
Variable — chronic administration for circadian effects
Typical protocol dose
10–20 mg / day
Russian bioregulator tradition dosing; not standardized in Western literature.
Duration
10–30 days per cycle
Traditional Khavinson protocol; cyclic administration common.
Clinical validation
None (PubMed indexed)

04Side Effects & Safety

Parameter
Adamax
Chonluten
Cardiovascular effects
ACTH(4-10) fragments may have pressor and cardioaccelerator actions at high dosesGruber 1984
Effects attenuated by α/β-receptor antagonists; observed at 30–1000 nmol/kg IV in rats.
Natriuretic effect
ACTH(4-10) exhibited natriuretic activity at lower doses (7 nmol/kg)Gruber 1984
Behavioral suppression
Suppression of aggression, reduced orientation-cognition reactions in rabbitsTeter 2001
May reflect anxiolytic or stress-dampening profile.
Long-term safety
Unknown — chronic human safety data lacking
Documented adverse events
No published safety data in PubMed-indexed literature
Theoretical risks
Peptide hypersensitivity, GI intolerance (uncharacterized)
Drug interactions
Unknown — no pharmacokinetic studies available
Pregnancy / lactation
No data — avoid
Absolute Contraindications
Adamax
  • ·Pregnancy and lactation (precautionary; no data)
  • ·Active cardiovascular instability (due to potential pressor effects)
Chonluten
  • ·Known hypersensitivity to peptide components
Relative Contraindications
Adamax
  • ·Hypertension (monitor BP if using higher doses)
  • ·Renal impairment (natriuretic effects may alter electrolyte balance)
Chonluten
  • ·Pregnancy and lactation (insufficient data)
  • ·Active malignancy (theoretical bioregulator concern)

05Administration Protocol

Parameter
Adamax
Chonluten
1. Reconstitution (if lyophilised)
Add sterile water or bacteriostatic water to lyophilised vial per manufacturer guidance. Roll gently — do not shake. Ensure clarity before use.
Typically supplied as capsules or sublingual tablets. No reconstitution required. Store in cool, dry place away from light.
2. Route
Intranasal administration is the primary route in animal and exploratory human studies. Delivered via nasal spray or dropper to ensure mucosal absorption.Dolotov 2006Smolnik 2000
Swallow capsule with water, 20–30 minutes before meals or as directed. Traditional Khavinson protocol emphasizes empty stomach for absorption.
3. Timing
Variable. Single-dose protocols for acute cognitive tasks; chronic daily dosing for circadian rhythm normalization and sustained neuroprotection.
Place tablet under tongue, allow dissolution for 1–2 minutes. Avoid swallowing immediately. Claimed to bypass first-pass metabolism.
4. Storage
Lyophilised: room temperature, light-protected. Reconstituted: refrigerate 2–8 °C, use within manufacturer-specified timeframe.
Morning dose preferred; may split into twice-daily if higher dose used. Consistency emphasized in bioregulator protocols.
5. Cycle protocol
10–30 day cycles common in Russian tradition. Rest period of 1–3 months between cycles often recommended, though no published evidence for this approach.

06Stack Synergy

Adamax
+ Semax
Moderate
View Semax

Both Adamax and Semax are ACTH(4-10)-derived nootropics acting via melanocortin receptors and BDNF upregulation. Adamax has distinct amino acid modifications at positions 8-10, potentially offering complementary receptor binding profiles or metabolic stability. Stacking may amplify neurotrophic signaling and cognitive enhancement, though direct synergy studies are absent. Theoretical multi-pathway benefit.

Adamax
Research dose intranasal
Semax
300–600 mcg intranasal
Frequency
Once daily, morning or pre-cognitive task
Primary benefit
Enhanced BDNF upregulation, cognitive performance, neuroprotection
Chonluten
— no documented stacks