Side-by-side · Research reference
AdipotidevsSelank
Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.
AAnimal-StrongHUMAN-REVIEWED15/49 cited
BHuman-MechanisticAUTO-DRAFTED11/40 cited
Adipotide
Pro-apoptotic Vascular-Targeting Peptide · Preclinical Only
IV · Systemic · Preclinical Protocols OnlyHossen 2013
Selank
Anxiolytic + Cognitive · Russian Pharma
Intranasal · 2–3×/day during stress / cognitive demand
01Mechanism of Action
Parameter
Adipotide
Selank
Primary target
Prohibitin-1 (PHB1) on adipose vasculature endotheliumHossen 2013
Monoamine system (serotonin / GABA modulation) + immunomodulation via tuftsin domainZaderej 2014
Pathway
CKGGRAKDC domain binds PHB1 → Peptide internalisation → D(KLAKLAK)₂ mitochondrial membrane disruption
Tuftsin-derived immune signaling + CNS monoamine modulation → reduced anxiety + improved mood / cognitionMedvedev 2007
Downstream effect
Endothelial apoptosis → Adipose vascular collapse → Adipocyte involution → Weight loss
Anxiolytic + cognitive enhancement; immunomodulation via increased IL-6 + IFN-γMedvedev 2007Zaderej 2014
Feedback intact?
N/A — Direct apoptotic mechanism, non-hormonal
No GABA-receptor binding; no dependence reportedMedvedev 2007
Origin
Synthetic bioconjugate: PHB1-targeting homing peptide + pro-apoptotic KLA sequence
Synthetic 7-AA peptide derived from human tuftsin (immune-system tetrapeptide)Zaderej 2014
Antibody development
—
—
02Dosage Protocols
Parameter
Adipotide
Selank
Animal dose (mouse)
Low dose (not specified in abstract)Hossen 2013
Systemic injection in diet-induced obesity (DIO) models.Hossen 2013
—
Route
Intravenous (systemic injection)
—
Frequency
Not specified in available data
2–3× per day during stress
Evidence basis
Preclinical animal models only
Human-mechanistic + Russian clinical trialsMedvedev 2007
Human data
None — no clinical trials reported
—
Lower / starter dose
—
75 mcg / dose
Duration
—
10–14 day cycles, repeated as needed
Reconstitution
—
Pre-formulated nasal spray (commercial); research vial: bacteriostatic water
Timing
—
Morning + early afternoon preferred
Half-life
—
Short (minutes plasma); CNS effect lasts ~3 hr
03Metabolic / Fat Loss Evidence
Parameter
Adipotide
Selank
Primary fat target
White adipose tissue (all depots)
—
Body weight reduction
Significant reduction in DIO miceHossen 2013
Absolute values not provided in abstract.
—
Leptin levels
Significant decrease
Parallel to adipose mass reduction.
—
Effect on adipocytes
Antiobesity effect on dysfunctional adipose cells (adipocytes + macrophages)Hossen 2013
—
Ectopic fat
Reduction in ectopic fat depositionHossen 2013
Marker of dysfunctional adipose tissue / metabolic syndrome.
—
Species tested
Obese rhesus monkeys, DIO mice
—
Human translation
Unknown — no clinical trials
—
04Side Effects & Safety
Parameter
Adipotide
Selank
Safety profile
Unknown — preclinical data only
—
Vascular selectivity
Targets adipose vasculature; off-target vascular effects unknown
—
Apoptotic mechanism risk
Pro-apoptotic payload may affect unintended tissues if selectivity incomplete
—
Kidney / liver toxicity
Not reported in available data
—
Immunogenicity
Not assessed in available data
—
Nasal irritation
—
Mild burning or congestion (transient)
Cognitive impairment
—
None — opposite effect (enhancement)
Allergic reaction
—
Rare hypersensitivity
Long-term safety
—
Limited Western RCT data
Pregnancy / OB
—
Avoid — insufficient data
Absolute Contraindications
Adipotide
- ·Human use — not approved, no clinical safety data
Selank
- ·Pregnancy / breastfeeding
- ·Hypersensitivity to peptide
Relative Contraindications
Adipotide
- ·Any condition requiring intact adipose-tissue vascularisation
Selank
- ·Active autoimmune disease (theoretical via immunomodulation)
05Administration Protocol
Parameter
Adipotide
Selank
1. Route
Intravenous injection (systemic) in preclinical models. No human protocols exist.
Pre-formulated nasal spray (commercial) or research vial reconstituted with bacteriostatic water.
2. Formulation
Bioconjugate peptide. May also be encapsulated in nanoparticles (prohibitin-targeted nanoparticle formulation, KLA-PTNP, showed superior efficacy vs. free bioconjugate in mice).Hossen 2013
Intranasal — 1–3 sprays per nostril per dose. Tilt head slightly back.
3. Preclinical dosing
Low-dose systemic injection (exact dosing not specified in available abstract). Frequency and duration not detailed.Hossen 2013
Morning + early afternoon for cognitive demand; PRN for acute anxiety.
4. Storage
Not specified — likely requires peptide-grade lyophilised storage and reconstitution.
Refrigerate after reconstitution; ≤30 days. Light-protected.
5. Caveat
—
Avoid co-administration with strong sedatives or other anxiolytics initially.