Acts as a cofactor for sirtuins (SIRT1–7) and PARP enzymes — the proteins that repair DNA damage and regulate gene expression. When NAD+ levels drop, these enzymes stall, accelerating cellular aging across every organ system.

Anyone over 35 experiencing fatigue, brain fog, or slow recovery. Widely used in longevity protocols, anti-aging clinics ($500–1,000/session IV), and addiction recovery programs.

Activates the AMPK pathway — the same cellular energy sensor triggered by exercise and caloric restriction. Signals cells to shift from glucose to fat oxidation, improving metabolic flexibility and reducing adipose tissue accumulation.

Those targeting fat loss, metabolic health, or longevity. Particularly effective for individuals with insulin resistance, elevated blood sugar, or sluggish metabolism. Also used in aging research for its lifespan-extending properties.

CJC-1295 (no DAC) stimulates GHRH receptors in the pituitary — triggering GH synthesis. Ipamorelin activates ghrelin receptors (GHS-R1a) — a completely separate pathway. Used together, they produce a compounded GH pulse 2–5x greater than either alone, without affecting cortisol or prolactin.

Anyone wanting to improve body composition, sleep quality, or recovery speed. Especially effective for those over 30 experiencing GH decline. Also popular for anti-aging and muscle preservation during fat loss phases.

BPC-157 upregulates VEGFR2 receptors to accelerate angiogenesis and tissue repair. TB-500 (Thymosin Beta-4) mobilizes stem cells and reduces fibrin formation in damaged tissue. GHK-Cu activates the SP1 transcription factor, resetting over 4,000 genes associated with youthful tissue function.

Active injuries, chronic joint pain, gut inflammation, post-surgery recovery, and skin aging. One of the most versatile compounds on this menu — effective for nearly everyone with a recovery or aesthetic goal.

Binds melanocortin receptors and rapidly upregulates BDNF and NGF (Nerve Growth Factor) in the hippocampus and prefrontal cortex. Also modulates dopamine and serotonin neurotransmission, producing cognitive enhancement alongside mood stabilization.

High-output cognitive work, studying, creative projects, or anyone managing brain fog, low motivation, or mild depression. Also used in clinical settings for neuroprotection and stroke recovery.

Inhibits enkephalin-degrading enzymes (enkephalinase), extending the half-life of endogenous enkephalins in circulation. Simultaneously modulates GABAergic and serotonin systems to produce anxiolytic effects without receptor downregulation — meaning no tolerance development over time.

Anxiety, chronic stress, social performance, or sleep quality improvement. Also effective as a complement to Semax — Semax drives focus and motivation while Selank smooths the anxious edge that high-output work can create. Known as the "Russian duo."

GLP-1 activation suppresses appetite centrally and slows gastric emptying. GIP activation reduces adipogenesis and improves insulin signaling in fat tissue. Glucagon receptor activation increases hepatic fat oxidation and raises basal metabolic rate. All three work simultaneously for unmatched fat loss efficacy.

Anyone targeting significant fat loss — especially visceral and abdominal fat. Superior to GLP-1 monotherapy for individuals who have plateaued on semaglutide or tirzepatide. Also improves metabolic markers including blood sugar and triglycerides.

Activates the SP1 transcription factor which controls over 31 genes related to collagen synthesis, anti-inflammatory response, and tissue remodeling. Also activates TGF-β signaling and promotes VEGF (angiogenesis), accelerating wound healing and tissue renewal at the cellular level.

Skin aging, collagen loss, fine lines, UV damage, hair thinning, wound healing, and post-procedure skin recovery. Unlike topical copper peptide serums (which cannot penetrate dermis), injectable GHK-Cu works systemically with dramatically superior bioavailability.

Transported into cells via PepT1 (a di/tripeptide transporter), where it directly inhibits NF-κB nuclear translocation — blocking the central inflammatory cascade at the source. Unlike NSAIDs or corticosteroids, it does not suppress the immune system broadly, targeting inflammation specifically.

Anyone with chronic gut inflammation (IBD, Crohn's, IBS, leaky gut), inflammatory skin conditions, or systemic inflammation. Also effective for post-workout inflammation reduction and general immune modulation without the suppressive side effects of traditional anti-inflammatory drugs.