Head to head

5-Amino-1MQ vs Tesamorelin

MetabolicGH secretagogue

A comparison decided mostly by evidence: Tesamorelin has been studied in people to a degree the other has not.

Verdict

One has been tested in people; the other has not

If your priority is the compound with the strongest published support, that is Tesamorelin. 5-Amino-1MQ is not therefore worse — it is less examined, which is a different thing — but the gap is the single most defensible difference on this page, and it is the one most comparisons quietly skip.

What you are actually choosing between

These sit in different classes. 5-Amino-1MQ is a metabolic compound; Tesamorelin is a growth hormone secretagogue. They get compared because of where they overlap, not because they are interchangeable.

The overlap is fat loss and metabolic health. On this site's goal weighting — an editorial priority score, not a measure of effect size — 5-Amino-1MQ rates 4/5 for fat loss and Tesamorelin rates 5/5.

The evidence

This is the part that decides most of it. Tesamorelin has an approved label and the randomized trial package behind it — the label is for HIV-associated lipodystrophy, not general fat loss. 5-Amino-1MQ has animal and cell data only, and no controlled human dosing trials — dose figures are extrapolated from vendor and community practice. That gap is the headline, and it is a statement about the literature rather than a promise about you: a compound with trial data can still do nothing for your case, and one without it is unproven rather than disproven.

How they differ in practice

5-Amino-1MQ is taken by mouth; Tesamorelin is a subcutaneous injection. That is the difference most people actually feel: Tesamorelin means reconstituting a vial and injecting; 5-Amino-1MQ does not require either. If needles are the deciding factor, this line settles it before any of the rest matters.

Tesamorelin has a characterized half-life of 36 min; 5-Amino-1MQ does not have one published here at all. That asymmetry is worth more than it looks — it usually tracks how much formal pharmacology has been done on a compound.

Committed time differs: 5-Amino-1MQ runs 12 weeks, Tesamorelin runs 26 weeks.

Risk and difficulty

The contraindication lists are not the same: Tesamorelin flags active malignancy, which 5-Amino-1MQ does not. If any of those describe you they remove a compound from consideration outright, regardless of everything above.

Source notes

What the evidence actually says

Verbatim, so you can check the verdict above against what it was built from.

5-Amino-1MQ

A small-molecule nicotinamide N-methyltransferase (NNMT) inhibitor, not a peptide. Evidence is preclinical: it reduced fat mass in diet-induced obese mice without changing food intake, and there are cell and rodent data on muscle stem cells. There are no published controlled human trials, so every dose figure here is extrapolated from vendor and community practice rather than clinical data — treat the range as low confidence. It is taken orally in capsules: 50-150 mg daily, with 100 mg typical, which in the microgram units used throughout this dataset is 50,000-150,000 mcg (100 mg = 100,000 mcg). It is swallowed as capsules rather than reconstituted, so the reconstitution fields do not apply.

Tesamorelin

The only compound in this class with a real FDA label. Tesamorelin is a stabilised GHRH (1-44) analogue approved as Egrifta to reduce excess visceral abdominal fat in HIV-infected patients with lipodystrophy, supported by two phase 3 randomized placebo-controlled trials over 26 weeks with a 26-week extension. Label dosing is 2 mg subcutaneously once daily (Egrifta and Egrifta SV); the reformulated Egrifta WR is 1.28 mg once daily, which is why the range here starts at 1280 mcg. Approved dosing applies ONLY to that HIV lipodystrophy indication - use for general body composition, and any product bought as a research chemical, is off-label and unapproved. Not studied in and not indicated for weight loss in the general population. Note that the Egrifta label directs administration immediately after reconstitution with the supplied diluent; the 30-day figure here reflects bacteriostatic-water reconstitution of multi-dose vials, which is not a labeled practice.

Side by side

The numbers

5-Amino-1MQ compared with Tesamorelin
Attribute5-Amino-1MQTesamorelin
ClassMetabolicGH secretagogue
RoutesOralSubcutaneous
Dose range50 mg–150 mg (typical 100 mg)1.28 mg–2 mg (typical 2 mg)
FrequencyOnce dailyOnce daily
Half-lifeNot characterized36 min
Cycle length12 weeks26 weeks
ExperienceIntermediateIntermediate
EvidenceAnimal / cell data onlyApproved (FDA/EMA)
Contraindications
  • Pregnant / nursing
  • Under 18
  • Pregnant / nursing
  • Active malignancy
  • Under 18
Side effects
  • Insomnia or restlessness if taken late in the day
  • Mild nausea or stomach upset
  • Headache
  • Jitteriness in sensitive users
  • Injection site erythema, pruritus, pain or bruising, the most common label reaction
  • Arthralgia and peripheral edema
  • Myalgia and paraesthesia or hypoaesthesia
  • Carpal tunnel-type symptoms in the hands
  • Rising IGF-1 and reduced glucose tolerance, so glucose should be monitored
  • Hypersensitivity or rash

Turn a typical dose into a mark on the syringe: Tesamorelin

Goals

Where they overlap, and where they do not

Goal5-Amino-1MQTesamorelin
fat loss
5-Amino-1MQ: 4/5
Tesamorelin: 5/5
metabolic health
5-Amino-1MQ: 4/5
Tesamorelin: 3/5
muscle growth
5-Amino-1MQ: 2/5
Tesamorelin: 2/5
longevityone only
5-Amino-1MQ: 2/5
Tesamorelin:
recovery and sleepone only
5-Amino-1MQ:
Tesamorelin: 2/5
focus and cognitionone only
5-Amino-1MQ:
Tesamorelin: 1/5

They overlap on 3 goals and diverge on 3. Weights are this site’s editorial priority score out of 5 — how central a goal is to why people use a compound. They are not effect sizes and two 5s do not mean two equal results.

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Related

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Educational information only, not medical advice. Talk to a licensed clinician before starting, changing, or stopping anything.