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Originally posted by @mommycurrie on TikTok · 71s|Watch on TikTok
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Auto-generated transcript of @mommycurrie's video. Quoted here for educational fact-check commentary; original creator retains all rights to the video content.

  1. 0:00I lost 7.4 pounds in seven days and two inches off my waist.
  2. 0:03Well, that's what she said after taking the bikini in a bottle.
  3. 0:06It's got to be the best nickname for a supplement yet.
  4. 0:10Oh, so accurate, not osempic. It is too very powerful.
  5. 0:15Short chain amino acid formula. Support your metabolism and your fat loss
  6. 0:20without the side effects, without the hair loss, the nausea, the muscle decline.
  7. 0:25Abilism boosted up. You got to keep your muscle. Five amino one MQ
  8. 0:29is the first short chain amino acid hoping to maintain your NAD plus
  9. 0:33loads to boost your cellular energy and your fat burning potential.
  10. 0:37Sloop 33 helps to trigger your master metabolic switch.
  11. 0:41AMPK to increase your fat burning and help to reduce the puffiness, the
  12. 0:46inflammation in your body. That's why she called it bikini in a bottle.
  13. 0:49Using them together in that orange tablet, your body burn more fat,
  14. 0:54decrease the puffiness and build a maintain lean muscle mass.
  15. 0:58And improve your insulin sensitivity and maybe even your collagen production.
  16. 1:02I don't know about you, but isn't that what we're all trying to do?
  17. 1:04See a later pyramid in Puzzle Belly. Comment Aminos. I will share the details
  18. 1:08with you before it all sells out.

5-Amino-1MQ and SLU-PP-332: separating hype from actual data

Cindy Currie | Aging Well

TikTok creator

3.9K viewsWatch on TikTok

Quick answer

5-Amino-1MQ is an NNMT inhibitor with preclinical evidence of fat mass reduction in rodent models, while SLU-PP-332 is an ERR agonist shown to enhance mitochondrial activity and endurance in mice (Deng et al., 2023, Nature Communications). Neither compound has published human clinical trial data supporting fat loss, metabolic improvement, or the safety profile implied in this video. The 7.4-pound, seven-day weight reduction described is physiologically inconsistent with fat loss and most likely reflects fluid shifts.

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For 5-Amino-1MQ and SLU-PP-332: separating hype from actual data, FormBlends checks the page topic against primary trials, systematic reviews, guidelines, and current PubMed-indexed literature where available. These citations are context, not medical advice, proof of eligibility, or a claim that every study applies to every patient.

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What this exact clip is really saying

This FormBlends review is specific to "5-Amino-1MQ and SLU-PP-332: separating hype from actual data" from Cindy Currie | Aging Well. We read the clip as a Peptide social video fact-checks claim about Peptide social video fact-checks, then separate the useful signal from what a short social video cannot prove. The page-specific claim focus is: 5-Amino-1MQ is an NNMT inhibitor with preclinical evidence of fat mass reduction in rodent models, while SLU-PP-332 is an ERR agonist shown to enhance mitochondrial activity and endurance in mice (Deng et al.

The reason this review is not generic is the source wording and the canonical claim label "peptides 7 4lbs and 2 gone in just 7 days these aren t meds they re a." In this clip, the useful excerpt is: "I lost 7." That wording changes the review because it points to Peptide social video fact-checks evidence, safety, and patient-fit context, not a one-size-fits-all protocol.

The source trail for this page is checked against Once-Weekly Semaglutide in Adults with Overweight or Obesity (2021), Effect of Continued Weekly Subcutaneous Semaglutide vs Placebo on Weight Loss Maintenance (2021), and Effect of Weekly Subcutaneous Semaglutide vs Daily Liraglutide on Body Weight (2022), plus the creator's own wording. Peptide social video fact-checks decisions still need an eligibility review, medication-interaction screen, access check, and quality-control review before anyone treats a social clip as medical advice.

SLU-PP-332 improved exercise endurance in sedentary mice in a 2023 Nature Communications study, but has not been tested for fat loss in humans.
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Claim being checked

5-Amino-1MQ is an NNMT inhibitor with preclinical evidence of fat mass reduction in rodent models, while SLU-PP-332 is an ERR agonist shown to enhance mitochondrial activity and endurance in mice (Deng et al.

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What it helps with

  • 5-Amino-1MQ is an NNMT inhibitor with preclinical evidence of fat mass reduction in rodent models, while SLU-PP-332 is an ERR agonist shown to enhance mitochondrial activity and endurance in mice (Deng et al., 2023, Nature Communications). Neither compound has published human clinical trial data supporting fat loss, metabolic improvement, or the safety profile implied in this video. The 7.4-pound, seven-day weight reduction described is physiologically inconsistent with fat loss and most likely reflects fluid shifts.
  • 5-Amino-1MQ has shown fat mass reduction in rodent models (Kannt et al., 2018, Scientific Reports), but zero published human clinical trials exist for fat loss.
  • SLU-PP-332 improved exercise endurance in sedentary mice in a 2023 Nature Communications study, but has not been tested for fat loss in humans.

What it may miss

  • It may not cover eligibility, contraindications, medication interactions, lab history, or dose escalation.
  • Compound access, legal status, and product quality still need a separate safety check.
  • Social video captions rarely show the full evidence base behind a claim.

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What You'll Learn

  • 5-Amino-1MQ has shown fat mass reduction in rodent models (Kannt et al., 2018, Scientific Reports), but zero published human clinical trials exist for fat loss.
  • SLU-PP-332 improved exercise endurance in sedentary mice in a 2023 Nature Communications study, but has not been tested for fat loss in humans.
  • A 7.4-pound weight drop in seven days is inconsistent with fat loss physiology; the maximum rate of fat oxidation in a significant caloric deficit is roughly 1 to 2 pounds of actual fat per week.
  • Neither compound is FDA-approved or has an established human safety profile, making side-effect comparisons to semaglutide unsupported.
  • AMPK activation is a legitimate metabolic concept, but SLU-PP-332 does not directly activate AMPK; the mechanistic framing in the video is imprecise.
  • The urgency tactic of "before it all sells out" combined with a single anecdote is a known consumer manipulation pattern, not clinical evidence.
  • Anyone considering these compounds should consult a licensed provider, as research-stage compounds sold in retail formats carry unknown long-term risks.

Our take · Written by FormBlends editorial team · Reviewed by FormBlends Medical Team · This is not a transcript. It is our independent review of the video above.

What did @mommycurrie actually say?

The creator claimed a customer lost "7.4 pounds in seven days and two inches off my waist" using a supplement combining 5-Amino-1MQ and SLU-PP-332, which she nicknamed "bikini in a bottle." She positioned these compounds as a safer alternative to semaglutide, saying they work "without the hair loss, the nausea, the muscle decline." She said 5-Amino-1MQ supports NAD+ levels to boost cellular energy and fat burning, while SLU-PP-332 triggers AMPK, your "master metabolic switch," to reduce inflammation and increase fat oxidation. She also floated claims about improved insulin sensitivity and collagen production. The pitch ended with a classic urgency hook: "before it all sells out."

To be clear, she is describing unregulated research compounds being sold in tablet form, and she is attributing dramatic, measurable body composition changes to them over the course of a single week.

Does the science back this up?

For 5-Amino-1MQ, there is some legitimate early science. For SLU-PP-332, human data is essentially nonexistent. Neither compound has clinical trial data supporting the claims made in this video.

5-Amino-1MQ is an NNMT (nicotinamide N-methyltransferase) inhibitor. Research in mice, including work by Kannt et al. (2018, Scientific Reports), showed NNMT inhibition reduced fat mass and improved metabolic markers. That is promising. But mouse models do not translate directly to human outcomes, and no peer-reviewed human trials on 5-Amino-1MQ for fat loss currently exist.

SLU-PP-332 is an ERR (estrogen-related receptor) agonist studied primarily for its AMPK-adjacent effects on muscle endurance. A 2023 study by Deng et al. in Nature Communications showed SLU-PP-332 improved exercise endurance in sedentary mice, essentially mimicking some effects of aerobic exercise at the cellular level. That is interesting science. It is not a human fat-loss clinical trial.

The claim that AMPK activation directly translates to measurable fat loss in humans over seven days, through an oral tablet, is not supported by any published evidence.

What did they get wrong (or right)?

The AMPK framing is not entirely wrong. But the leap from mechanism to outcome is enormous, and the creator does not flag that gap.

What they got directionally right: AMPK is genuinely involved in fat oxidation and metabolic regulation. NAD+ metabolism is a legitimate area of longevity and metabolic research. NNMT inhibition does have a plausible mechanistic connection to fat mass reduction based on preclinical data. These are real concepts, not invented ones.

What they got wrong, plainly: The 7.4 pounds in seven days framing is not credible as a fat-loss number. That scale of weight loss in one week almost certainly reflects water and glycogen loss, not fat tissue. Presenting it as evidence that these peptides "work" is misleading, whether or not that was the intent.

  • Comparing these compounds to semaglutide without acknowledging that semaglutide has extensive Phase 3 clinical trial data and these compounds have none is a false equivalence.
  • The collagen production claim came with an "I don't know about you" hedge, which is the creator's way of floating an unsupported claim with plausible deniability.
  • Neither compound is FDA-approved, and their long-term safety profiles in humans are unknown.

What should you actually know?

These are research-stage compounds being sold directly to consumers, and that gap between lab and retail shelf matters.

Both 5-Amino-1MQ and SLU-PP-332 are available through research chemical suppliers and some compounding-adjacent telehealth platforms. Neither has completed human clinical trials for fat loss. The fact that they are described as "amino-based peptides" rather than drugs does not change their regulatory or safety profile. Mechanism-of-action claims, even accurate ones, are not the same as clinical evidence that a product works safely in your body at a given dose over a given time period.

If you are a woman over 40 dealing with midlife metabolic changes, that is a real and frustrating experience. But the urgency framing, "before it all sells out," combined with a single anecdotal result is a sales tactic, not a health recommendation. A one-week weight drop of 7.4 pounds is almost never adipose tissue. It is water. Anyone who tells you otherwise is either uninformed or not being straight with you.

Consult a licensed provider before using any unregulated peptide compound. The preclinical science here is genuinely interesting, but interesting science and safe consumer products are two very different things.

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About the Creator

Cindy Currie | Aging Well · TikTok creator

3.9K views on this video

🎉 7.4lbs and 2” gone in just 7 days... These aren't meds — they're amino-based peptides that help your body do what it used to do naturally: 5-Amino-1MQ: supports fat metabolism + boosts cellular energy SLU-PP-332: activates AMPK — your body's built-in fat- burning switch Together, they support fat loss, reduce inflammation, protect lean muscle, and help you feel like yourself again…..especially during perimenopause when everything seems to be going sideways. Comment AMINOS and I'll get you th

Frequently asked questions

Quick answers based on this video and our medical team review.

What does the video say about 5-amino-1mq has shown fat mass reduction in rodent models (kannt?

5-Amino-1MQ has shown fat mass reduction in rodent models (Kannt et al., 2018, Scientific Reports), but zero published human clinical trials exist for fat loss.

What does the video say about slu-pp-332 improved exercise endurance in sedentary mice in a 2023?

SLU-PP-332 improved exercise endurance in sedentary mice in a 2023 Nature Communications study, but has not been tested for fat loss in humans.

What does the video say about a 7.4-pound weight drop in seven days?

A 7.4-pound weight drop in seven days is inconsistent with fat loss physiology; the maximum rate of fat oxidation in a significant caloric deficit is roughly 1 to 2 pounds of actual fat per week.

What does the video say about neither compound?

Neither compound is FDA-approved or has an established human safety profile, making side-effect comparisons to semaglutide unsupported.

What does the video say about ampk activation?

AMPK activation is a legitimate metabolic concept, but SLU-PP-332 does not directly activate AMPK; the mechanistic framing in the video is imprecise.

What does the video say about the urgency tactic of "before it all sells out" combined?

The urgency tactic of "before it all sells out" combined with a single anecdote is a known consumer manipulation pattern, not clinical evidence.

Sources & references

Citations extracted from our medical team's review. Click any citation to search PubMed.

Educational use only. This fact-check is editorial content for general information. Nothing here is medical advice. Talk to a licensed provider about your specific situation before starting, stopping, or changing any supplement, peptide, or medication regimen.

Read More on This Topic

Our written guides go deeper with dosing details, comparison tables, and medical-team reviewed protocols.

Not medical advice. This video was made by Cindy Currie | Aging Well, not by FormBlends. Our write-up above is an editorial review, not a medical recommendation. Talk to your doctor before making any decisions about medications or treatments.