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Protocols

BAM15 protocols in the published literature

StatusPreclinical only

PeptideHound Staff · Last editorially reviewed · 14 sources

Every published amount of BAM15 is an animal amount, and most of them are not amounts at all in the usual sense: they are a percentage of the food. No study among the research behind this page gave BAM15 to a person, so no human figure exists to report.

The commonest design mixes it into chow or a high-fat diet at 0.1 to 0.2 percent by weight, and the mice then eat as much as they like. Two experiments in diabetic mice used exactly that pair of figures and found the higher one did more. A ten-week study in aged obese mice used the lower one.

Injected amounts appear only in the disease models. One 2025 artery study gave 5 mg per kilogram per day under the skin. A tumour study injected 50 nanograms per millilitre directly into the tumour, which is a concentration in a small volume of tissue rather than a dose to a body.

None of this converts. A percentage of a mouse's food is a figure that depends on what and how much that mouse eats, and the published human record it would have to be checked against does not exist in these sources.

Evidence: Not dosing guidance - every figure below is an animal study parameter, reported as such - most are a percentage of the animals' food by weight - no amount for a person exists among these sources

What amounts of BAM15 did the published studies use?

animal model

The figures below are study parameters, reported as such, and the unit changes with the experiment. The 2023 diabetic-mouse study compared calorie restriction against BAM15 at two doses of 0.1% and 0.2% (w/w) admixed in diet, with one group also fed only within a set window.1 The 2025 side-by-side comparison of 15 uncouplers used a similar pair, feeding mice chow with 0.15% BAM15 (w/w) or chow with 0.2% BAM15 (w/w).2

The 2022 muscle-ageing study used the lower end, giving aged obese mice BAM15 at 0.1% w/w in high fat diet for ten weeks.3 Away from the food-based designs, a 2025 artery study evaluated BAM15 at 5 mg/kg/day given under the skin in mice.4 Those are the four designs that recur. Everything else in this literature is a cell-culture concentration.

Amounts given to mice in the studies described above. Animal amounts studied, not converted to a person, and not a dosing guide.
StudyAnimalAmount studiedHow given
2023 diabetic-mouse studyDiabetic mice0.1% or 0.2% w/wMixed into the diet
2025 comparison of 15 uncouplersMice0.15% or 0.2% w/wMixed into chow
2022 muscle-ageing studyAged obese mice0.1% w/wIn high fat diet for ten weeks
2025 artery studyMice5 mg/kg/dayUnder the skin

Who received those amounts?

animal model

Mice, almost entirely, and mice chosen for a disease rather than for being ordinary. The 2023 study used male db/db mice, a strain carrying a genetic fault that produces severe hyperglycemia, obesity, hypertriglyceridemia, and fatty liver.1 The 2022 muscle study worked at the other end of life, randomising eighty-week-old male C57BL/6J mice with obesity to ten weeks of treatment.3

Other species appear at the edges of the literature: a 2022 ageing study gave 50 µM BAM15 to nematode worms, and a 2020 imaging experiment infused it into two pigs.6 Reading an amount without reading who received it is how a mouse figure becomes a human protocol. Every number on this page belongs to an animal with a named strain, a named diet and a named illness.

Why is the amount a percentage rather than a milligram figure?

animal model

Because the compound was mixed into food rather than given as a measured dose, and that is a deliberate choice rather than sloppiness. A percentage by weight, written w/w, means grams of BAM15 per hundred grams of diet, as in the 2024 fatty-liver study where treatments were admixed in diet and mice were pair-fed to control for drug intake.7

Pair-feeding means each treated animal gets the same quantity of food as its control, so differences cannot be explained by one group eating more. The design suits what an uncoupler does, because the 2020 obesity work found that BAM15 reduced body fat in mice without altering food intake, which keeps the delivered quantity steady across groups.8 The consequence for a reader is blunt. A figure expressed as a share of a rodent's diet has no equivalent outside that cage, and converting it would mean inventing the mouse's appetite, its weight and its absorption.

How was BAM15 administered?

animal model

Three routes appear, and the choice follows the question being asked rather than any judgement about which works best. Giving it by mouth dominates the metabolic work. That is possible because the 2020 obesity study found that BAM15 is orally bioavailable, which means enough of it survives the gut to reach the blood.8 The 2025 artery study used a shot under the skin, written s. c. in the paper, with the full figure recorded as 5 mg/kg/day.4

A 2023 sepsis study injected it at fixed intervals instead, giving mice BAM15 at 0, 6, or 12 hours after the surgical procedure that induced illness.9 A 2025 tumour study kept it local, reporting intratumoral injection of 50 ng/mL BAM15, which means a shot into the tumour itself.5 A strength injected into a lump of tissue is not the same kind of number as a daily amount eaten for weeks, although both get reported as doses.

How long did the studies run?

animal model

Weeks, in the metabolic work, and the two commonest durations are four and ten. The 2025 comparison phenotyped its mice over 4 weeks of treatment before analysing tissue and plasma.2 The 2024 fatty-liver study ran its animals on a fattening diet for 38 weeks before stratification and randomization to treatments for 8 weeks.7

The longest BAM15 exposure covered here is the muscle-ageing experiment's ten weeks of high fat diet in mice already eighty weeks old.3 Ten weeks in an aged mouse is a substantial fraction of what remains of its life, which is why that study carries weight. It is still ten weeks, and nothing covered here describes a year.

Did more produce more?

animal model

In the diabetic-mouse work, partly, and the shape of the answer is more interesting than a yes. In those mice, the 2023 study found that low-dose 0.1% BAM15 did not affect body mass but partially improved glucose tolerance to a similar degree as 50% calorie restriction.1 Its own conclusion draws the line: the smaller amount showed that the gains in glucose control are independent of weight loss.1

The 2025 comparison saw the same pattern, reporting that BAM15 dose-dependently improved body weight and metabolic parameters in db/db mice, with the larger share of food doing more across weight, glucose and liver measures.2 Two amounts is not a curve. What those studies show is that the smaller amount did something different from the larger one, and not where any ceiling sits.

Is there a BAM15 dosage chart?

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Not one built from this literature, and a chart assembled honestly from it would be unusable as a protocol. It would have four rows, three of them expressed as a percentage of mouse chow, one as milligrams per kilogram injected under the skin of a mouse, and a column headed species that read mouse all the way down.

Charts are also harder to justify in this class than in most, because a 2025 comparison of 15 uncouplers concluded that mitochondrial uncouplers should not be generalized and each uncoupler molecule needs to be considered by its own actions in well-defined experimental conditions.2 If one uncoupler's numbers cannot be read across to another, a figure copied out of a mouse study certainly cannot be read across to a person. A chart that leaves the species column off is not simplifying the evidence, it is deleting it.

Is there a human amount?

primary research

No study among the research behind this page gave BAM15 to a person, so there is no human amount to report, and the nearest approaches show how far off that is. The closest is a 2020 imaging study whose preliminary dose response experiments were conducted in two pigs, infusing BAM15 into the heart arteries to shift a radioactive tracer.10

The authors describe what they were measuring, reporting a maximum depolarization of 10 mV as a result of the BAM15 infusion.10 That is an imaging endpoint in an anaesthetised animal, not a therapeutic amount, and it was delivered into a coronary artery rather than swallowed. Describing it as the human-adjacent figure would overstate it twice over.

Can an animal amount be converted?

animal model

Not here, and refusing the conversion is a position about the evidence rather than caution for its own sake. Two of the three published routes do not have a quantity to convert in the first place, since a percentage of chow and a concentration in a tumour both describe an environment rather than a dose to a body.

Even the molecule's distribution refuses the simplification, because a 2021 study tracked where it went and found BAM15 in adipose, liver, and tumor tissue with low abundance in skeletal muscle in mice.11 A compound that concentrates in fat and liver in one species does not necessarily do so in another, and body-surface-area arithmetic has nothing to say about that. Any figure produced that way would be a recommendation wearing a calculation.

Does the form it is in change the amount needed?

animal model

Substantially, and this is one of the few places where this literature is unusually clear. A 2022 formulation study built albumin nanoparticles precisely because they improve aqueous solubility and half-life of BAM15, which is to say the plain molecule dissolves badly and leaves quickly.12 A 2023 sepsis study found the packaging changed the result as well, reporting that BAM15 particles but not free BAM15 alleviated liver injury induced by a bacterial toxin in mice.13

That second finding is the important one. Same molecule, same animals, different carrier, and one worked where the other did not. An amount is therefore inseparable from the preparation it was given in, and none of the preparations in these studies is what material sold under this name would be.

Why do the published amounts differ so much?

animal model

Because the experiments were asking unrelated questions, and each one chose the delivery that suited its own endpoint. A metabolic study needs steady exposure over weeks, which is why the 2025 comparison benchmarked its uncouplers against a lifestyle intervention of 35% calorie restriction in mice.2

A cancer study needs the compound where the tumour is, which is why a 2025 paper used local injection and reported that low-dose BAM15 promoted signalling and the TCA cycle without increasing cell proliferation or inducing cell death in vitro.5 A sepsis study needs timing above all, which is why the 2023 kidney work gave it at three separate points and found BAM15 reduced mortality, even after 12 hours, when mice were ill.9 The spread in the numbers is therefore not disagreement about an amount. It is four different experimental questions, and none of them was what quantity a person should take.

Does any of this apply to material bought under this name?

primary research

No, and the gap is wider than it would be for most compounds covered on this site. Every figure above describes a compound of verified structure, weighed into a known quantity of diet or dissolved to a known concentration by the people who synthesised it. Structure is not a technicality in this class, since the 2015 chemistry paper showed the importance of the furazan, pyrazine, and aniline rings as well as pKa in maintaining its effective protonophore activity.14

No analysis among the research behind this page has measured what is inside any vial sold under this name, so neither its identity nor its strength can be checked against the figures above. What is documented about harm, and what the older uncouplers did to people, is taken apart on the BAM15 safety page. What the animal amounts actually produced is on the BAM15 benefits page, and the wider picture is on the BAM15 overview.

What we don’t know

The gaps in the evidence matter as much as the findings.

  1. 01Any amount for a person. No study among the research behind this page gave BAM15 to one, and the nearest approach was an infusion into the heart arteries of two pigs.
  2. 02What a percentage of mouse chow corresponds to. It depends on how much that mouse eats, what the diet is made of and how much is absorbed, and none of these sources reports those values together.
  3. 03Whether there is a ceiling. The metabolic studies covered here tested two amounts each, which shows a direction and not a curve.
  4. 04Whether a schedule or a break matters. No study among these sources tested cycling, tapering or stopping and restarting in any species.
  5. 05How often it would need to be given. None of these sources reports a half-life for BAM15 itself, only for chemical derivatives of it.
  6. 06What a safe upper figure would be in any species. The animal studies covered here were designed to test effect, and their blood-marker screens were an end-of-study check rather than a dose-finding exercise.
  7. 07Whether the injected and dietary figures are comparable. One is a daily quantity per kilogram and the other a share of food, and no study covered here ran both in the same animals.
  8. 08What is in material sold under this name. No analysis among these sources has measured its identity, strength or sterility.

Sources

  1. 1Targeting negative energy balance with calorie restriction and mitochondrial uncoupling in db/db mice Mol Metab 2023. doi:10.1016/j.molmet.2023.101684animal model
  2. 2Diverse actions of 15 structurally unrelated mitochondrial uncouplers in cells and mice Mol Metab 2025. doi:10.1016/j.molmet.2025.102204animal model
  3. 3Mitochondrial uncoupling attenuates sarcopenic obesity by enhancing skeletal muscle mitophagy and quality control J Cachexia Sarcopenia Muscle 2022. doi:10.1002/jcsm.12982animal model
  4. 4BAM15 inhibits endothelial pyroptosis via the NLRP3/ASC/caspase-1 pathway to alleviate atherosclerosis Atherosclerosis 2025. doi:10.1016/j.atherosclerosis.2025.119226animal model
  5. 5Tumor metabolome remolded by low dose mitochondrial uncoupler elicites robust CD8(+) T cell response Cell Death Discov 2025. doi:10.1038/s41420-025-02584-9in vitro
  6. 6BAM15 Relieves Neurodegeneration in Aged Caenorhabditis elegans and Extends Lifespan Metabolites 2022. doi:10.3390/metabo12111129animal model
  7. 7Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease Acta Physiol (Oxf) 2024. doi:10.1111/apha.14217animal model
  8. 8Mitochondrial uncoupler BAM15 reverses diet-induced obesity and insulin resistance in mice Nat Commun 2020. doi:10.1038/s41467-020-16298-2animal model
  9. 9BAM15 treats mouse sepsis and kidney injury, linking mortality, mitochondrial DNA, tubule damage, and neutrophils J Clin Invest 2023. doi:10.1172/JCI152401animal model
  10. 10In-vivo Imaging of Mitochondrial Depolarization of Myocardium With Positron Emission Tomography and a Proton Gradient Uncoupler Front Physiol 2020. doi:10.3389/fphys.2020.00491primary research
  11. 11Breast cancer growth and proliferation is suppressed by the mitochondrial targeted furazano[3,4-b]pyrazine BAM15 Cancer Metab 2021. doi:10.1186/s40170-021-00274-5animal model
  12. 12Self-assembly drug-albumin nanocomposites for nonalcoholic fatty liver disease treatment Int J Biol Macromol 2022. doi:10.1016/j.ijbiomac.2022.06.167animal model
  13. 13Polymeric Particle BAM15 Targeting Macrophages Attenuates the Severity of LPS-Induced Sepsis: A Proof of Concept for Specific Immune Cell-Targeted Therapy Pharmaceutics 2023. doi:10.3390/pharmaceutics15122695animal model
  14. 14Structure-activity relationships of furazano[3,4-b]pyrazines as mitochondrial uncouplers Bioorg Med Chem Lett 2015. doi:10.1016/j.bmcl.2015.06.040primary research