BAM15

BAM15

BAM15

BAM15

BAM15 is a mitochondrial-selective protonophore uncoupler engineered to discharge the inner mitochondrial membrane proton gradient without depolarizing the cell plasma membrane. By uncoupling oxidative phosphorylation from ATP synthase, BAM15 elevates mitochondrial oxygen consumption rate (OCR), accelerates fatty acid oxidation, and suppresses mitochondrial reactive oxygen species (ROS) generation across broad concentration windows.

 

 

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What is BAM15?

BAM15 (known chemically as N5,N6-bis(2-fluorophenyl)-[1,2,5]oxadiazolo[3,4-b]pyrazine-5,6-diamine) is a pioneer selective mitochondrial protonophore uncoupler. Developed to overcome the severe plasma membrane depolarization and narrow therapeutic windows of legacy uncouplers (such as 2,4-dinitrophenol / DNP and FCCP), BAM15 selectively translocates protons across the inner mitochondrial membrane while remaining completely inert at the plasma membrane barrier.

By dissipating the proton motive force without arresting cellular ATP production, BAM15 forces cells to increase nutrient oxidation rates to maintain basal energy demands. This stimulates robust oxygen consumption rates (OCR), drives mitochondrial lipid oxidation, and reduces oxidative stress by suppressing mitochondrial superoxide generation.

Batch-verified for high analytical purity at Modern Aminos, BAM15 is offered as a standardized reference material for cell culture and biochemical bioenergetics research. Researchers evaluating uncoupled cellular respiration, fatty acid oxidation flux, and anti-obesity metabolic mechanisms evaluate BAM15 alongside complementary metabolic reference standards available on the site, such as SLU-PP-332, DADA (Diisopropylamine Dichloroacetate), AICAR, and MOTS-C.

Chemical and Molecular Data

Compound Name BAM15 (Mitochondrial Protonophore Uncoupler)
Quantity / Formats Offered High-Purity Dry Reference Powder / Solid Unit Material
Chemical Structure Fluorinated Oxadiazolopyrazinediamine Derivative
Synonyms / Alt Names BAM15, BAM-15, N5,N6-bis(2-fluorophenyl)-[1,2,5]oxadiazolo[3,4-b]pyrazine-5,6-diamine
CAS Number 210344-95-9
Chemical Formula C16H10F2N6O
Molecular Weight 340.29 g/mol
IUPAC Name N5,N6-bis(2-fluorophenyl)-[1,2,5]oxadiazolo[3,4-b]pyrazine-5,6-diamine
InChIKey InChIKey=VFUQOQAWLKIXCA-UHFFFAOYSA-N
SMILES Code C1=CC=C(C(=C1)NC2=NC3=NON=C3N=C2NC4=CC=CC=C4F)F

What are the Mechanisms of Action?

The biochemical pathways and cellular targets include:

  • Plasma Membrane-Sparing Mitochondrial Proton Leak: BAM15 binds protons in the intermembrane space and shuttles them across the mitochondrial inner membrane into the matrix, bypassing ATP synthase. Crucially, BAM15 exhibits zero activity at the plasma membrane, preventing cytosolic acidification, cell depolarization, and plasmalemmal cytotoxicity.
  • Stimulation of Oxygen Consumption Rate (OCR) & Nutrient Oxidation: Uncoupling mitochondrial respiration from ATP production forces cells to maximize substrate oxidation. In cell culture assays, BAM15 drives maximal uncoupled oxygen consumption rates (OCR), accelerating glucose and long-chain fatty acid oxidation flux.
  • Mitochondrial Reactive Oxygen Species (ROS) Suppression: High mitochondrial inner membrane potential (ΔΨm) drives electronic back-pressure in Complex I and Complex III, accelerating electron leak and ROS generation. Mild proton uncoupling mediated by BAM15 lowers ΔΨm slightly, suppressing oxidative stress without triggering cell death.

What do Preclinical & Academic Studies Show for BAM15?

Evaluating research efficacy and published scientific literature:

  • Mitochondrial Uncoupling & Subtype Kinetics (PubMed): Landmark bioenergetic studies cataloged on PubMed (PMID: 24828558) demonstrate that BAM15 stimulates maximal respiration across a broader concentration range than FCCP without causing plasma membrane depolarization or off-target cell death.
  • Energy Expenditure & Metabolic Disease Modeling (PMC): Comprehensive biomedical reviews archived in PMC (PMC4074404) document BAM15’s capacity to protect against diet-induced obesity, hepatic steatosis, and renal ischemia-reperfusion injury by enhancing tissue-specific energy expenditure.
  • Chemical Profiling & Identification (PubChem): Official structural characterization maintained on PubChem verifies the molecular mass (340.29 g/mol), fluorinated oxadiazolopyrazine geometry, and HPLC mass spectrometry profile of CAS 210344-95-9.

How does BAM15 compare to other compounds?

To evaluate uncoupling mechanisms, plasma membrane safety, and bioenergetic efficiency, researchers compare BAM15 against alternative reference standards available at Modern Aminos:

BAM15 vs. Legacy Protonophores (DNP and FCCP)

In cellular respiration and mitochondrial bioenergetics research, protonophore selectivity dictates toxicity profiles:

  • BAM15: Highly selective mitochondrial protonophore. Uncouples inner mitochondrial membrane respiration without depolarizing plasma membranes, maintaining high cell viability across broad concentration gradients.
  • Legacy Uncouplers (DNP / FCCP): Non-selective protonophores. Depolarize both inner mitochondrial membranes and plasma membranes simultaneously, causing rapid ATP depletion, cytosolic calcium influx, and cytotoxicity at narrow concentration thresholds.
Compound / Reference Chemical Structure & Class Core Mechanism of Action Research Focus & Profile
BAM15 Fluorinated Oxadiazolopyrazinediamine Uncoupler Discharges mitochondrial inner membrane proton gradient to uncouple OXPHOS from ATP synthesis without plasma membrane effect Focuses on plasma membrane-sparing uncoupled respiration, oxygen consumption rate (OCR) elevation, and ROS suppression
SLU-PP-332 Pan-ERR Nuclear Receptor Agonist Binds ERRα/β/γ receptors to recruit PGC-1α and upregulate mitochondrial OXPHOS gene transcription Focuses on nuclear receptor exercise mimetics, oxidative muscle fiber switching, and de novo mitochondrial biogenesis
DADA (Diisopropylamine Dichloroacetate) PDK Kinase Inhibitor / Vasodilator Salt Inhibits Pyruvate Dehydrogenase Kinase to maintain active PDH, driving pyruvate into mitochondrial oxidative phosphorylation Focuses on glucose oxidation, extracellular lactate suppression, and microvascular oxygen delivery assays
AICAR Nucleoside Analog Master AMPK Agonist Mimics AMP to directly phosphorylate and activate AMP-activated protein kinase (AMPK) independent of cellular ATP levels Focuses on master metabolic switch activation, glucose uptake, GLUT4 translocation, and metabolic signaling pathways

Frequently Asked Questions (FAQs)

1. Is Modern Aminos a reliable place to buy BAM15?

Yes, Modern Aminos is a highly trusted vendor for high-purity research chemicals and reference compounds. Every batch undergoes strict third-party analytical testing (including HPLC and Mass Spectrometry) to verify minimum 98%+ chemical purity, correct molecular weight (340.29 g/mol), exact protonophore activity, and complete absence of heavy metals or synthesis impurities.

2. What is BAM15 and how is it classified chemically?

BAM15 (N5,N6-bis(2-fluorophenyl)-[1,2,5]oxadiazolo[3,4-b]pyrazine-5,6-diamine) is a synthetic fluorinated oxadiazolopyrazinediamine derivative. It is classified chemically as a selective mitochondrial protonophore uncoupler.

3. How does BAM15 uncouple oxidative phosphorylation without depolarizing the plasma membrane?

BAM15 selectively translocates protons across the inner mitochondrial membrane, dissipating the proton motive force used by ATP synthase. Unlike legacy uncouplers, it lacks affinity for plasma membrane lipids, preserving cell membrane potential and preventing plasma membrane depolarization.

4. Why is plasma membrane depolarization a limitation in traditional uncouplers like DNP or FCCP?

Traditional uncouplers like DNP and FCCP depolarize both mitochondrial and plasma membranes. Plasma membrane depolarization disrupts ion homeostasis, induces calcium influx, and causes cell necrosis at narrow therapeutic ranges. BAM15 avoids this off-target effect.

5. What role does BAM15 play in cellular oxygen consumption rate (OCR) and ROS reduction?

By uncoupling respiration, this compound forces cells to consume oxygen at maximal rates to maintain energy equilibrium. Concurrently, mild dissipation of inner membrane potential (ΔΨm) reduces electron back-pressure, suppressing mitochondrial reactive oxygen species (ROS) formation.

6. How does BAM15 compare to nuclear receptor exercise mimetics like SLU-PP-332?

BAM15 is a chemical protonophore that directly dissipates mitochondrial proton gradients to increase oxygen consumption. SLU-PP-332 is a nuclear receptor agonist that binds ERRs to upregulate transcriptional expression of mitochondrial gene networks over hours and days.

7. How does Modern Aminos verify the chemical purity and mass identity of BAM15?

Modern Aminos utilizes High-Performance Liquid Chromatography (HPLC) to confirm active chemical purity exceeding 98% and Mass Spectrometry (MS) to verify exact molecular weight (340.29 g/mol) and structural identity prior to batch release.

8. What are the recommended storage and stability parameters for BAM15 reference material?

Dry-fill reference materials should be stored tightly sealed in a cool, dry environment (15°C to 25°C) or refrigerated for long-term preservation. Protect from direct heat, light exposure, and atmospheric moisture to maintain solid-state chemical stability.

Disclaimer: All compounds and research materials provided by Modern Aminos are strictly for laboratory and research professional use only. They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA). These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

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  • You are a qualified professional or entity with the necessary knowledge, training, and facilities to handle chemical reagents safely and appropriately.
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Prohibited Uses

  • This product is not to be used as an active pharmaceutical ingredient (API) in compounding or manufacturing drugs for human or veterinary use.
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