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Synonyms: Bongkrek Acid

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $1,790 | 7-10 days | 7-10 days |
| Description | Bongkrekic acid (ammonium salt) is a natural product, a mitochondrial adenine nucleotide translocase (ANT) inhibitor that induces neutrophil extracellular trap formation through signaling pathways such as p38 and ERK, and is used for research on mitochondrial function and immune response. |
| Targets & IC50 | MDA-MB-231 cells:34.14 μM (EC50), LTED:2.58 μM (EC50), MCF-7 cells:> 50 μM (EC50) |
| In vitro | Methods: Rat liver mitochondria and bovine heart submitochondrial particles were used, and [³H]ADP uptake was measured. Bongkrekic acid was incubated at concentrations of 1–10 μM for 15–20 seconds. Results: At pH 6.0, 1–5 μM Bongkrekic acid significantly inhibited ADP uptake (inhibition rate >80%); at pH 7.4, 5–10 μM showed approximately 30% inhibition, confirming its pH-dependent inhibition of the ADP/ATP carrier.[1] Methods: HepG2 cells were used, and oxygen consumption rate (OCR) was measured by Seahorse extracellular flux analyzer. Bongkrekic acid concentration was 20 μM, with 1-hour pre-incubation. Results: Bongkrekic acid alone significantly inhibited OCR; addition before Oligomycin blocked its induced proton uncoupling, but addition after uncoupling occurred had no reversing effect.[2] |
| In vivo | Methods: Zebrafish embryos were exposed to Bongkrekic acid (0.01, 0.05, 0.1, 1 mg/L, in water) at 4 hours post-fertilization for 96 hours to assess developmental toxicity. Results: Mortality rates reached 79% in the 0.1 mg/L group and 100% in the 1 mg/L group; exposure to ≥0.05 mg/L resulted in decreased cardiac function and neurobehavioral abnormalities; exposure to ≥0.1 mg/L caused morphological malformations, liver damage, acidosis, and ionoregulatory disorders. [3] |
| Synonyms | Bongkrek Acid |
| Molecular Weight | 486.60 |
| Formula | C28H38O7 |
| Cas No. | 11076-19-0 |
| Smiles | C(\C=C\[C@H](C/C=C/CC/C=C/C=C\C[C@H](/C(=C\C=C(\C(O)=O)/C)/C)OC)C)(/CC(O)=O)=C\C(O)=O |
| Storage | Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (164.41 mM), Sonication is recommended. H2O: 1 mg/mL (2.06 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | |||||||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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