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Bongkrekic acid

(Synonyms: Bongkrek Acid) Copy Product Info
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Synonyms: Bongkrek Acid

Catalog No. T36067 Copy Product Info
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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.
Bongkrekic acid
Cas No. 11076-19-0
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$1,7907-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
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]
SynonymsBongkrek Acid
Chemical Properties
Molecular Weight486.60
FormulaC28H38O7
Cas No.11076-19-0
SmilesC(\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 & Solubility Information
StorageStore 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
1mg5mg10mg50mg
1 mM2.0551 mL10.2754 mL20.5508 mL102.7538 mL
DMSO
1mg5mg10mg50mg
5 mM0.4110 mL2.0551 mL4.1102 mL20.5508 mL
10 mM0.2055 mL1.0275 mL2.0551 mL10.2754 mL
20 mM0.1028 mL0.5138 mL1.0275 mL5.1377 mL
50 mM0.0411 mL0.2055 mL0.4110 mL2.0551 mL
100 mM0.0206 mL0.1028 mL0.2055 mL1.0275 mL
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.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Keywords

Related Tags: Bongkrekic acid chemical structure | Bongkrekic acid in vivo | Bongkrekic acid in vitro | Bongkrekic acid formula | Bongkrekic acid molecular weight