Bongkrekic Acid (Synonyms: Bongkrek Acid) |
| カタログ番号GC42965 |
ボンクレキン酸 (アンモニウム塩) は、シュードモナス ココベネナンス菌によって分泌されるミトコンドリア毒素です。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 11076-19-0
Sample solution is provided at 25 µL, 10mM.
Bongkrekic acid is a natural toxin first isolated from coconut tempeh contaminated with bacteria. It is a polyunsaturated long-chain fatty acid derivative that acts as a potent inhibitor of the mitochondrial adenine nucleotide (ADP/ATP) translocase (Ki < 2 nM). [1][2][3]Despite its high affinity, bongkrekic acid has a slow rate of action in intact preparations, as it must permeate the inner mitochondrial membrane to bind the translocase.[3]
Reference:
[1]. Henderson, P.J.F., and Lardy, H.A. Bongkrekic acid. An inhibitor of the adenine nucleotide translocase of mitochondria. The Journal of Biological Chemisty 245(6), 1319-1326 (1970).
[2]. Dahout-Gonzalez, C., Hury, H., Trézéguet, V., et al. Molecular, functional, and pathological aspects of the mitochondrial ADP/ATP carrier. Physiology (Bethesda) 21, 242-249 (2006).
[3]. Klingenberg, M. The ADP and ATP transport in mitochondria and its carrier. Biochimica et Biophysica Acta 1778(10), 1978-2021 (2008).
| Cas No. | 11076-19-0 | SDF | |
| 同義語 | Bongkrek Acid | ||
| Chemical Name | 20-(carboxymethyl)-6R-methoxy-2,5,17S-trimethyl-2E,4Z,8Z,10E,14E,18E,20Z-docosaheptaenedioic acid | ||
| Canonical SMILES | OC(/C=C(CC(O)=O)\C=C\[C@@H](C)C/C=C/CC/C=C/C=C\C[C@@H](OC)/C(C)=C\C=C(C(O)=O)/C)=O | ||
| Formula | C28H38O7 | M.Wt | 486.6 |
| 溶解度 | DMSO : 100 mg/mL (205.51 mM; Need ultrasonic and warming) | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
|
1 mg | 5 mg | 10 mg |
| 1 mM | 2.0551 mL | 10.2754 mL | 20.5508 mL |
| 5 mM | 0.411 mL | 2.0551 mL | 4.1102 mL |
| 10 mM | 0.2055 mL | 1.0275 mL | 2.0551 mL |
Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
g
μL
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 17 reference(s) in Google Scholar.)
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