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Antimycin A1

Catalog No.GC42818

Antimycin A, an antibiotic produced by Streptomyces species that demonstrates antifungal, insecticidal, nematocidal, and piscicidal properties, is a mixture of Antimycins A1, A2, A3, and A4.

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Antimycin A1 Chemical Structure

Cas No.: 642-15-9

Size Price Stock Qty
500μg
$256.00
In stock
2.5mg
$1,088.00
In stock

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Sample solution is provided at 25 µL, 10mM.

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Description of Antimycin A1

Antimycin A, an antibiotic produced by Streptomyces species that demonstrates antifungal, insecticidal, nematocidal, and piscicidal properties, is a mixture of Antimycins A1, A2, A3, and A4. [1] It blocks mitochondrial respiration and can deplete cellular levels of ATP via inhibition of complex III of the mitochondrial electron transport chain (ETC). Antimycin A prevents the transfer of electrons between the b-cytochromes and ubiquinone at the Q(inner) site of complex III. This results in the stabilization of the ubisemiquinone radical at the Q(outer) site of complex III, leading to increased production of superoxide. [2][3] Antimycin A is widely used in research to shunt electron flow through the ETC in order to study the chemical details of oxygen respiration. Additionally, antimycin A has been shown to inhibit Bcl-2 and Bcl-xL proteins, inducing apoptosis.[3][4][5]

Reference:
[1]. Seipke, R.F., and Hutchings, M.I. The regulation and biosynthesis of antimycins. Beilstein J.Org.Chem. 9, 2556-2563 (2013).
[2]. Muller, F., Crofts, A.R., and Kramer, D.M. Multiple Q-cycle bypass reactions at the Qo site of the cytochrome bc1 complex. Biochemistry 41(25), 7866-7874 (2002).
[3]. Muller, F.L., Roberts, A.G., Bowman, M.K., et al. Architecture of the Qo site of the cytochrome bc1 complex probed by superoxide production. Biochem. 42(21), 6493-6499 (2003).
[4]. Azmi, A.S., and Mohammad, R.M. Non-peptidic small molecule inhibitors against Bcl-2 for cancer therapy. J.Cell Physiol. 218(1), 13-21 (2009).
[5]. Marton, A., Mihalik, R., Bratincsak, A., et al. Apoptotic cell death induced by inhibitors of energy conservation--Bcl-2 inhibits apoptosis downstream of a fall of ATP level. Eur. J. Biochem. 250(2), 467-475 (1997).

Chemical Properties of Antimycin A1

Cas No. 642-15-9 SDF
Chemical Name 2(or 3)-methyl-butanoic acid, (2R,3S,6S,7R,8R)-3-[[3-(formylamino)-2-hydroxybenzoyl]amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl ester
Canonical SMILES CC(C)CC(O[C@H]([C@H]1CCCCCC)[C@H](C)OC([C@@H](NC(C2=CC=CC(NC([H])=O)=C2O)=O)[C@@H](C)OC1=O)=O)=O
Formula C28H40N2O9 M.Wt 548.6
Solubility Soluble in ethanol, methanol, DMSO, DMF Storage Store at -20°C, protect from light
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.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Antimycin A1

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1 mg 5 mg 10 mg
1 mM 1.8228 mL 9.1141 mL 18.2282 mL
5 mM 0.3646 mL 1.8228 mL 3.6456 mL
10 mM 0.1823 mL 0.9114 mL 1.8228 mL
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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. )

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Average Rating: 5 ★★★★★ (Based on Reviews and 35 reference(s) in Google Scholar.)

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