AAL Toxin TE1

CAS# 176590-37-7

AAL Toxin TE1

2D Structure

Catalog No. BCN1737----Order now to get a substantial discount!

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Quality Control of AAL Toxin TE1

3D structure

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AAL Toxin TE1

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Chemical Properties of AAL Toxin TE1

Cas No. 176590-37-7 SDF Download SDF
PubChem ID 102004520 Appearance Powder
Formula C27H49NO9 M.Wt 531.68
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-[2-[(3R,4R,5S,7S,16S)-17-acetamido-4,16-dihydroxy-3,7-dimethylheptadecan-5-yl]oxy-2-oxoethyl]butanedioic acid
SMILES CCC(C)C(C(CC(C)CCCCCCCCC(CNC(=O)C)O)OC(=O)CC(CC(=O)O)C(=O)O)O
Standard InChIKey XRIPCOGRCJFLJK-AZFHZTBSSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of AAL Toxin TE1

The Alternaria alternata f. sp. lycopersici

Biological Activity of AAL Toxin TE1

Description1. AAL-toxin has a wide range of phytotoxicity, it has potential as a natural herbicide because several important weeds including jimsonweed, black nightshade, prickly sida and hemp sesbania are quite sensitive, while some crops such as cotton and maize are not affected.
TargetsAntifection

AAL Toxin TE1 Dilution Calculator

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AAL Toxin TE1 Molarity Calculator

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Preparing Stock Solutions of AAL Toxin TE1

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8808 mL 9.4042 mL 18.8083 mL 37.6166 mL 47.0208 mL
5 mM 0.3762 mL 1.8808 mL 3.7617 mL 7.5233 mL 9.4042 mL
10 mM 0.1881 mL 0.9404 mL 1.8808 mL 3.7617 mL 4.7021 mL
50 mM 0.0376 mL 0.1881 mL 0.3762 mL 0.7523 mL 0.9404 mL
100 mM 0.0188 mL 0.094 mL 0.1881 mL 0.3762 mL 0.4702 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on AAL Toxin TE1

Product ion filtering with rapid polarity switching for the detection of all fumonisins and AAL-toxins. [Pubmed:26467225]

Rapid Commun Mass Spectrom. 2015 Nov 30;29(22):2131-9.

Fumonisins and AAL-toxins are structurally similar mycotoxins that contaminate agricultural crops and foodstuffs. Traditional analytical screening methods are designed to target the known compounds for which standards are available but there is clear evidence that many other derivatives exist and could be toxic. A fast, semi-targeted method for the detection of all known fumonisins, AAL-toxins(eg. AAL Toxin TE1) and related emerging toxins is required. METHODS: Strains of Fusarium verticillioides, Alternaria arborescens and Aspergillus welwitschiae were grown on their associated crops (maize, tomatoes, and grapes, respectively). Extracts were first analyzed in negative mode using product ion filtering to detect the tricarballylic ester product ion that is common to fumonisins and AAL-toxins (m/z 157.0142). During the same liquid chromatography (LC) run, rapid polarity switching was then used to collect positive mode tandem mass spectrometric (MS(2) ) data for characterization of the detected compounds. RESULTS: Fumonisin B1 , B2 , B3 and B4 were detected on Fusarium contaminated maize, AAL-toxins TA, TB, TD, TE(include AAL Toxin TE1 and AAL Toxin TE2) were detected on Alternaria inoculated tomatoes and fumonisin B2 , B4 and B6 on Aspergillus contaminated grapes. Additionally, over 100 structurally related compounds possessing a tricarballylic ester were detected from the mould inoculated plant material. These included a hydroxyl-FB1 from F. verticillioides inoculated maize, keto derivatives of AAL-toxins from A. arborescens inoculated tomatoes, and two previously unreported classes of non-aminated fumonisins from Asp. welwitschiae contaminated grapes. CONCLUSIONS: A semi-targeted method for the detection of all fumonisins and AAL-toxins in foodstuffs was developed. The use of the distinctive tricarballylic ester product anion for detection combined with rapid polarity switching and positive mode MS(2) is an effective strategy for differentiating between known isomers such as FB1 and FB6 . This analytical tool is also effective for the identification of new compounds as evident from the discoveries of the previously unreported hydroxyl-FB1 , keto-AAL-toxins, and the two new families of non-aminated fumonisins.

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