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AAL Toxin TC2
AAL Toxin TC2
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name AAL Toxin TC2
Price:
CAS No.: 176590-34-4
Catalog No.: CFN00009
Molecular Formula: C25H47NO8
Molecular Weight: 489.65 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: From Alternaria alternata f. sp. lycopersici
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: 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.
Targets: Antifection
AAL Toxin TC2 Description
Source: From Alternaria alternata f. sp. lycopersici
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0423 mL 10.2114 mL 20.4228 mL 40.8455 mL 51.0569 mL
5 mM 0.4085 mL 2.0423 mL 4.0846 mL 8.1691 mL 10.2114 mL
10 mM 0.2042 mL 1.0211 mL 2.0423 mL 4.0846 mL 5.1057 mL
50 mM 0.0408 mL 0.2042 mL 0.4085 mL 0.8169 mL 1.0211 mL
100 mM 0.0204 mL 0.1021 mL 0.2042 mL 0.4085 mL 0.5106 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Journal of Agricultural and Food Chemistry, 1994, 42(2):327-333.
Structural characterization of three new AAL toxins produced by Alternaria alternata f. sp. lycopersici[Reference: WebLink]

METHODS AND RESULTS:
Three new pairs of biologically active regioisomeric toxins (toxins TC, TD, and TE) were isolated from liquid cultures of alternata f.sp. lycopersici, purified using standard chromatographic procedures, and their structures elucidated following interpretation of spectra obtained from and mass spectrometry experiments. Each of the toxin congeners is structurally similar to the toxin TA, which was characterized earlier from culture filtrates of this fungus. toxin TC resembles TA but differs in its lack of at C4 and C5. toxin TE is the N-acetylated form of TC. Spectroscopic data are reported to confirm that TB is similar to TA but lacks a at C5, as suggested earlier. toxin TD is the N-acetylated form of TB.
CONCLUSIONS:
All five pairs of regioisomers arise as products of fungal and do not appear to be generated during isolation. All regioisomeric pairs induce the genotype-specific necrosis characteristic of toxin TA in bioassays but differ markedly in relative toxicity.
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