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Aflavarin
Aflavarin
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Aflavarin
Price:
CAS No.: 144429-67-4
Catalog No.: CFN89117
Molecular Formula: C24H22O9
Molecular Weight: 454.43 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Source: The secondary metabolites of Aspergillus flavus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
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
Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Aflavarin exhibits potent antifeedant activity against the fungivorous beetle Carpophilus hemipterus.
In vitro:
Fungal Genet Biol. 2017 Jul;104:29-37.
Aspergillus flavus aswA, a gene homolog of Aspergillus nidulans oefC, regulates sclerotial development and biosynthesis of sclerotium-associated secondary metabolites.[Pubmed: 28442441]

METHODS AND RESULTS:
Aspergillus flavus aswA (AFLA_085170) is a gene encoding a Zn(II)2Cys6 DNA-binding domain and a transcriptional activation domain, DUF3468. Disruption of aswA yielded strains that made a truncated gene transcript and generated a fungus that produced a greatly increased number of sclerotia. These sclerotia were odd-shaped and non-pigmented (white) and different from oval and pigmented (dark brown to black) mature sclerotia. Transcriptomic analysis of the ΔaswA strain grown on potato dextrose agar plates and Wickerham agar plates showed that expression of clustering genes involved in the biosynthesis of three sclerotium-associated secondary metabolites was down-regulated. These included gene clusters of asparasone, aflatrem, and Aflavarin. In contrast, those of aflatoxin, cyclopiazonic acid and kojic acid were not affected.
CONCLUSIONS:
Metabolite analyses confirmed that the non-pigmented sclerotia contained aflatoxin and cyclopiazonic acid but not other aforementioned metabolites, three asparasone analogs and dihydroxyaflavinine commonly present in mature sclerotia. Impairment in aswA gene function stalls normal sclerotial development, which in turn prevents biosynthesis and accumulation of sclerotium-specific metabolites.
Journal of Natural Products, 1992, 55(8):1080-1086.
Aflavarin and β-Aflatrem: New Anti-Insectan Metabolites from the Sclerotia of Aspergillus flavus[Reference: WebLink]

METHODS AND RESULTS:
Aflavarin [3], a new bicoumarin, and beta-aflatrem [11], an isomer of the tremorgen aflatrem, were isolated from the sclerotia of Aspergillus flavus. The structures were determined through a series of 1D and 2D nmr experiments, assisted by spectral comparisons with known compounds. Aflavarin exhibits potent antifeedant activity against the fungivorous beetle Carpophilus hemipterus. Beta-aflatrem causes a significant reduction in the growth rate of the corn earworm Helicoverpa zea.
CONCLUSIONS:
The presence of nominine [13] as a minor metabolite of A. flavus is reported for the first time.
Aflavarin Description
Source: The secondary metabolites of Aspergillus flavus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2006 mL 11.0028 mL 22.0056 mL 44.0112 mL 55.014 mL
5 mM 0.4401 mL 2.2006 mL 4.4011 mL 8.8022 mL 11.0028 mL
10 mM 0.2201 mL 1.1003 mL 2.2006 mL 4.4011 mL 5.5014 mL
50 mM 0.044 mL 0.2201 mL 0.4401 mL 0.8802 mL 1.1003 mL
100 mM 0.022 mL 0.11 mL 0.2201 mL 0.4401 mL 0.5501 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.
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