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9,10-dihidro derivate of aflatoxin G1. A potent hepatotoxic and hepatocarcinogenic mycotoxin
Aflatoxin G2 is a fungal secondary toxic metabolite synthesized by Aspergillus parasiticus, Aspergillus flavus, and Aspergillus nomius, species that are found in tropical and subtropical regions of the world. Aflatoxin Gs (AFGs) are derivatives of difuranocoumarin and contain a bifuran group linked to a coumarin nucleus and a lactone ring.
| CAS | 7241-98-7 |
|---|---|
| Synonyms | AFLATOXIN G2 [HSDB] | 1H,12H-Furo(3',2':4,5)furo(2,3-h)pyrano(3,4-c)(1)benzopyran-1,12-dione, 3,4,7a,9,10,10a-hexahydro-5-methoxy-, (7aR,10aS)- | Aflatoxin G2 in Acetonitrile | 2MS0D8WA29 | (3S,7R)-11-methoxy-6,8,16,20-tetraoxapentacyclo[10.8.0.02,9.03,7. |
| Specifications & Purity | ≥98%(HPLC) |
| Storage | Store at -20°C |
| Shipped In | Ice chest + Ice pads |
| Product Description | 9,10-dihidro derivate of aflatoxin G1. A potent hepatotoxic and hepatocarcinogenic mycotoxin Product description Aflatoxin G2 is a fungal secondary toxic metabolite synthesized by Aspergillus parasiticus, Aspergillus flavus, and Aspergillus nomius, species that are found in tropical and subtropical regions of the world. Aflatoxin Gs (AFGs) are derivatives of difuranocoumarin and contain a bifuran group linked to a coumarin nucleus and a lactone ring. |
| Pubchem Sid | 504760881 |
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504760881 |
| Solubility | DMSO or Methanol |
| Sensitivity | Light Sensitive;Moisture sensitive |
| Mdl Number | MFCD00078141 |
| EC Number | 230-643-4 |
| PubChem CID | 2724362 |
| Molecular Formula | C17H14O7 |