| Weight | 328.276 g/mol |
|---|---|
| Formula | C17H12O7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
ST50405313 (1165-39-5)
aflatoxin G1
Score:
#134 in Microbiology
,
#421 in Biochemistry
,
#1418 in Biology
,
#1659 in Chemistry
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- Total syntheses of aflatoxins M1 and G1 and an improved synthesis of aflatoxin B1 (Journal of the American Chemical Society, 1971)
- Identification of O-methylsterigmatocystin as an aflatoxin B1 and G1 precursor in Aspergillus parasiticus. (Applied and Environmental Microbiology, 1987)
- Dillapiol and Apiol as Specific Inhibitors of the Biosynthesis of Aflatoxin G1 in Aspergillus parasiticus (Bioscience, Biotechnology, and Biochemistry, 2007)
- The production of aflatoxin B1 or G1 by Aspergillus parasiticus at various combinations of temperature and water activity is related to the ratio of aflS to aflR expression (Mycotoxin Research, 2010)
- Detoxification of aflatoxins by seed extracts of the medicinal plant, Trachyspermum ammi (L.) Sprague ex Turrill - Structural analysis and biological toxicity of degradation product of aflatoxin G1 (Food Control, 2010)
- Comparison of aflatoxin B1 and aflatoxin G1 binding to cellular macromolecules in vitro, in vivo and after peracid oxidation; characterisation of the major nucleic acid adducts (Chemico-Biological Interactions, 1979)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - aflatoxin G1
-
SMILESCOC1=C2C3=C(C(=O)OCC3)C(=O)OC2=C4C5C=COC5OC4=C1
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InChIKeyXWIYFDMXXLINPU-UHFFFAOYSA-N
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