| Identification | Back Directory | [Name]
averantin | [CAS]
5803-62-3 | [Synonyms]
averantin
Averantin
DISCONTINUED
1,3,6,8-Tetrahydroxy-2-(1-hydroxyhexyl)-anthraquinone
ANTHRAQUINONE,2-(1-HYDROXYHEXYL)-1,3,6,8-TETRAHYDROXY-
(-)-1,3,6,8-Tetrahydroxy-2-(1-hydroxyhexyl)-9,10-anthracenedione
1,3,6,8-Tetrahydroxy-2-[(1S)-1-hydroxyhexyl]-9,10-anthracenedione | [Molecular Formula]
C20H20O7 | [MDL Number]
MFCD32644887 | [MOL File]
5803-62-3.mol | [Molecular Weight]
372.37 |
| Chemical Properties | Back Directory | [Boiling point ]
694.5±34.0 °C(Predicted) | [density ]
1.490±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO: soluble; Methanol: soluble | [form ]
A crystalline solid | [pka]
6.04±0.20(Predicted) | [color ]
Orange |
| Hazard Information | Back Directory | [Description]
Averantin is an anthraquinone fungal metabolite that has been found in Aspergillus. It is an intermediate in the biosynthesis of aflatoxin B1 . Averantin is active against B. subtilis bacteria and the plant pathogenic fungus F. solani in vitro (MICs = 16-32 μg/ml). | [Uses]
Averantin is the minor metabolite of the fungus Cercospora arachidicola[1]. Averantin is an aflatoxin B1 precursor that can be used in the biosynthetic pathway[2]. | [Definition]
ChEBI: A tetrahydroxyanthraquinone that is 1,3,6,8-tetrahydroxy-9,10-anthraquinone bearing a 1-hydroxyhexyl substituent at position 2. | [storage]
+4°C | [References]
[1] ALBERT STOESS, et al. Minor anthraquinonoid metabolites of Cercospora arachidicola. S. Can. J. Chem. 63, 1258 (1985).
[2] J W Bennett, et al. Identification of averantin as an aflatoxin B1 precursor: placement in the biosynthetic pathway. Appl Environ Microbiol. 1980 Apr;39(4):835-9. DOI:10.1128/aem.39.4.835-839.1980 |
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