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averantin

Product Name
averantin
CAS No.
5803-62-3
Chemical Name
averantin
Synonyms
averantin;Averantin DISCONTINUED;Averantin, Aflatoxin B1 percursor;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
CBNumber
CB61373602
Molecular Formula
C20H20O7
Formula Weight
372.37
MOL File
5803-62-3.mol
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averantin Property

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
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
28059
Product name
Averantin
Packaging
5mg
Price
$399
Updated
2024/03/01
Usbiological
Product number
207080
Product name
Averantin
Packaging
1mg
Price
$316
Updated
2021/12/16
Adipogen Life Sciences
Product number
BVT-0169-M005
Product name
Averantin
Purity
≥98%(HPLC;NMR)
Packaging
5mg
Price
$320
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
MTB0000627
Product name
AVERANTIN
Purity
95.00%
Packaging
5MG
Price
$500.26
Updated
2021/12/16
Crysdot
Product number
CD32000921
Product name
Averantin
Purity
95+%
Packaging
5mg
Price
$802
Updated
2021/12/16
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averantin Chemical Properties,Usage,Production

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

averantin Preparation Products And Raw materials

Raw materials

Preparation Products

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5803-62-3, averantinRelated Search:

4,4'-Dihydroxybenzophenone 1,3-DIHYDROXY-2-METHYLANTHRAQUINONE 2,4,4'-TRIHYDROXYBENZOPHENONE averufin LUCIDIN 1,3,8-TRIHYDROXY-2-(1-HYDROXYHEXYL)-6-METHOXY-9,10-ANTHRACENEDIONE averantin 2,2',4,4'-Tetrahydroxybenzophenone

  • averantin
  • 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-(1-hydroxyhexyl)-anthraquinone
  • 1,3,6,8-Tetrahydroxy-2-[(1S)-1-hydroxyhexyl]-9,10-anthracenedione
  • Averantin DISCONTINUED
  • Averantin, Aflatoxin B1 percursor
  • 5803-62-3