Aspergillic acid

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Aspergillic acid
Aspergillsäure.svg
Names
IUPAC name
6-Butan-2-yl-1-hydroxy-3-(2-methylpropyl)pyrazin-2-one
Systematic IUPAC name
1-Hydroxy-6-(2-butanyl)-3-isobutyl-2(1H)-pyrazinone
Other names
  • 6-sec-Butyl-1-hydroxy-3-isobutyl-2(1H)-pyrazinone
  • 6-sec-Butyl-3-isobutylpyrazinol 1-oxide
  • 2-Hydroxy-3-isobutyl-6-(1-methylpropyl)pyrazine 1-oxide
  • 3-Isobutyl-6-sec-butyl-2-hydroxypyrazine 1-oxide
Identifiers
  • 28696-18-6 checkY
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/C12H20N2O2/c1-5-9(4)11-7-13-10(6-8(2)3)12(15)14(11)16/h7-9,16H,5-6H2,1-4H3
    Key: IUZCDJYHMMWBBE-UHFFFAOYSA-N
  • CCC(C)C1=CN=C(C(=O)N1O)CC(C)C
Properties
C12H20N2O2
Molar mass 224.304 g·mol−1
Appearance Pale yellow needles
Density 1.163 g/cm3
Melting point 98 °C (208 °F; 371 K)
log P 1.7
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Aspergillic acid is an organic chemical compound with the molecular formula C12H20N2O2. It has a pale yellow crystalline appearance. Aspergillic acid is most commonly known as an antibiotic and antifungal agent that is derived from certain strains of the fungus Aspergillus flavus.[1][2]

History[]

In 1940 and discovered that a fungal strain of Aspergillus flavus growing in a surface culture on a tryptone-salt was capable of producing a bactericidal filtrate. It has also been shown to be a bactericidal for some Gram-negative as well as Gram-positive bacteria. Over the next few years they worked off this discovery and succeeded to isolate the active material in the crystalline form. In 1943 they managed to isolate this antibiotic compound and called it aspergillic acid primarily because of its origin and acidic properties. Scientists have since been working with the Asperigillus flavus strain to produce various types of antibacterial substances.[3][4]

Structure[]

The structure of aspergillic acid was made by Dutcher and Spring and his co-workers. They suggested that it is a cyclic hydroxamic acid related to pyridine. It can be reduced to a neutral deoxyaspergillic acid, which is a racemization product found by Newbold, et al. to be identical with 3-isobutyl-6-sec-butyl-2-hydroxypyrazine. Because of this, aspergillic acid has been assigned the corresponding l-oxide or tautomeric pyridine hydroxamic acid structure show below.[4]

Aspergillic acid analog

Toxicity[]

The toxicity of aspergillic acid is controlled by the hydroxamic acid functionality, and there is little effect on toxicity observed between the differences in the 3 and 6 position side chain substituents. Chelation of physiologically important ions, such as calcium by aspergillic acid appears to be the likely mechanism of its toxic action.[5]

Synthesis[]

Different Aspergillus strains are capable of making various derivatives. Aspergillus flavus is used to produce an antibiotic substance called . Flavacol is then added to cultures of and is N-hydroxylated into . It is then hydroxylated in the side-chain in order to make [6]

Other studies show that aspergillic acid can also be derived from one molecule of L-leucine and one molecule of L-isoleucine in Aspergillus flavus.[6]

Reactions[]

When aspergillic acid reactions with iron trichloride (FeCl3), there is the formation of green cupric salt. This suggests that aspergillic acid is a hydroxamic acid derivative, which is also confirmed by the formation of deoxyaspergillic acid by dry distillation with copper chromite catalyst.

Bromination of aspergillic acid followed by reduction with zinc and acetic acid gives a diketopiperazine. Hydrolysis with HBr yields a mixture of DL-leucine and DL-isoleucine. These reaction schemes can be seen below:[7]

Aspergillic acid reactions 2[7]

References[]

  1. ^ James C. MacDonald (1961). "Biosynthesis of Aspergillic Acid" (PDF). Journal of Biological Chemistry. 236 (2).
  2. ^ Lewis, Robert A. (1998). Lewisʼ Dictionary of Toxicology. ISBN 9781566702232.
  3. ^ James D. Dutcher. "Aspergillic Acid: An Antibiotic Substance Produced by Aspergillus Flavus I. General Properties; Formation of Desoxyaspergillic acid; Structural Conclusions" (PDF). Journal of Biological Chemistry.
  4. ^ a b Masaki Mitsuo (1966). "Total Syntheses of Racemic Aspergillic Acid and Neoaspergillic Acid". The Journal of Organic Chemistry. 31 (12): 4143–4146. doi:10.1021/jo01350a062.
  5. ^ Deshpande, S. S. (28 August 2002). Handbook of Food Toxicology. ISBN 9780203908969.
  6. ^ a b Bu'Lock, J. D. (1977). Biosynthesis: A Review of the Literature Published During 1970 and 1971. ISBN 9780851865430.
  7. ^ a b Brossi, Arnold (1986-12-01). The Alkaloids. ISBN 9780124695290.
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