Tenuazonic acid

Tenuazonic acid
Names
	IUPAC name (5S)-3-Acetyl-5-[(2S)-butan-2-yl]-4-hydroxy-2,5-dihydro-1H-pyrrol-2-one
Identifiers
CAS Number	610-88-8 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:9440;
ChEMBL	ChEMBL511015 ;
ChemSpider	19953674 ;
ECHA InfoCard	100.164.201
PubChem CID	101949;
UNII	Y2J8Y1TO29 ;
CompTox Dashboard (EPA)	DTXSID701017805 ;
	InChI InChI=1S/C10H15NO3/c1-4-5(2)8-9(13)7(6(3)12)10(14)11-8/h5,8,13H,4H2,1-3H3,(H,11,14)/t5-,8-/m0/s1 Key: CEIZFXOZIQNICU-XNCJUZBTSA-N ;
	SMILES O=C1C(C(C)=O)=C(O)[C@@]([C@H](CC)C)([H])N1;
Properties
Chemical formula	C10H15NO3
Molar mass	197.234 g·mol−1
Appearance	White crystalline powder
Acidity (pKa)	3.5
Hazards
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	* 182 mg kg−1 (Mice, ♂, oral) 225 mg kg−1 (Mice, ♂, oral); 81 mg kg−1 (Mice, ♀, oral);
Pharmacology
Routes of; administration	Ingested or Inhaled
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Tenuazonic acid is a mycotoxin produced by Alternaria species.^[4] It is a powerful eukaryotic protein synthesis inhibitor.^[5]

In 1991 Tenuazonic acid was reported to inhibit skin tumor promotion in mice.^[6]

References

^ "Tenuazonic Acid". Cayman Chemical.
^ ^a ^b Miller, F. A. et al.; Nature, 200 (1963), S. 1338–1339
^ Smith, E. R. et al.; Cancer Chemother. Rep. 52 (1968), S. 579–585.
^ Alisa D. Hocking (Editor), John I. Pitt (Editor) and Robert A. Samson (Editor): Advances in Food Mycology. Springer 2006; ISBN 978-0-387-28385-2; p. 23
^ Dilip K. Arora and Arora K. Arora: Fungal Biotechnology in Agricultural, Food, and Environmental Applications. Marcel Dekker Inc; illustrated edition 2003; ISBN 978-0-8247-4770-1; p. 336
^ Tenuazonic acid page from Fermentek

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