105088-14-0 Usage
Description
Zearalenone-4-glucopyranoside is a masked mycotoxin derived from Fusarium species, which is a type of fungus commonly found in various plant sources. It is characterized by the presence of a glucose molecule attached to the zearalenone molecule through a β-D-glucopyranosidic linkage. This modification alters the chemical properties and biological activity of the parent compound, zearalenone, making it a unique and interesting molecule for study and potential applications.
Uses
Used in Agricultural and Food Safety Applications:
Zearalenone-4-glucopyranoside is used as a biomarker for the presence of Fusarium mycotoxins in agricultural products and foodstuffs. Its detection can help in monitoring and controlling the contamination of crops and food by harmful mycotoxins, ensuring the safety and quality of the final products.
Used in Pharmaceutical and Biochemical Research:
Zearalenone-4-glucopyranoside serves as a valuable research tool for studying the structure-activity relationships of mycotoxins and their biological effects. It can be used to investigate the mechanisms of action, toxicity, and potential therapeutic applications of zearalenone and its derivatives.
Used in Environmental and Ecological Studies:
Zearalenone-4-glucopyranoside can be employed as an indicator of the presence and activity of Fusarium species in various ecosystems. This information can be useful for understanding the ecological roles of these fungi, their impact on plant health, and their potential as biocontrol agents against other harmful organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 105088-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,8 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105088-14:
(8*1)+(7*0)+(6*5)+(5*0)+(4*8)+(3*8)+(2*1)+(1*4)=100
100 % 10 = 0
So 105088-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H32O10/c1-13-6-5-9-15(26)8-4-2-3-7-14-10-16(11-17(27)19(14)23(31)32-13)33-24-22(30)21(29)20(28)18(12-25)34-24/h3,7,10-11,13,18,20-22,24-25,27-30H,2,4-6,8-9,12H2,1H3/b7-3+
105088-14-0Relevant articles and documents
Glycosylation of mycotoxins
Grabley,Gareis,Bockers,Thiem
, p. 1078 - 1080 (1992)
Glycoconjugates of some mycotoxins were prepared by the phase-transfer catalyzed glycosylation procedure. With zearalenone a regio- and stereospecific glucosylation gave the natural derivative which proved to be a 'masked mycotoxin'. In the case of ochrat
