51550-28-8 Usage
Description
(3beta,7alpha)-8-oxo-12,13-epoxytrichothec-9-ene-3,7,15-triyl triacetate is a complex chemical compound characterized by a trichothecene backbone and three acetate groups attached at different positions. Trichothecenes are a class of mycotoxins produced by various fungi species, known for their toxicity to humans and animals. The unique structure of this compound suggests potential biological activity, likely due to its capacity to engage with cellular processes and enzymes. However, its highly intricate and potentially hazardous nature necessitates further research to fully comprehend its properties and possible applications.
Uses
Due to the provided materials not specifying any particular applications for (3beta,7alpha)-8-oxo-12,13-epoxytrichothec-9-ene-3,7,15-triyl triacetate, it is not possible to list its uses as was done for Glycerol in the example. However, given its potential biological activity and the fact that it belongs to the trichothecene family, it could potentially be studied for applications in areas such as:
Used in Pharmaceutical Research:
(3beta,7alpha)-8-oxo-12,13-epoxytrichothec-9-ene-3,7,15-triyl triacetate could be used as a research compound for investigating its interaction with cellular processes and enzymes, which may lead to the development of new pharmaceutical agents or a better understanding of its toxicological profile.
Used in Toxicological Studies:
Understanding the toxicity and mechanism of action of this compound could be crucial for toxicological studies, potentially informing the development of antidotes or preventive measures against exposure to similar mycotoxins.
Check Digit Verification of cas no
The CAS Registry Mumber 51550-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,5 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51550-28:
(7*5)+(6*1)+(5*5)+(4*5)+(3*0)+(2*2)+(1*8)=98
98 % 10 = 8
So 51550-28-8 is a valid CAS Registry Number.
51550-28-8Relevant articles and documents
Trichothecene mycotoxin interconversions: Partial syntheses of calonectrin and deoxynivalenol, and of a trichothecene epi-epoxide, 3α,4β,15-triacetoxy-12,13-epi-epoxytrichothec-9-ene
Cameron,Colvin
, p. 887 - 895 (2007/10/02)
The partial syntheses of two trichothecenes, calonectrin (4β,15-diacetoxy-12,13-epoxytrichothec-9-ene) and deoxynivalenol (3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-ene), from a readily available trichothecene, anguidine (4β,15-diacetoxy-3α-hydroxy-12,13-epoxytrichothec-9-ene) are described. In addition, and in order to provide further insight into the mode of action of the trichothecene mycotoxins, 3α,4β,15-tricetoxy-12,13-epi-epoxytrichothec-9-ene, of the first semisynthetic trichothecene epi-epoxides, has been prepared and its X-ray crystal structure determined. In significant contrast to its natural isomer, epi-epoxide proved to be biologically inactive.
Chemical Deoxygenation of the Trichothecenes, Diacetoxyscirpenol and Deoxynivalenol
Colvin, Ernest W.,Cameron, Stuart
, p. 1084 - 1085 (2007/10/02)
Based on a model study using the bicyclic epoxides (9) and (10), an efficient one-step procedure for the selective removal of the 12,13-epoxide ring of the trichothecene toxins has been devised.
Chemical deoxygenation of the epoxide moiety in deoxynivalenol (vomitoxin)
King, Russell R.,Greenhalgh, Roy
, p. 1089 - 1092 (2007/10/02)
Reaction of triacetoxydeoxynivalenol (3) with hydrobromic acid - acetic acid at reflux temperatures yielded 3α,7α,13,15-tetraacetoxy-2-bromo apotrichothec-9-en-8-one (5) and 3α,7α,15-triacetoxy-13-bromo-12-hydroxytrichothec-9-en-8-one (4).Dehalohydrination of the 13,12-bromohydrin derivative with Zn - acetic acid followed by deacetylation with sodium ethoxide gave 3α,7α,15-trihydroxytrichothec-9,12-dien-8-one (2).This compound proved identical to the transformation product isolated from incubation of deoxynivalenol (vomitoxin) in vitro with rumen microorganisms.
