6795-16-0 Usage
Description
DHST, also known as sterigmatocystin, is a secondary metabolite of Aspergillus flavus and other fungi. It is a mycotoxin with a unique chemical structure, featuring a xanthone ring system ortho-fused to a dihydrofuranofuran moiety. DHST has been a subject of interest due to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
DHST is used as a starting material for the synthesis of various pharmaceutical compounds, including antibiotics and anticancer drugs. Its unique chemical structure allows for the development of novel therapeutic agents with potential applications in treating various diseases.
Used in Chemical Research:
DHST serves as a valuable compound for chemical research, particularly in the study of fungal metabolites and their biosynthetic pathways. Understanding the properties and mechanisms of DHST can contribute to the development of new chemical processes and the discovery of new bioactive compounds.
Used in Mycotoxin Detection and Prevention:
Due to its toxic nature, DHST is used as a target for the development of detection methods and preventive measures against mycotoxin contamination in the food and feed industry. Identifying and controlling the presence of DHST can help ensure the safety and quality of agricultural products.
Used in Environmental Monitoring:
DHST can be utilized as a biomarker for monitoring the presence of specific fungi in the environment. This can be particularly useful in assessing the risk of mycotoxin contamination in various settings, such as agriculture, food processing, and indoor air quality.
Check Digit Verification of cas no
The CAS Registry Mumber 6795-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6795-16:
(6*6)+(5*7)+(4*9)+(3*5)+(2*1)+(1*6)=130
130 % 10 = 0
So 6795-16-0 is a valid CAS Registry Number.
6795-16-0Relevant articles and documents
Ordering the reductive and cytochrome P450 oxidative steps in demethylsterigmatocystin formation yields general insights into the biosynthesis of aflatoxin and related fungal metabolites
Henry, Kevin M.,Townsend, Craig A.
, p. 3724 - 3733 (2007/10/03)
The biosynthesis of the potent environmental carcinogen aflatoxin B1 involves ca. 15 steps beyond the first polyketide intermediate. Central among these is the rearrangement of the anthraqinone versicolorin A to the xanthone demethylsterigmatocystin. Gene
