39546-16-2 Usage
Description
Flavoskyrin is an anthraquinoid mycotoxin that exhibits extreme toxicity towards various organisms, including cultured Helas, the protozoan Tetrahymena pyriformis, and Escherichia coli mutants. Its potent toxic properties make it a compound of interest for further research and potential applications in specific industries.
Uses
Used in Pharmaceutical Industry:
Flavoskyrin is used as a research compound for its potent toxic effects on various organisms. Its application in the pharmaceutical industry is primarily for the development of new drugs or therapies that can target specific pathogens or cancer cells by leveraging the toxin's properties.
Used in Agricultural Industry:
In the agricultural industry, Flavoskyrin could potentially be utilized as a biopesticide due to its toxicity towards certain organisms. However, its use would require thorough research and development to ensure safety and efficacy, as well as to minimize any potential harm to non-target species and the environment.
Used in Research and Development:
Flavoskyrin's extreme toxicity makes it a valuable tool in research and development, particularly in the fields of microbiology, cell biology, and toxicology. It can be used to study the mechanisms of action of various toxins and their effects on different cell types, leading to a better understanding of cellular processes and potential therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 39546-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,4 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39546-16:
(7*3)+(6*9)+(5*5)+(4*4)+(3*6)+(2*1)+(1*6)=142
142 % 10 = 2
So 39546-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H24O10/c1-9-3-11-19(13(31)5-9)26(37)22-16(34)7-15(33)21-23(22)28(11)40-30-24(21)17(35)8-18(36)25(30)27(38)20-12(29(30)39)4-10(2)6-14(20)32/h3-6,15,17,21,24,31-33,35,37-38H,7-8H2,1-2H3
39546-16-2Relevant articles and documents
Synthesis of (-)-Flavoskyrins by Catalyst-Free Oxidation of (R)-Configured Dihydroanthracenones in Aqueous Media and Its (Bio)synthetic Implications
Mondal, Amit,De, Arijit,Husain, Syed Masood
, p. 8511 - 8515 (2020/11/12)
A catalyst-free method for the synthesis of dimeric (-)-flavoskyrins has been developed. It involves the autoxidation of chemoenzymatically synthesized (R)-configured dihydroanthracenones in the presence of molecular oxygen in buffer of pH 6.0 followed by spontaneous [4 + 2] cycloaddition in stereocontrolled exo-anti fashion to form (-)-flavoskyrins. The method is applied to obtain several homo- A s well as heterodimerized flavoskyrins (nine examples) in 27-72% yield and implies the involvement of a similar pathway in the (bio)synthesis of modified bisanthraquinones and their analogues.
