475-54-7 Usage
Uses
Used in Pharmaceutical Applications:
Oosporein is used as a pharmaceutical agent for its diverse biological activities. These activities include potential applications in the development of new drugs targeting various diseases and conditions.
Used in Anticancer Applications:
Oosporein is used as an anticancer agent due to its ability to exhibit cytotoxic effects on cancer cells. It may be employed in the development of novel cancer treatments, targeting specific cancer cell types and potentially enhancing the efficacy of existing therapies.
Used in Drug Delivery Systems:
Oosporein can be used in the development of drug delivery systems to improve the bioavailability and targeting of therapeutic agents. Its unique properties may allow for the creation of innovative drug carriers, enhancing the delivery and effectiveness of various medications.
Used in Agricultural Applications:
Oosporein is used as a biopesticide in the agricultural industry. Its mycotoxin properties make it a potential candidate for the development of environmentally friendly and targeted pest control solutions.
Used in Research Applications:
Oosporein is used as a research tool in the field of biology and pharmacology. Its diverse biological activities and potential applications make it a valuable compound for studying various cellular processes and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 475-54-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 475-54:
(5*4)+(4*7)+(3*5)+(2*5)+(1*4)=77
77 % 10 = 7
So 475-54-7 is a valid CAS Registry Number.
475-54-7Relevant academic research and scientific papers
An efficient synthesis of oosporein
Love, Brian E.,Bonner-Stewart, Jeffrey,Forrest, Lori A.
body text, p. 5050 - 5052 (2009/12/05)
Fungal metabolite oosporein was prepared in four steps and 24% overall yield starting from 2,5-dimethoxytoluene. It was demonstrated that treatment of phoenicin with pyrrolidine and copper(II) acetate led to oosporein, whereas similar treatment of the isomeric 'isophoenicin' produced a benzofuran diquinone. No chromatography was required during any step of the synthesis.
